Linear motifs confer functional diversity onto splice variants

被引:56
作者
Weatheritt, Robert J. [1 ]
Davey, Norman E. [1 ,2 ]
Gibson, Toby J. [1 ]
机构
[1] European Mol Biol Lab, Struct & Computat Biol Unit, D-69117 Heidelberg, Germany
[2] European Mol Biol Lab, Chem Biol Core Facil, D-69117 Heidelberg, Germany
关键词
IN-VIVO; DOMAIN; P53; IDENTIFICATION; SPECIFICITY; EXPRESSION; DATABASE; BINDING; GENE; PROTEINS;
D O I
10.1093/nar/gks442
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The pre-translational modification of messenger ribonucleic acids (mRNAs) by alternative promoter usage and alternative splicing is an important source of pleiotropy. Despite intensive efforts, our understanding of the functional implications of this dynamically created diversity is still incomplete. Using the available knowledge of interaction modules, particularly within intrinsically disordered regions (IDRs), we analysed the occurrences of protein modules within alternative exons. We find that regions removed or included by pre-translational variation are enriched in linear motifs suggesting that the removal or inclusion of exons containing these interaction modules is an important regulatory mechanism. In particular, we observe that PDZ-, PTB-, SH2- and WW-domain binding motifs are more likely to occur within alternative exons. We also determine that regions removed or included by alternative promoter usage are enriched in IDRs suggesting that protein isoform diversity is tightly coupled to the modulation of IDRs. This study, therefore, demonstrates that short linear motifs are key components for establishing protein diversity between splice variants.
引用
收藏
页码:7123 / 7131
页数:9
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