Putative alternative trans-splicing of leukocyte adhesion-GPCR pre-mRNAs generates functional chimeric receptors

被引:5
作者
Chiu, Pei-Ling [2 ,3 ]
Ng, Boon Han [1 ]
Chang, Gin-Wen [4 ]
Gordon, Siamon [4 ]
Lin, Hsi-Hsien [1 ]
机构
[1] Chang Gung Univ, Coll Med, Dept Microbiol & Immunol, Tao Yuan, Taiwan
[2] Chang Gung Univ, Coll Med, Dept Med Biotechnol, Tao Yuan, Taiwan
[3] Chang Gung Univ, Coll Med, Sci Labs, Tao Yuan, Taiwan
[4] Univ Oxford, Sir William Dunn Sch Pathol, Oxford OX1 3RE, England
来源
FEBS LETTERS | 2008年 / 582卷 / 05期
基金
英国医学研究理事会;
关键词
adhesion-GPCR; EGF-TM7; LNB-TM7; alternative splicing; trans-splicing;
D O I
10.1016/j.febslet.2008.02.004
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 EGF-TM7 receptors, a subfamily of. adhesion-GPCRs mostly restricted to leukocytes, are known to express multiple functional protein isoforms through extensive alternative cis-splicing. Here, we demonstrate that EGF-TM7 pre-mRNAs also undergo the rare trans-splicing, leading to the generation of functional chimeric receptors. RT-PCR and in silico analyses of EMR2 transcripts identified unique fragments containing the EGF-like motif 3 of a closely related EGF-TM7 gene, CD97, in addition to the alternative cis-spliced products. The sequence swapping is restricted to the EGF-3 exon, generating unique EMR2(1-2-3*-5) and EMR2(1-2-3*-4-5) molecules, which are functional in ligand-binding as the wild-type EMR2(1-2-3-4-5) and CD97(1-2-3-4-5) receptors. Our results suggest that human leukocytes employ trans-splicing as well as cis-splicing to increase the repertoire of functional adhesion-GPCRs. (c) 2008 Federation of European Biochemical Societies. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:792 / 798
页数:7
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