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急性淋巴细胞白血病中染色体易位产生的嵌合癌蛋白。

Chimaeric oncoproteins resulting from chromosomal translocations in acute lymphoblastic leukaemia.

作者信息

Hunger S P, Cleary M L

机构信息

Department of Pathology, Stanford University Medical Center, CA 94305.

出版信息

Semin Cancer Biol. 1993 Dec;4(6):387-99.

PMID:8142624
Abstract

A major mode of proto-oncogene activation by chromosomal translocations concerns the creation of fusion genes which encode chimaeric proteins. The largest class of oncogenes identified to date is the transcription factors, which are involved in control of cellular proliferation and differentiation via regulation of target gene transcription. Protein chimaeras that result from translocations in childhood ALL include two which involve the 19p13.3 gene E2A and a large heterogeneous group involving HRX located at chromosome band 11q23. Functional studies demonstrate that E2A fusion proteins function as chimaeric transcription factors, and structural features suggest that HRX fusion proteins may have analogous properties.

摘要

染色体易位激活原癌基因的一种主要方式涉及融合基因的产生,这些融合基因编码嵌合蛋白。迄今为止鉴定出的最大一类癌基因是转录因子,它们通过调控靶基因转录参与细胞增殖和分化的控制。儿童急性淋巴细胞白血病(ALL)中因易位产生的蛋白质嵌合体包括两种涉及19p13.3基因E2A的嵌合体,以及一大类涉及位于染色体11q23带的HRX的异质群体。功能研究表明,E2A融合蛋白作为嵌合转录因子发挥作用,结构特征表明HRX融合蛋白可能具有类似特性。

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