Analysis of ACAT1 gene variants in a patient with β-ketothiolase deficiency.
10.3760/cma.j.cn511374-20200121-00045
- Author:
Chuntao SUN
1
;
Qigang ZHANG
;
Lingli KONG
;
Yumei WANG
;
Li ZHANG
Author Information
1. Department of Child Health Care, Huai'an Maternal and Child Health Care Hospital, Huai'an, Jiangsu 223002, China. zlacwb @126.com.
- Publication Type:Journal Article
- MeSH:
Acetyl-CoA C-Acetyltransferase/genetics*;
Acetyl-CoA C-Acyltransferase/genetics*;
Amino Acid Metabolism, Inborn Errors/genetics*;
Female;
High-Throughput Nucleotide Sequencing;
Humans;
Infant, Newborn;
Male;
Mutation
- From:
Chinese Journal of Medical Genetics
2021;38(2):166-169
- CountryChina
- Language:Chinese
-
Abstract:
OBJECTIVE:To explore the genetic etiology of a child suspected for β-ketothiolase deficiency by neonatal screening.
METHODS:All coding exons and flanking sequences of the ACAT1 gene were subjected to targeted capture and high-throughput sequencing. Suspected variants were verified by Sanger sequencing and bioinformatic analysis.
RESULTS:The child was found to harbor compound heterozygous variants of the ACAT1 gene, namely c.121-3C>G and c.275G>A (p. Gly92Asp). The c.121-3C>G variant was also detected in his father and two sisters, while the c.275G>A (p. Gly92Asp) was a de novo variant. A c.334+ 172C>G (rs12226047) polymorphism was also detected in his mother and two sisters. Sanger sequencing has verified that the c.275G>A (p. Gly92Asp) and c.334+172C>G (rs12226047) variants are located on the same chromosome. Bioinformatics analysis suggested both c.121-3C>G and c.275G>A (p.G92D) variants to be damaging. Based on the American College of Medical Genetics and Genomics standards and guidelines, the c.275G>A variant of the ACAT1 gene was predicted to be pathogenic (PS2+ PM2+ PM3+ PP3+PP4), the c.121-3C>G variant to be likely pathogenic (PM2+ PM3+ PP3+PP4).
CONCLUSION:The c.121-3C>G and c.275G>A variants of the ACAT1 gene probably underlay the pathogenesis of the child. Above finding has enriched the variant spectrum of the ACAT1 gene.
