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EWS/FLI1诱导的躁狂边缘蛋白使NIH 3T3细胞具有致瘤性。

EWS/FLI1-induced manic fringe renders NIH 3T3 cells tumorigenic.

作者信息

May W A, Arvand A, Thompson A D, Braun B S, Wright M, Denny C T

机构信息

Department of Pediatrics, University of Alabama at Birmingham School of Medicine, USA.

出版信息

Nat Genet. 1997 Dec;17(4):495-7. doi: 10.1038/ng1297-495.

Abstract

EWS/FLI1, a fusion gene found in Ewing's sarcoma, encodes a transcriptional regulator and promotes cellular transformation by modulating the transcription of specific target genes. We have found that EWS/FLI1 and structurally related fusion proteins upregulate manic fringe (MFNG), a recently described member of the Fringe gene family instrumental in somatic development. MFNG is also expressed in human tumour-derived cell lines expressing EWS/FLI1. Overexpression of MFNG in NIH 3T3 cells renders them tumorigenic in mice with severe combined immunodeficiency disease (SCID). These data demonstrate that part of the oncogenic effect of EWS/FLI1 is to transcriptionally deregulate a member of a family of morphogenic genes.

摘要

EWS/FLI1是在尤因肉瘤中发现的一种融合基因,编码一种转录调节因子,并通过调节特定靶基因的转录促进细胞转化。我们发现EWS/FLI1和结构相关的融合蛋白上调了躁狂边缘蛋白(MFNG),这是最近描述的在体细胞发育中起重要作用的边缘基因家族的成员。MFNG也在表达EWS/FLI1的人肿瘤衍生细胞系中表达。在NIH 3T3细胞中过表达MFNG会使其在患有严重联合免疫缺陷疾病(SCID)的小鼠中具有致瘤性。这些数据表明EWS/FLI1的致癌作用部分是通过转录失调一个形态发生基因家族的成员来实现的。

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