Polymorphisms in the breakpoint cluster region of bcr gene.
- Author:
Hong TIAN
1
;
Shu-Yun ZHOU
Author Information
1. Department of Hematology, Fuzhou General Hospital, Nanjing Military Area, Fuzhou 350025, Fujian Province, China.
- Publication Type:Journal Article
- MeSH:
Base Sequence;
Chromosome Breakage;
Fusion Proteins, bcr-abl;
genetics;
Humans;
Leukemia, Myelogenous, Chronic, BCR-ABL Positive;
genetics;
Molecular Sequence Data;
Polymorphism, Single Nucleotide;
Proto-Oncogene Proteins c-bcr;
genetics
- From:
Journal of Experimental Hematology
2008;16(3):659-662
- CountryChina
- Language:Chinese
-
Abstract:
This study was aimed to explore the single nucleotide polymorphism (SNPs) of breakpoint cluster region of bcr gene in Chinese people and the relationship between SNPs and chronic myelogenous leukemia (CML). A 3.12 kb region spanning from exon 13 to exon 15 in the bcr region were screened by DNA pooling and denaturing high performance liquid chromatography (dHPLC), and the results were verified by sequencing. The results indicated that 6 novel SNP sites and 2 bases different from reference sequence were confirmed in the region studied, and the frequency of 6 novel SNP sites in studied population was obtained, one SNP of which was found in exon 13 and caused a nonsynonymous mutation. The gene frequencies of novel SNPs had no significant difference between CML and control people. It is concluded that sequence polymorphisms in the major breakpoint cluster region of bcr gene are found, most of which are SNPs, No relationship can be confirmed between SNPs and CML disease.
