Chromatin and epigenetic regulation of pre-mRNA processing

被引:72
作者
Brown, Seth J. [4 ]
Stoilov, Peter [1 ,2 ]
Xing, Yi [3 ,4 ]
机构
[1] W Virginia Univ, Dept Biochem, Morgantown, WV 26506 USA
[2] W Virginia Univ, Mary Babb Randolph Canc Ctr, Morgantown, WV 26506 USA
[3] Univ Iowa, Dept Biomed Engn, Iowa City, IA 52242 USA
[4] Univ Iowa, Dept Internal Med, Iowa City, IA 52242 USA
基金
美国国家卫生研究院;
关键词
POLYMERASE-II; HISTONE H3; IN-VIVO; EUKARYOTIC GENOMES; DNA METHYLATION; EXON DEFINITION; SPLICING CODE; NUCLEOSOME; TRANSCRIPTION; INTRON;
D O I
10.1093/hmg/dds353
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
New data are revealing a complex landscape of gene regulation shaped by chromatin states that extend into the bodies of transcribed genes and associate with distinct RNA elements such as exons, introns and polyadenylation sites. Exons are characterized by increased levels of nucleosome positioning, DNA methylation and certain histone modifications. As pre-mRNA splicing occurs co-transcriptionally, changes in the transcription elongation rate or epigenetic marks can influence exon splicing. These new discoveries broaden our understanding of the epigenetic code and ascribe a novel role for chromatin in controlling pre-mRNA processing. In this review, we summarize the recently discovered interplay between the modulation of chromatin states and pre-mRNA processing with the particular focus on how these processes communicate with one another to control gene expression.
引用
收藏
页码:R90 / R96
页数:7
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