Objective Premature ovarian insufficiency(POI)is defined as the depletion of ovarian function before 40years of age,affecting approximately 3.7%of women in their reproductive age worldwide.Previous studies revealed se...Objective Premature ovarian insufficiency(POI)is defined as the depletion of ovarian function before 40years of age,affecting approximately 3.7%of women in their reproductive age worldwide.Previous studies revealed several genes involved in the Fanconi anaemia(FA)pathway participate in the pathogenesis of POI,such as FANCA and FANCM.FA pathway maintains rapid proliferation in the developing primordial germ cells by deregulating transcription-replication conflicts,which is crucial for the establishment of sufficient ovarian reserve.FANCJ encodes a DNA helicase located downstream of the FA pathway promoting DNA damage repair and cell proliferation.Recently,two heterozygous FANCJ missense variants have been reported in patients with POI,suggesting haploinsufficiency of FANCJ participates in the pathogenesis of the disease.In this study,to further explore the contribution of FANCJ variants in POI,we reported a rare homozygous FANCJ start-loss variation in one patient with POI and illustrated its pathogenicity by in vitro functional studies.Methods The loss-of-function(LoF)variants of FANCJ were screened in our internal whole-exome sequencing(WES)database of POI.Sanger sequencing and WES analysis were employed on the proband and the patient’s family members to illustrate the origin of the bi-allelic variant.Cycloheximide chase assay was performed to demonstrate the impact of the variant on the protein stability of FANCJ.Protein ubiquitination assay was performed to confirm the accelerated degradation pathway of FANCJ protein.ResultsThrough the variation screening,a bi-allelic variant of FANCJ(NM_032043.3:c.1A>G,p.Met1Val)was identified in one case.The functional study showed that the start-loss variant affected FANCJ protein stability by accelerated protein degradation through the ubiquitinproteasome pathway.Conclusion Our findings provide further genetic evidence of the FANCJ variant participating in the pathogenesis of POI,expand the inherited mode and highlight the essential role of the FA pathway in maintaining ovarian function.展开更多
基金supported by the National Key Research&Development Program of China(2022YFC2703800,2022YFC2703000)the National Natural Science Foundation of China(82125014,32070847)+5 种基金the Basic Science Center Program of NFSC(31988101)the Key Project of Natural Science Foundation of Shandong Province(ZR202105250005)the Program for Excellent Young Scholars of Shandong Province(ZR2022YQ69)the Taishan Scholars Program for Young Experts of Shandong Provincethe Jinan Shizhong District key Industry Leading Talent ProgramThe Fundamental Research Funds of Shandong University。
文摘Objective Premature ovarian insufficiency(POI)is defined as the depletion of ovarian function before 40years of age,affecting approximately 3.7%of women in their reproductive age worldwide.Previous studies revealed several genes involved in the Fanconi anaemia(FA)pathway participate in the pathogenesis of POI,such as FANCA and FANCM.FA pathway maintains rapid proliferation in the developing primordial germ cells by deregulating transcription-replication conflicts,which is crucial for the establishment of sufficient ovarian reserve.FANCJ encodes a DNA helicase located downstream of the FA pathway promoting DNA damage repair and cell proliferation.Recently,two heterozygous FANCJ missense variants have been reported in patients with POI,suggesting haploinsufficiency of FANCJ participates in the pathogenesis of the disease.In this study,to further explore the contribution of FANCJ variants in POI,we reported a rare homozygous FANCJ start-loss variation in one patient with POI and illustrated its pathogenicity by in vitro functional studies.Methods The loss-of-function(LoF)variants of FANCJ were screened in our internal whole-exome sequencing(WES)database of POI.Sanger sequencing and WES analysis were employed on the proband and the patient’s family members to illustrate the origin of the bi-allelic variant.Cycloheximide chase assay was performed to demonstrate the impact of the variant on the protein stability of FANCJ.Protein ubiquitination assay was performed to confirm the accelerated degradation pathway of FANCJ protein.ResultsThrough the variation screening,a bi-allelic variant of FANCJ(NM_032043.3:c.1A>G,p.Met1Val)was identified in one case.The functional study showed that the start-loss variant affected FANCJ protein stability by accelerated protein degradation through the ubiquitinproteasome pathway.Conclusion Our findings provide further genetic evidence of the FANCJ variant participating in the pathogenesis of POI,expand the inherited mode and highlight the essential role of the FA pathway in maintaining ovarian function.
