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小鼠过氧化物酶体增殖物激活受体γ(mPPARγ)基因的结构组织:不同启动子的使用和不同的剪接产生两种mPPARγ亚型。

Structural organization of mouse peroxisome proliferator-activated receptor gamma (mPPAR gamma) gene: alternative promoter use and different splicing yield two mPPAR gamma isoforms.

作者信息

Zhu Y, Qi C, Korenberg J R, Chen X N, Noya D, Rao M S, Reddy J K

机构信息

Department of Pathology, Northwestern University Medical School, Chicago, IL 60611, USA.

出版信息

Proc Natl Acad Sci U S A. 1995 Aug 15;92(17):7921-5. doi: 10.1073/pnas.92.17.7921.

DOI:10.1073/pnas.92.17.7921
PMID:7644514
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC41258/
Abstract

To gain insight into the regulation of expression of peroxisome proliferator-activated receptor (PPAR) isoforms, we have determined the structural organization of the mouse PPAR gamma (mPPAR gamma) gene. This gene extends > 105 kb and gives rise to two mRNAs (mPPAR gamma 1 and mPPAR gamma 2) that differ at their 5' ends. The mPPAR gamma 2 cDNA encodes an additional 30 amino acids N-terminal to the first ATG codon of mPPAR gamma 1 and reveals a different 5' untranslated sequence. We show that mPPAR gamma 1 mRNA is encoded by eight exons, whereas the mPPAR gamma 2 mRNA is encoded by seven exons. Most of the 5' untranslated sequence of mPPAR gamma 1 mRNA is encoded by two exons, whereas the 5' untranslated sequence and the extra 30 N-terminal amino acids of mPPAR gamma 2 are encoded by one exon, which is located between the second and third exons coding for mPPAR gamma 1. The last six exons of mPPAR gamma gene code for identical sequences in mPPAR gamma 1 and mPPAR gamma 2 isoforms. The mPPAR gamma 1 and mPPAR gamma 2 isoforms are transcribed from different promoters. The mPPAR gamma gene has been mapped to chromosome 6 E3-F1 by in situ hybridization using a biotin-labeled probe. These results establish that at least one of the PPAR genes yields more than one protein product, similar to that encountered with retinoid X receptor and retinoic acid receptor genes. The existence of multiple PPAR isoforms transcribed from different promoters could increase the diversity of ligand and tissue-specific transcriptional responses.

摘要

为深入了解过氧化物酶体增殖物激活受体(PPAR)亚型的表达调控机制,我们确定了小鼠PPARγ(mPPARγ)基因的结构组织。该基因长度超过105 kb,可产生两种mRNA(mPPARγ1和mPPARγ2),它们在5'端存在差异。mPPARγ2 cDNA在mPPARγ1第一个ATG密码子的N端额外编码30个氨基酸,并揭示了不同的5'非翻译序列。我们发现mPPARγ1 mRNA由8个外显子编码,而mPPARγ2 mRNA由7个外显子编码。mPPARγ1 mRNA的大部分5'非翻译序列由两个外显子编码,而mPPARγ2的5'非翻译序列和额外的30个N端氨基酸由一个外显子编码,该外显子位于编码mPPARγ1的第二个和第三个外显子之间。mPPARγ基因的最后6个外显子在mPPARγ1和mPPARγ2亚型中编码相同的序列。mPPARγ1和mPPARγ2亚型从不同的启动子转录。使用生物素标记的探针通过原位杂交将mPPARγ基因定位到6号染色体E3 - F1区域。这些结果表明,至少有一个PPAR基因会产生不止一种蛋白质产物,这与视黄酸X受体和视黄酸受体基因的情况类似。从不同启动子转录产生多种PPAR亚型的现象可能会增加配体和组织特异性转录反应的多样性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b55d/41258/c1799932eb82/pnas01495-0328-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b55d/41258/c1799932eb82/pnas01495-0328-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b55d/41258/c1799932eb82/pnas01495-0328-a.jpg

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