多种机制对人融合癌基因RUNX1-RUNX1T1 mRNA多样性的贡献

Ilya M. Ilyushonak, A. Migas, A. Sukhareuski, Aksana Schneider, V. Grinev
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引用次数: 1

摘要

在这项工作中,我们使用了一组综合的融合癌基因RUNX1-RUNX1T1替代外显子来分析其mRNA的生成模式。我们发现大部分的备选外显子都是规范外显子的修饰变体,并且转录本,包括这些外显子,具有非常低的表达水平。“热区”,包括外显子4a、6、8b、9、11和12,产生了大约80%的这种变异。我们还描述了RUNX1-RUNX1T1的一个新的转录起始区,并提供了融合rna与正常和缩短的3 ' - utr在白血病细胞中共表达的证据。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The contribution of various mechanisms to mRNA diversity of human fusion oncogene RUNX1-RUNX1T1
In this work, we used a comprehensive set of the fusion oncogene RUNX1-RUNX1T1 alternative exons to analyze the patterns of its mRNA generation. We found that the waste majority of alternative exons are modified variants of canonical exons, and the transcripts, including such exons, have a very low expression level. The «hot regions», including exons 4a, 6, 8b, 9, 11 and 12, produces about 80 % of such variants. Also we described a new transcription start region of RUNX1-RUNX1T1 and provide the evidences of co-expression of the fusion RNAs with normal and shortened 3′-UTRs in leukemic cells.
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