An anthropoid-specific locus of orphan C to U RNA-editing enzymes on chromosome 22

被引:607
作者
Jarmuz, A
Chester, A
Bayliss, J
Gisbourne, J
Dunham, I
Scott, J
Navaratnam, N
机构
[1] Univ London Imperial Coll Sci Technol & Med, Fac Med, Genet & Genomics Res Inst, London W12 ONN, England
[2] Sanger Ctr, Cambridge CB10 1SB, England
[3] MRC, Ctr Clin Sci, RNA Editing Grp, London W12 ONN, England
关键词
APOBEC gene cluster; neoplasia;
D O I
10.1006/geno.2002.6718
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
The cytidine (C) to uridine (U) editing of apolipoprotein (apo) B mRNA is mediated by tissue-specific, RNA-binding cytidine deaminase APOBEC1. APOBEC1 is structurally homologous to Escherichia coli cytidine deaminase (ECCDA), but has evolved specific features required for RNA substrate binding and editing. A signature sequence for APOBEC1 has been used to identify other members of this family. One of these genes, designated APOBEC2, is found on chromosome 6. Another gene corresponds to the activation-induced deaminase (AID) gene, which is located adjacent to APOBEC1 on chromosome 12. Seven additional genes, or pseudogenes (designated APOBEC3A to 3G), are arrayed in tandem on chromosome 22. Not present in rodents, this locus is apparently an anthropoid-specific expansion of the APOBEC family. The conclusion that these new genes encode orphan C to U RNA-editing enzymes of the APOBEC family comes from similarity in amino acid sequence with APOBEC1, conserved intron/exon organization, tissue-specific expression, homodimerization, and zinc and RNA binding similar to APOBEC1. Tissue-specific expression of these genes in a variety of cell lines, along with other evidence, suggests a role for these enzymes in growth or cell cycle control.
引用
收藏
页码:285 / 296
页数:12
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