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10.15252/embj.201386433

http://scihub22266oqcxt.onion/10.15252/embj.201386433
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C4194127!4194127!24843044
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suck abstract from ncbi


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pmid24843044      EMBO+J 2014 ; 33 (12): 1397-415
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  • Eaf5/7/3 form a functionally independent NuA4 submodule linked to RNA polymerase II-coupled nucleosome recycling #MMPMID24843044
  • Rossetto D; Cramet M; Wang AY; Steunou AL; Lacoste N; Schulze JM; Côté V; Monnet-Saksouk J; Piquet S; Nourani A; Kobor MS; Côté J
  • EMBO J 2014[Jun]; 33 (12): 1397-415 PMID24843044show ga
  • The NuA4 histone acetyltransferase complex is required for gene regulation, cell cycle progression, and DNA repair. Dissection of the 13-subunit complex reveals that the Eaf7 subunit bridges Eaf5 with Eaf3, a H3K36me3-binding chromodomain protein, and this Eaf5/7/3 trimer is anchored to NuA4 through Eaf5. This trimeric subcomplex represents a functional module, and a large portion exists in a native form outside the NuA4 complex. Gene-specific and genome-wide location analyses indicate that Eaf5/7/3 correlates with transcription activity and is enriched over the coding region. In agreement with a role in transcription elongation, the Eaf5/7/3 trimer interacts with phosphorylated RNA polymerase II and helps its progression. Loss of Eaf5/7/3 partially suppresses intragenic cryptic transcription arising in set2 mutants, supporting a role in nucleosome destabilization. On the other hand, loss of the trimer leads to an increase of replication-independent histone exchange over the coding region of transcribed genes. Taken together, these results lead to a model where Eaf5/7/3 associates with elongating polymerase to promote the disruption of nucleosomes in its path, but also their refolding in its wake.
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