Okumura Masayo, Kondo Shinichi, Ogata Maiko, Kanemoto Soshi, Murakami Tomohiko, Yanagida Kanta, Saito Atsushi, Imaizumi Kazunori
Division of Structural Cellular Biology, The Graduate School of Biological Sciences, Nara Institute of Science and Technology (NAIST), 8916-5 Takayama, Ikoma, Nara 630-0101, Japan.
Biochem Biophys Res Commun. 2005 Aug 19;334(1):23-9. doi: 10.1016/j.bbrc.2005.06.057.
Gene expression can be regulated not only by transcription and post-transcriptional modifications, but also by splicing regulation. Recent genome-wide analyses have indicated that up to 70% of human genes may have alternatively spliced forms, suggesting that splicing regulation affects a wide range of gene expression. Tumor tissues show significantly altered protein expressions, and this is also thought to be affected by alternative splicing. Although some alternative splicing events have been reported to be cancer specific and others have been predicted from database analyses, the process of alternative splicing and its regulatory machinery are hardly understood. We searched for and detected alternative splicing events that alter protein splicing in all or a subset of tumor tissues. The results revealed tissue-specific alterations of splicing regulation by tumorigenesis, and regulatory cis-element analyses further suggested that multiple splicing regulatory machineries were affected by this process.
基因表达不仅可以通过转录和转录后修饰来调控,还可以通过剪接调控来实现。最近的全基因组分析表明,高达70%的人类基因可能具有可变剪接形式,这表明剪接调控会影响广泛的基因表达。肿瘤组织显示出明显改变的蛋白质表达,并且这也被认为受可变剪接的影响。尽管已报道一些可变剪接事件具有癌症特异性,并且其他一些事件已通过数据库分析预测得出,但可变剪接过程及其调控机制却几乎不为人所知。我们搜索并检测了在所有或部分肿瘤组织中改变蛋白质剪接的可变剪接事件。结果揭示了肿瘤发生导致的剪接调控的组织特异性改变,并且调控顺式元件分析进一步表明多个剪接调控机制受此过程影响。