Maternal gene Ooep may participate in homologous recombination-mediated DNA double-strand break repair in mouse oocytes

Da-Jian He,Lin Wang,Zhi-Bi Zhang,Kun Guo,Jing-Zheng Li,Xie-Chao He,Qing-Hua Cui,Ping Zheng,＊

1 Yunnan Key Laboratory of Animal Reproduction,Kunming Institute of Zoology,Chinese Academy of Sciences,Kunming Yunnan 650223,China

2 Laboratory of Biochemistry and Molecular Biology,School of Life Sciences,Yunnan University,Kunming Yunnan 650091,China

3 Kunming College of Life Science,University of Chinese Academy of Sciences,Kunming Yunnan 650204,China

ABSTRACT DNA damage in oocytes can cause infertility and birth defects.DNA double-strand breaks(DSBs)are highly deleterious and can substantially impair genome integrity.Homologous recombination(HR)-mediated DNA DSB repair plays dominant roles in safeguarding oocyte quantity and quality.However,little is known regarding the key players of the HR repair pathway in oocytes.Here,we identified oocyte-specific gene Ooep as a novel key component of the HR repair pathway in mouse oocytes.OOEP was required for efficient ataxia telangiectasia mutated(ATM)kinase activation and Rad51 recombinase(RAD51)focal accumulation at DNA DSBs.Ooep null oocytes were defective in DNA DSB repair and prone to apoptosis upon exogenous DNA damage insults.Moreover,Ooep null oocytes exhibited delayed meiotic maturation.Therefore,OOEP played roles in preserving oocyte quantity and quality by maintaining genome stability.Ooep expression decreased with the advance of maternal age,suggesting its involvement in maternal aging.

Keywords:Ooep;Homologous recombination;DNA double-strand break repair;ATM;RAD51

INTRODUCTION

During the long period of meiotic arrest,oocytes are exposed to endogenous and exogenous genotoxic insults and tend to accumulate DNA damage.DNA damage can occur as single-stranded breaks(SSBs)or double-strand breaks(DSBs),the latter of which are highly deleterious and can substantially impair genomic integrity and cell viability. Two major pathways are involved in DNA DSB repair,non-homologous end joining(NHEJ)-and homologous recombination(HR)-mediated repair. In oocytes,defection of the error-free HR pathway can cause a decline in oocyte quantity and quality in natural and pathological reproductive aging in both mice and humans(Day et al.,2015;Perry et al.,2013;Titus et al.,2013;Wang et al.,2014).Therefore,HR-based DNA DSB repair in oocytes plays a key role in regulating female reproductive performance.This repair has been intensively studied in somatic cells,with many players identified(Adamson et al.,2012);however,little information is available regarding the components of the HR repair pathway in oocytes.Identifying essential participants will shed light on understanding oocyte and ovarian aging.

Oocyte-expressed protein(Ooep)is an oocyte-specific maternal-effect gene. The OOEP protein localizes at the subcortical region of an oocyte and interacts with four other maternal proteins,including MATER,FILIA,PADI6,and TLE6,to form a subcortical maternal complex(SCMC)in mouse and human oocytes(Li et al.,2008;Zhu et al.,2015).Depletion of OOEP or its interaction proteins can lead to embryo arrest at the 2-cell stage with uncharacterized molecular mechanisms in mice(Li et al.,2008;Tong et al.,2000;Yu et al.,2014;Yurttas et al.,2008;Zheng&Dean,2009). We recently utilized mouse embryonic stem cells as a model to explore the function of FILIA and uncovered its critical roles in safeguarding the genomic stability of pluripotent stem cells(Zhao et al.,2015).This finding prompted our hypothesis that OOEP may be involved in regulating genome stability in oocytes.Thus,in this study,we carefully examined the function of OOEP in DNA DSB repair in oocytes.

MATERIALS AND METHODS

Animals

The mouse line with targeted mutation of Ooep(background C57BL/B6×Sv129)was kindly provided by Dr.Jurrien Dean from the National Institutes of Health,USA.These Ooeptm/tmfemale mice do not express the OOEP protein in oocytes(Li et al.,2008).Mice were maintained in specific pathogen-free conditions. All experimental procedures and animal care were performed according to the protocols approved by the Ethics Committee of the Kunming Institute of Zoology,Chinese Academy of Sciences.

DNA damage treatment of oocytes and ovaries

Germinal vesicle(GV)-stage oocytes were cultured according to standard procedures(Marangos&Carroll,2012).Ovaries were collected from newborn mice at postnatal day 5(P5)and cultured according to standard protocols(Gonfloni et al.,2009).

Antibodies

Rabbit anti-OOEP serum was raised against the 1–19 amino acids of the OOEP protein(Li et al.,2008),and antibody specificity was verified by utilizing Ooep null oocytes.Other primary and secondary antibodies were obtained commercially,with relevant information shown in Table 1.

Table 1 Information on primary and secondary antibodies for immunofluorescence staining(IF)and immunoblotting(IB)

Immunofluorescence staining and foci intensity quantification

Immunofluorescence staining of oocytes and ovaries was performed according to standard procedures(Guo et al.,2016;Xiong et al.,2008). DNA was labeled with 4′,6-diamidino-2-phenylindole(DAPI,Sigma,Germany).Images were analyzed using FV10-ASW 2.1 viewer software.The intensities of the foci were quantified using Image J software.

Comet assay

Alkaline comet assay was performed according to standard procedures(Berthelot-Ricou et al.,2011;Tice et al.,2000).Comets were analyzed using CASP comet assay analysis software(Andor Technology,UK).Three independent repeats were performed.

Detection of apoptosis by TUNEL staining

Frozen ovarian sections were permeabilized with 0.1%Triton X-100 in phosphate-buffered saline(PBS),followed by incubation with the TUNEL reaction solution from the In-Situ Cell Death Detection Kit,Fluorescein(Roche Diagnostics,USA).All staining procedures were performed according to the manufacturer’s instructions.DNA was labeled with DAPI.

Hematoxylin and eosin(HE)staining and primordial and primary follicle counting

Ovarian sections were incubated with the HE reaction solution(BOSTER,USA)at room temperature(RT).All staining procedures were performed according to the manufacturer’s instructions.Oocytes residing in primordial and primary follicles were counted,as described previously(Myers et al.,2004;Skaznik-Wikiel et al.,2007).

Construction of OOEP-GFP expression plasmid

The protein-coding region of Ooep was amplified by polymerase chain reaction (PCR) and inserted into pc DNA3.1/CT-GFP-TOPO(Invitrogen,USA).Integrity was confirmed by DNA sequencing.

In vitro transcription and mRNA microinjection of GV oocytes

Ooep-Gfp expressing plasmids were linearized with ScaI(New England Biolabs,USA).The mRNA was synthesized using an in vitro transcription kit(mMessage mMachine T7 kit,Ambion,USA),and purified with a RNeasy MinElute Cleanup Kit(Qiagen,Germany).The mRNA was then dissolved in nuclease-free water and stored at?80°C.We microinjected 500 ng/μL of mRNA in injection buffer(10 mmol/L Tris-HCl(pH 7.5)and 0.1 mmol/L EDTA)into the cytoplasm of Ooep-/-GV oocytes.

Single-oocyte c DNA amplification and quantitative RT-PCR

Briefly,c DNA was prepared from a single GV oocyte and amplified by 20 cycles of PCR according to published protocols(Tang et al.,2010).Glyceraldehyde 3-phosphate dehydrogenase(Gapdh)was used as the housekeeping control.Primers for amplification of Gapdh and Ooep included:Ooep forward:5′-GTCATAGGCACAGACCAAGCG-3′,Ooep reverse:5′-GGCCGCCATGTTCAAGAGAAT-3′;Gapdh forward:5′-TTGAGGTCAATGAAGGGGTC-3′,Gapdh reverse:5′-TCG TCCCGTAGACAAAATGG-3′.GraphPad Prism 5 software was used for statistical analysis.

Statistical analyses

Quantitative analyses were based on at least three independent repeats and results were represented as means±SEM.Data were first tested by the homogeneity of variance test. For non-normal distribution,the data were subjected to nonparametric tests.Otherwise,the data were analyzed by t-tests.We considered P＜0.05 as statistically significant.

RESULTS

Ooep participates in DNA double-strand break repair in mouse oocytes

Upon DNA damage,histone H2AX is phosphorylated at Ser139(γ-H2AX)and recruited to the damaged sites to form visible foci under confocal microscopy(Rogakou et al.,1998).γ-H2AX foci formation is generally considered as a marker of DNA damage.In the fully-grown GV oocytes,depletion of OOEP caused a significant increase in γ-H2AX foci intensity compared to wild-type oocytes(Figure 1A),suggesting more endogenous DNA damage in Ooeptm/tmoocytes.To validate this observation,we performed comet assay,an unambiguous method that measures the extent of DNA damage on a single cell basis(Berthelot-Ricou et al.,2011;Tice et al.,2000).The GV oocytes from Ooeptm/tmfemales displayed significantly longer comet tails than those from the wild-type counterparts(Figure 1B),confirming that Ooeptm/tmoocytes contained more endogenous DNA damage.

Figure 1 Ooep depletion causes DNA damage in mouse oocytes

The accumulation of DNA damage in Ooeptm/tmoocytes suggested inefficiency in DNA damage repair.To test this hypothesis,we treated wild-type and mutant GV oocytes with 50μg/mL of etoposide,a topoisomerase II inhibitor,to induce DNA DSBs(Marangos&Carroll,2012;Nagy&Soutoglou,2009),and compared the dynamics of γ-H2AX resolution.Immediately after treatment,wild-type and mutant oocytes had comparable γ-H2AX levels,as measured by immunostaining(Figure 2A)and immunoblotting analyses(Figure 2B).Following several hours of DNA repair recovery,γ-H2AX was significantly resolved in the wild-type oocytes,reflecting efficient DNA damage repair. In sharp contrast,γ-H2AX remained at a higher level in the Ooeptm/tmoocytes than in the wild-type oocytes,indicating compromised DNA damage repair(Figure 2A,B).To further validate the role of OOEP in DNA damage repair,we performed a rescue experiment by micro-injecting Gfp(green fluorescent protein)-tagged Ooep mRNA into the Ooeptm/tmoocytes.Consistently,the OOEP-complemented oocytes resolved γ-H2AX more efficiently than the Ooeptm/tmoocytes after etoposide treatment and recovery(Figure 2C).These data together support the notion that maternal protein OOEP is necessary for efficient DNA DSB repair in oocytes.In line with this role,the protein expression of OOEP was slightly induced by etoposide treatment in GV oocytes(Figure 2D).

Figure 2 Ooep participates in DNA double-strand break repair in mouse oocytes

Ooep may be involved in HR-mediated DNA DSB repair

In oocytes,DNA DSB is predominantly repaired via the HR-mediated pathway,in which ataxia telangiectasia mutated(ATM)kinase plays a central orchestration role(Oktay et al.,2015;Titus et al.,2013).ATM activation by DSBs initiates robust checkpoint signaling as well as DSB repair processes in somatic cells(Behrens et al.,2014;Jackson&Bartek,2009)and germ cells(Di Giacomo et al.,2005;Oktay et al.,2015).In mouse GV oocytes,ATM can be activated by certain levels of etoposide-induced DNA DSBs.We therefore treated the oocytes with 50μg/mL of etoposide for 3 h,as per previous study(Marangos&Carroll,2012),and examined the effect of OOEP on ATM activation by phosphorylation at serine 1981 residue(p-ATM)(Lavin&Kozlov,2007).Co-immunostaining analysis showed that fewer p-ATM foci were formed and co-localized with γ-H2AX foci in the Ooeptm/tmoocytes than in the wild-type oocytes,despite γ-H2AX level being comparable(Figure 3A).Immunoblotting analysis of p-ATM further validated this observation.Under normal conditions,very little p-ATM was detected in either wild-type or mutant oocytes.However,higher levels of p-ATM were induced in wild-type oocytes compared with mutant oocytes following etoposide treatment(Figure 3B).These results suggest that OOEP regulates ATM activation upon DNA DSBs.

Figure 3 OOEP is required for ATM activation and RAD51 recruitment to DNA damage sites

RAD51 is an essential recombinase downstream of ATM in the HR pathway(Oktay et al.,2015,Perez et al.,2007).After DNA DSBs,the RAD51 protein is recruited and binds to resected single-strand DNA to form DNA-protein filaments(RAD51 foci),which facilitate the searching and pairing of DNA homologues during recombination(Jasin&Rothstein,2013).Upon etoposide treatment,RAD51 foci were formed at damage sites labeled with γ-H2AX in wild-type oocytes.However,fewer RAD51 foci were detected in Ooeptm/tmoocytes(Figure 3C).Thus,the absence of OOEP in oocytes impaired RAD51 focal accumulation at DNA damage sites.Taken together,these data demonstrate that OOEP may function in the HR-mediated DNA DSB repair pathway by regulating ATM activation and RAD51 recruitment to DSB sites in mouse oocytes.

Ooep protects oocytes from DNA DSB-induced apoptosis and meiosis delay

Persistent DNA DSBs can evoke p63-mediated apoptosis of oocytes in primordial and primary follicles(Gonfloni et al.,2009;Suh et al.,2006).OOEP is necessary for HR-mediated DNA DSB repair in oocytes,suggesting that Ooeptm/tmoocytes might be sensitive to exogenous or endogenous DNA damage insults and prone to apoptosis. To test this hypothesis,we compared the apoptosis susceptibility of oocytes to exogenous DNA damage insults between wild-type and Ooeptm/tmfemales at the early postnatal stage.Five-day-old(P5)mouse ovaries,which contained mostly primordial follicles,were collected and cultured for 12 h with various doses of DNA cross-linking agent cisplatin(Gonfloni et al.,2009).At the concentration of 3 mg/L,cisplatin was able to induce mild apoptosis(～13.5%)in wild-type ovaries and was therefore utilized in the following studies.After in vitro treatment,ovarian sections from Ooeptm/tmand wild-type females were counterstained with DDX4(a germ cell specific marker)and TUNEL.The percentages of apoptotic oocytes(DDX4+TUNEL+)were significantly higher in Ooeptm/tminfants than in wild-type counterparts(Figure 4A),suggesting that Ooeptm/tmoocytes were more sensitive than wild-type oocytes to exogenous DNA damage insults due to compromised HR repair.To understand the in vivo effect of OOEP depletion under the physiological conditions,we collected ovaries from 4-week-old and 16-week-old wild-type and Ooeptm/tmfemales and compared the number of oocytes within primordial and primary follicles,which express P63 and are subject to DNA damage-induced atresia(Suh et al.,2006). Intriguingly,at 4-week old,the numbers of oocytes in primordial and primary follicles were significantly higher in Ooeptm/tmfemales than in wild-type females.This probably reflected the developmental halt caused by the accumulated endogenous DNA damage in part of the oocytes.In contrast,at 16-week old,the numbers of oocytes in primordial and primary follicles were statistically lower in Ooeptm/tmfemales than in wild-type females(Figure 4B).Together,these results support that OOEP protects oocytes from endogenous or exogenous DNA DSB-induced apoptosis and preserves oocyte quantity under DNA damage insults.

DNA damage in fully grown oocytes compromises the completion of meiosis by inducing a delay in meiosis resumption(germinal vesicle breakdown,GVBD)(Marangos&Carroll,2012)and the activation of spindle assembly checkpoint(SAC)at metaphase I(Collins et al.,2015;Marangos et al.,2015).We investigated the influence of OOEP loss on the kinetics of GVBD and the first polar body extrusion(PBE)during oocyte in vitro maturation. Under normal conditions,the Ooeptm/tmoocytes showed a 4-h delay in reaching 50%-GVBD compared with wild-type oocytes. In addition,～20%less oocytes completed GVBD in the absence of OOEP compared with the wild-type counterparts at the end of culture(Figure 4C).Likewise,the Ooeptm/tmoocytes displayed a 2-h delay in reaching 50%-PBE.At the end of culture,20%less oocytes completed PBE compared with the wild-type counterparts(Figure 4D).Thus,OOEP was essential for efficient meiosis resumption and completion by preserving oocyte genomic integrity.Decline in DNA DSB repair competence is considered a major factor contributing to oocyte and ovarian aging at advanced maternal age(Oktay et al.,2014,2015;Titus et al.,2013;Xu et al.,2015).We examined if Ooep expression declined with maternal aging.mRNA expression levels of the Ooep gene measured in single GV oocytes of old females(40-week old)were lower than those from young females(8-week old)(Figure 4E).Thus,Ooep expression exhibited age-dependent decline and may contribute to ovarian failure and reproductive aging under physiological or pathological conditions.

DISCUSSION

DNA damage in oocytes can cause infertility,abortion,and birth defects,leading to reproductive failure. Among all types of DNA damage,DSBs are the most deleterious and can substantially impair genome integrity.Experimental and clinical studies on mice and humans have revealed that intact DNA DSB repair in oocytes is necessary to preserve oocyte quantity and quality.Decline in DNA DSB repair has a causal relationship with ovarian failure,menopause,and infertility(Oktay et al.,2014,2015;Titus et al.,2013;Xu et al.,2015).Genome-wide association studies on menopause timing have also highlighted the strong association of early menopause with DNA damage response pathways where many genes are involved in DNA repair,particularly the HR pathway(e.g.,BRCA1 pathway)and checkpoint response(cell cycle response and apoptosis)(Day et al.,2015;Perry et al.,2013).Thus,investigating how oocytes respond to DNA DSBs and what molecules are involved in HR-mediated DSB repair will shed light on oocyte and ovarian aging. In this study,we presented the following lines of evidence to support the notion that OOEP may participate in HR-mediated DNA DSB repair by regulating the ATM-RAD51 axis in oocytes.Firstly,after etoposide treatment,γ-H2AX foci,which monitor DNA DSBs,were gradually resolved in wild-type oocytes but persisted in Ooep null oocytes,although this defect was rescued by re-expression of OOEP.Secondly,wild-type oocytes evoked the activation of ATM,a central coordinator in DNA DSB repair processes,in response to exogenous DNA damage.However,Ooep-/-oocytes failed to efficiently ignite ATM activation and this defect could be rescued by the re-introduction of OOEP proteins into mutant oocytes.Finally,RAD51,a recombinase essential for HR-mediated DNA DSB repair,was recruited to damage sites and formed foci in wild-type oocytes in response to etoposide treatment.In contrast,fewer RAD51 proteins were recruited to and formed foci at DNA DSBs in Ooep-/-oocytes,although this defect could also be rescued by exogenous OOEP.

Due to the compromised DNA damage repair,Ooep-/-oocytes displayed an accumulation of endogenous DNA damage,as determined by the comet assay,an unambiguous method that measures the extent of DNA damage on a single cell basis. As DNA damage can induce atresia of oocytes in primordial and primary follicles through the p63-mediated pathway(Gonfloni et al.,2009;Suh et al.,2006),we proposed that the accumulation of endogenous DNA damage in Ooep-/-oocytes may drive the atresia of oocytes and decrease the oocyte number in primordial and primary follicles under physiological conditions.Indeed,in young adult mice(16-week old),a mild but statistically significant decrease in oocyte quantity within the primordial and primary follicles was detected in the Ooep-/-ovaries compared to the wild-type counterparts.Oocytes in primordial and primary follicles from Ooep-/-females also displayed higher sensitivity to exogenous DNA insults and were prone to apoptosis. These observations suggest that OOEP is necessary for the preservation of oocyte quantity in normal and DNA-damaged conditions.OOEP depletion not only impairs the survival of oocytes within primordial and primary follicles,but also affects meiotic maturation and early embryonic development.Compared with wild-type oocytes,Ooep-/-GV oocytes exhibited delays in meiosis resumption as well as progression to the metaphase II stage.Moreover,embryos derived from Ooep-/-oocytes were arrested at the 2-cell stage(Li et al.,2008). This developmental arrest could be due to the DNA damage-induced cell cycle checkpoint(Xu et al.,2015).Thus,OOEP is essential for preserving oocyte quality.Interestingly,the mRNA expression of Ooep in mouse oocytes was reduced with advanced maternal age.Several key HR pathway genes,including Brca1,Mre11,Atm,and Rad51,also display age-dependent expression decrease in both human and mouse oocytes(Day et al.,2015;Oktay et al.,2015;Titus et al.,2013).Therefore,the coordinated decrease in the expression of Ooep and other canonical HR genes contributes to ovarian failure and reproductive aging under physiological and pathological conditions. OOEP is conservatively expressed in human oocytes(Zhu et al.,2015),implying that it may play similar roles in repairing DNA DSBs via the HR pathway in human oocytes.

Figure 4 Ooep protects oocytes from DNA DSB-induced apoptosis and meiosis delay

OOEP proteins are distributed in cytoplasm and localized at the subcortex of mouse and human oocytes(Li et al.,2008;Zhu et al.,2015).OOEP was also excluded from the DNA DSB sites in oocytes treated with etoposide(data not shown).Thus,the functions of OOEP in regulating HR-mediated DNA DSB repair are likely indirect.OOEP is predicted to contain an atypical hnRNP K homology(KH)domain implicated in RNA binding(Wang et al.,2014).RNA binding proteins have been recognized as crucial players in the HR repair pathway(Adamson et al.,2012).The involvement of RBPs in regulating ovarian aging has also been reported(Day et al.,2015).For instance,RNA binding protein FMRP encoded by fragile X mental retardation(Fmr1)gene plays an essential role in preserving ovarian function in mice and humans(Ascano et al.,2012;Lu et al.,2012).In the future,elucidating the molecular mechanism of OOEP is warranted to better understand the function of RBPs in preserving the genome integrity of germ cells and early embryos.

CONCLUSIONS

To the best of our knowledge,this work is the first to provide evidence that maternal OOEP may participate in HR-mediated DNA DSB repair by regulating the ATM-RAD51 axis in oocytes.Thus,OOEP may participate in the regulation of genome stability in oocytes and contribute to ovarian failure and reproductive aging under physiological or pathological conditions.

COMPETING INTERESTS

The authors declare that they have no competing interests.

AUTHORS’CONTRIBUTIONS

P.Z.designed the study.P.Z.and Q.H.C.supervised the study.D.J.H.,L.W.,Z.B.Z.,K.G.,J.Z.L.,and X.C.H.performed the experiments.P.Z.wrote the manuscript.

ACKNOWLEDGEMENTS

We thank Dr.Jurrien Dean from the National Institutes of Health,USA,for providing the Ooeptm/tmmice.