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人ADP-核糖基化因子的分子克隆、序列分析及mRNA表达

Molecular cloning, sequence analysis and mRNA expression of human ADP-ribosylation factor.

作者信息

Peng Z G, Calvert I, Clark J, Helman L, Kahn R, Kung H F

机构信息

Program Resources, Inc., National Cancer Institute-Frederick Cancer Research Facility, MD 21701.

出版信息

Biofactors. 1989 Mar;2(1):45-9.

PMID:2535313
Abstract

The ADP-ribosylation factor (ARF) is the small (21 kb) GTP-binding protein required for the efficient cholera toxin-catalyzed ADP-ribosylation of purified Gs, the stimulating regulatory component of adenylate cyclase. Human ARF cDNA clones were obtained from a human cDNA library by cross-species hybridization with bovine ARF1, and the nucleotide and deduced amino acid sequences were determined. Comparison of the sequences of human and bovine ARF1 showed 90% identity at the nucleotide level and 100% identity at the amino acid level, demonstrating the highly conserved nature of the ARF protein. Using human ARF cDNA as the probe, we have detected ARF messenger RNA (approximately 2.2-2.3 kb) in a wide variety of human tissues and tumor cell lines.

摘要

ADP核糖基化因子(ARF)是一种小的(21 kb)GTP结合蛋白,它是霍乱毒素高效催化纯化的Gs(腺苷酸环化酶的刺激调节成分)进行ADP核糖基化所必需的。通过与人ARF1进行跨物种杂交,从人cDNA文库中获得了人ARF cDNA克隆,并测定了其核苷酸和推导的氨基酸序列。人和牛ARF1序列的比较显示,在核苷酸水平上有90%的同一性,在氨基酸水平上有100%的同一性,这表明ARF蛋白具有高度保守性。以人ARF cDNA为探针,我们在多种人体组织和肿瘤细胞系中检测到了ARF信使RNA(约2.2 - 2.3 kb)。

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