外显子
生物
RNA剪接
选择性拼接
遗传学
增强子
外显子剪接增强剂
拼接因子
计算生物学
基因
转录因子
核糖核酸
作者
Amir Goren,Oren Ram,Maayan Amit,Hadas Keren,Galit Lev-Maor,Ida Vig,Tal Pupko,Gil Ast
出处
期刊:Molecular Cell
[Elsevier BV]
日期:2006-06-01
卷期号:22 (6): 769-781
被引量:300
标识
DOI:10.1016/j.molcel.2006.05.008
摘要
Exonic splicing regulatory sequences (ESRs) are cis-acting factor binding sites that regulate constitutive and alternative splicing. A computational method based on the conservation level of wobble positions and the overabundance of sequence motifs between 46,103 human and mouse orthologous exons was developed, identifying 285 putative ESRs. Alternatively spliced exons that are either short in length or contain weak splice sites show the highest conservation level of those ESRs, especially toward the edges of exons. ESRs that are abundant in those subgroups show a different distribution between constitutively and alternatively spliced exons. Representatives of these ESRs and two SR protein binding sites were shown, experimentally, to display variable regulatory effects on alternative splicing, depending on their relative locations in the exon. This finding signifies the delicate positional effect of ESRs on alternative splicing regulation.
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