Lack of MECP2 gene transcription on the duplicated alleles of two related asymptomatic females with Xq28 duplications and opposite X‐chromosome inactivation skewing. Issue 11 (5th August 2021)

• Record Type: Journal Article
• Authors: Sun, Yixi; Yang, Yali; Luo, Yuqin; Chen, Min; Wang, Liya; Huang, Yingzhi; Yang, Yanmei; Dong, Minyue
• Is Part Of: Human mutation. Volume 42:Issue 11(2021)
• Page Start: 1429
• Page End: 1442
• Publication Date: 2021-08-05
• Subjects: allele‐specific expression (ASE) -- androgen receptor (AR) assay -- MECP2 duplication -- RNA sequencing -- skewed X‐chromosome inactivation (XCI); Human chromosome abnormalities -- Periodicals; Mutation (Biology) -- Periodicals; 616.04205
• DOI: 10.1002/humu.24262
• Languages: English
• ISSNs: 1059-7794

Abstract

Abstract: Xq28 duplication syndrome (MIM# 300815) is a severe neurodevelopmental disorder in males due to MeCP2 overexpression. Most females with MECP2 duplication are asymptomatic carriers, but there are phenotypic heterogeneities. Skewed X‐chromosome inactivation (XCI) can protect females from exhibiting clinical phenotypes. Herein we reported two asymptomatic females (mother and grandmother) with interstitial Xq28 duplication. AR and RP2 assays showed that both had extremely skewed XCI, the Xq28 duplicated chromosome was inactivated in the mother, but was surprisingly activated in the grandmother. Interestingly, by combining RNA sequencing and whole‐exome sequencing, we confirmed that XIST only expressed in the Xq28 duplication chromosomes of the two females, indicating that the Xq28 duplication chromosomes were inactive. Meanwhile, MECP2 and most XCI genes in the duplicated X‐chromosomes were not transcriptionally expressed or upregulated, precluding major clinical phenotypes in the two females, especially the grandmother. We showed that XCI status detected using RNA sequencing was more relevant for establishing the clinical phenotype of MECP2 duplication in females. It suggested that there were other factors maintaining the XCI status in addition to DNA methylation, a possible additional inhibition mechanism occurred at the transcriptional level in the unmethylated X‐chromosome, counter balancing the MECP2 duplication's detrimental phenotype effects. Abstract : Lack of MECP2 gene transcription on the duplicated alleles of two related assympomatic females with Xq28 duplications and opposite X‐chromosome inactivation skewing.