4.8 Article

C2H2 zinc finger proteins greatly expand the human regulatory lexicon

期刊

NATURE BIOTECHNOLOGY
卷 33, 期 5, 页码 555-U181

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NATURE PORTFOLIO
DOI: 10.1038/nbt.3128

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资金

  1. Canadian Institutes of Health Research [MOP-77721, MOP-111007, MOP-272138]
  2. Canadian Institutes for Advanced Research
  3. Canadian Institutes of Health Research Banting Fellowship
  4. European Molecular Biology Organization postdoctoral fellowship
  5. Natural Science and Engineering Research Council CGS-M

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Cys2-His2 zinc finger (C2H2-ZF) proteins represent the largest class of putative human transcription factors. However, for most C2H2-ZF proteins it is unknown whether they even bind DNA or, if they do, to which sequences. Here, by combining data from a modified bacterial one-hybrid system with protein-binding microarray and chromatin immunoprecipitation analyses, we show that natural C2H2-ZFs encoded in the human genome bind DNA both in vitro and in vivo, and we infer the DNA recognition code using DNA-binding data for thousands of natural C2H2-ZF domains. In vivo binding data are generally consistent with our recognition code and indicate that C2H2-ZF proteins recognize more motifs than all other human transcription factors combined. We provide direct evidence that most KRAB-containing C2H2-ZF proteins bind specific endogenous retroelements (EREs), ranging from currently active to ancient families. The majority of C2H2-ZF proteins, including KRAB proteins, also show widespread binding to regulatory regions, indicating that the human genome contains an extensive and largely unstudied adaptive C2H2-ZF regulatory network that targets a diverse range of genes and pathways.

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