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From transposon to transcription factor: Genome-wide functional studies of the conserved primate CSB-PGBD3 fusion protein.

机译:从转座子到转录因子:保守的灵长类CSB-PGBD3融合蛋白的全基因组功能研究。

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摘要

The CSB-PGBD3 fusion protein arose over 43 million years ago when a 2.5 kb piggyBac 3 (PGBD3) transposon inserted into intron 5 of the Cockayne syndrome Group B (CSB) gene in the common ancestor of all higher primates. As a result, full length CSB is now coexpressed with an abundant CSB-PGBD3 fusion protein by alternative splicing of CSB exons 1-5 to the PGBD3 transposase. An internal deletion of the piggyBac transposase ORF also gave rise to 889 dispersed, 140 bp MER85 elements which were mobilized in trans by PGBD3 transposase. Here, we show that the CSB-PGBD3 fusion protein binds MER85s in vitro, and induces a strong interferon-like innate antiviral immune response when expressed in CSB-null UVSS1KO cells. To explore the connection between DNA binding and gene expression changes induced by CSB-PGBD3, we investigated the genome-wide DNA binding profile of the fusion protein. CSB-PGBD3 binds to 363 MER85 elements in vivo, but these sites do not correlate with gene expression changes induced by the fusion protein. Instead, CSB-PGBD3 is enriched at AP-1, TEAD1, and CTCF motifs, presumably through protein-protein interactions with the cognate transcription factors; moreover, recruitment of CSB-PGBD3 to AP-1 and TEAD1 motifs correlates with nearby genes regulated by CSB-PGBD3 expression in UVSS1KO cells and downregulated by CSB rescue of mutant CS1AN cells. We also examined close PGBD3 homologs in galago monkeys, which have no domesticated PGBD3, and the freshwater cnidarian Hydra magnipapillata to show that as many as 30 mutations lead to the domestication of PGBD3. We conclude that horizontal transfer of PGBD3 created the CSB-PGBD3 fusion protein, which substantially reshapes the transcriptome in CS patient CS1AN, and that continued expression of the CSB-PGBD3 fusion protein in the absence of functional CSB may affect the clinical presentation of CS patients by directly altering the transcriptional program.
机译:CSB-PGBD3融合蛋白产生于4300万年前,当时一个2.5 kb的piggyBac 3(PGBD3)转座子插入了所有高级灵长类动物共同祖先Cockayne综合征B组(CSB)基因的内含子5中。结果,现在通过将CSB外显子1-5与PGBD3转座酶选择性剪接,全长CSB现在与丰富的CSB-PGBD3融合蛋白共表达。 piggyBac转座酶ORF的内部缺失也产生了889个分散的140bp MER85元件,其被PGBD3转座酶反式动员。在这里,我们显示CSB-PGBD3融合蛋白在体外结合MER85s,并在无CSB的UVSS1KO细胞中表达时诱导强烈的干扰素样先天性抗病毒免疫应答。为了探索CSB-PGBD3诱导的DNA结合与基因表达变化之间的联系,我们研究了融合蛋白的全基因组DNA结合谱。 CSB-PGBD3在体内与363个MER85元件结合,但这些位点与融合蛋白诱导的基因表达变化不相关。取而代之的是,CSB-PGBD3富含AP-1,TEAD1和CTCF基序,大概是通过蛋白质与同源转录因子的相互作用。此外,CSB-PGBD3募集到AP-1和TEAD1基序与附近基因受UVSS1KO细胞中CSB-PGBD3表达的调控以及CSB拯救突变CS1AN细胞的调控。我们还检查了没有驯化的PGBD3的加拉加猴中接近的PGBD3同源物,以及淡水的刺id蛇(Hydra magnipapillata)显示多达30个突变导致PGBD3驯化。我们得出的结论是,PGBD3的水平转移产生了CSB-PGBD3融合蛋白,该融合蛋白实质上重塑了CS患者CS1AN中的转录组,并且在没有功能性CSB的情况下CSB-PGBD3融合蛋白的持续表达可能会影响CS患者的临床表现通过直接改变转录程序。

著录项

  • 作者

    Gray, Lucas.;

  • 作者单位

    University of Washington.;

  • 授予单位 University of Washington.;
  • 学科 Chemistry Biochemistry.
  • 学位 Ph.D.
  • 年度 2012
  • 页码 165 p.
  • 总页数 165
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

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