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Zhang, Ya‐Xin; He, Wen‐Bin; Xiao, Wen‐Juan; Meng, Lan‐Lan; Tan, Chen; Du, Juan; Lu, Guang‐Xiu; Lin, Ge; Tan, Yue‐Qiu
Molecular genetics & genomic medicine, April 2020, Volume: 8, Issue: 4Journal Article
Background Premature ovarian insufficiency (POI) is one major cause of female infertility, minichromosome maintenance complex component 8 (MCM8) has been reported to be responsible for POI. Methods Whole‐exome sequencing was performed to identify the genetic variants of women with POI. Sanger sequencing was used to validate the variants in all the family members. Various bioinformatic software was used for the pathogenicity assessment. Reverse transcription polymerase chain reaction (RT‐PCR), real‐time quantitative PCR, and a chromosomal instability study induced by mitomycin C were performed to analyze the functional effects of the variant. Results A novel homozygous frameshift mutation (NM_032485.4:c.351_354delAAAG) of MCM8 gene was identified in the patients, segregated with POI in this family. This mutation is predicted to produce truncated MCM8 protein and to be pathogenic. Reverse transcription polymerase chain reaction revealed that the frameshift mutation led to a remarkably reduced level of MCM8 transcript products, and chromosomal instability study showed that the ability of mutant MCM8 to repair DNA breaks was impaired. Conclusion We identified a novel homozygous frameshift mutation in the MCM8 gene in two affected sisters with POI, and functional analysis revealed that this mutation is pathogenic. Our findings enrich the MCM8 mutation spectrum and might help clinicians to make a precise diagnosis, thereby allowing better family planning and genetic counseling. In our study, a novel homozygous frameshift mutation in the MCM8 gene was identified in a consanguineous Han Chinese family by whole‐exome sequencing, which segregates with POI in this family. Furthermore, functional characterization revealed that this frameshift mutation is pathogenic.
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