2 CLOSELY LINKED BUT SEPARABLE PROMOTERS FOR HUMAN NEURONAL NITRIC-OXIDE SYNTHASE GENE-TRANSCRIPTION

被引:80
作者
XIE, JL
RODDY, P
RIFE, TK
MURAD, F
YOUNG, AP
机构
[1] OHIO STATE UNIV,OHIO STATE BIOCHEM PROGRAM,CTR NEUROBIOTECHNOL,COLUMBUS,OH 43210
[2] OHIO STATE UNIV,COLL PHARM,DIV PHARMACOL,COLUMBUS,OH 43210
[3] MOLEC GERIATR CORP,LAKE BLUFF,IL 60044
关键词
NEURONAL GENE EXPRESSION; CPG ISLANDS; TRANSIENT EXPRESSION; EXON MAPPING;
D O I
10.1073/pnas.92.4.1242
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
In this report we demonstrate that the human cerebellum contains neuronal nitric oxide synthase (nNOS) mRNAs with two distinct 5'-untranslated regions that are encoded through use of closely linked but separate promoters. nNOS cDNA clones were shown to contain different 5' terminal exons spliced to a common exon 2. Genomic cloning and sequence analysis demonstrate that the unique exons are positioned within 300 bp of each other but separated from exon 2 by an intron that is at least 20 kb in length. A CpG island engulfs the downstream 5'-terminal exon. In contrast, most of the upstream exon resides outside of this CpG island. Interestingly, the upstream exon includes a GT dinucleotide repeat. A fusion gene with a 414-bp nNOS genomic fragment that includes a portion of the upstream 5'-terminal exon and its immediate 5'-flanking DNA is expressed in transfected HeLa cells. Also expressed is a fusion gene that contains the luciferase reporter under transcriptional control by a 308-bp genomic fragment that includes the region separating both d'-terminal exons. These results indicate that expression of these exons is subject to transcriptional control by separate promoters. However, the proximity of these promoters raise the possibility that complex interactions may be involved in regulating nNOS gene expression at these sites.
引用
收藏
页码:1242 / 1246
页数:5
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