Structural and promoter regions of the murine pyruvate carboxylase gene

被引:22
|
作者
Jitrapakdee, S
Petchamphai, N
Sunyakumthorn, P
Wallace, JC
Boonsaeng, V
机构
[1] Mahidol Univ, Fac Sci, Dept Biochem, Bangkok 10400, Thailand
[2] Univ Adelaide, Dept Mol Biosci, Adelaide, SA 5005, Australia
基金
澳大利亚研究理事会;
关键词
pyruvate carboxylase; biotin-dependent enzyme; gluconeogenesis; lipogenesis; gene regulation; gene structure;
D O I
10.1006/bbrc.2001.5599
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
We have cloned and sequenced the gene encoding mouse pyruvate carboxylase (mPC) [EC 6.4.1.1]. The coding region contains 19 exons, one 5'-untranslated region exon, and 19 introns in 22 kb of genomic DNA. This gene's exon/intron organization is highly conserved with respect to rat and human PC genes. The mPC gene promoter lacks canonical TATA and CCAAT boxes, in common with a number of housekeeping genes. Transient expressions in COS-1 of a luciferase reporter gene under the control of 5'-nested deletions of the 5'-flanking sequence of the mPC gene have identified the 166-bp minimal sequence required for basal transcription. Alternative splicing at the 5'-untranslated region exon of the mouse PC gene results in the production of two alternate transcripts bearing different 5'-noncoding regions. Both transcripts are highly expressed in kidney and liver and moderately expressed in heart and testis and expressed at a low level in spleen. (C) 2001 Academic Press.
引用
收藏
页码:411 / 417
页数:7
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