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大鼠脑前脑啡肽原mRNA。cDNA克隆、一级结构及其在中枢神经系统中的分布。

Rat brain preproenkephalin mRNA. cDNA cloning, primary structure, and distribution in the central nervous system.

作者信息

Yoshikawa K, Williams C, Sabol S L

出版信息

J Biol Chem. 1984 Nov 25;259(22):14301-8.

PMID:6548748
Abstract

A cDNA-clone library was constructed from poly-adenylated RNA of Fischer rat striatum and screened for inserts coding for the enkephalin precursor preproenkephalin. The insert of one positive clone, pRPE2, was sequenced and found to contain the coding sequence (810 bases), as well as 316 and 155 bases of the 3' and 5' untranslated regions, respectively, of rat preproenkephalin mRNA. The primary structure of rat preproenkephalin (269 amino acids, Mr 30,932) is similar to those of previously sequenced bovine and human preproenkephalins (78 and 82% matched residues, respectively), and contains four copies of Met-enkephalin, one of Leu-enkephalin, one of Met-enkephalin-Arg6-Gly7-Leu8, and one of Met-enkephalin-Arg6-Phe7. Cell-free translation of rat striatal mRNA selected by hybridization with pRPE2 DNA resulted in the synthesis of a 31,000-Da protein. Southern analysis of rat genomic DNA with 32P-labeled pRPE2 fragments is consistent with a single preproenkephalin gene. A 32P-labeled pRPE2 fragment hybridized specifically with preproenkephalin mRNA (approximately 1500 bases) on Northern blots of polyadenylated or total RNA of all brain regions but not liver. Relative abundances of preproenkephalin mRNA in total RNA of specific regions of the rat central nervous system, determined by a sensitive dot-blot hybridization assay, had the following order: striatum much greater than hypothalamus, pons-medulla, spinal cord greater than cerebellum, midbrain, frontal cortex greater than hippocampus, thalamus. The pRPE2 probe is useful for the analysis of the dynamics of preproenkephalin mRNA in rat neurons.

摘要

从费希尔大鼠纹状体的多聚腺苷酸化RNA构建了一个cDNA克隆文库,并筛选编码脑啡肽前体前脑啡肽原的插入片段。对一个阳性克隆pRPE2的插入片段进行测序,发现其包含大鼠前脑啡肽原mRNA的编码序列(810个碱基),以及3'和5'非翻译区的316个和155个碱基。大鼠前脑啡肽原(269个氨基酸,Mr 30,932)的一级结构与先前测序的牛和人前脑啡肽原相似(分别有78%和82%的匹配残基),并包含四个甲硫氨酸脑啡肽拷贝、一个亮氨酸脑啡肽拷贝、一个甲硫氨酸脑啡肽-精氨酸6-甘氨酸7-亮氨酸8拷贝和一个甲硫氨酸脑啡肽-精氨酸6-苯丙氨酸7拷贝。用pRPE2 DNA杂交选择的大鼠纹状体mRNA进行无细胞翻译,产生了一种31,000道尔顿的蛋白质。用32P标记的pRPE2片段对大鼠基因组DNA进行Southern分析,结果与单个前脑啡肽原基因一致。一个32P标记的pRPE2片段在所有脑区而非肝脏的多聚腺苷酸化或总RNA的Northern印迹上与前脑啡肽原mRNA(约1500个碱基)特异性杂交。通过灵敏的点杂交分析测定,大鼠中枢神经系统特定区域总RNA中前脑啡肽原mRNA的相对丰度顺序如下:纹状体远大于下丘脑、脑桥-延髓、脊髓大于小脑、中脑、额叶皮质大于海马体、丘脑。pRPE2探针可用于分析大鼠神经元中前脑啡肽原mRNA的动态变化。

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