肺泡横纹肌肉瘤癌基因PAX3-FKHR的基因分析。

B E Kempf, P K Vogt
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引用次数: 0

摘要

人肺泡横纹肌肉瘤PAX3-FKHR融合蛋白由PAX3的dna结合域和FKHR的转录激活域组成。它在鸡胚成纤维细胞(CEFs)培养中诱导致癌转化。pax3 - fkhr转化的cef连续培养1年以上;静息时,部分培养物分化成几种不同的细胞类型。缺失分析表明,DNA结合和转录激活是诱导pax3 - fkhr转化的细胞表型所必需的。与表达野生型PAX3-FKHR的CEFs不同,DNA结合或反活化减少的突变PAX3-FKHR蛋白会诱导细胞形态和生长行为的改变。完全缺乏DNA结合或转激活潜能的突变蛋白无法转化。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A genetic analysis of PAX3-FKHR, the oncogene of alveolar rhabdomyosarcoma.

The PAX3-FKHR fusion protein of human alveolar rhabdomyosarcoma consists of the DNA-binding domains of PAX3 and the transcriptional activation domain of FKHR. It induces oncogenic transformation in cultures of chicken embryo fibroblasts (CEFs). PAX3-FKHR-transformed CEFs have been kept in continuous culture for more than 1 year; when quiescent, portions of the cultures differentiate into several distinct cell types. Deletion analysis suggests that both DNA binding and transcriptional activation are required for the induction of the PAX3-FKHR-transformed cellular phenotype. Mutant PAX3-FKHR proteins with reduced DNA binding or transactivation induce altered cellular morphologies and growth behavior distinct from that of CEFs expressing wild-type PAX3-FKHR. Mutant proteins that completely lack DNA binding or transactivation potential fail to transform.

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