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RBM4介导的全转录组可变剪接靶点及其在癌症中的潜在作用

Transcriptome-wide targets of alternative splicing by RBM4 and possible role in cancer.

作者信息

Markus M Andrea, Yang Yee Hwa J, Morris Brian J

机构信息

Basic & Clinical Genomics Laboratory, School of Medical Sciences and Bosch Institute, The University of Sydney, Sydney, New South Wales, Australia.

School of Mathematics and Statistics, The University of Sydney, Sydney, New South Wales, Australia.

出版信息

Genomics. 2016 Apr;107(4):138-44. doi: 10.1016/j.ygeno.2016.02.003. Epub 2016 Feb 17.

Abstract

This study determined transcriptome-wide targets of the splicing factor RBM4 using Affymetrix GeneChip(®) Human Exon 1.0 ST Arrays and HeLa cells treated with RBM4-specific siRNA. This revealed 238 transcripts that were targeted for alternative splicing. Cross-linking and immunoprecipitation experiments identified 945 RBM4 targets in mouse HEK293 cells, 39% of which were ascribed to "alternative splicing" by in silico pathway analysis. Mouse embryonic stem cells transfected with Rbm4 siRNA hairpins exhibited reduced colony numbers and size consistent with involvement of RBM4 in cell proliferation. RBM4 cDNA probing of a cancer cDNA array involving 18 different tumor types from 13 different tissues and matching normal tissue found overexpression of RBM4 mRNA (p<0.01) in cervical, breast, lung, colon, ovarian and rectal cancers. Many RBM4 targets we identified have been implicated in these cancers. In conclusion, our findings reveal transcriptome-wide targets of RBM4 and point to potential cancer-related targets and mechanisms that may involve RBM4.

摘要

本研究使用Affymetrix GeneChip(®) Human Exon 1.0 ST芯片以及用RBM4特异性小干扰RNA(siRNA)处理的HeLa细胞,确定了剪接因子RBM4在全转录组范围内的靶标。这揭示了238个发生可变剪接的转录本。交联免疫沉淀实验在小鼠HEK293细胞中鉴定出945个RBM4靶标,通过计算机通路分析,其中39%归因于“可变剪接”。用Rbm4 siRNA发夹转染的小鼠胚胎干细胞显示集落数量和大小减少,这与RBM4参与细胞增殖一致。对来自13种不同组织的18种不同肿瘤类型及匹配的正常组织的癌症cDNA阵列进行RBM4 cDNA探针检测,发现RBM4 mRNA在宫颈癌、乳腺癌、肺癌、结肠癌、卵巢癌和直肠癌中过表达(p<0.01)。我们鉴定出的许多RBM4靶标都与这些癌症有关。总之,我们的研究结果揭示了RBM4在全转录组范围内的靶标,并指出了可能涉及RBM4的潜在癌症相关靶标和机制。

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