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大鼠前促生长抑素原mRNA的克隆与特性分析

Cloning and characterization of a mRNA-encoding rat preprosomatostatin.

作者信息

Funckes C L, Minth C D, Deschenes R, Magazin M, Tavianini M A, Sheets M, Collier K, Weith H L, Aron D C, Roos B A, Dixon J E

出版信息

J Biol Chem. 1983 Jul 25;258(14):8781-7.

PMID:6134733
Abstract

An undecanucleotide extended hybridization probe has been used to screen a rat medullary thyroid carcinoma cDNA library for clones which contain preprosomatostatin sequences. The nucleotide sequence encoding rat preprosomatostatin is reported. The sequence of cDNA contains 67 nucleotides in the 3'-noncoding region, 84 nucleotides in the 5'-untranslated region, and 458 bases corresponding to the coding region. The mRNA codes for a somatostatin precursor 116 amino acids in length (Mr = 12,773). The preprosomatostatin has a sequence of hydrophobic amino acids at the NH2 terminus, followed by a peptide of approximately 78 residues, which precedes somatostatin-14. The amino acid sequences of rat and human preprosomatostatin (Shen, L. P., Pictet, R. L., and Rutter, W. J. (1982) Proc. Natl. Acad. Sci. U.S.A. 79, 4575-4579) differ by only 4 amino acid residues. Translation of rat poly(A) RNA in a rabbit reticulocyte cell-free system followed by immunoprecipitation with antisera directed against somatostatin-14 demonstrated the synthesis of a single protein having a molecular weight of 15,000. Two proteins having molecular weights of 14,000 and 15,000 are immunoprecipitated from a wheat germ cell-free translation mixture. Northern analysis of the somatostatin mRNA indicated that it is approximately 850 nucleotides in length. Analysis of several medullary thyroid carcinomas demonstrated that one tumor, designated WF, had immunoreactive somatostatin-14 in concentrations of 350 ng of somatostatin-14/mg of protein and somatostatin mRNA that represented 10% of the cellular poly(A) RNA. Cell lines derived from this tumor may provide an attractive system to investigate the regulation of somatostatin gene expression.

摘要

一种十一核苷酸延伸杂交探针已被用于筛选大鼠甲状腺髓样癌cDNA文库,以寻找包含前促生长抑素原序列的克隆。报道了编码大鼠前促生长抑素原的核苷酸序列。该cDNA序列在3'非编码区含有67个核苷酸,在5'非翻译区含有84个核苷酸,以及与编码区对应的458个碱基。该mRNA编码一个长度为116个氨基酸的生长抑素前体(Mr = 12,773)。前促生长抑素原在NH2末端有一段疏水氨基酸序列,接着是一个约78个残基的肽段,该肽段先于生长抑素-14。大鼠和人类前促生长抑素原的氨基酸序列(沈立平、皮克特、鲁特,(1982年)《美国国家科学院院刊》79卷,4575 - 4579页)仅相差4个氨基酸残基。在兔网织红细胞无细胞体系中对大鼠多聚腺苷酸RNA进行翻译,然后用针对生长抑素-14的抗血清进行免疫沉淀,结果表明合成了一种分子量为15,000的单一蛋白质。从麦胚无细胞翻译混合物中免疫沉淀出两种分子量分别为14,000和15,000的蛋白质。对生长抑素mRNA的Northern分析表明其长度约为850个核苷酸。对几种甲状腺髓样癌的分析表明,其中一个名为WF的肿瘤,其免疫反应性生长抑素-14的浓度为350 ng生长抑素-14/mg蛋白质,生长抑素mRNA占细胞多聚腺苷酸RNA的10%。源自该肿瘤的细胞系可能为研究生长抑素基因表达的调控提供一个有吸引力的系统。

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