Analysis of MECP2 gene variants and X chromosome inactivation in four children with Rett syndrome.
10.3760/cma.j.cn511374-20241112-00588
- Author:
Chen WEI
1
;
Rong QIANG
;
Wenwen YU
Author Information
1. Genetic Medicinal Center, Northwest Women's and Children's Hospital, Xi'an, Shaanxi 710061, China. 306602637@qq.com.
- Publication Type:English Abstract
- MeSH:
Child;
Humans;
Chromosomes, Human, X/genetics*;
Exome Sequencing;
Methyl-CpG-Binding Protein 2/genetics*;
Mutation;
Rett Syndrome/genetics*;
X Chromosome Inactivation/genetics*
- From:
Chinese Journal of Medical Genetics
2025;42(5):568-573
- CountryChina
- Language:Chinese
-
Abstract:
OBJECTIVE:To investigate the X-chromosome inactivation (XCI) patterns and origin in four children with Rett syndrome (RTT), and to explore the genetic basis of their phenotypic variability.
METHODS:Four pediatric RTT cases diagnosed at Northwest Women's and Children's Hospital between August 1, 2022 and October 31, 2024 were enrolled. Clinical data were collected, and whole exome sequencing (WES) and Sanger sequencing were performed on the children and their parents to identify pathogenic variants. XCI analysis and linkage studies were conducted to determine the origin of variants and assess skewed XCI. This study was approved by the Medical Ethics Committee of the Northwest Women's and Children's Hospital (Ethics No. 21-036).
RESULTS:WES and Sanger sequencing revealed that the four children carried the following MECP2 (NM_001110792.2) variants. c.916C>T (p.Arg306Cys), c.842delG (p.G281Afs*20), c.763C>T (p.R255X), and c.686C>T (p.Pro229Leu). The c.916C>T variant was maternally inherited, while the other three were de novo. All four variants have been previously reported: c.916C>T, c.842delG, and c.763C>T were classified as pathogenic, whereas c.686C>T was deemed likely pathogenic. XCI analysis demonstrated skewed inactivation in child 2 and 3 and their mothers, with maternal X-chromosome recombination during gametogenesis observed in child 3. All variants were located on the maternal X chromosome.
CONCLUSION:Skewed XCI is a common pathogenic mechanism in MECP2-related RTT, and MECP2 variants may exhibit a maternal origin bias. Clinical evaluation should incorporate XCI status for comprehensive genetic analysis.
