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J Clin Invest. 2013 July 1; 123(7): 3124–3134.
Published online 2013 June 3. doi:  10.1172/JCI67260
PMCID: PMC3696544

Dominant protein interactions that influence the pathogenesis of conformational diseases

Abstract

Misfolding of exportable proteins can trigger endocrinopathies. For example, misfolding of insulin can result in autosomal dominant mutant INS gene–induced diabetes of youth, and misfolding of thyroglobulin can result in autosomal recessive congenital hypothyroidism with deficient thyroglobulin. Both proinsulin and thyroglobulin normally form homodimers; the mutant versions of both proteins misfold in the ER, triggering ER stress, and, in both cases, heterozygosity creates potential for cross-dimerization between mutant and WT gene products. Here, we investigated these two ER-retained mutant secretory proteins and the selectivity of their interactions with their respective WT counterparts. In both cases and in animal models of these diseases, we found that conditions favoring an increased stoichiometry of mutant gene product dominantly inhibited export of the WT partner, while increased relative level of the WT gene product helped to rescue secretion of the mutant partner. Surprisingly, the bidirectional consequences of secretory blockade and rescue occur simultaneously in the same cells. Thus, in the context of heterozygosity, expression level and stability of WT subunits may be a critical factor influencing the effect of protein misfolding on clinical phenotype. These results offer new insight into dominant as well as recessive inheritance of conformational diseases and offer opportunities for the development of new therapies.

Introduction

Several human “conformational diseases” of the secretory pathway are caused by mutations in exportable proteins blocking their export from the ER (1). Loss of function in post-ER compartments is often observed as autosomal recessive disease. By contrast, other disorders caused by gain-of-toxic-function mutations can ultimately lead to cell death that may trigger autosomal dominant disease (2).

Given that both autosomal dominant and recessive mutations can be found in exportable proteins that form homodimers and the much higher frequency of heterozygosity than homozygosity in the global population, it is critical to understand how cross-dimerization between WT and mutant gene products might influence clinical phenotypes. To study this, we have examined mutant forms of proinsulin (linked to autosomal dominant disease) and thyroglobulin (Tg) (linked to autosomal recessive disease).

Proinsulin, the major protein synthesized by pancreatic β cells, is cotranslationally translocated into the ER. In the ER, proinsulin is thought to form noncovalent homodimers that proceed in the distal secretory pathway to form homohexamers that undergo endoproteolytic processing to mature insulin and C-peptide (3). Recently, 26 distinct coding sequence mutations in proinsulin have been found responsible for a gain of toxic function underlying the autosomal dominant syndrome of mutant INS gene–induced diabetes of youth (MIDY), in which secretion of coexpressed WT proinsulin is inhibited, resulting in insulin-deficient diabetes (4). When expressed recombinantly, MIDY proinsulin mutants, including proinsulin-G(B23)V, are not appreciably secreted from heterologous cells (5). Curiously, however, some MIDY mutants expressed in Min6 pancreatic β cells, including proinsulin-G(B23)V, undergo successful anterograde transport in the secretory pathway, even to the extent of becoming endoproteolytically processed in secretory granules (6). The difference in the secretory fate of proinsulin-G(B23)V in cells lacking a WT proinsulin allele compared with that of β cells that express endogenous proinsulin raises the question of whether WT proinsulin could impact transport of the mutant proinsulin-G(B23)V.

Such a question is also interesting when considering Tg, the major protein product of the thyroid gland that serves as precursor for thyroid hormone synthesis. The large Tg primary structure comprises 3 disulfide-rich upstream regions (“I-II-III”) followed by the cholinesterase-like (ChEL) domain (7). Similar to proinsulin, Tg forms noncovalent homodimers in the ER (8). The ChEL domain functions as an intramolecular chaperone to promote oxidative folding of I-II-III but also functions in Tg homodimerization (9, 10). In the disorder known as congenital hypothyroidism with deficient Tg, ChEL is a commonly affected mutation site both in humans (11) and rodent models (1214). Homozygous rdw/rdw dwarf rats express a single ChEL point mutation [equivalent to G(2298)R of mature mouse Tg] and develop thyroid atrophy (15) from thyrocyte cell death (16). When coexpressed, mutant rdw-Tg can cross-dimerize with WT Tg (17).

Understanding the cell biological behaviors of misfolded versions of exportable proteins in the presence of their properly folded partners is of great importance for understanding potential therapeutic approaches to conformational diseases. In this study, we have investigated the selectivity of interactions between 2 ER-retained mutant secretory proteins and their WT counterparts.

Results

Transdominant retention of a well-folded WT secretory protein partner.

To test whether simple ER retention of one homodimerization partner can confer retention to a WT bystander, we expressed various epitope-tagged proinsulin constructs: human proinsulin (hPro) bearing or not bearing a Myc- or SuperfolderGFP-tag within the C-peptide sequence (hPro-CpepMyc and hPro-CpepSfGFP, respectively) or mouse proinsulin (mPro). Epitope tagging the C-peptide does not significantly affect the folding or ER export of WT proinsulin (18). We also expressed proinsulin(s) bearing a C-terminal KDEL sequence reported to confer proinsulin retention within the ER (19). All of these recombinant proinsulins were comparably expressed, and the expression level for each protein could be experimentally controlled (although the mutant hProG[B23]V-CpepMyc is less stable; see below), as it was proportional to the amount of plasmid DNA included in our transfections (Supplemental Figure 1A; supplemental material available online with this article; doi: 10.1172/JCI67260DS1). hPro-CpepSfGFP-KDEL was retained intracellularly in INS1 β cells (Supplemental Figure 1B), primarily in the same compartment as that marked by a ER-RFP, a red fluorescent protein bearing the KDEL retention signal (6).

Interestingly, when cotransfected with hPro-CpepSfGFP-KDEL plasmid, the intracellular content of WT hPro-CpepMyc increased, and its secretion decreased (Figure (Figure1A).1A). Intracellular WT hPro-CpepMyc coimmunoprecipitated with hPro-CpepSfGFP-KDEL, perhaps to an even greater extent than its coprecipitation with WT hPro-CpepSfGFP (Figure (Figure1B,1B, bottom row). Nevertheless, even as increasing doses of mPro-KDEL dramatically inhibited secretion of WT hPro (Figure (Figure1C,1C, top, measured by hPro radioimmunoassay [RIA]), secretion of WT TgGFP was largely unaffected in the same cells (Figure (Figure1C,1C, bottom). These results suggest that blockade of export of the well-folded WT secretory protein partner involves specific interactions with its ER-retained dimerization partner. Indeed, as shown in Figure Figure1D,1D, secretion of WT hPro-CpepMyc was largely restored upon overexpression of WT mPro “competitor,” even in the presence of mPro-KDEL.

Figure 1
Proinsulin-KDEL interacts with and inhibits secretion of WT proinsulin.

Misfolded mutant secretory protein also assembles with and impairs secretion of its WT partner.

We have previously suggested that, in the autosomal dominant disease called MIDY, misfolded mutant proinsulin can inhibit WT proinsulin export by recruitment of the WT gene product into aberrant protein complexes within the ER (5, 18). Indeed, when WT hPro-CpepMyc was coexpressed with misfolded mutant mProG(B23)V in place of WT mPro, the WT hPro-CpepMyc secretion was impaired in trans (Figure (Figure2A).2A). By contrast, the mutant rdw Tg functions as an autosomal recessive allele (15); nevertheless, surprisingly, we found that coexpression of rdw-Tg also could greatly decrease the secretion of WT Tg3xMyc (Figure (Figure2B),2B), with the extent of this dominant-negative inhibition dependent upon the relative abundance of mutant versus WT gene products (see below). Unlike secreted WT Tg3xMyc, WT Tg3xMyc retained intracellularly in the presence of coexpressed rdw-Tg was recovered in an endoglycosidase H–sensitive (EndoH-sensitive) state, indicating molecules that had not advanced to the Golgi complex (Figure (Figure2B).2B). The rdw-Tg has a point mutation in the ChEL domain that is involved in Tg homodimerization (10, 17). To test whether the rdw ChEL domain can indeed associate with the WT Tg ChEL domain, WT ChEL-HA was coexpressed with rdw-ChEL-Myc. Similar to the situation with the mutant proinsulin hProG(B23)V-CpepMyc (Figure (Figure2C,2C, bottom), we found that mutant rdw-ChEL could coprecipitate with its WT dimerization partner (Figure (Figure2D,2D, bottom).

Figure 2
Cross-dimerization of mutant/WT proinsulin and mutant/WT Tg.

WT mutant cross-dimerization offers secretory rescue to the mutant gene product.

In INS1 cells, WT hPro-CpepSfGFP efficiently reached secretory granules and was well secreted, whereas hProC(A7)Y-CpepSfGFP (which harbors the same mutation as that found in the Akita mouse) was retained in the ER (Figure (Figure3A)3A) rather than being secreted (Figure (Figure3A)3A) (20). Interestingly, however, recombinant hProG(B23)V-CpepSfGFP showed intermediate behavior, with partial ER retention and a partial secretory granule distribution, and an intermediate level of secretion — consistent with a previous report (6). This stands in contrast to findings that secretion of mutant hProG(B23)V is negligible in heterologous cells that do not express endogenous WT proinsulin (5). We therefore considered whether secretion of hProG(B23)V might be improved in cells expressing a WT proinsulin partner. To test this, we expressed WT hPro-CpepSfGFP in the mouse pituitary cell line AtT20 (which forms secretory granules containing ACTH but does not express proinsulin). In this cell line, WT hPro-CpepSfGFP colocalized with endogenous ACTH in secretory granules that accumulate at the distal tips of cellular processes (Figure (Figure3B).3B). When expressed by itself, hProG(B23)V-CpepSfGFP exhibited primarily an ER distribution and did not reach secretory granules (Figure (Figure3B).3B). However, when coexpressed with WT hPro-CpepMyc, the hProG(B23)V-CpepSfGFP was partially rescued, becoming visible in secretory granules (Figure (Figure3B).3B). These results indicate that expression of WT proinsulin enhances intracellular transport of mutant hProG(B23)V.

Figure 3
Intracellular distribution of mutant proinsulins in regulated secretory cells coexpressing or not coexpressing WT proinsulin.

To determine the selectivity of this rescue, 293T cells were cotransfected with fixed equimolar amounts of hProG(B23)V-CpepMyc and rdw-TgGFP and simultaneously cotransfected with either WT mPro or WT Tg (empty vector was included to keep constant the total DNA in each transfection). Secretory rescue of hProG(B23)V was provided selectively by WT mPro (Figure (Figure4A,4A, top; confirmed by immunoblotting in Figure Figure4B)4B) but not by WT Tg (Figure (Figure4A,4A, top), as measured by hPro-specific RIA. Conversely, rescue of rdw-TgGFP secretion was conferred upon coexpression of WT Tg (17) but not by WT mPro (lane M, Figure Figure4A,4A, bottom). This phenotype involved authentic intracellular transport through the secretory pathway (rather than cell death), as rescue was blocked in cells treated with brefeldin A (which blocks anterograde transport; Figure Figure4C).4C). Thus, not only can an ER-retained dimerization partner impair secretion of its WT counterpart (Figures (Figures11 and and2),2), but expression of a WT dimerization partner augments secretion of its misfolded counterpart (Figures (Figures33 and and44).

Figure 4
Cross-dimerization as a basis for secretory rescue of mutant proinsulin or Tg is specific to respective WT partners.

WT dimerization partners dose-dependently stabilize their misfolded counterparts for secretory rescue.

To examine the stability of hProG(B23)V-CpepMyc, we used metabolic pulse labeling of cells with 35S-amino acids and measured the fraction of newly synthesized protein remaining at 20 hours after synthesis. hProG(B23)V-CpepMyc stability was significantly increased by coexpression of WT mPro (Figure (Figure5A).5A). In parallel, WT Tg3xMyc increased both the intracellular as well as secreted amounts of rdw-TgGFP — indeed, these observations were dependent on the dose of WT Tg3xMyc (Figure (Figure5B).5B). Rescue of hProG(B23)V-CpepMyc also was observed with increasing concentrations of coexpressed WT mPro (Figure (Figure5C).5C). Notably, rescue appeared more dependent upon the ratio between WT and mutant proteins than the absolute amount of WT protein expressed, because increasing rescue was also observed with decreasing expression of misfolded mutant rdw-TgGFP rather than when the amount of WT Tg3xMyc was raised (Figure (Figure55D).

Figure 5
Secretory rescue and stabilization of mutant proinsulin or Tg by their WT counterparts is linked to the WT/mutant expression ratio.

Rescue of mutant and blockade of WT proinsulin and Tg occur within the (patho)physiological context.

To determine whether the effects of altering WT/mutant stoichiometric ratio in heterologous cells also are observed in pancreatic β cells, we expressed 2 different doses of hProG(B23)V-CpepSfGFP in INS1E cells that are known to secrete endogenous proinsulin and insulin under basal conditions and at greater levels in response to elevated glucose. Unsurprisingly, INS1E cells transfected with less plasmid expressed less mutant proinsulin (Figure (Figure5E).5E). Interestingly, INS1E cells expressing less mutant proinsulin (and thus a higher WT/mutant stoichiometric ratio) exhibited higher fractional secretion of the mutant protein under both basal and glucose-stimulated conditions, including both unprocessed hProG(B23)V-CpepSfGFP and its CpepGFP-processing product (Figure (Figure55E).

We next wished to extend these findings to tissues of animals with diseases of protein misfolding in the ER. First, we looked directly at the rescue of mutant rdw-Tg3xMyc in thyroid tissue from animals lacking or bearing WT Tg. For this, we prepared an rdw-Tg3xMyc transgene whose expression in the thyroid gland was driven by a Tg promoter. The rdw-Tg protein was expressed in thyroid tissue of otherwise WT C57BL/6 mice or mutant cog/cog mice (with homozygous expression of mutant Tg-L2263P) in a C57BL/6 background. Both strains of mice expressed the rdw-Tg protein in the thyroid gland (Supplemental Figure 2), and both strains can iodinate secreted proteins (21). However, in thyroid tissue from the cog/cog background (lacking WT Tg), no rdw-Tg could become iodinated, indicating an inability of rdw-Tg to reach the iodination site (Figure (Figure6A).6A). By contrast, in thyroid tissue of C57BL/6 control mice expressing WT Tg, some mutant rdw-Tg was rescued based on the ability to become iodinated — moreover, the iodinated rdw-Tg was endoH resistant, indicative of molecules that had undergone normal intracellular transport through Golgi/post-Golgi compartments (Figure (Figure66A).

Figure 6
Rescue of mutant Tg and blockade of WT proinsulin in primary tissue from animal models of disease.

We also wished to determine whether decreased WT/mutant stoichiometry can promote blockade of the WT gene product. For this, we examined mice expressing the Akita-like mutant hProC(A7)Y-CpepGFP transgene (22), with deletion of either one allele or homozygous knockout of endogenous Ins2 to progressively decrease WT proinsulin expression. We then used mPro-specific immunofluorescence to examine the intracellular distribution of the remaining endogenous (primarily Ins1) gene product. In WT, Ins2+/–, and Ins2–/– mice lacking the mutant transgene, most pancreatic β cells exhibit strong proinsulin immunostaining in the Golgi region, consistent with previous reports (20, 23). However, in the presence of the mutant hProC(A7)Y-CpepGFP (which itself is entrapped in the ER; ref. 22), more cells began to appear with endogenous mPro in an ER-like pattern (colocalizing with calnexin; Figure Figure6B,6B, top 2 rows). There is published evidence that endogenous proinsulin synthesis/content is heterogeneous in the population of islet β cells (24, 25). Nevertheless, in Ins2–/– mice, as the ratio of WT/mutant proinsulin decreased, the fraction of cells exhibiting endogenous WT proinsulin in an ER-staining pattern increased — and this effect was apparent in mice matched for random blood glucose levels ≤250 mg/dl (Figure (Figure6B).6B). These findings demonstrate that, in tissues from actual conformational disease models, both mutant secretory protein rescue (Figure (Figure6A)6A) and WT secretory protein blockade (Figure (Figure6B)6B) are influenced by the ratio of WT/mutant secretory protein in the ER.

Can secretory rescue and secretory blockade occur simultaneously?

To examine whether both rescue (of mutant) and blockade (of WT) dimerization partners can occur simultaneously, we first transfected 293T cells with WT mPro or hProG(B23)V or both. We then independently measured mPro and hPro secretion by species-specific immunoassay. Secretion of WT mPro was significantly diminished by the presence of hProG(B23)V (Figure (Figure7A).7A). Remarkably, from the same cells, hProG(B23)V secretion was improved by the coexpression of WT mPro (Figure (Figure7A).7A). Similarly, when transfecting with progressively increasing ratios of WT Tg3xMyc to mutant rdw-TgGFP, rdw-TgGFP secretion improved (Figure (Figure7B),7B), whereas WT Tg3xMyc was markedly diminished when the ratio favored rdw-TgGFP (Figure (Figure7B).7B). Intermediate ratios showed both rescue and blockade (Figure (Figure7B).7B). Both sets of data in Figure Figure77 indicate that these effects occur simultaneously in the same cells.

Figure 7
Bidirectional consequences of interactions between mutant and WT cross-dimerization partners.

Is secretory rescue of misfolded proinsulin unique to the G(B23)V substitution?

Multiple MIDY mutants cause dominant-negative blockade of WT proinsulin export (5). Structurally, MIDY can be subdivided into those mutants that cause the gain or loss of a Cys residue to create an unpaired cysteine, and other mutants affecting conserved hydrophobic residues that perturb disulfide pairing of the natural cysteine partners (4). To see which class of mutants could be rescued by coexpression of WT proinsulin, we compared secretion of a series of coexpressed MIDY mutants. Notably, secretion of most proinsulin mutants containing an unpaired cysteine, such as C(A6)Y, C(B19)H, or the C(A7)Y mutant responsible for diabetes in the Akita mouse, was not improved by coexpression of WT proinsulin (Figure (Figure8).8). By contrast, secretion of several other misfolded MIDY proinsulins [e.g., A(SP24)D, H(B5)D, G(B8)S] was rescued in addition to G(B23)V. These data suggest that this mechanism does not work in all cases; nevertheless, cross-dimerization of proinsulin (Figure (Figure1B1B and Figure Figure2C)2C) or Tg (Figure (Figure2D)2D) exhibits plasticity, highlighting the potential for intracellular transport rescue of a variety of misfolded exportable proteins by their WT counterparts.

Figure 8
Secretory rescue by WT proinsulin is restricted to a subset of MIDY mutants.

Discussion

There are a large number of disorders linked to misfolding, ER entrapment (26), and degradation of exportable proteins (27), and several new approaches have been proposed for the development of therapies for these diseases. Some of these proposals include pharmacological modification of the rate of protein synthesis to avoid overloading protein folding capacity (28), others involve manipulation of the intraluminal ER ionic milieu (29, 30) or modulating ER-associated degradation (ERAD) (31), and still others involve pharmacologic chaperones (32) or modulators of endogenous ER chaperone activity (33, 34), including preemptive induction of unfolded protein response (35). Each of these therapies is designed to manipulate the ER quality control environment, altering the ratio of protein folding to protein folding capacity.

In addition to these critical features, we also note that there has been unrecognized selection pressure for exportable proteins to evolve as oligomeric species (36). Indeed, even upon initial description of the ER hsp70 chaperone, BiP, its ability to confer ER retention was found to be linked to its selective association with unassembled subunits of exportable protein oligomers (37). Oligomerization limits chaperone rebinding and helps to relieve ER entrapment (38, 39), often by limiting exposure of unpaired Cys residues that can frequently be associated with ER retention (4042). Typically, monomer folding precedes oligomerization (43), but there are examples in which oligomer formation may be a very early folding step (44). Either way, for many exportable proteins, achieving an oligomeric state is a critical decision point in determining anterograde transport versus ERAD (45).

It has been shown that expression of misfolded mutant proteins has the potential to cause WT (bystander) dimerization partners to be retained in the ER (5, 18, 4649). Protein-specific rather than general enhancement — lowering the levels of the mutant partner (50) and raising WT levels — has been proposed as one of the more efficacious therapeutic approaches, by maintaining general protein homeostasis while allowing escape from ER entrapment of a specific disease-linked gene product (51, 52). In this study, we emphasize that one potential consequence of raising the WT/mutant protein ratio is that an increased fraction of mutant protein may cross-dimerize with WT, allowing for novel, protein-specific enhancement of protein export. Our findings are unequivocal, because we have selectively epitope tagged the respective WT and mutant partners and experimentally controlled the expression levels of the respective products (Figures (Figures11 and and557). In this report, we have studied proinsulin mutants causing MIDY and Tg mutants causing congenital hypothyroidism as 2 genetically unrelated representatives of a broad class of conformational diseases of exportable proteins. The organs affected by these diseases appear quite different in terms of their ability to expand tissue mass, and they might have different intrinsic susceptibility to ER stress (a goiter can grow large, whereas expansion of pancreatic β cell mass is more limited), yet studying these molecules in parallel has allowed us to address persistent questions about the extent to which phenotypes linked to cross-dimerization are protein specific and the extent to which the pathogenesis of these diseases is secondary to generalized ER stress.

In this study, we demonstrate that retention of proinsulin-KDEL, via a mechanism involving neither misfolding nor ER stress, is sufficient to induce export blockade of its WT dimerization partner (Figure (Figure1,1, A and C) in conjunction with direct physical association between the partners (Figure (Figure1B).1B). Also, further addition of WT proinsulin competes with the proinsulin-KDEL to allow escape from this blockade (Figure (Figure1D).1D). In the same cells, WT Tg secretion continues unimpeded in the face of proinsulin blockade, demonstrating specificity (Figure (Figure1C).1C). We have every reason to believe that the initial pathogenesis of MIDY is based on a similar underlying cell biological principle: in the case of mutant versions of exportable proteins, chaperone-mediated retention of the misfolded gene product is the rule (53). While formation of misfolded protein complexes was once thought to be nonspecific (54), we have found that expression of the proinsulin-G(B23)V mutant selectively coprecipitates its WT partner (Figure (Figure2C)2C) and blocks secretion of that partner (Figure (Figure2A)2A) while neither associating with nor blocking WT Tg in the same cells (Figure (Figure1C1C and data not shown). This dominant effect on WT proinsulin appears to account for the dominant inheritance of MIDY (Figure (Figure9),9), producing insulin deficiency from the WT allele (4). Moreover, expressing the Akita-like hProC(A7)Y-CpepGFP transgene in mice first with heterozygous and then with homozygous loss of endogenous Ins2 (i.e., changing the relative expression of the 2 protein partners) results in progressive blockade of remaining WT proinsulin, independent of changes in random blood glucose (Figure (Figure66B).

Figure 9
Model of bidirectional intermolecular interactions of misfolded and native proteins.

Despite an autosomal recessive pattern of inheritance, we found surprisingly similar molecular behavior for the genetically unrelated Tg protein. The rdw-Tg, which bears a mutation in the ChEL domain and causes thyrocyte cell death only when expressed in homozygotes (16), also exhibits cross-dimerization with WT Tg in heterozygotes (17). Herein, we show that the molecular mechanism involves direct interactions between the mutant and WT dimerization (ChEL) domains (Figure (Figure2D).2D). Remarkably, we found that expression of the recessive rdw-Tg can also dominantly block export of its WT Tg partner (Figure (Figure2B),2B), and this phenotype is linked to lowering the WT/mutant protein ratio (Figure (Figure7B).7B). The fact that heterozygosity does not generate hypothyroidism in vivo indicates that rdw/+ rats express a Tg protein ratio favoring the WT gene product. Further, when expression of the WT gene product is favored, rescue phenotypes become apparent. Such rescue was directly demonstrated in thyroid tissues of mice expressing a mutant rdw-Tg3xMyc transgene in a WT genetic background: unlike in cog/cog mice, rdw-Tg3xMyc acquired endoH resistance and even became iodinated in animals making endogenous WT Tg (Figure (Figure6A).6A). Moreover, rescue is also observed for proinsulin mutations that are ordinarily transmitted with autosomal dominant inheritance. In pancreatic β cells, partial rescue of proinsulin-G(B23)V to secretory granules was already in evidence (Figure (Figure3A),3A), conferring enhanced secretion under both basal and stimulated conditions (Figure (Figure5E5E and ref. 6), and such an effect can be directly attributed to coexpression of WT proinsulin (Figure (Figure3B).3B). Moreover, rescue of mutant proinsulin-G(B23)V or rdw-Tg is also protein specific: in cells coexpressing both mutants, secretory rescue of proinsulin-G(B23)V was accomplished exclusively by WT proinsulin, whereas secretory rescue of rdw-Tg was accomplished exclusively by WT Tg (Figure (Figure44).

All evidence points to the idea that secretory rescue is a consequence of intracellular stabilization of the mutant gene product: this was true for both proinsulin-G(B23)V (Figure (Figure5A)5A) and rdw-Tg (Figure (Figure5B).5B). And for both mutant proteins, the magnitude of the stabilization and secretory rescue is linked to the ratio of WT/mutant protein expression (Figure (Figure5,5, C and D). Most remarkable of all, rescue (of mutant) and blockade (of WT) secretion occurred simultaneously in the same cells (Figure (Figure7).7). Thus, for both proteins, there is a dynamic bidirectional balance between retention and anterograde transport of mutant cross-dimers (Figure (Figure99).

We posit that, for the many conformational diseases affecting exportable proteins that oligomerize in the ER, a dominant versus recessive pattern of inheritance is in part a reflection of the balance of these two activities (blockade versus rescue; see Figure Figure9).9). In the case of MIDY and other dominantly inherited diseases, the balance favors net retention of protein, whereas, in the case of congenital hypothyroidism with defective Tg, the balance favors net export. The minimum plasmid ratio at which we observed secretory rescue was consistent with this hypothesis: rescue of proinsulin-B23V required higher WT/mutant ratios than the rescue of rdw-Tg secretion (Figure (Figure55).

In conclusion, the data presented herein indicate that both secretory blockade and rescue involve direct cross-dimerization between WT and mutant gene products. As cross-dimerization in the secretory pathway is certainly not limited to proinsulin and Tg (55), we expect that similar cooperativity will be observed for other exportable proteins. While the effects described in this report appear limited to protein-specific protein rescue of mutant oligomerization partners, the results imply a broader significance for understanding disease pathophysiology. Specifically, our studies have potential relevance for the finding of ER accumulation of secretory proteins, even in the absence of any mutations. For example, WT proinsulin is prone to misfolding under conditions of increased insulin demand (56, 57), and its accumulation may contribute to β cell failure (58, 59). If oligomerization plays an important role in the retention of WT proinsulin and other WT secretory proteins, then protecting/stabilizing the interaction interface (such as with small molecule interactors) might allow ER escape of an increased fraction of exportable protein, despite the presence of a misfolded subset of such molecules. Such methods might be used in combination therapy with other approaches to alter the ER environment (described above), opening remarkable new avenues for treatment of diseases of misfolding of exportable proteins.

Methods

Materials.

Lipofectamine 2000, DMEM, RPMI 1640 medium, fetal bovine serum, Zysorbin, penicillin, and streptomycin were from Invitrogen. Glucose, 3-isobutyl-1-methylxanthine (IBMX), tolbutamide, and brefeldin A were from Sigma-Aldrich. EndoH was from New England Biolabs. Complete protease inhibitor cocktail was from Roche. Citrisolv was from Fisher Scientific. Rabbit anti-Myc and anti-GFP and chicken anti-Myc were from Immunology Consultants. Mouse mAb anti-HA was from Covance. Rabbit anti-ACTH antibody was a gift from M. Low (University of Michigan). hPro-specific RIA was from Millipore. mPro-specific ELISA and mPro-specific antibody was from Alpco. Trans35S label and Na125I were from Perkin Elmer.

Cell culture and transfection.

293, 293T, and AtT20 cells were cultured in DMEM with 10% fetal bovine serum and penicillin (100 U/ml) and streptomycin (100 μg/ml). INS1 and INS1E cells were cultured in RPMI 1640 medium supplemented with 10% fetal bovine serum, 1 mM pyruvate, 10 mM HEPES, penicillin (100 U/ml), streptomycin (100 μg/ml), and 50 mM 2-mercaptoethanol. Proinsulin and Tg variants were expressed in pCDNA3.1 or pTarget mammalian expression vectors. The hPro-CpepSfGFP-KDEL vector was a gift from E. Snapp (AECOM). Transfections using Lipofectamine 2000 were performed in 12-well plates. Total plasmid DNA was held constant within each experiment by addition of empty vector. Cells were harvested 24–48 hours after transfection and lysed in boiling SDS gel buffer (4% SDS, 20% glycerol, 120 mM Tris, pH 6.8), RIPA buffer (0.1 M NaCl, 0.2% deoxycholate, 25 mM Tris, pH 7.4, 1% Triton X-100, 0.1% SDS, 10 mM EDTA, pH 8.0, and proteinase inhibitor cocktail), NP40-CoIP buffer (1% NP40, 0.1 M NaCl, 2 mM EDTA, 25 mM Tris, pH 7.4), or TX-CoIP buffer (0.1% Triton X-100, 0.1 M NaCl, 5 mM EDTA, 25 mM Tris, pH 7), as indicated. For glucose-stimulated secretion measurements, cells were preincubated in 2.8 mM glucose for 30 minutes. Fresh basal media (2.8 mM glucose) was then collected for 90 minutes, followed by stimulation media (21 mM glucose, 1 mM tolbutamide, 1 mM IBMX) for 90 minutes, with cell lysis thereafter in SDS gel buffer.

Generation of mouse lines.

Mice expressing hProC(A7)Y-CpepGFP transgene driven by the Ins1 promoter, bearing heterozygous/homozygous disruption of endogenous Ins2, were as previously described (22). A full description of rdw-Tg3xMyc transgenic mice is forthcoming; briefly, a transgene consisting of the bovine Tgn promoter (60) immediately upstream of the full-length mouse Tgn ORF encoding rdw-Tg plus a triple-Myc epitope tag (i.e., rdw-Tg3xMyc) (10) was expressed in C57BL/6 mice. These rdw-Tg3xMyc transgenic mice in a Tgn+/+ genetic background were crossed and then backcrossed with Tgncog/cog mice to generate Tgn+/cog mice and then Tgncog/cog mice with or without the rdw-Tg3xMyc transgene. All animals were used in accordance with the University of Michigan’s University Committee on Use and Care of Animals.

Confocal imaging.

Formaldehyde-fixed cells were permeabilized with 0.4% TX100, blocked (TBS containing 3% BSA and 0.2% TX100), and then either directly mounted or stained overnight at 4°C with primary antibodies: chicken anti-Myc (1:5,000 dilution) and rabbit anti-ACTH (1:25,000). Thereafter, slides were rinsed and incubated with secondary antibody conjugates, mounted with ProLong Gold with DAPI (Invitrogen), and imaged by confocal epifluorescence with a ×60 oil objective. GFP intensity in granule (ACTH staining) and nongranule regions was quantified using MetaMorph (Molecular Devices). For cells transfected with hPro-CpepMyc, only cells positively staining with chicken anti-Myc antibodies were quantified.

For imaging of mouse islets, excised pancreata were fixed, paraffin embedded, microsectioned, and deparaffinized with Citrisolv. Sections underwent antigen retrieval (RetrieveALL-1), were blocked with 3% BSA, and were immunostained overnight at 4°C with mouse anti-mPro, guinea pig anti-insulin, and rabbit anti-calnexin antibodies. After rinsing and incubation with secondary antibody conjugates, slides were mounted with ProLong Gold with DAPI and by confocal epifluorescence as above. For quantification of WT mPro localization, investigators were blinded to mouse genotype. Four to five islets per mouse were analyzed, with each nucleated cell expressing proinsulin scored as either “majority ER” (colocalizing with calnexin) or “majority Golgi” (perinuclear crescent of increased signal intensity).

Metabolic labeling, immunoprecipitation, and EndoH digestion.

Twenty-four hours after transfection, cells were trypsinized and replated on poly-d-lysine–coated plates. After 6 hours, cells were pulse labeled with 35S-amino acids for 10 minutes and chased as indicated with cells lysed in RIPA buffer. For measurement of mutant proinsulin stability, lysate and media were combined, precleared with zysorbin, and immunoprecipitated with anti-insulin or anti-Myc. Immunoprecipitates (normalized to TCA-precipitable counts) were analyzed by reducing 4%–12% acrylamide gradient SDS-PAGE, phosphorimaging, and band quantitation (ImageQuant).

For 125I labeling of secreted rdw-Tg3xMyc, thyroid glands were labeled for 30 minutes at 37°C in 200 μl complete medium containing 0.1 μM NaI plus 1.0 μCi/μl Na125I. After labeling, samples were washed thrice with ice-cold PBS, sonicated in 200 μl RIPA buffer, diluted to 1 ml, and immunoprecipitated with rabbit anti-Myc antibody normalized to total DNA in the lysate.

EndoH digestion was performed according to manufacturer instructions; EndoH-sensitive and -resistant rdw-Tg3xMyc standards were from transfected 293T cells radiolabeled with 35S-amino acids. EndoH digests were analyzed by SDS 5%-PAGE and phosphorimaging. Controls establish that anti-Myc does not immunoprecipitate untagged endogenous Tg (data not shown).

Coimmunoprecipitation.

After lysis in ice-cold coimmunoprecipitation (CoIP) buffer, lysates were precleared and then immunoprecipitated with the indicated antibodies, washed, and analyzed by reducing SDS-PAGE and immunoblotting.

Proinsulin measurements and Western blotting.

At 24 hours after transfection, an overnight incubation in fresh media was initiated, and cells were lysed in RIPA buffer. Secreted and cellular proinsulin was measured by hPro-specific RIA or mPro-specific ELISA normalized to total protein in the lysate. For Western blotting, proteins (10 μg per lane) were resolved by 4%–12% acrylamide gradient SDS-PAGE, electrotransferred to nitrocellulose, and immunoblotted with the indicated antibodies. Horseradish peroxidase–conjugated secondary antibodies were from Jackson ImmunoResearch, with proteins visualized by ECL (Millipore). α-Tubulin was measured as a loading control. Western blot bands were quantified using ImageJ and ImageQuant software. The location of relevant molecular weight markers (kDa) is indicated in the figures.

Statistics.

Statistical analyses were conducted using GraphPad Prism software. Data are presented as mean ± SEM, unless otherwise noted (as in the legend for Figure Figure8).8). Two-tailed Student’s t test was used to assess statistical significance, with a threshold for significance of P < 0.05.

Study approval.

Handling and euthanizing of mice were performed entirely in accordance with national guidelines and with approval from the Committee on Use and Care of Animals at the University of Michigan.

Supplementary Material

Supplemental data:

Acknowledgments

This work was supported by NIH R01DK48280 and R01DK40344 with additional support from March of Dies grant no. 6-FY11-357 as well as support from training grants NIH F30DK095504, T32GM007863, T32GM008322, and T32HD007505. The authors thank Stephen Lentz at the Morphology and Image Analysis Core and the Transgenic Animal Model Core, both supported by the Michigan Diabetes Research Center (NIH P30DK020572) and Michigan Gastrointestinal Peptide Research Center (NIH P30DK034933). We thank Ann Soliman, Ali Reda, and Kathryn Hutchison for technical assistance.

Footnotes

Conflict of interest: The authors have declared that no conflict of interest exists.

Citation for this article:J Clin Invest. 2013;123(7):3124–3134. doi:10.1172/JCI67260.

References

1. Aridor M, Hannan LA. Traffic jam: a compendium of human diseases that affect intracellular transport processes. Traffic. 2000;1(11):836–851. doi: 10.1034/j.1600-0854.2000.011104.x. [PubMed] [Cross Ref]
2. Kim PS, Arvan P. Endocrinopathies in the family of endoplasmic reticulum (ER) storage diseases: disorders of protein trafficking and the role of ER molecular chaperones. Endocr Rev. 1998;19(2):173–202. doi: 10.1210/er.19.2.173. [PubMed] [Cross Ref]
3. Dodson G, Steiner D. The role of assembly in insulin’s biosynthesis. Curr Opin Struct Biol. 1998;8(2):189–194. doi: 10.1016/S0959-440X(98)80037-7. [PubMed] [Cross Ref]
4. Liu M, et al. Proinsulin misfolding and diabetes: mutant INS gene-induced diabetes of youth. Trends Endocrinol Metab. 2010;21(11):652–659. [PMC free article] [PubMed]
5. Liu M, et al. Mutant INS-gene induced diabetes of youth: proinsulin cysteine residues impose dominant-negative inhibition on wild-type proinsulin transport. PLoS One. 2010;5(10):e13333. doi: 10.1371/journal.pone.0013333. [PMC free article] [PubMed] [Cross Ref]
6. Rajan S, et al. In vitro processing and secretion of mutant insulin proteins that cause permanent neonatal diabetes. Am J Physiol Endocrinol Metab. 2010;298(3):E403–E410. doi: 10.1152/ajpendo.00592.2009. [PubMed] [Cross Ref]
7. Arvan P, Di Jeso B. The Thyroid. 2004. Thyroglobulin structure, function, and biosynthesis. In: Braverman LE, Utiger R, eds. pp. 77–95. Philadelphia, Pennsylvania, USA: Lippincott Williams and Wilkins;
8. Kim PS, Arvan P. Folding and assembly of newly synthesized thyroglobulin occurs in a pre-Golgi compartment. J Biol Chem. 1991;266(19):12412–12418. [PubMed]
9. Lee J, Di Jeso B, Arvan P. The cholinesterase-like domain of thyrogobulin functions as an intramolecular chaperone. J Clin Invest. 2008;118(8):2950–2958. doi: 10.1172/JCI35164. [PubMed] [Cross Ref]
10. Lee J, Wang X, Di Jeso B, Arvan P. The cholinesterase-like domain, essential in thyroglobulin trafficking for thyroid hormone synthesis, is required for protein dimerization. J Biol Chem. 2009;284(19):12752–12761. doi: 10.1074/jbc.M806898200. [PubMed] [Cross Ref]
11. Targovnik HM, Esperante SA, Rivolta CM. Genetics and phenomics of hypothyroidism and goiter due to thyroglobulin mutations. Mol Cell Endocrinol. 2010;322(1–2):44–55. doi: 10.1016/j.mce.2010.01.009. [PubMed] [Cross Ref]
12. Kim PS, Hossain SA, Park YN, Lee I, Yoo SE, Arvan P. A single amino acid change in the acetylcholinesterase-like domain of thyroglobulin causes congenital goiter with hypothyroidism in the cog/cog mouse: a model of human endoplasmic reticulum storage diseases. Proc Natl Acad Sci U S A. 1998;95(17):9909–9913. doi: 10.1073/pnas.95.17.9909. [PubMed] [Cross Ref]
13. Hishinuma A, Furudate S, Oh-Ishi M, Nagakubo N, Namatame T, Ieiri T. A novel missense mutation (G2320R) in thyroglobulin causes hypothyroidism in rdw rats. Endocrinology. 2000;141(11):4050–4055. doi: 10.1210/en.141.11.4050. [PubMed] [Cross Ref]
14. Kim PS, et al. A missense mutation G2320R in the thyroglobulin gene causes non-goitrous congenital primary hypothyroidism in the WIC-rdw rat. Mol Endocrinol. 2000;14(12):1944–1953. doi: 10.1210/me.14.12.1944. [PubMed] [Cross Ref]
15. Umezu M, Kagabu S, Jiang J, Sato E. Evaluation and characterization of congenital hypothyroidism in rdw dwarf rats. Lab Anim Sci. 1998;48(5):496–501. [PubMed]
16. Menon S, et al. Oxidoreductase interactions include a role for ERp72 engagement with mutant thyroglobulin from the rdw/rdw rat dwarf. J Biol Chem. 2007;282(9):6183–6191. doi: 10.1074/jbc.M608863200. [PMC free article] [PubMed] [Cross Ref]
17. Wang X, et al. Cis and trans actions of the cholinesterase-like domain within the thyroglobulin dimer. J Biol Chem. 2010;285(23):17564–17573. doi: 10.1074/jbc.M110.111641. [PubMed] [Cross Ref]
18. Hodish I, et al. Misfolded proinsulin affects bystander proinsulin in neonatal diabetes. J Biol Chem. 2010;285(1):685–694. doi: 10.1074/jbc.M109.038042. [PubMed] [Cross Ref]
19. Gupta S, McGrath B, Cavener DR. PERK (EIF2AK3) regulates proinsulin trafficking and quality control in the secretory pathway. Diabetes. 2010;59(8):1937–1947. doi: 10.2337/db09-1064. [PMC free article] [PubMed] [Cross Ref]
20. Haataja L, et al. Proinsulin intermolecular interactions during secretory trafficking in pancreatic β cells. J Biol Chem. 2013;288(3):1896–1906. doi: 10.1074/jbc.M112.420018. [PubMed] [Cross Ref]
21. Fogelfeld L, Harel G, Beamer WG, Schneider AB. Low-molecular-weight iodoproteins in the congenital goiters of cog/cog mice. Thyroid. 1992;2(4):329–335. doi: 10.1089/thy.1992.2.329. [PubMed] [Cross Ref]
22. Hodish I, et al. In vivo misfolding of proinsulin below the threshold of frank diabetes. Diabetes. 2011;60(8):2092–2101. doi: 10.2337/db10-1671. [PMC free article] [PubMed] [Cross Ref]
23. Orci L, Ravazzola M, Amherdt M, Madsen O, Vassalli JD. Direct identification of prohormone conversion site in insulin-secreting cells. Cell. 1985;42(2):671–681. doi: 10.1016/0092-8674(85)90124-2. [PubMed] [Cross Ref]
24. Schuit FC, In’t Veld PA, Pipeleers DG. Glucose stimulates proinsulin biosynthesis by a dose-dependent recruitment of pancreatic β cells. Proc Natl Acad Sci U S A. 1988;85(11):3865–3869. doi: 10.1073/pnas.85.11.3865. [PubMed] [Cross Ref]
25. Kiekens R, In ‘t Veld P, Mahler T, Schuit F, Van De Winkel M, Pipeleers D. Differences in glucose recognition by individual rat pancreatic B cells are associated with intercellular differences in glucose-induced biosynthetic activity. J Clin Invest. 1992;89(1):117–125. doi: 10.1172/JCI115551. [PMC free article] [PubMed] [Cross Ref]
26. Nehls S, et al. Dynamics and retention of misfolded proteins in native ER membranes. Nat Cell Biol. 2000;2(5):288–295. doi: 10.1038/35010558. [PubMed] [Cross Ref]
27. Guerriero CJ, Brodsky JL. The delicate balance between secreted protein folding and endoplasmic reticulum-associated degradation in human physiology. Physiol Rev. 2012;92(2):537–576. doi: 10.1152/physrev.00027.2011. [PMC free article] [PubMed] [Cross Ref]
28. Hulleman JD, Balch WE, Kelly JW. Translational attenuation differentially alters the fate of disease-associated fibulin proteins. FASEB J. 2012;26(11):4548–4560. doi: 10.1096/fj.11-202861. [PubMed] [Cross Ref]
29. Yu T, Chung C, Shen D, Xu H, Lieberman AP. Ryanodine receptor antagonists adapt NPC1 proteostasis to ameliorate lipid storage in Niemann-Pick type C disease fibroblasts. Hum Mol Genet. 2012;21(14):3205–3214. doi: 10.1093/hmg/dds145. [PMC free article] [PubMed] [Cross Ref]
30. Wang F, Chou A, Segatori L. Lacidipine remodels protein folding and Ca 2+ homeostasis in Gaucher’s disease fibroblasts: a mechanism to rescue mutant glucocerebrosidase. Chem Biol. 2011;18(6):766–776. doi: 10.1016/j.chembiol.2011.04.008. [PubMed] [Cross Ref]
31. Yu T, Chung C, Shen D, Xu H, Lieberman AP. Ryanodine receptor antagonists adapt NPC1 proteostasis to ameliorate lipid storage in Niemann-Pick type C disease fibroblasts. Hum Mol Genet. 2012;21(14):3205–3214. doi: 10.1093/hmg/dds145. [PMC free article] [PubMed] [Cross Ref]
32. Conn PM, Janovick JA. Drug development and the cellular quality control system. Trends Pharmacol Sci. 2009;30(5):228–233. doi: 10.1016/j.tips.2009.02.002. [PubMed] [Cross Ref]
33. Balch WE, Morimoto RI, Dillin A, Kelly JW. Adapting proteostasis for disease intervention. Science. 2008;319(5865):916–919. doi: 10.1126/science.1141448. [PubMed] [Cross Ref]
34. Lukacs GL, Verkman AS. CFTR: folding, misfolding and correcting the ΔF508 conformational defect. Trends Mol Med. 2012;18(2):81–91. doi: 10.1016/j.molmed.2011.10.003. [PMC free article] [PubMed] [Cross Ref]
35. Lu PD, et al. Cytoprotection by pre-emptive conditional phosphorylation of translation initiation factor 2. EMBO J. 2004;23(1):169–179. doi: 10.1038/sj.emboj.7600030. [PubMed] [Cross Ref]
36. Hurtley SM, Helenius A. Protein oligomerization in the endoplasmic reticulum. Annu Rev Cell Biol. 1989;5:277–307. doi: 10.1146/annurev.cb.05.110189.001425. [PubMed] [Cross Ref]
37. Bole DG, Hendershot LM, Kearney JF. Posttranslational association of immunoglobulin heavy chain binding protein with nascent heavy chains in nonsecreting hybridomas. J Cell Biol. 1986;102(5):1558–1566. doi: 10.1083/jcb.102.5.1558. [PMC free article] [PubMed] [Cross Ref]
38. Doms RW. Oligomerization and protein transport. Methods Enzymol. 1990;191:841–854. [PubMed]
39. Leitzgen K, Knittler MR, Haas IG. Assembly of immunoglobulin light chains as a prerequisite for secretion. A model for oligomerization-dependent subunit folding. J Biol Chem. 1997;272(5):3117–3123. doi: 10.1074/jbc.272.5.3117. [PubMed] [Cross Ref]
40. Kerem A, Kronman C, Bar-Nun S, Shafferman A, Velan B. Interrelations between assembly and secretion of recombinant human acetylcholinesterase. J Biol Chem. 1993;268(1):180–184. [PubMed]
41. Reddy PS, Corley RB. Assembly, sorting, and exit of oligomeric proteins from the endoplasmic reticulum. Bioessays. 1998;20(7):546–554. doi: 10.1002/(SICI)1521-1878(199807)20:7<546::AID-BIES5>3.0.CO;2-I. [PubMed] [Cross Ref]
42. Anelli T, et al. Thiol-mediated protein retention in the endoplasmic reticulum: the role of ERp44. EMBO J. 2003;22(19):5015–5022. doi: 10.1093/emboj/cdg491. [PubMed] [Cross Ref]
43. Kim P, Bole D, Arvan P. Transient aggregation of nascent thyroglobulin in the endoplasmic reticulum: relationship to the molecular chaperone, BiP. J Cell Biol. 1992;118(3):541–549. doi: 10.1083/jcb.118.3.541. [PMC free article] [PubMed] [Cross Ref]
44. Lodish HF, Kong N, Wikstrom L. Calcium is required for folding of newly made subunits of the asialoglycoprotein receptor within the endoplasmic reticulum. J Biol Chem. 1992;267(18):12753–12760. [PubMed]
45. De Jaco A, et al. A mutation linked with autism reveals a common mechanism of endoplasmic reticulum retention for the alpha,beta-hydrolase fold protein family. J Biol Chem. 2006;281(14):9667–9676. doi: 10.1074/jbc.M510262200. [PubMed] [Cross Ref]
46. Hahn MK, Robertson D, Blakely RD. A mutation in the human norepinephrine transporter gene (SLC6A2) associated with orthostatic intolerance disrupts surface expression of mutant and wild-type transporters. J Neurosci. 2003;23(11):4470–4478. [PubMed]
47. Cordat E, et al. Dominant and recessive distal renal tubular acidosis mutations of kidney anion exchanger 1 induce distinct trafficking defects in MDCK cells. Traffic. 2006;7(2):117–128. doi: 10.1111/j.1600-0854.2005.00366.x. [PubMed] [Cross Ref]
48. Mendes HF, Cheetham ME. Pharmacological manipulation of gain-of-function and dominant-negative mechanisms in rhodopsin retinitis pigmentosa. Hum Mol Genet. 2008;17(19):3043–3054. doi: 10.1093/hmg/ddn202. [PubMed] [Cross Ref]
49. Kagan A, Yu Z, Fishman GI, McDonald TV. The dominant negative LQT2 mutation A561V reduces wild-type HERG expression. J Biol Chem. 2000;275(15):11241–11248. doi: 10.1074/jbc.275.15.11241. [PubMed] [Cross Ref]
50. Butler DC, McLear JA, Messer A. Engineered antibody therapies to counteract mutant huntingtin and related toxic intracellular proteins. Prog Neurobiol. 2012;97(2):190–204. doi: 10.1016/j.pneurobio.2011.11.004. [PMC free article] [PubMed] [Cross Ref]
51. Li C, Xiao P, Gray SJ, Weinberg MS, Samulski RJ. Combination therapy utilizing shRNA knockdown and an optimized resistant transgene for rescue of diseases caused by misfolded proteins. Proc Natl Acad Sci U S A. 2011;108(34):14258–14263. doi: 10.1073/pnas.1109522108. [PubMed] [Cross Ref]
52. Sandefur CI, Schnell S. A model of threshold behavior reveals rescue mechanisms of bystander proteins in conformational diseases. Biophys J. 2011;100(8):1864–1873. doi: 10.1016/j.bpj.2011.03.006. [PubMed] [Cross Ref]
53. Navarro D, Qadri I, Pereira L. A mutation in the ectodomain of herpes simplex virus 1 glycoprotein B causes defective processing and retention in the endoplasmic reticulum. Virology. 1991;184(1):253–264. doi: 10.1016/0042-6822(91)90842-Y. [PubMed] [Cross Ref]
54. Marquardt T, Helenius A. Misfolding and aggregation of newly synthesized proteins in the endoplasmic reticulum. J Cell Biol. 1992;117(3):505–513. doi: 10.1083/jcb.117.3.505. [PMC free article] [PubMed] [Cross Ref]
55. Kittanakom S, Cordat E, Akkarapatumwong V, Yenchitsomanus PT, Reithmeier RA. Trafficking defects of a novel autosomal recessive distal renal tubular acidosis mutant (S773P) of the human kidney anion exchanger (kAE1). J Biol Chem. 2004;279(39):40960–40971. doi: 10.1074/jbc.M405356200. [PubMed] [Cross Ref]
56. Wang J, Chen Y, Yuan Q, Tang W, Zhang X, Osei K. Control of precursor maturation and disposal is an early regulative mechanism in the normal insulin production of pancreatic beta-cells. PLoS One. 2011;6(4):e19446. doi: 10.1371/journal.pone.0019446. [PMC free article] [PubMed] [Cross Ref]
57. Liu M, Li Y, Cavener D, Arvan P. Proinsulin disulfide maturation and misfolding in the endoplasmic reticulum. J Biol Chem. 2005;280(14):13209–13212. doi: 10.1074/jbc.C400475200. [PMC free article] [PubMed] [Cross Ref]
58. Laybutt DR, et al. Endoplasmic reticulum stress contributes to beta cell apoptosis in type 2 diabetes. Diabetologia. 2007;50(4):752–763. doi: 10.1007/s00125-006-0590-z. [PubMed] [Cross Ref]
59. Scheuner D, Kaufman RJ. The unfolded protein response: a pathway that links insulin demand with beta-cell failure and diabetes. Endocr Rev. 2008;29(3):317–333. doi: 10.1210/er.2007-0039. [PubMed] [Cross Ref]
60. Ledent C, Parmentier M, Vassart G. Tissue-specific expression and methylation of a thyroglobulin-chloramphenicol acetyltransferase fusion gene in transgenic mice. Proc Natl Acad Sci U S A. 1990;87(16):6176–6180. doi: 10.1073/pnas.87.16.6176. [PubMed] [Cross Ref]

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