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四氢生物蝶呤辅因子生物合成:大鼠脑和颈上神经节中鸟苷三磷酸环化水解酶I信使核糖核酸的表达

Tetrahydrobiopterin cofactor biosynthesis: GTP cyclohydrolase I mRNA expression in rat brain and superior cervical ganglia.

作者信息

Hirayama K, Lentz S I, Kapatos G

机构信息

Department of Psychiatry, Wayne State University School of Medicine, Detroit, Michigan 48201.

出版信息

J Neurochem. 1993 Sep;61(3):1006-14. doi: 10.1111/j.1471-4159.1993.tb03614.x.

Abstract

GTP cyclohydrolase I (GTPCH) is the rate-limiting enzyme in the biosynthesis of tetrahydrobiopterin, the reduced pteridine cofactor required for catecholamine (CA), indoleamine, and nitric oxide biosynthesis. We have used the reverse transcription-polymerase chain reaction technique, based on the published cDNA sequence for rat liver GTPCH, to clone a portion of the GTPCH transcript from rat adrenal gland mRNA and have used this clone for the analysis of GTPCH mRNA in brain and other tissues of the rat by northern blot, nuclease protection assay, and in situ hybridization. Two GTPCH mRNA transcripts of 1.2 and 3.8 kb in length were detected by northern blot, with the 1.2-kb form predominating in the liver and the 3.8-kb form in the pineal gland, adrenal gland, brainstem, and hypothalamic neurons maintained in culture. In situ hybridization studies localized GTPCH mRNA to CA-containing perikarya in the locus ceruleus, ventral tegmental area, and substantia nigra, pars compacta. Levels of GTPCH mRNA in central and peripheral catecholamine neurons determined by nuclease protection assay were increased twofold 24 h after a single injection of the CA-depleting drug reserpine; both the 1.2- and 3.8-kb transcripts were increased in the adrenal gland. Low levels of GTPCH mRNA were also detected by nuclease protection assay in the striatum, hippocampus, and cerebellum, brain regions that do not contain monoaminergic perikarya.

摘要

鸟苷三磷酸环化水解酶I(GTPCH)是四氢生物蝶呤生物合成中的限速酶,四氢生物蝶呤是儿茶酚胺(CA)、吲哚胺和一氧化氮生物合成所需的还原型蝶呤辅因子。我们基于已发表的大鼠肝脏GTPCH的cDNA序列,使用逆转录-聚合酶链反应技术,从大鼠肾上腺mRNA中克隆了一部分GTPCH转录本,并将该克隆用于通过Northern印迹、核酸酶保护分析和原位杂交来分析大鼠脑和其他组织中的GTPCH mRNA。通过Northern印迹检测到两种长度分别为1.2 kb和3.8 kb的GTPCH mRNA转录本,1.2 kb的形式在肝脏中占主导,而3.8 kb的形式在松果体、肾上腺、脑干和培养的下丘脑神经元中占主导。原位杂交研究将GTPCH mRNA定位到蓝斑、腹侧被盖区和黑质致密部中含CA的核周体。通过核酸酶保护分析确定,单次注射CA耗竭药物利血平24小时后,中枢和外周儿茶酚胺神经元中的GTPCH mRNA水平增加了两倍;肾上腺中1.2 kb和3.8 kb的转录本均增加。通过核酸酶保护分析在纹状体、海马体和小脑中也检测到低水平的GTPCH mRNA,这些脑区不含单胺能核周体。

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