Transcription of human neuronal nitric oxide synthase mRNAs derived from different first exons is partly controlled by exon 1-specific promoter sequences

被引:39
作者
Bros, M
Boissel, JP
Gödtel-Armbrust, U
Förstermann, U
机构
[1] Johannes Gutenberg Univ Mainz, Dept Pharmacol, D-55101 Mainz, Germany
[2] Johannes Gutenberg Univ Mainz, Dept Dermatol, D-55101 Mainz, Germany
关键词
alternative splicing; reporter gene assays; RT real-time PCR; cortex; hippocampus; skin; skeletal muscle; heart; testis; kidney;
D O I
10.1016/j.ygeno.2005.11.013
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
The human neuronal nitric oxide synthase (NOSI) gene is subject to extensive splicing. A total of 12 NOSI mRNA species have been identified. They differ in their 5' ends and are derived from 12 different first exons (termed exons Ia to II). Various cell lines whose NOSI first exon expression patterns were representative of human brain, skin, and skeletal muscle were identified. These included A673 neuroepithelioma cells, SK-N-MC neuroblastoma cells, HaCaT keratinocyte-like cells, and C2C12 myocyte-like cells. In these cell lines, correlations were found between the exon I variants preferentially expressed and the promoter activities of their cognate 5' flanking sequences. These data demonstrate that expression of the different exon I-related splice variants of NOSI mRNA is controlled directly (at least in part) by the associated 5' flanking sequences. (c) 2005 Elsevier Inc. All rights reserved.
引用
收藏
页码:463 / 473
页数:11
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