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Microcephaly is a clinical characteristic for human nijmegen breakage syndrome (NBS, mutated in NBS1 gene), a chromosomal instability syndrome. However, the underlying molecular pathogenesis remains elusive. In the present study, we demonstrate that neuronal disruption of NBS (Nbn in mice) causes microcephaly characterized by the reduction of cerebral cortex and corpus callosum, recapitulating neuronal anomalies in human NBS. Nbs1-deficient neocortex shows accumulative endogenous DNA damage and defective activation of Ataxia telangiectasia and Rad3-related (ATR)-Chk1 pathway upon DNA damage. Notably, in contrast to massive apoptotic cell death in Nbs1-deficient cerebella, activation of p53 leads to a defective neuroprogenitor proliferation in neocortex, likely via specific persistent induction of hematopoietic zinc finger (Hzf) that preferentially promotes p53-mediated cell cycle arrest whilst inhibiting apoptosis. Moreover, Trp53 mutations substantially rescue the microcephaly in Nbs1-deficient mice. Thus, the present results reveal the first clue that developing neurons at different regions of brain selectively respond to endogenous DNA damage, and underscore an important role for Nbs1 in neurogenesis.
Nijmegen breakage syndrome (NBS), caused by hypomorphic mutation in NBS1 1, is a chromosomal instability syndrome, characterized by chromosomal instability, immunodeficiency, radiosensitivity, cancer predisposition and microcephaly. The Nbs1/Nibrin/p95 protein is a component of the Mre11/Rad50/Nbs1 (MRN) complex that acts as a DNA double-strand break (DSB) sensor and functions in cell cycle checkpoint in response to DNA damage and DNA repair together with Ataxia telangiectasia mutated (ATM), Ataxia telangiectasia and Rad3-related (ATR), mediator of DNA damage checkpoint protein 1 (MDC1) and H2AX 2. Following DSBs in DNA, Nbs1 interacts with phosphorylated H2AX (γH2AX) and is responsible for the nuclear translocation of the Mre11/Rad50 repair complex to the sites of DNA damage to sense DNA strand breaks and activate ATM 3, 4, 5. In addition, Nbs1 is phosphorylated by ATM, activating downstream molecules including p53, BRCA1 and Chk2 to control cell cycle progression 6, 7. Moreover, it has also been demonstrated that the MRN complex plays a role in single-strand break (SSB) -mediated ATR activation and subsequent phosphorylation of Chk1 8, 9. Thus, Nbs1 or MRN also participates in mediating activation of ATM and ATR directly or indirectly 2, 10, 11.
Genetic defects in DNA damage response (DDR) lead to human microcephaly syndromes, such as Nijmegen breakage syndrome, ATR Seckel syndrome (mutated in ATR 12), and primary microcephaly (MCPH) caused by mutations in MCPH1 13. These syndromes share overlapping neuronal defects, indicating that microcephaly may be caused by alterations of neuronal progenitors in response to DNA damage.
To study the molecular pathogenesis of microcephaly induced by DDR defects in humans, attempts have been made using mouse models with disruption of NBS1 (known as Nbn in mice) and ATR. Due to their essential nature in cellular function, null mutation of Nbn and ATR in mice lead to embryonic lethality 14, 15. Although mice with hypomorphic mutations of Nbn are viable, they do not show obvious brain phenotypes seen in human NBS 16. When we specifically deleted Nbn in mouse central nervous system (CNS) using Cre-loxP, these mice (NbnCNS-del mice) exhibited growth retardation and early onset of cataracts 17. The most striking phenotype of these mice is an early postnatal ataxia caused by the agenesis of the cerebellum with decreased proliferation in neuronal progenitors, and massive cell death in cerebellar neuronal cells 18. In addition, NbnCNS-del mice displayed microcephaly and severely affected white matter integrity, retina and astrocyte functionality 19, 20, 21. However, the nature of cerebral reduction and the underlying molecular mechanism in NbnCNS-del mice have not been investigated.
Macroscopically, the size and shape of the cerebrum was greatly reduced in the NbnCNS-del mice compared to its counterpart starting from postnatal day 7 (P7), becoming more evident at P14 and P21. The maximum width of hemisphere in 2-month-old NbnCNS-del and NbnCNS-ctr mice is around 4.3 ± 2 mm and 5.2 ± 2.3 mm, respectively (averaged from more than 20 mice of each group, P < 0.01 (t-test), Figure 1A). To study the effect of neuronal deletion of Nbn in cerebrum, we performed histological analysis on the NbnCNS-del brain between P7 and P21 and revealed a general (~20%) reduction in thickness of the cerebral cortex compared to their littermate controls (Figure 1B). To examine the distinct morphological identities of cerebral cortex in details, we performed immunostaining with a neuronal-specific marker, neuronal nuclei (NeuN; Figure 1C). The cortex of the control mice is characterized by six laminas, which could be distinguished by packing density and neural morphology (Figure 1C). This laminar cortical structure was altered in NbnCNS-del mice (Figure 1C). Although the layer I that contains Cajal-Retzius cells was similar to that in the NbnCNS-ctr cortex, the thickness of layer II/III that contains small pyramidal cells was reduced with less neuron cellularity (~76% of that in the NbnCNS-ctr cortex, Figure 1C and and1D).1D). In addition, layers IV and V, where granule cells (GC) and large pyramidal cells localize, respectively, were less recognizable and their thickness and the cellularity was also decreased (~78% of that in the NbnCNS-ctr cortex, Figure 1C and and1D).1D). However, the layer VI contained the similar number of polymorphic cells compared to that in NbnCNS-ctr cerebral cortex (Figure 1C and and1D1D).
Similar to NBS patients, the thickness of the corpus callosum (CC) was reduced in NbnCNS-del brain (Figure 1B, ,1E1E and and1F).1F). As CC is composed by tightly packed neural axon wrapped with myelin sheath of glial cells, we further examined myelin basic protein (MBP) and found that the density and thickness of MBP-stained neural fibers were markedly decreased (Figure 1E). There was a dramatic reduction of the number of medial habenular neurons (Mhb) (Figure 1B), and mild alterations of the fasciole cinereum (fc) in NbnCNS-del mice (Figure 1B). The size of thalamic and hypothalamic region in NbnCNS-del mice was also proportionally reduced compared to that in control brains (Figure 1B). Neurons in the CA1, CA3 field and dentate gyrus (DG) of NbnCNS-del hippocampus were less densely packed from P7 to P21 (Figure 1E). In addition, NbnCNS-del mice displayed an increased number of neurons in the polymorph layer DG (PoDG, Figure 1E). The microcephaly has been observed in NbnCNS-del mice of 129/SV × C57/BL6 mixed background originated from two independent ES clones.
Strikingly, NbnCNS-del mice displayed a severely altered olfactory bulb (OB). At low magnification, NeuN immunostaining showed that the morphology of the NbnCNS-del OB differed from that of the NbnCNS-ctr mice (Supplementary information, Figure S1A). For instance, in the NbnCNS-ctr OB, each cell population was laminated at the defined structure, whereas NbnCNS-del OB displayed a reduced cellularity and less defined laminar structure (Supplementary information, Figure S1A, left panel). Further examination of the OB structure under high magnification revealed three major differences between NbnCNS-ctr and NbnCNS-del mice. First, although olfactory nerve layer (ONL) and glomerular layer (GL), where the dendrites of second-order neurons form spheroidal structure, glomeruli, were present in NbnCNS-del mice, the number of the periglomerular neurons was reduced (arrows, Supplementary information, Figure S1A). Second, the superficial external plexiform layer (EPL) and the laminar structure of the mitral cell layer (ML) were less defined in the NbnCNS-del mice (Supplementary information, Figure S1A). Third, a significant decrease in the number of GCs was observed in all NbnCNS-del OBs analyzed from P1 to P21 (Supplementary information, Figure S1A and data not shown).
The OB is formed postnatally 22. Immature neurons generated from neural stem cells in the subventricular zone (SVZ) migrate towards each other in chains through the rostral migratory stream (RMS) to the OB (Supplementary information, Figure S1B). To investigate the defect of olfactory neurogenesis in NbnCNS-del mice, we pulse labeled mice with bromodeoxyuridine (BrdU). From P0 to P7, proliferating neuroprogenitors in the SVZ of the lateral ventricles (LV) were greatly reduced in the NbnCNS-del mice compared to that in the controls (Supplementary information, Figure S1B). In addition, BrdU-positive neurons in the RMS were also reduced in the NbnCNS-del mice compared to that in the controls (Supplementary information, Figure S1B).
Nbs1 is a key DDR molecule and DDR is critical for the development of the CNS 23. We next evaluated the level of endogenous DNA damage in NbnCNS-del neocortex by immunohistochemical analysis on a DNA strand break marker, phosphorylated H2AX (γH2AX). In contrast to NbnCNS-ctr neocortex, increased γH2AX not only occurred in proliferating neural precursor cells at ventricular zone (VZ), but also aggregated in postmitotic neurons at the mantle zone (MZ) of Nbn-deficient brain (Figure 2A). This suggests that Nbs1 deficiency leads to accumulation of endogenous DNA damage in line with spatial and temporal proliferation pattern during the cerebral development. Therefore, we speculated that stalled replication forks during cell proliferation and oxidative damage from cellular metabolism contribute to physiological endogenous DNA damage, which could activate ATM/ATR signaling through Nbs1 or MRN complex and subsequently induce activation of downstream substrate p53 to control cell proliferation and/or apoptosis (Figure 2B).
We further explored the role of Nbs1 deficiency in ATM and ATR signaling during cerebral genesis in vivo. As proliferation of cerebral neuroprogenitors in ventricular zone start at E11-E12, we analyzed damage response signaling in embryonic cerebra from E12.5 to E18.5 by western blotting. We found an efficient deletion of Nbs1 after E12.5, and nearly complete absence of Nbs1 protein at E15.5 and E18.5 (Figure 2C). Notably, ATR-mediated phosphorylation of Chk1 at serine-345 (Chk1-S345p) in NbnCNS-del embryonic cortex (E15.5-E18.5) was largely compromised (Figure 2C). However, compatible with the NbnCNS-ctr brain, endogenous DNA damage in the NbnCNS-del brain activated ATM indicated by phosphorylation of ATM at serine-1987 (ATM-S1987p, equivalent to Ser1981 of human ATM), and also phosphorylated its downstream target Chk2 (Supplementary information, Figure S2).
To further investigate Nbs1-mediated activation of ATR signaling at a single cell level, we analyzed the phosphorylation of Chk1 (Chk1-S345p) in primary cultured neural progenitors verified by nestin immunoactivity (Figure 3A). In response to hydroxylurea (HU)-induced replication fork blockage, Chk1-S345p was recruited to the sites of replication fork and formed foci in Nbs1-proficient neurons (Figure 3A). Consistent with western blot analysis (Figure 2C), Nbs1-deficient neurons were devoid of Chk1-S345p foci in response to HU-induced replication fork blockage (Figure 3A). As Nbs1 and ATR have been shown in regulating BRCA1 protein focus formation responding to DNA damage 24, 25, immunofluorescence staining of BRCA1 revealed that replication fork blockage caused by HU failed to induce BRCA1 foci in Nbs1-deficient neurons (Figure 3B). However, Nbs1 deficiency did not affect the phosphorylated histone H2AX (γH2AX) focus formation in HU-treated developing neuron (Figure 3C). The nature of Nbs1-deficient primary neuron was verified by the lack of Mre11 and Rad50 foci, and Mre11 retained in the cytoplasm in the absence of Nbs1 in response to replication blockage (Figure 3D and data not shown). These results indicate that in neocortex, Nbs1 deficiency mainly affects ATR-mediated DNA damage response.
Since ATM-Chk2 signaling remains functional in Nbs1-deficient neocortex (Supplementary information, Figure S2), we next explored the consequence of phosphorylation of ATM and Chk2 occurring in Nbs1-deficient developing cortex. Immunostaining and western blot analysis of ATM downstream target p53 revealed an accumulation of the p53 protein in the VZ and MZ in Nbs1-deficient developing cortex (Figure 4A and and4B).4B). In addition, immunoactivity of p21 and its mRNA level were detected in the VZ and MZ of Nbs1 mutant mice (Figure 4A and and4C),4C), suggesting a defective proliferation of cortical neuroprogenitors. To further confirm the impact of increased p53 and p21 on cell proliferation, we performed histological assay by in vivo labeling with BrdU. During neurogenesis, proliferating neuroprogenitors (BrdU-positive cells) at VZ exit from cell cycle and migrate to the MZ, becoming postmitotic neurons (Figure 4D). Consistent with the role of Nbs1 in cerebellar neuroprogenitors 18 and in the lens epithelium 17, Nbs1 deficiency led to a significant reduction of BrdU-positive neuroprogenitors at E12.5 and E15.5 compared to their NbnCNS-ctr counterparts (Figure 4D and and4E,4E, data not shown).
Since p53 activation by Nbs1 deficiency leads to massive apoptosis in cerebella 18, we next evaluated the cell death in NbnCNS-del neocortex. Histological analysis of NbnCNS-del and control neocortex revealed no apparent pyknotic cells from E15.5 (Figure 5A) to E18.5 (data not shown), and negative for active caspase 3 immunoactivity. On the contrary, pyknotic cells with fragmented nuclei that are positive for active caspase 3 immunoactivity were frequently observed in NbnCNS-del medullar oblongata compared to that in NbnCNS-Ctr mice (Figure 5A, active caspase 3 positive cells/field at 40× original magnification: 12.4 ± 2.3 versus 1.4 ± 1.1, n = 8, P < 0.001).
In NbnCNS-del brain, although p53 was activated ubiquitously (Figure 4A), the impact of Nbs1 deficiency on neuronal apoptosis in different regions of the brain seems different. DDR-mediated p53 activation determines cellular outcome by regulating the expression of diverse genes that control cell cycle arrest and apoptosis. To explore the molecular mechanism of its functional diversities in apoptotic response, we first examined the expression levels of p53 proapoptotic targets, such as Bax, Noxa and Puma. Although the expression levels of Bax, Noxa and Puma proteins were significantly increased in Nbs1-deficient cerebella at P7 (as for positive control of apoptosis 18, Figure 5B), activation of p53 did not induce the expression of these proapoptotic proteins in neocortex of E13.5 embryos and cerebral cortex at P7 (Figure 5B). Notably, expression of antiapoptotic molecule Bcl-2 in Nbs1-deficient neocortex at E13.5 and cerebral cortex at P7 was comparable to that in Nbs1 control mice.
To further investigate the changes of p53-dependent proapoptotic proteins in NbnCNS-del brain were regulated at the transcriptional level, total RNAs from mouse neocortex and cerebella were subjected to quantitative real-time PCR analysis. Nbs1 deficiency significantly increased Bax, Noxa, and Puma mRNA levels in cerebella at P7 (Figure 5C), but had no obvious effect on these gene expression in neocortex at E15.5 (Figure 5D) and in cerebral cortex at P7 (Supplementary information, Figure S3).
Recent studies suggest that transactivation of p53-dependent target genes can be modulated by different p53-interacting partners, thereby regulating cell cycle arrest and/or apoptosis 26. It has been shown that hematopoietic zinc finger (Hzf), a zinc finger-containing p53 target gene, is induced by genotoxic and oxidative stress in a p53-dependent manner. Upon binding to p53, Hzf preferentially transactivates pro-arrest p53 target genes like p21 over its proapoptotic target genes such as Bax, Noxa and Puma, resulting in growth arrest and apoptosis inhibition 27. Thus, the ability of p53 to recruit to the promoters of cell cycle arrest target genes is directly regulated by Hzf. To investigate whether Hzf plays a role in Nbs1-deficient neuron, we first performed immunostaining for Hzf in Nbs1-deficient and -proficient neocortex at E12.5 and E15.5. Concomitant with p53 activation, the expression of Hzf was very high in the VZ of NbnCNS-del developing cortex but was nearly absent in NbnCNS-ctr neocortex at E12.5 (Figure 5E). Although Das et al. has demonstrated in vitro that following prolonged exposure to DNA damage or extended p53 expression/activation leads to Hzf protein degradation, which in turn induces activation of proapoptotic p53 targets such as Bax, Puma and Noxa, resulting in apoptosis, we found that the induction of Hzf by p53 activation existed persistently in NbnCNS-del neocortex from E12.5 to E15.5, but not in medulla oblongata and primordial cerebellar neurons (Figure 5E and data not shown). Western blot analysis also showed that expression of Hzf was profoundly upregulated both in E15.5 and P7 NbnCNS-del cortex, but neuronal Nbs1 deficiency did not affect the expression of Hzf in cerebella at P7 (Figure 5F). This suggests that Hzf appears a different pattern of expression in response to endogenous DNA damage caused by Nbs1 deficiency during neurogenesis.
In addition to Hzf, we also analyzed other p53-interacting proteins in Nbs1-deficient neocortex. ASPP family members ASPP1 and ASPP2 interact with p53 and specifically enhance p53-induced apoptosis 28, while their inhibitor iASPP prevents p53 transcriptional activity from proapoptotic promoters by competing with ASPP1 and ASPP2 to bind p53 29. The human cellular apoptosis susceptibility protein hCAS/CSE1L associates with chromatin and regulates induction of selective p53 target genes and apoptosis 30. In contrast to Hzf expression in NbnCNS-del cortex and cerebella, the expression of ASPP2, iASPP and hCAS/CSE1L remained unchanged compared to that in control mice (Figure 5G). Thus, Hzf likely plays a key role in sustaining p53-mediated cell cycle arrest and defective proliferation of neuroprogenitors in Nbs1-deficient neocortex.
DNA damage in different areas of NbnCNS-del brain induces activation of ATM target p53 protein (Figures 4A, ,4B4B and and6A),6A), which controls genes expression, leading to developmental defects of brain 18. To further evaluate the potential role of p53 in Nbs1-deficient microcephaly, we introduced Trp53 mutations in NbnCNS-del mice. Histopathological analysis of NbnCNS-del;Trp53+/+ cerebra revealed microcephaly and all identical cerebral defects seen in NbnCNS-del mice (data not shown). Trp53 heterozygosity had a marginal effect on the loss of brain weight and cerebral development defects in NbnCNS-del mice (Figure 6B and and6C;6C; data not shown). Notably, null mutation of Trp53 significantly increased brain weight (Figure 6B), and substantially rescued the thickness of cortex (Cx) and CC in NbnCNS-del mice (Figure 6C). Moreover, null mutation of Trp53 largely increased granule cell numbers and improved the laminar structure in NbnCNS-del OB (Supplementary information, Figure S1C).
To further understand the role of p53 on Hzf expression in Nbs1-deficient brain, we next investigated the expression level of Hzf in Nbn/Trp53 double mutant cortex and cerebella. Consistent with Nbs1-deficient neocortex, NbnCNS-del;Trp53+/− cortex displayed an increased expression level of Hzf (Figure 6D), and Trp53 null mutation markedly reduced Hzf expression in NbnCNS-del cortex. Interestingly, Trp53 null mutation did not affect the expression of Hzf protein in NbnCNS-del cerebella (Figure 6D), implying that during neurogenesis p53-induced Hzf expression in NbnCNS-del brain is indeed in a region-specific manner.
In the present study, we have shown that neural inactivation of Nbs1 leads to microcephaly in mice characterized by reduced size of cerebral cortex and thickness of CC, resembling neuronal abnormalities of human NBS patients 31.
Development of the cerebral cortex is a strictly regulated process whereby neural progenitor cells from the proliferative pseudostratified ventricular zone go through massive expansion before they exit the cell cycle and form cortical neurons 32. Neuroprogenitors are rapidly proliferating and potentially generate high level of oxidative damage, which may lead to a high level of lesions encountered at the replication fork 33. Several pathways may execute to recognize and repair these lesions, unrepaired DNA strand breaks can cause detrimental outcome, including chromosomal instability, cell death, developmental defects and neoplastic transformation 34. In particular, the nervous system is susceptible to DNA repair deficiency, which can lead to neurodegeneration, microcephaly or brain tumors 33. Our study using developmental brain provides direct evidence that endogenous DNA damage caused by SSBs/replication fork blockage or DSBs activates ATR-Chk1 and ATM-Chk2-p53 pathways. Thus, it is likely that both ATM and ATR pathways participate in monitoring endogenous DNA damage during neurogenesis (see Figure 7).
It has been shown that Nbs1 is required to modulate ATM or ATR activation in vitro and in vivo 3, 8, 11, 25, 35. Notably, we show in the present study that Nbs1 dysfunction impairs the ATR-Chk1 signaling (see Figures 2 and and3),3), rather than the ATM-Chk2 pathway (see Supplementary information, Figure S2). It is likely that during neurogenesis, endogenous DNA damage caused by Nbs1 deficiency mainly leads to SSBs, such as replication fork blockage that activate ATR pathway. Although MRN complex activate ATM kinase 3, deletion of Nbs1 retained accumulation of Mre11 at cytoplasmic compartment, presumably inactivating the MRN function 36 (see Figure 3D). However, it has been shown recently that in neuroprogenior cells, ATM activation responding to DNA damage may not require Nbs1 37. Thus, defects in ATR-Chk1 signaling in Nbs1-deficient neocortical neurons may convert unrepaired replication fork to DSBs and result in a progressive accumulation of persistent DSBs throughout the brain, which in turn activate cell cycle checkpoint mediated by ATM-p53 pathway, leading to proliferation defects and microcephaly 38 (see Figure 7). In supporting this hypothesis, inactivation of Trp53 largely rescues microcephaly in NbnCNS-del brain.
We have shown previously that Nbs1-deficient cerebellar neuroprogenitors are susceptible to DNA damage and postmitotic neurons with accumulation of DNA damage and chromosomal aberrations are cleared by massive cell death through activation of ATM-p53 signaling that leads to agenesis of cerebellum 18. In the present study, although Nbs1-deficient cortical neuroprogenitors are susceptible to endogenous DNA damage that slows down proliferation (see Figure 4), distinct from cerebellar and medulla oblongata neurons, neocortical postmitotic neurons are more tolerable to DNA damage-induced cell death (see Figure 5A). Thus, the cerebrum continues to develop into microcephaly, which is likely due to proliferation defects. This functional difference of neurons in a specific region to endogenous DNA damage may be caused by a specific overactivation of Hzf upon ATM-p53 signaling in neocortex (see Figure 5), which favors cell cycle arrest over apoptosis by selectively recruiting p53 to promoters of pro-arrest target gene such as p21, resulting in proliferation arrest 27. In contrast, in Nbs1-deficient cerebella endogenous DNA damage enhanced p53-mediated cell death and proliferation arrest. Therefore, Hzf acts both as a p53 target (Figure 6) and as an important regulator in p53-mediated cell fate determination during cortical neurogenesis (see Figure 7). Thus, this study may partly explain the respective neuropathology in human that neurons at different regions of brain respond differently to endogenous DNA damage during neurogenesis.
In conclusion, the present study shows a role of Nbs1 in neocortical neurons by regulating ATR-Chk1 pathway in monitoring endogenous DNA damage. Neuronal Nbs1 deletion causes defective proliferation by activation of p53-Hzf signaling in neocortex, but not p53-mediated proapototic pathway, leading to microcephaly, and neurons display a region-specific response to endogenous DNA damage during neurogenesis. Thus, Nbs1-deficient mice present a useful model for further dissection of the molecular mechanisms of human NBS.
The generation and genotyping of Nbs1F6/F6;nestin-Cre+ (referred to as NbnCNS-del) and Trp53-deficient NbnCNS-del mice has been described previously 18. All animal experiments were approved by and performed in accordance with the guidelines of the International Agency for Research on Cancer's Animal Care and Use Committee and IBMS/PUMC's Animal Care and Use Committee.
Animals were euthanized by carbon dioxide at the indicated time points. Whole mouse brains were fixed in 4% paraformaldehyde, followed by dehydration and paraffin embedding. Histopathological analysis was carried out on 3-μm-thick sections stained with hematoxylin and eosin (H&E). Immunohistochemical staining was performed as described previously 39. Antibodies included those specific for: mouse anti-NeuN (Millipore, Chemicon, Temecula, USA), rabbit anti-γH2AX (Abcam, Cambridge, UK), mouse anti-5-bromo-2′-deoxyuridine (BrdU, Sigma, Steinheim, Germany), rabbit anti-p53 (NovoCastra, Newcastle, UK), mouse anti-p21 (BD Pharmingen, San Jose, USA), and rabbit anti-active caspase 3 (Cell Signaling Technology, Danvers, USA), mouse anti-Hzf (Abnova, TaiPei, Taiwan). For the in vivo proliferation assay, we injected pregnant females intraperitoneally with 50 μg BrdU/g body weight. Embryos were collected 6 h after injection and fixed in 4% paraformaldehyde.
Quantifications of BrdU and active caspase-positive cells were performed from at least 5 to 10 embryos of each genotype, six high power fields (×40) of each, and the thickness of CC was measured at a point between CA1 and CA3 using a Zeiss Axioskop fluorescence microscope.
Proteins extracted from tissue and cells in RIPA buffer (20 mM HEPES pH 7.6, 20% glycerol, 0.5 M NaCl, 1.5 mM MgCl2, 0.2 mM EDTA pH 8.0, 0.5% NP-40, 1 mM DTT, 1 mM PMSF, 5 μg/ml leupeptin, 2 μg/ml aprotinin, 1mM β-glycerolphosphate, 1 mM Na3VO4 and 10 mM NaF) were resolved by SDS-PAGE, blotted and stained with antibodies in TBST containing 5% non-fat dried milk, followed by incubation with horseradish peroxidase-conjugated secondary antibodies and detected by the ECL reagents (Amersham Biosciences). The following antibodies were used: rabbit anti-Nbs1 (Oncogene, Swampscott, USA), mouse anti-ATM (Novus, Littleton, USA), mouse anti-ATM-S1987p (Rockland, Gilbertsville, USA), mouse anti-Chk2 (Millipore, Upstate, Temecula, USA), mouse anti-PARP-1 (R&D systems, Minneapolis, USA), rabbit anti-ATR (Novus), rabbit anti-Chk1-S345p (Cell Signaling Technology), rabbit anti-Puma (Abcam), rabbit anti-Noxa (Abcam), rabbit anti-Bax (Millipore, Upstate, Temecula, USA), rabbit anti-Bcl-2 (Millipore, Upstate, Temecula, USA), mouse anti-p53 (Cell Signaling Technology, Danvers, USA), rabbit anti-Hzf (Santa Cruz Biotechnology, Santa Cruz, USA), mouse anti-ASPP2 (Sigma, St Louis, USA), mouse anti-iASPP (Sigma), rabbit anti-hCAS/CSE1L (Abcam) and mouse anti-β-actin (Santa Cruz Biotechnology).
Primary neurons from embryonic cortex at E13.5 were cultured as described previously 18. To induce focus formation, cells were plated onto poly-D-lysine-coated coverslips, treated with or without 2 mM HU for 3 h, and fixed. Immunofluorescence staining was performed as described previously 40. Briefly, cells were washed once in PBS with 1 mM glycerolphosphate, 1 mM Na3VO4, 10 mM NaF and 1 mM PMSF, and further treated with a hypotonic lysis solution containing 10 mM Tris-HCl pH 7.4, 2.5 mM MgCl2, 1 mM PMSF, 1 mM glycerolphosphate, 1 mM Na3VO4, 10 mM NaF and 0.5% Nonidet P-40 for 8 min on ice. Subsequently cells were fixed in ice-cold acetone-methanol (1:1) for 30 min on ice. The slides were then incubated with appropriate primary antibody in TBST containing 5% non-fat dried milk. Slides were mounted in Vectashield mounting medium with DAPI (Vector Laboratories) and visualized under a Zeiss Axioskop fluorescence microscope equipped with a CCD imaging system (IP Lab Spectrum). A cell with at least five distinct foci in the nucleus was scored as focus positive, and at least 150 cells per staining were analyzed. Antibodies were specific for: mouse anti-nestin (Millipore, Chemicon, Temecula, USA), rabbit anti-phosphorylated H2AX (γH2AX, Millipore, Upstate, Temecula, USA), rabbit anti-Mre11 (Novus), rabbit anti-Chk1-S345p (Cell Signaling Technology) and rabbit anti-BRCA1 41.
Total RNA was extracted from E15.5 mouse neocortex, P7 cerebella and cerebral cortex in TRIzol (Invitrogen), followed by chloroform extraction. First-strand cDNA synthesis from total RNA template (2 μg) was performed with ReverTra Ace qPCR RT Kit (TOYOBO), oligo dT and random primers. The cDNA was amplified with a Bio-Rad iQTM5 Multicolor Real-Time PCR Detection System, using SYBR Green Realtime PCR Master Mix (TOYOBO) and PAGE-purified primers (invitrogen). Primer sequences were as follows: p21 (forward: 5′-ACATCTCAGGGCCGAAAAC-3′ reverse: 5′-CCTGACCCACAGCAGAAGA-3′), Puma (forward: 5′-CGTGTGGAGGAGGAGGAGT-3′ reverse: 5′-GGGAGGAGTCCCATGAAGA-3′), Noxa (forward: 5′-TGGAGTGCACCGGACATAAC-3′ reverse: 5′-AGCACACTCGTCCTTCAAGTCT-3′), Bax (forward: 5′-GCAGAGGATGATTGCTGACG-3′ reverse, 5′- GGGCCTTGAGCACCAGTTT-3′), and β-actin (forward: 5′-TGTTACCAACTGGGACGACA-3′ reverse: 5′- GGGGTGTTGAAGGTCTCAAA-3′).
All data were presented as mean values and standard error of mean (SEM). Differences between groups were compared by analysis of variance followed by t test using Sigma plot software. P value < 0.05 was considered to be statistically significant.
This work was initiated in the International Agency for Research on Cancer (IARC), Lyon, France. We thank D Galendo (IARC) for the maintenance of the animal colonies, PO Frappart, N Lyndrate, C Carreira (IARC), L Lin and SY Hu (IBMS/PUMC) for technical support. We are also grateful to Dr E van Dyke (IARC) for helpful discussions and Dr CX Deng (NIH, USA) for BRCA1 antibody. This work was supported in part by La Ligue Nationale contre le Cancer, France, IBMS/PUMC Director's Fund (2007RC03), the National Natural Science Foundation of China (30970602), the National Novel Drug Development Fund (2009ZX09303-008) and 111 Project (B08007). ZQW is supported by Association for International Cancer Research (AICR), UK and the Deutschen Forschungsgemeinschaft (DFG), Germany. YGY is supported by the Hundred Talents Program of the Chinese Academy of Sciences.
(Supplementary information is linked to the online version of the paper on the Cell Research website.)
Nbs1 deficiency disrupted laminar structure and reduced cellularity of olfactory bulb.
Western lot analysis of ATM and Chk2 in Nbs1-deficient developing brain.
Nbs1 deficiency has no obvious effect on expression levels of p53-mediated proapoptotic target genes Bax, Noxa, Puma in P7 Nbs1-deficient cerebral cortex.