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Nucleosome organization in sequences of alternative events in human genome

机译:人类基因组中其他事件序列中的核小体组织

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摘要

Recent studies indicate that precursor mRNA splicing occurs cotranscriptionally and that nucleosome positioning may influence inclusion of internal exon sequences. In eukaryotic genomes, most genes are subject to alternative splicing. Nucleosome occupancy in sequences of different types of alternative events was investigated by analyzing genome-wide nucleosome positioning data sets from human. Nucleosomes were found to be preferentially positioned within constitutive exons and/or constitutive portions of alternative exons, which was not associated with gene expression or states of cells but was based on sequence and positively related with the sequence conservation of splicing sites. In addition, the nucleosome distribution in an alternative acceptor exon was different from that in an alternative donor exon. Nucleosome occupancy around constitutive transcription start sites also showed stronger +1 nucleosome enrichment and weaker nucleosome occupancy in nucleosome free regions. These results provided a new approach for better appreciation of the connection between chromatin structure and gene expression regulation.
机译:最近的研究表明前体mRNA剪接共转录发生,核小体的定位可能会影响内部外显子序列的包含。在真核基因组中,大多数基因都需要进行可变剪接。通过分析人类全基因组范围的核小体定位数据集,研究了不同类型替代事件序列中的核小体占有率。发现核小体优先位于组成性外显子和/或替代性外显子的组成部分内,其与基因表达或细胞状态无关,而是基于序列,并且与剪接位点的序列保守性正相关。另外,替代受体外显子中核小体的分布不同于替代供体外显子中的核小体分布。组成性转录起始位点周围的核小体占据也显示出更强的+1核小体富集和较弱的无核小体区域中的核小体占有率。这些结果为更好地了解染色质结构与基因表达调控之间的联系提供了一种新方法。

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