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3pK,一种位于小细胞肺癌肿瘤抑制基因区域的新型丝裂原活化蛋白激酶激活的蛋白激酶。

3pK, a new mitogen-activated protein kinase-activated protein kinase located in the small cell lung cancer tumor suppressor gene region.

作者信息

Sithanandam G, Latif F, Duh F M, Bernal R, Smola U, Li H, Kuzmin I, Wixler V, Geil L, Shrestha S

机构信息

Biological Carcinogenesis and Development Program, PRI/DynCorp, National Cancer Institute, Frederick Cancer Research and Development Center, Maryland 21702-1201, USA.

出版信息

Mol Cell Biol. 1996 Mar;16(3):868-76. doi: 10.1128/MCB.16.3.868.

Abstract

NotI linking clones, localized to the human chromosome 3p21.3 region and homozygously deleted in small cell lung cancer cell lines NCI-H740 and NCI-H1450, were used to search for a putative tumor suppressor gene(s). One of these clones, NL1G210, detected a 2.5-kb mRNA in all examined human tissues, expression being especially high in the heart and skeletal muscle. Two overlapping cDNA clones containing the entire open reading frame were isolated from a human heart cDNA library and fully characterized. Computer analysis and a search of the GenBank database to reveal high sequence identity of the product of this gene to serine-threonine kinases, especially to mitogen-activated protein kinase-activated protein kinase 2, a recently described substrate of mitogen-activated kinases. Sequence identitiy was 72% at the nucleotide level and 75% at the amino acid level, strongly suggesting that this protein is a serine-threonine kinase. Here we demonstrate that the new gene, referred to as 3pK (for chromosome 3p kinase), in fact encodes a mitogen-activated protein kinase-regulated protein serine-threonine kinase with a novel substrate specificity.

摘要

定位于人类染色体3p21.3区域且在小细胞肺癌细胞系NCI-H740和NCI-H1450中纯合缺失的NotI连接克隆,被用于寻找一个假定的肿瘤抑制基因。这些克隆之一,NL1G210,在所有检测的人体组织中检测到一个2.5 kb的mRNA,在心脏和骨骼肌中表达尤其高。从人心脏cDNA文库中分离出两个包含完整开放阅读框的重叠cDNA克隆并进行了全面鉴定。通过计算机分析和对GenBank数据库的搜索,发现该基因产物与丝氨酸-苏氨酸激酶有高度的序列同源性,尤其是与丝裂原活化蛋白激酶激活的蛋白激酶2,这是一种最近描述的丝裂原活化激酶的底物。在核苷酸水平上序列同源性为72%,在氨基酸水平上为75%,强烈表明该蛋白是一种丝氨酸-苏氨酸激酶。在这里,我们证明这个新基因,称为3pK(3号染色体p臂激酶),实际上编码一种具有新底物特异性的丝裂原活化蛋白激酶调节的蛋白丝氨酸-苏氨酸激酶。

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