[Analysis of PCCA and PCCB gene mutations in patients with propionic acidemia]

Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2015 Feb;32(1):26-30. doi: 10.3760/cma.j.issn.1003-9406.2015.01.006.
[Article in Chinese]

Abstract

Objective: To analyze PCCA and PCCB gene mutations in 10 Chinese patients with propionic acidemia(PA).

Methods: Genomic DNA was extracted from peripheral blood leukocytes. The 39 exons and flanking sequences of the PCCA and PCCB genes were amplified with polymerase chain reaction and subjected to direct DNA sequencing.

Results: DNA sequencing has revealed that 7 patients have carried a PCCA gene mutation, 2 patients carried PCCB gene mutation and 1 patient carried mutations in both PCCA and PCCB genes. Ten PA mutations were confirmed, including 8 affecting the PCCA gene and 2 affecting the PCCB gene. Three PCCA mutations c.245G>A, IVS15+5del5, c.1288C>T and 2 PCCB mutations c.838insC, c.1087T>C were found for the first time.

Conclusion: Among Chinese patients with propionic acidemia patients, their genetic mutations are mainly found on the PCCA gene.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Child, Preschool
  • Female
  • Humans
  • Infant
  • Male
  • Methylmalonyl-CoA Decarboxylase / genetics*
  • Mutation*
  • Propionic Acidemia / genetics*

Substances

  • Methylmalonyl-CoA Decarboxylase