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JP designed and performed research, analyzed data and wrote paper. WYIC performed research. NKW performed research and analyzed data. AMS performed research. SK performed research. KK performed research. MEJ performed research. JRL analyzed data. AKK performed research. JF contributed essential reagents. DT analyzed data. KO performed research and analyzed data. GAF performed research and analyzed data. GL performed research and analyzed data. VK performed research and analyzed data. BG designed research, analyzed data and wrote paper.
Endoglin is an accessory receptor for TGF-β signalling and is required for normal hemangioblast, early hematopoietic and vascular development. We have previously shown that an upstream enhancer, Eng-8 together with the promoter region mediates robust endothelial expression yet is inactive in blood. To identify hematopoietic regulatory elements, we employed array based methods to determine chromatin accessibility across the entire locus. Subsequent transgenic analysis of candidate elements showed that an endothelial enhancer at Eng+9 when combined with an element at Eng+7 functions as a strong hemato-endothelial enhancer. ChIP-chip analysis demonstrated specific binding of Ets factors to the promoter as well as to the -8, +7 and +9 enhancers in both blood and endothelial cells. By contrast Pu.1, an Ets factor specific to the blood lineage, and Gata2 binding was only detected in blood. Gata2 was bound only at +7 and GATA motifs were required for hematopoietic activity. This modular assembly of regulators gives blood and endothelial cells the regulatory freedom to independently fine-tune gene expression and emphasizes the role of regulatory divergence in driving functional divergence.
Transcriptional regulation is a key mechanism controlling the formation and subsequent behaviour of hematopoietic stem cells (HSCs) 1. We have previously shown that clustering of Ets and Gata sites can be exploited in genome-wide computational screens to identify new hematopoietic stem/progenitor elements 2-5. These computational screens were performed using the Ets/Ets/Gata (E/E/G) signature (two conserved Ets and one conserved Gata site within a 50 base pair sequence window with defined spacing and orientation constraints) using the Scl +19 HSC enhancer as a template 3. Given these constraints, the predicted E/E/G elements have all been clustered within a single hematopoietic enhancer. The possibility that the E/E/G HSC signature could be assembled across multiple independent enhancers had not been tested.
During development, endothelium and blood arise from common or closely related progenitors and there are several signalling molecules and transcription factors (TFs) that are key regulators of both 6. Several lines of evidence support a role for Endoglin in blood and blood vessel development: Endoglin (ENG or CD105) is an accessory receptor for members of the transforming growth factor-beta (TGF-β) superfamily, including TGFβ1/3, activin and BMP2/7 and is expressed on the surface of proliferating endothelial cells and adult bone marrow HSCs 7,8; Eng-/- mice have severely anemic yolk sacs by E9.5 and die at E10.5-11.5 with cardiac and vascular abnormalities 9-11; Endoglin has also been shown to mark BL-CFCs, the in vitro equivalent of the hemangioblast, the embryonic progenitor of hematopoietic and endothelial lineages; Eng-/- BL-CFCs are reduced in number and have limited hematopoietic potential 12. Differential expression of Endoglin in various hematopoietic progenitor compartments has recently been utilized to define a functional hierarchy for myelo-erythroid progenitors 13.
Despite its functional relevance, the only comprehensive survey of tissue specific control of Endoglin expression has been limited to the endothelium. We have previously shown that Ets TFs act on the Eng promoter and a -8kb enhancer to regulate Endoglin expression in the endothelium 14. The TFs and cis-regulatory elements that regulate Endoglin expression during blood development however are not known. Taking advantage of new array based methodologies to identify chromatin accessibility and TF binding over large genomic regions, we investigated the transcriptional regulation of Endoglin during mouse embryonic hematopoiesis. We also sought to address the following general issues. First, can array based methods be used to identify functionally valid hematopoietic enhancers? Second, can the E/E/G HSC signature be assembled across multiple distinct hematopoietic enhancers rather than being confined to a single enhancer? Third, do components of the Fli1/Gata2/Scl triad which operates during early blood development and regulates master hematopoietic transcription factors such as Runx1 also regulate expression of Endoglin?
In situ hybridizations (ISH) were performed on paraffin or cryo sections using digoxigenin labelled riboprobes and detected with an alkaline phosphatase-conjugated anti-digoxigenin antibody as previously described 15.
HPC-7 cells were maintained as described 16. Bry-GFP ES cells were maintained and differentiated as described 17. Day 3 EBs were harvested, trypsinized, stained for GFP (Bry) and Flk1 expression and sorted for gene expression analyses. MS1 and BW5147 cells were maintained in DMEM and RPMI respectively each supplemented with 10% FCS.
Sorted E11.5 FL cells were counted and cultured in cytokine supplemented Methocult GF-3434 for erythroid and myeloid colony formation. Six plates each were seeded with 2 ×103 FDG+ or FDG- cells from transgenic FLs. Six plates of 2 × 103 FDG-treated WT FL cells were also set up as a control. The plates were cultured at 37°C, and colonies were scored at 10 days.
ChIP assays were performed on HPC-7, BW5147 and MS1 cells. Enrichment was measured by real-time PCR using Sybr Green (Stratagene) or labeled for array hybridization as described below. The levels of enrichment were normalized to that obtained with a control rabbit antibody and were calculated as a fold increase over that measured at a control region, Scl +21. Methods and Primers listed in SI.
DNA templates were prepared as detailed elsewhere 18. Briefly, nuclei were prepared from 5 million cells and incubated with 120 units of DNaseI (Ambion) on ice for 1 h. DNA was then extracted, RNase A treated and repaired with T4 polymerase (NE Biolabs), to provide double-stranded blunt ends. The DNA was then precipitated and re-suspended for ligation to a double stranded asymmetric biotinylated linker. Following ligation, the DNA was re-precipitated, re-suspended, and primer-extended. Primer-extended template was then purified from linker and digested genomic DNA, using streptavidin beads (Dynal) and labeled for array hybridization as described below.
The array design has been deposited in ArrayExpress under the accession A-MEXP-1020 and A-MEXP-1021. See SI for details.
Immunoprecipitated DNA was labeled with the Cy3 dye, mixed with Cy5 labeled control DNA and then precipitated with cot-1 DNA. Following pre-hybridization of the array slides with herring sperm DNA/cot-1 DNA, the samples were resuspended in hybridization buffer and hybridized to the slides for 45 h using an automated TECAN 400 hybridization station. Following hybridization, slides were scanned using an Agilent DNA microarray scanner. Mean spot intensities from images were quantified using GenePix 6.0 with background subtraction. The array results have been deposited in ArrayExpress under E-TABM-455. See SI for details
Detailed in SI
Candidate enhancer sequences were PCR amplified from human genomic DNA. Mutations were generated by PCR using oligonucleotides with mismatches and verified by DNA sequencing. F0 transgenic mouse embryos and the -8/P/lacZ/+7/+9 line were generated by pronuclear injection of lacZ reporter fragments 19. For histology, the embryos were embedded in paraffin, sectioned and counter stained with brazilin. Primers listed in SI.
Single cell suspensions of E11.5 and E12.5 FLs (L1091xWT) were stained with anti-CD105/PE (R&D Systems), - CD 150/APC (BioLegend), - CD48/PE, - CD41/PE, - cKit/APC, 7-AAD (all from BD Pharmingen) and the fluorescent substrate FDG (fluorescein di-β-D galactopyranoside; F-2756 - Sigma), analyzed on a FACSCalibur (BD Biosciences) and reported using FlowJo software.
Gene expression relative to βactin was quantified using SYBR-Green (Stratagene) or TaqMan real-time PCR. Primers are listed in SI.
Although Endoglin is expressed in adult HSCs and can be used to enrich adult bone marrow HSCs, its expression profile during fetal hematopoiesis is not known 13,20. During mouse development, the first long-term reconstituting HSCs are thought to be generated from the floor of the dorsal aorta (DA) in the aorta-gonad-mesonephros (AGM) region at E10.5 6. These putative HSCs are recognized as blood clusters and are thought to originate from the aortic endothelium or the underlying mesenchyme. HSC numbers are subsequently amplified in the fetal liver (FL) and other sites. Endoglin expression is first evident at E6.5 in the amniotic fold and developing allantois and at E7.5 and E8.5 in the yolk-sac, dorsal aorta and primitive heart tube (Figure S1 and 21). To demonstrate Endoglin expression in wild-type mice, we used in situ RNA hybridization on E10.5 (Figure 1A) and E11.5 (Figure 1B) mouse embryos. At E10.5, Endoglin transcripts are present in the endocardium (H), endothelia of small and large blood vessels including the DA (Figure 1A(i)), in hematopoietic intra-aortic clusters located in the floor of the DA (Figure 1A(ii)), and in the FL (Figure 1A(iii)). At E11.5, Endoglin expression persists in the hemogenic DA and in the FL (Figure 1B (i)) where ~ 3% of FL hematopoietic cells are Endoglin (CD105) positive, a majority of which also express the progenitor marker, c-kit (Figure 1B (ii)).
We have previously identified, using multispecies alignments of the Eng locus, nine regions (E1-E9; Figure 2A) with high sequence conservation across a wide range of mammals 14. Transgenic analysis demonstrated that E1 as a -8kb enhancer (Eng -8) together with the Eng promoter (E3) targeted Endoglin expression to the endothelium in transgenic mice 14. Eng -8 however did not target blood progenitors in developing embryos (Figure S2). To identify gene regulatory elements that direct Endoglin expression to blood progenitors, we mapped histone H3 acetylation status and DNaseI hypersensitivity sites in hematopoietic and endothelial cell lines (Figure 2).
Modifications to histones that package the genome are thought to contribute to the orchestration of gene expression and cellular state, by determining higher order chromatin structure 22. Histone acetylation can increase TF access to chromatin by counteracting higher order chromatin folding that may mask cis-elements 23. Potential gene regulatory regions can therefore be identified by chromatin immunoprecipitation (ChIP) using an antibody to acetylated histone H3. Alternatively cis-regulatory elements within actively transcribed gene loci can be mapped by their hypersensitivity to DNaseI digestion. By incorporating array technology, both ChIP and DNaseI hypersensitivity mapping have been successfully adapted to studying large genomic regions 24,25. We hypothesized that those regulatory elements that direct Endoglin expression to blood or endothelial cells would be accessible to TF binding and as such show active chromatin marks by one or both assays in representative cells.
In Endoglin expressing MS1 endothelial cells (Figure S3), active chromatin marks were seen at P (Eng promoter) and at -8 by both H3Ac ChIP-chip and array based DNaseI hypersensitivity mapping (ADHM) (Figure 2B). A conserved region at +9 was also accessible by both assays. By contrast, two ADHM sites, one at a poorly conserved region 5′ to the highly conserved +7 region and another at the +15 conserved region, did not show corresponding accessibility by H3Ac ChIP-chip. The HPC7 cell line expresses Endoglin (Figure S3), requires Stem Cell Factor for growth and has multi-lineage differentiation capacity in transplantation assays 16. As with MS1 endothelial cells, prominent active chromatin marks were seen at the Eng promoter (P) and Eng-8 enhancer (-8) in HPC-7 hematopoietic cells (Figure 2C) by both H3Ac ChIP-chip and ADHM. In addition, enrichments were also seen at genomic coordinates corresponding to +7 and +9 conserved regions in both assays. The DNaseI hypersensitive mark at +18 in HPC-7 cells did not correlate with enrichment of acetylated histones at this site. By contrast, BW5147 T-cells, which do not express Endoglin (Figure S3), lack active chromatin marks at the Eng promoter (P) (Figure 2D). Interestingly somewhat diminished ‘active’ marks remain at -8 but are absent from +7 and +9 regions. Taken together, these results show first that, promoter accessibility correlates with Endoglin expression irrespective of cell type. Second that, -8 and +9 non-coding conserved regions are accessible in both blood and endothelial cells whereas the +7 region is accessible in blood progenitors but not in endothelial cells. These results are summarized in Figure S4.
To test whether the genomic regions identified by profiling chromatin accessibility represent bona fide hematopoietic regulatory elements, we performed in vivo transgenic assays. The +7 and +9 regions are located in the first intron approximately +7 kb and +9 kb from the translation start site of human ENG (Figure 3A). We have previously established that the Eng promoter (P) targets lacZ reporter expression to subsets of endothelial cells, albeit weakly, and that the Eng-8 region significantly enhances promoter activity in the endothelium (14 and Figure 3B compare wholemount embryos and sections in (ii), (viii) and (xiv) with (i), (vii) and (xiii)). To evaluate the roles of the +7 and +9 regions as potential enhancers, we inserted 483bp (+7431/+7913) and 500bp (+8974/+9473) fragments corresponding to these regions, alone or in combination, downstream of either the Eng promoter (P/lacZ) or the Eng promoter/enhancer (-8/P/lacZ) reporter constructs (Figure 3B). Reporter gene expression was evident in FL hematopoietic cells in P/lacZ/+7 and P/lacZ/+9 transgenic embryos and both the frequency and intensity of expression was increased by combining +7 and +9 (Figure 3B compare wholemount embryos (v) with (iii) and (iv) and FL sections in (xvii) with (xv) and also with (xvi)). By adding the -8 enhancer to P/lacZ/+7/+9 and thus incorporating the complete chromatin accessibility profile seen in HPC-7 hematopoietic cells into a single reporter construct, the specificity of hemato-endothelial expression was enhanced (Figure 3B (vi), (xii) and (xviii)).
Transgenic embryos generated with Eng promoter constructs that included the +9 fragment showed strong endothelial/endocardial and hematopoietic reporter gene expression (Figure 3B (iv-vi)). This is consistent with the ADHM profiles in Figure 2 which show chromatin accessibility at the +9 region in both MS1 endothelial and HPC-7 hematopoietic cells. Also consistent with the chromatin accessibility profiles in Figure 2, transgenic embryos generated with the P/lacZ/+15 construct showed strong endothelial expression but lacked hematopoietic expression (Figure S5) and those generated with the P/lacZ/+7 construct showed blood but relatively weak endothelial staining. Finally, despite the prominent chromatin mark at Eng +18 in the ADHM profile in HPC-7 cells, P/lacZ/+18 transgenics did not show reporter gene expression in FL blood cells (Figure S6). Therefore by filtering, chromatin accessibility profiles using in vivo transgenics, we were able to identify bona fide hematopoietic enhancers in the Eng locus. This emphasizes the need to correlate chromatin accessibility profiles in individual cell types with appropriate in vivo models so that potential enhancers are tested not in isolation but with due regard to tissue development in the whole embryo.
To explore the surface phenotype of FL cells targeted by the Eng+7 and Eng+9 enhancers, we generated a stable mouse line expressing the -8/P/lacZ/+7/+9 transgene (L1091) that incorporated all of the regions with active chromatin marks identified by both H3Ac ChIP-chip and ADHM in HPC-7 cells (Figure 3B (vi)). The transgene is expressed as early as E7.5, where it targets cells in the blood band region in the proximal yolk sac (Figure S7). At E11.5, embryos show reporter expression in the yolk sac endothelium, hemogenic dorsal aorta and blood cells in the placenta and fetal liver (Figure 3C (i)). Fetal liver haematopoietic cells targeted by the -8/P/lacZ/+7/+9 transgene show greater multilineage growth potential assayed by in vitro colony-forming assays (compare FDG positive vs. negative fractions in Figure 3C (ii)). Flowcytometry of FL cells from -8/P/lacZ transgenic embryos (L1082) showed no reporter gene expression when stained with the fluorescent β-galactosidase substrate, FDG (Figure S2). However, when the Eng +7 and Eng +9 enhancers are added to the construct (-8/P/lacZ/+7/+9) approximately 3% of E11.5 FL cells do (Figure 3C (iii)). Furthermore, the majority of FL cells targeted by the transgene were also Endoglin (CD105) positive. Although most of the c-Kit positive cells in the FL do not express either CD105 or the -8/P/lacZ/+7/+9 transgene (Figure 1B (ii) and 3C (iv)), approximately 60% of cells targeted by the transgene are both CD105 and c-Kit positive (Figure 3C (v)). As shown in Figure S8, cells that express the -8/P/lacZ/+7/+9 transgene are also enriched for CD150+ blood stem/progenitor cells and show a relative paucity of lineage committed CD150-/ CD48-/ CD41- cells 26. This activity however does not persist in adult bone marrow (Figure S9) and could indicate that these elements may not be used to express Endoglin in adult bone marrow or more likely that the transgene is silenced with time. Taken together these data show that the - 8/P/lacZ/+7/+9 transgene targets FL blood progenitors and that in vivo activity of these non-coding conserved regions is consistent with endogenous Endoglin expression.
We have shown previously that clusters of highly conserved Ets and Gata sites are critical for the activity of early hematopoietic regulatory elements of the Scl, Lyl1, Fli1, Hhex and Gata2 genes 2-5,27. The Eng+7 enhancer has two conserved Gata binding sites within a large block of highly conserved sequence, flanked by two conserved Ets binding sites (Figure 4A). The Eng+9 enhancer has no Gata binding sites but has four Ets binding sites conserved down to opossum and an additional five conserved between human and mouse (Figure 4B). To establish the relative contribution of the various conserved Ets and Gata motifs, mutations were introduced and the activity of the enhancers tested in F0 transgenics (Figure 4C). Although the Eng+7 and Eng+9 enhancers in combination with the endogenous Eng promoter show hematopoietic activity, when combined with the SV promoter neither enhancer is sufficient on its own to target blood (compare Figure 4C (i) and (ii) with Figure 3B (iii) and (iv)). However when combined in a single construct, Eng+7 and Eng+9 enhancers show robust activity in blood (compare Figure 4C (iii) with Figure 3B (v). Eng+9 enhancer shows robust endothelial activity and deleting a core region with four highly conserved Ets binding sites reduces but does not eliminate this activity in all embryos (Figure 4C (ii)). This is probably due in part to the partially conserved Ets sites that are retained in Eng+9 (ΔEts) (yellow blocks in Figure 4B (ii)). Importantly, the Gata binding sites in Eng+7 are critical for the hematopoietic activity of the SV/lacZ/+7/+9 construct although some endothelial activity remains in SV/lacZ/+7(ΔG1G2)/+9 and SV/lacZ/+7(ΔG1G2)/+9 (ΔEts) transgenic embryos (Figure 4C (iii)).
Blood and endothelium develop from closely related mesodermal progenitors (reviewed in 6). Lineage tracing studies in zebrafish have confirmed earlier in vitro data that a proportion of blood and endothelial cells share a common progenitor, the hemangioblast 28. Nevertheless, following differentiation, ES cells in culture form colonies known as embryoid bodies (EBs) that contain mesodermal (Brachyury+) progenitors that display both blood and endothelial potential i.e. blast-colony forming cells (BL-CFC) 29. This transient population (day 2.5-4 of differentiation) represents the in vitro equivalent of the yolk-sac hemangioblast. The ES/EB model system has been applied to an ES cell line with GFP targeted to the Brachyury locus (GFP-Bry ES) 17. By sorting day 3-3.5 EBs based on GFP and Flk1 expression it is possible to identify three distinct cell populations, GFP-Flk1- (DN), GFP+Flk1- (SP) and GFP+Flk1+ (DP) that represent a developmental progression ranging from pre-mesoderm (DN) to pre-hemangioblast mesoderm (SP) to the hemangioblast mesoderm (DP).
Endoglin is required for development of hemangioblast equivalents and early hematopoiesis 12 and as shown in Fig. 5A (i), expression levels increase approximately 3.5 fold as cells transit from pre-hemangioblast mesoderm (SP) to the hemangioblast mesoderm (DP). We have previously shown that Fli1 and Gata2, together with Scl, form a recursively wired transcriptional subcircuit that operates during early endothelial and HSC development in the embryo 5. Pu.1 is an Ets TF that is expressed in blood but not endothelial cells and is indispensable for the maintenance of HSCs and for normal myeloid and B- lymphoid development 30. To determine the role of Fli1, Gata2, Scl and Pu.1 in regulating Endoglin expression during blood specification, we measured variations in the levels of these TFs in cell fractions from sorted day 3.5 and in unsorted day 4.5 EBs. The levels of Fli1, Gata2 and Scl increased dramatically in DP cells (Figure 5A (ii) and 5). A day later, with further hematopoietic differentiation, the levels of these TFs continued to increase. Pu.1 levels lagged behind but increased at day 4.5. All four transcription factors are also present in FL cells at E11.5 (Figure 5B and 5).
To correlate transgenic in vivo enhancer activity with in vivo TF occupancy, we performed ChIP-chip experiments with well characterized antibodies in ES cell derived HPC-7 cells which fulfil many functional requirements defining HSCs 16. All four transcription factors are expressed at high levels in these cells (16 and Figure S10). As shown in Figure 5C, Fli1 and Pu.1 are enriched at the Eng promoter (P), Eng -8, Eng+7 and Eng+9 enhancers. The enrichments of these Ets factors are consistent with both chromatin accessibility (Figure 2C) and the presence of conserved Ets binding sites (14 and Figure 4A and B). Gata2 enrichment was most prominent at Eng+7, which has two highly conserved Gata binding sites (Figure 4A). Scl is expressed in HPC-7 cells (Figure S10 and 16) but is not enriched at the Eng locus despite the presence of a E-box element at Eng -8 that is highly conserved in mammals (mm9: Chr2: 32,493,775-800). Similar enrichment profiles were also seen in 416B blood progenitors (data not shown). By contrast, in MS1 endothelial cells, although the Fli1 enrichment profile mirrors that in HPC-7 cells, Gata2 is not enriched at the Eng locus (Figure 5C). Peaks of enrichment for Fli1, Pu.1 and Gata2 are also seen at Eng +30 (marked with an asterix). The corresponding tile has a palindromic 8bp region with two overlapping GATA and two Ets binding sites (ggatatcc). The corresponding region shows a degree of chromatin accessibility in HPC-7 and MS1 cells and is worthy of further study.
In this report we show first that, array based chromatin accessibility surveys are useful in identifying tissue specific enhancers but that in vivo validation is required to filter false positives. Second that, the Ets/ Gata transcriptional programme that regulates hematopoietic gene expression is not necessarily confined to a single hematopoietic enhancer and can be assembled across multiple tissue specific enhancers. Third, that by distributing the Ets/Gata code across separate enhancers, hemangioblasts, blood stem/progenitors and endothelial cells can regulate expression of genes such as Endoglin that are functionally important to each, in a cell type specific manner despite the overlap in their respective transcriptional programmes. Fourth, that Pu.1 and Gata2 drive Endoglin expression in blood stem/progenitors but not endothelial cells; a mechanism that could be a paradigm for expressing other genes shared between both tissues.
Characterisation of transcriptional networks has become a major focus of developmental biology as these networks govern the spatial variation and temporal sequence of gene expression. Within these networks, combinatorial interactions of transcription factors control the expression of key effector genes including those involved in signal transduction such as Endoglin. Individual cis-regulatory elements are key components of transcriptional networks because they function as information processing units by integrating the inputs of their respective upstream regulators into tightly controlled spatiotemporal expression patterns. However, functional characterisation of transcriptional regulatory elements has traditionally been a laborious process thus limiting our ability to reconstruct transcriptional regulatory networks.
Recent array based methods have greatly facilitated chromatin accessibility surveys as a means to identify candidate gene regulatory regions spread across large genomic intervals. However, it remains unknown to what extent even comprehensive chromatin profiling across multiple tissues will be able to accurately identify tissue-specific regulatory elements. This comprehensive survey of the Endoglin locus shows that although there is broad agreement between techniques, the chromatin accessibility sites identified by surveying histone modifications and DNaseI accessibility can differ. Some of these differences, and indeed the validity of the predicted elements as bona fide tissue specific enhancers, can be resolved using in vivo transgenics. Indeed, the best predictor of tissue specificity of an element in transgenic assays was consistency between histone acetylation and DNaseI accessibility profiles. Our current data therefore suggest that although informative, recently reported genome-wide chromatin accessibility profiles 31,32 should be interpreted with caution when drawing conclusions about true in vivo activities of any regions flagged as candidate regulatory elements.
Blood and endothelial cells share a close developmental link and based on experiments in chick, the existence of a shared progenitor called the hemangioblast was proposed 33,34. Bi-potential precursors have also been demonstrated in mouse and human ES cell cultures 29,35 and from cells derived from the gastrulating mouse embryo 36. However, estimates of the in vivo frequency of these bi-potential progenitors vary. On the one hand, single cell resolution fate mapping in zebrafish embryos showed that approximately 12.5% of labeled cells give rise to both blood and endothelial progeny and to no other cell type 28. On the other hand however, fate-mapping analyses both by transplantation using early mouse embryos 37 as well as in chimeras generated using differentially labeled mouse ES cells 38 suggest that the majority of yolk sac blood and endothelial cells develop independently from mesodermal precursors without necessarily originating from a shared progenitor. However, later during embryogenesis, blood stem cells are thought to be specified from hemogenic endothelium of the dorsal aorta 39 again suggesting a close relationship between endothelium and blood stem/progenitor cells.
Despite the above controversies likely to be caused by differences between what individual cells can do when placed in specific culture conditions as opposed to what they will do in an intact embryo, a wide range of genetic evidence supports a close biological relationship between endothelial and early blood cells. Both gain and loss of function studies for a number of genes result in phenotypes affecting both lineages 40-42 and endoglin is of course a member of this growing list of genes 9. Extensive functional overlap between endothelial and blood stem/progenitor cells has also been identified at the level of transcriptional regulation. In particular, regulatory elements containing clusters of Ets and Gata binding sites are active in both lineages 2,27 and indeed an E/E/G signature has been used successfully for the computational identification of additional enhancers with this dual specificity 3,4. However, several regulatory elements with little or no hematopoietic activity have also been identified and these are generally characterized by the presence of multiple Ets sites but no Gata sites 14,43.
Unlike other genes studied to date that are co-expressed in endothelium and blood stem/progenitor cells, the endoglin locus does not contain a typical Ets/Gata responsive enhancer. Instead, the Ets/Gata regulatory code is assembled across distinct elements with the intriguing consequence that Gata2 control of endoglin expression becomes restricted to hematopoietic cells. Disentanglement of regulatory programmes has recently emerged as a potential major driver of evolution in lower eukaryotes 44. Similarly, the modular assembly (and disassembly) of the Ets/Gata code across multiple tissue specific regulatory elements appears to allow a degree of regulatory freedom so that when blood and endothelial cells co-express a gene they can disentangle these enhancers and recruit only those elements they need to fine tune gene expression to suit individual needs. This dynamic interaction and potential for alternative TF/ cis-regulatory element interactions may be particularly important when expressing a functionally important gene against the changing transcriptional landscape of a progenitor transiting towards a definitive cellular phenotype.
Within the endoglin locus, Gata2 binding to the +7 enhancer is specific to the blood lineage and is required for hematopoietic activity of +9, an otherwise endothelial enhancer. It is striking that by co-opting the +7 region, the +9 endothelial enhancer is converted into a robust hemato-endothelial enhancer. Although the precise temporal and spatial emergence of blood and endothelial cells in the extra-embryonic yolk sac is debated, the endothelium predates the emergence of HSCs from the dorsal aorta. This raises the possibility that the regulatory network that specifies blood diverged from a pre-existing endothelial regulatory network.
Gata2 is expressed in endothelial cells yet cannot access the +7 enhancer due at least in part to compacted chromatin. Accessibility at the +7 enhancer in the blood lineage is of fundamental importance and could be established in mesodermal precursors by pioneer transcription factors that are expressed in these progenitors and in blood but not in endothelium. FoxA, for example, opens compacted chromatin and by interacting with the albumin enhancer in endoderm precursors maintains enhancer accessibility in liver cells but not in tissues where FoxA is not expressed 45. Pu.1 has been shown to act as a pioneer transcription factor at the c-fms locus 46, is expressed in blood but not endothelium and binds the +7 enhancer with Gata2. Low-level Pu.1 expression is present in Brachyury +/Flk1+ mesodermal precursors and increases substantially with hematopoietic differentiation and could play a role in +7 enhancer accessibility in the blood lineage and Gata2 binding at this site. Potential synergism of Pu.1 and Gata2 in driving the early hematopoietic programme is in stark contrast to the well established antagonism between Pu.1 and Gata1, widely seen as one of the key mechanisms driving lineage commitment of differentiating common myeloid progenitor cells 47. However, cooperative interactions between Pu.1 and Gata2 are not without precedent. For example, the differentiation of mast cells, which like stem cells depend on Stem Cell Factor signaling, can be induced through cooperative action of Pu.1 and Gata2 48.
Like endoglin, both Pu.1 and Gata2 play important roles in blood stem/progenitor cells and it is tempting to speculate that at least some of the phenotypic consequences of loss of Pu.1 or Gata2 could be explained by reduced levels of endoglin. Moreover, it is interesting that Pu.1 when disrupted is leukaemogenic 49 as Endoglin itself was first identified from a pre-B acute lymphoblastic leukaemia cell line. Endoglin is also a marker of tumour vascularity and soluble Endoglin, a product of the native protein that is cleaved from the cell surface, is aetiologically linked with preeclampsia 50. Underlying both is the overexpression of Endoglin in the vasculature. Unravelling the transcriptional programmes that drive Endoglin expression therefore not only sheds light on normal development but also opens up possible avenues to control the abnormal expression implicated in a range of pathologies.
We thank Michelle Hammett, Sandie Piltz, and Paula Braker for generating transgenic mice, Catherine Porcher (Oxford University) for the anti-Scl antibody used in ChIP, Richard Auburn from FlyChip for printing the arrays. This work was supported by grants from the Biotechnology and Biological Sciences Research Council, the Leukaemia Research Fund, Cancer Research UK, a C.J. Martin/R.G. Menzies fellowship from the National Health and Medical Research Council (Australia) to J.E.P and fellowships from the Kay Kendall Leukaemia Fund to K.O. and the Canadian Institutes for Health Research to J.R.L.