Gene organization of human transporter associated with antigen processing-like (TAPL, ABCB9): analysis of alternative splicing variants and promoter activity

被引:22
作者
Kobayashi, A [1 ]
Hori, S [1 ]
Suita, N [1 ]
Maeda, M [1 ]
机构
[1] Osaka Univ, Grad Sch Pharmaceut Sci, Lab Biochem & Mol Biol, Suita, Osaka 5650871, Japan
基金
日本学术振兴会;
关键词
ABCB9; alternative splicing; gene structure; promoter; TAP-like; transporter;
D O I
10.1016/j.bbrc.2003.08.081
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The gene organization of human TAPL (TAP-like, ABCB9) was determined. The TAPL gene consists of 12 exons including the first non-coding exon on human chromosome 12q23.34. Three alternative splicing variants of the 12th exon have been identified by 3'RACE using RNA from human cell lines and isolated lymphocytes. As expected from the similarity of the amino acid sequences of TAP1, TAP2, and TAPL, the intron insertion points in these three genes are essentially the same. However, the TAP2 and TAPL genes are closely related, since each has common non-coding exon and splicing isoforms. The novel splicing variants of TAPL termed 12B and 12C have shorter carboxyl terminal amino acid sequences than 12A, reportedly a conserved isoform in rodents and human. The proximal promoter region of the TAPL gene lacks a canonical TATA-box but contains several GC-box elements. The 60 bp upstream sequence containing two GC-boxes from the human TAPL transcriptional start site confers basal promoter activity. (C) 2003 Elsevier Inc. All rights reserved.
引用
收藏
页码:815 / 822
页数:8
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