A novel homozygous missense variant in BTG4 causes zygotic cleavage failure and female infertility

被引:11
|
作者
Liu, Ruyi [1 ,2 ]
Zhou, Yifan [3 ]
Li, Qiaoli [1 ,2 ]
Chen, Biaobang [4 ]
Zhou, Zhou [1 ,2 ]
Wang, Lan [3 ]
Wang, Lei [1 ,2 ]
Sang, Qing [1 ,2 ]
Jin, Lei [3 ]
机构
[1] Fudan Univ, Childrens Hosp, Inst Pediat, Inst Biomed Sci, Shanghai 200032, Peoples R China
[2] Fudan Univ, State Key Lab Genet Engn, Shanghai 200032, Peoples R China
[3] Huazhong Univ Sci & Technol, Tongji Hosp, Tongji Med Coll, Reprod Med Ctr, Wuhan 430030, Peoples R China
[4] Fudan Univ, NHC Key Lab Reprod Regulat, Shanghai Inst Biomed & Pharmaceut Technol, Shanghai 200032, Peoples R China
基金
上海市自然科学基金; 中国国家自然科学基金;
关键词
BTG4; Variant; Female infertility; Zygotic cleavage failure; MUTATIONS;
D O I
10.1007/s10815-021-02340-9
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Purpose "Zygotic cleavage failure" is an embryonic phenotype that causes female infertility and failure of in vitro fertilization and/or intracytoplasmic sperm injection. We aimed to identify pathogenic variants in a female infertility patient from a consanguineous family with the "zygotic cleavage failure" phenotype. Methods Whole-exome sequencing was performed in the affected patient; Sanger sequencing was used to confirm the identified variant. The functional effect of the identified variant was further investigated in HeLa cells. Results We identified a novel homozygous missense mutation in BTG4 (c.285G > C, p.W95C) in the affected individual. Co-immunoprecipitation in HeLa cells showed the complete loss of the interaction between the p.W95C BTG4 variant protein and CNOT7. Conclusion This study confirms our previous research and expands the mutational spectrum of BTG4. Our findings complement the diagnostic genetic basis for "zygotic cleavage failure" patients and suggest that BTG4 may be a good target for future therapeutic strategies.
引用
收藏
页码:3261 / 3266
页数:6
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