Multiple gene duplication and expression of mouse bcl-2-related genes, A1

被引:64
作者
Hatakeyama, S
Hamasaki, A
Negishi, I
Loh, DY
Sendo, F
Nakayama, K
Nakayama, K
机构
[1] Kyushu Univ, Med Inst Bioregulat, Dept Mol & Cellular Biol, Higashi Ku, Fukuoka 8128582, Japan
[2] Kyushu Univ, Med Inst Bioregulat, Lab Embryon & Genet Engn, Higashi Ku, Fukuoka 8128582, Japan
[3] Yamagata Univ, Sch Med, Dept Immunol & Parasit, Yamagata 9909585, Japan
[4] Gumma Univ, Sch Med, Dept Dermatol, Maebashi, Gumma 3718571, Japan
[5] Nippon Roche Res Ctr, Dept Biol, Kamakura, Kanagawa 2470063, Japan
关键词
apoptosis; gene cloning; neutrophil;
D O I
10.1093/intimm/10.5.631
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Here we report the genomic cloning and characterization of the murine A1 genes, which belong to the bcl-2 gene family. Southern analysis indicated the existence of at least four A1 genes in the murine genome and four different A1 genes, designated A1-a, -b, -c and -d, were cloned from the murine genomic library. The Al-a, -b and -d genes consisted of two exons, whereas the A1-c gene contained 1 bp insertion in the coding region which may result in an aberrant and truncated protein by frame-shift. With the exception of A1-c, the coding regions among A1 genes are highly conserved at >97% at the nucleotide level and at >96% at the amino acid level. A1-a, -b and -d genes appeared to be expressed specifically in organs containing many neutrophils, In neutrophils, A1-a, -b and -d transcripts were detected at a comparable level. Our data suggest that the multiple Al genes in mice were generated by gene duplication and each of them may function as anti-apoptotic molecules in neutrophils.
引用
收藏
页码:631 / 637
页数:7
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