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通过代表性差异分析鉴定尤因肉瘤EWS/FLI融合蛋白的靶基因

Identification of target genes for the Ewing's sarcoma EWS/FLI fusion protein by representational difference analysis.

作者信息

Braun B S, Frieden R, Lessnick S L, May W A, Denny C T

机构信息

Molecular Biology Institute, University of California, Los Angeles 90024, USA.

出版信息

Mol Cell Biol. 1995 Aug;15(8):4623-30. doi: 10.1128/MCB.15.8.4623.

Abstract

The EWS/FLI-1 fusion gene results from the 11;22 chromosomal translocation in Ewing's sarcoma. The product of the gene is one of a growing number of structurally altered transcription factors implicated in oncogenesis. We have employed a subtractive cloning strategy of representational difference analysis in conjunction with a model transformation system to identify genes transcribed in response to EWS/FLI. We have characterized eight transcripts that are dependent on EWS/FLI for expression and two transcripts that are repressed in response to EWS/FLI. Three of the former were identified by sequence analysis as stromelysin 1, a murine homolog of cytochrome P-450 F1 and cytokeratin 15. Stromelysin 1 is induced rapidly after expression of EWS/FLI, suggesting that the stromelysin 1 gene may be a direct target gene of EWS/FLI. These results demonstrate that expression of EWS/FLI leads to significant changes in the transcription of specific genes and that these effects are at least partially distinct from those caused by expression of germ line FLI-1. The representational difference analysis technique can potentially be applied to investigate transformation pathways activated by a broad array of genes in different tumor systems.

摘要

EWS/FLI-1融合基因源于尤因肉瘤中的11;22染色体易位。该基因的产物是越来越多与肿瘤发生相关的结构改变的转录因子之一。我们采用了代表性差异分析的消减克隆策略,并结合模型转化系统来鉴定响应EWS/FLI而转录的基因。我们已经鉴定出八个依赖EWS/FLI表达的转录本和两个响应EWS/FLI而被抑制的转录本。通过序列分析,前三个被鉴定为基质金属蛋白酶1、细胞色素P-450 F1的小鼠同源物和细胞角蛋白15。基质金属蛋白酶1在EWS/FLI表达后迅速被诱导,这表明基质金属蛋白酶1基因可能是EWS/FLI的直接靶基因。这些结果表明,EWS/FLI的表达导致特定基因转录的显著变化,并且这些效应至少部分不同于由种系FLI-1表达引起的效应。代表性差异分析技术有可能应用于研究不同肿瘤系统中由多种基因激活的转化途径。

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