A case of complex structural variants in the Xq28 region diagnosed by whole genome sequencing.
10.3760/cma.j.cn511374-20250217-00082
- Author:
Yulai YANG
1
,
2
;
Chuang LI
;
Ming GAO
;
Yuan LYU
Author Information
1. Department of Gynecology and Obstetrics, Shengjing Hospital Affiliated to China Medical University, Key Laboratory of Maternal-Fetal Medicine of Liaoning Province, Shenyang, Liaoning 110004, China. hawk.lv@
2. com.
- Publication Type:English Abstract
- MeSH:
Humans;
Female;
Chromosomes, Human, X/genetics*;
DNA Copy Number Variations/genetics*;
Whole Genome Sequencing/methods*;
Methyl-CpG-Binding Protein 2/genetics*;
Pregnancy;
Male;
Adult
- From:
Chinese Journal of Medical Genetics
2025;42(3):355-359
- CountryChina
- Language:Chinese
-
Abstract:
OBJECTIVE:To re-analyze a likely pathogenic variant in the Xq28 region identified by copy number variation sequencing (CNV-seq) through whole genome sequencing (WGS).
METHODS:A fetus found to harbor a duplication in the Xq28 region by CNV-seq at Shengjing Hospital Affiliated to China Medical University in May 2023 was selected as the study subject. WGS was carried out for the fetus and its parents. Bioinformatic software was used to analyze the chromosomal structure and CNVs. Quantitative PCR (qPCR) was applied to determine the expression level of the MECP2 gene. This study has been approved by the Ethics Committee of Shengjing Hospital (Ethic No. 2013PS33K).
RESULTS:A duplication (ChrX:153302641_153503563) and four breakpoints were identified on the X chromosome of the fetus' father. Bioinformatic analysis revealed that the duplicated region has involved exons 1 to 3 and part of the 5'-UTR of the MECP2 gene, which was inserted into the Xp11 region. Additionally, an inversion was detected in the Xp11 region adjacent to the duplicated segment. RT-PCR results showed normal level of MECP2 mRNA expression. The Xq28 duplication has not encompassed the entire MECP2 gene, nor disrupted its structure or altered its expression.
CONCLUSION:WGS has enabled more precise diagnosis of chromosomal structural variants and provided guidance for accurate genetic counseling for the affected families.
