Gene structure and expression of the mouse adipocyte enhancer-binding protein

被引:38
作者
Ro, HS [1 ]
Kim, SW [1 ]
Wu, DG [1 ]
Webber, C [1 ]
Nicholson, TE [1 ]
机构
[1] Dalhousie Univ, Fac Med, Dept Biochem & Mol Biol, Halifax, NS B3H 4H7, Canada
基金
加拿大自然科学与工程研究理事会;
关键词
adipocyte differentiation; differential splicing; protein truncation; reverse transcription-polymerase chain reaction: northern blotting; Immunoprecipitation;
D O I
10.1016/S0378-1119(01)00771-5
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
The adipocyte enhancer-binding protein (AEBP1) is a transcriptional repressor with carboxypeptidase activity. AEBP1 expression is down-regulated during adipogenesis. Aortic carboxypeptidase-like protein (ACLP) is a non-nuclear isoform of AEBP1 that has an N-terminal extension of 380 amino acids. ACLP expression is up-regulated during vascular smooth muscle cell differentiation. To gain insight into the regulation of AEBP1 isoform expression, we have determined the structural organization of the mouse AEBP1 gene. This gene extends over 10 kb, has 21 exons, and gives rise to two mRNAs (AEBP1 and ACLP). The 9th intron is retained in the mature AEBP1 transcript. Thus, ACLP encodes an additional 380 amino acids N-terminal to the first ATG codon of AEBP1 which is located in exon 10. RTPCR experiments showed that both transcripts are expressed ubiquitously in all mouse tissues examined, while Western blot analysis suggested that expression is translationally regulated. Our results provide evidence that two isoforms of AEBP1 with very different functions are produced by an alternative splicing mechanism. This represents a new example of regulation of subcellular localization by protein truncation. (C) 2001 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:123 / 133
页数:11
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