Variable promoter usage and alternative splicing in five mouse connexin genes

被引:23
作者
Anderson, CL [1 ]
Zundel, MA [1 ]
Werner, R [1 ]
机构
[1] Univ Miami, Sch Med, Dept Biochem & Mol Biol, Miami, FL 33136 USA
关键词
D O I
10.1016/j.ygeno.2004.11.007
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
Recent work from our lab has demonstrated the importance of alternative promoters and variable 5' UTRs in the regulation of two connexin genes. To see whether other connexins also utilize multiple promoters to produce different mRNA isoforms, we screened the mouse EST database for variations in the 5' ends of each connexin EST in UniGene. 5'-RACE analysis of mouse embryo cDNA targeting five candidate genes, Cx31, Cx40, Cx45, Cx46, and Cx47 (approved gene symbols Gjb3, Gja5, Gja7, Gja3, and Gja12, respectively), revealed the existence of multiple previously unknown exons upstream of the coding region that result in variations in the 5' UTR of the mRNA. RTPCR from 17 different mouse tissues revealed that many isoforms are expressed in a tissue-specific manner, with some being the predominant exons found in the tissues tested. Many of the novel 5' UTRs include upstream open reading frames, suggesting varying translational efficiencies. The expression of alternative 5' UTRs suggests that connexins, like many genes involved in development, require complex regulation at both transcriptional and translational levels. (C) 2004 Elsevier Inc. All rights reserved.
引用
收藏
页码:238 / 244
页数:7
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