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[细胞分化和肿瘤发生过程中同工酶基因表达的改变]

[Alteration of isozyme gene expression during cell differentiation and oncogenesis].

作者信息

Yamada K, Noguchi T

机构信息

Department of Nutrition and Physiological Chemistry, Osaka University Medical School.

出版信息

Nihon Rinsho. 1995 May;53(5):1112-8.

PMID:7602764
Abstract

Rat pyruvate kinase (PK) has four isozymes, called the M1-, M2-, L-, and R-types. The M1- and M2-type isozymes of PK are produced from the PKM gene by alternative splicing, whereas the L- and R-type isozymes of PK are produced from the PKL gene by use of different tissue-specific promoters. In early development, only M2-type PK expresses in all tissues. After late morphogenesis, M1-, L-, and R-type PK express tissue-specifically. In contrast, cell proliferation such as regenerating liver and oncogenesis lead to decrease or cessation of the expression of tissue-specific PK isozymes and to stimulation of the expression of M2-type PK. These phenomena from the point of view transcriptional regulatory apparatus of the PKM and PKL gene are discussed.

摘要

大鼠丙酮酸激酶(PK)有四种同工酶,分别称为M1型、M2型、L型和R型。PK的M1型和M2型同工酶由PKM基因通过可变剪接产生,而PK的L型和R型同工酶由PKL基因通过使用不同的组织特异性启动子产生。在早期发育过程中,只有M2型PK在所有组织中表达。在晚期形态发生后,M1型、L型和R型PK进行组织特异性表达。相反,诸如再生肝脏和肿瘤发生等细胞增殖会导致组织特异性PK同工酶的表达减少或停止,并刺激M2型PK的表达。本文从PKM和PKL基因转录调控机制的角度对这些现象进行了讨论。

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