Wang Zefeng, Rolish Michael E, Yeo Gene, Tung Vivian, Mawson Matthew, Burge Christopher B
Department of Biology, Massachusetts Institute of Technology, Cambridge, MA 02139, USA.
Cell. 2004 Dec 17;119(6):831-45. doi: 10.1016/j.cell.2004.11.010.
Exonic splicing silencers (ESSs) are cis-regulatory elements that inhibit the use of adjacent splice sites, often contributing to alternative splicing (AS). To systematically identify ESSs, an in vivo splicing reporter system was developed to screen a library of random decanucleotides. The screen yielded 141 ESS decamers, 133 of which were unique. The silencer activity of over a dozen of these sequences was also confirmed in a heterologous exon/intron context and in a second cell type. Of the unique ESS decamers, most could be clustered into groups to yield seven putative ESS motifs, some resembling known motifs bound by hnRNPs H and A1. Potential roles of ESSs in constitutive splicing were explored using an algorithm, ExonScan, which simulates splicing based on known or putative splicing-related motifs. ExonScan and related bioinformatic analyses suggest that these ESS motifs play important roles in suppression of pseudoexons, in splice site definition, and in AS.
外显子剪接沉默子(ESSs)是一种顺式调控元件,可抑制相邻剪接位点的使用,常常导致可变剪接(AS)。为了系统地鉴定ESSs,开发了一种体内剪接报告系统来筛选随机十聚体文库。该筛选产生了141个ESS十聚体,其中133个是独特的。其中十几个序列的沉默子活性也在异源外显子/内含子环境和第二种细胞类型中得到了证实。在独特的ESS十聚体中,大多数可以聚集成组,产生七个假定的ESS基序,有些类似于由hnRNPs H和A1结合的已知基序。使用一种名为ExonScan的算法探索了ESSs在组成型剪接中的潜在作用,该算法基于已知或假定的剪接相关基序模拟剪接。ExonScan和相关的生物信息学分析表明,这些ESS基序在假外显子的抑制、剪接位点的定义和可变剪接中发挥重要作用。