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编码来自转化人淋巴细胞的一种假定磷脂酶C的完整互补DNA。

Complete cDNA encoding a putative phospholipase C from transformed human lymphocytes.

作者信息

Ohta S, Matsui A, Nazawa Y, Kagawa Y

机构信息

Department of Biochemistry, Jichi Medical School, Tochigi-ken, Japan.

出版信息

FEBS Lett. 1988 Dec 19;242(1):31-5. doi: 10.1016/0014-5793(88)80979-7.

Abstract

Phosphoinositide-specific phospholipase C (PLC) is a crucial enzyme in transmembrane signaling. A cDNA encoding the putative phospholipase C was cloned from human lymphocytes that were transformed by infection with Epstein-Barr virus. The deduced amino acid sequence of the cDNA accounted for 146.1 kDa of the molecular mass of the complete enzyme and showed 50.2% sequence similarity to bovine brain PLC. This cDNA contained regions, the sequences of which were similar to those of some tyrosine kinase-related oncogene products. Northern blotting demonstrated that the mRNA for this PLC is expressed in human promyelocytic leukemia cells (HL-60). Since the other cloned cDNAs for PLCs could not hybridize with the RNA from this cell, it is strongly suggested that the gene obtained here encodes an additional isozyme of PLC in blood cells.

摘要

磷酸肌醇特异性磷脂酶C(PLC)是跨膜信号传导中的一种关键酶。从被爱泼斯坦-巴尔病毒感染而转化的人淋巴细胞中克隆出了编码假定磷脂酶C的cDNA。该cDNA推导的氨基酸序列占完整酶分子量的146.1 kDa,与牛脑PLC的序列相似性为50.2%。此cDNA包含一些区域,其序列与某些酪氨酸激酶相关癌基因产物的序列相似。Northern印迹法表明,该PLC的mRNA在人早幼粒细胞白血病细胞(HL-60)中表达。由于其他克隆的PLC cDNA不能与此细胞的RNA杂交,强烈提示此处获得的基因编码血细胞中一种额外的PLC同工酶。

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