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首页> 外文期刊>Human Molecular Genetics >Predominant patterns of splicing evolution on human, chimpanzee and macaque evolutionary lineages
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Predominant patterns of splicing evolution on human, chimpanzee and macaque evolutionary lineages

机译:人类,黑猩猩和猕猴进化谱系拼接演化的主要模式

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摘要

Although splicing is widespread and evolves rapidly among species, the mechanisms driving this evolution, as well as its functional implications, are not yet fully understood. We analyzed the evolution of splicing patterns based on transcriptome data from five tissues of humans, chimpanzees, rhesus macaques and mice. In total, 1526 exons and exon sets from 1236 genes showed significant splicing differences among primates. More than 60% of these differences represent constitutive-to-alternative exon transitions while an additional 25% represent changes in exon inclusion frequency. These two dominant evolutionary patterns have contrasting conservation, regulation and functional features. The sum of these features indicates that, despite their prevalence, constitutive-to-alternative exon transitions do not substantially contribute to long-term functional transcriptome changes. Conversely, changes in exon inclusion frequency appear to be functionally relevant, especially for changes taking place in the brain on the human evolutionary lineage.
机译:虽然拼接是普遍的并且在物种之间迅速发展,但尚未完全理解驱动这种进化的机制以及其功能影响。我们分析了基于来自人,黑猩猩,恒河猴和小鼠的五种组织的转录组数据的剪接模式的演变。总共,来自1236个基因的1526个外显子和外显子组在灵长类内显示出显着的剪接差异。超过60%的这些差异代表了组成型替代的外显子过渡,而另外25%代表外显子包含频率的变化。这两个主导的进化模式具有对比的节约,调节和功能特征。这些特征的总和表明,尽管它们流行,因此组成型替代的外显子转变对长期功能转录组变化没有基本贡献。相反,外显子包含频率的变化似乎是在功能上相关的,特别是对于人类进化谱系发生的大脑发生的变化。

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  • 来源
    《Human Molecular Genetics 》 |2018年第8期| 共12页
  • 作者单位

    Chinese Acad Sci Shanghai Inst Biol Sci Max Planck Partner Inst Computat Biol Shanghai 200031;

    Chinese Acad Sci Shanghai Inst Biol Sci Max Planck Partner Inst Computat Biol Shanghai 200031;

    Univ Dundee JBC WTB Bioctr Dundee DD1 5EH Scotland;

    Chinese Acad Sci Shanghai Inst Biol Sci Max Planck Partner Inst Computat Biol Shanghai 200031;

    Chinese Acad Sci Shanghai Inst Biol Sci Max Planck Partner Inst Computat Biol Shanghai 200031;

    Helmholtz Assoc MDC Max Delbruck Ctr Mol Med D-13125 Berlin Germany;

    Chinese Acad Sci Shanghai Inst Biol Sci Max Planck Partner Inst Computat Biol Shanghai 200031;

    Skolkovo Inst Sci &

    Technol Skolkovo 143025 Russia;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 医学遗传学 ;
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