MECP2 germline mosaicism plays an important part in the inheritance of Rett syndrome: a study of MECP2 germline mosaicism in males

• Published in: BMC medicine Vol. 21; no. 1; p. 155
• Main Authors: Wen, Yongxin, Wang, Jiaping, Zhang, Qingping, Yang, Xiaoxu, Wei, Liping, Bao, Xinhua
• Format: Journal Article
• Language: English
• Published: England BioMed Central Ltd 20.04.2023; BioMed Central; BMC
• Subjects: Adult; Binomial distribution; Blood; Care and treatment; Daughters; De novo; Diagnosis; Disease prevention; Disorders; Families & family life; Family medical history; Fathers; Female; Gene mutations; Genetic aspects; Genetic disorders; Genetics; Germ Cells; Germline; Health aspects; Humans; Male; Males; MECP2; MeCP2 protein; Men; Methyl-CpG binding protein; Mosaicism; Mutation; Mutation hot spots; Offspring; Phenotype; Rett syndrome; Rett Syndrome - genetics; Semen; Software; Sperm; Statistical analysis; China; MECP2; Mosaicism; De novo; Germline; Rett syndrome
• ISSN: 1741-7015; 1741-7015
• DOI: 10.1186/s12916-023-02846-2

Germline mosaicisms could be inherited to offspring, which considered as "de novo" in most cases. Paternal germline MECP2 mosaicism has been reported in fathers of girls with Rett syndrome (RTT) previously. For further study, we focused on MECP2 germline mosaicism in males, not only RTT fathers. Thirty-two fathers of RTT girls with MECP2 pathogenic mutations and twenty-five healthy adult males without history and family history of RTT or other genetic disorders were recruited. Sperm samples were collected and ten MECP2 hotspot mutations were detected by micro-droplet digital PCR (mDDPCR). And routine semen test was performed at the same time if the sample was sufficient. Additionally, blood samples were also detected for those with sperm MECP2 mosaicisms. Nine fathers with RTT daughters (28.1%, 9/32) were found to have MECP2 mosaicism in their sperm samples, with the mutant allele fractions (MAFs) ranging from 0.05% to 7.55%. Only one father with MECP2 c.806delG germline mosaicism (MAF 7.55%) was found to have mosaicism in the blood sample, with the MAF was 0.28%. In the group of healthy adult males, MECP2 mosaicism was found in 7 sperm samples (28.0%, 7/25), with the MAFs ranging from 0.05% to 0.18%. None of the healthy adult males with MECP2 germline mosaicisms were found with MECP2 mosaicism in blood samples. There were no statistical differences in age, or the incidence of asthenospermia between fathers with RTT daughters and healthy adult males with MECP2 germline mosaicisms. Additionally, there was no linear correlation between MAFs of MECP2 mosaicisms and the age of males with germline MECP2 mosaicisms. Germline MECP2 mosaicism could be found not only in fathers with RTT daughters but also in healthy adult males without family history of RTT. As germline mosaic mutations may be passed on to offspring which commonly known as "de novo", more attention should be paid to germline mosaicism, especially in families with a proband diagnosed with genetic disorders.