Open AccessChromatin remodeller Fun30Fft3 induces nucleosome disassembly to facilitate RNA polymerase II elongation
Author(s) -
Junwoo Lee,
Eui Sung Choi,
Hogyu David Seo,
Keunsoo Kang,
Joshua M. Gilmore,
Laurence Florens,
Michael P. Washburn,
Joonho Choe,
Jerry L. Workman,
Daeyoup Lee
Publication year - 2017
Publication title -
nature communications
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.559
H-Index - 365
ISSN - 2041-1723
DOI - 10.1038/ncomms14527
Subject(s) - nucleosome , chromatin , rna polymerase ii , microbiology and biotechnology , histone , transcription (linguistics) , biology , chemistry , genetics , dna , gene , promoter , gene expression , linguistics , philosophy
Previous studies have revealed that nucleosomes impede elongation of RNA polymerase II (RNAPII). Recent observations suggest a role for ATP-dependent chromatin remodellers in modulating this process, but direct in vivo evidence for this is unknown. Here using fission yeast, we identify Fun30 Fft3 as a chromatin remodeller, which localizes at transcribing regions to promote RNAPII transcription. Fun30 Fft3 associates with RNAPII and collaborates with the histone chaperone, FACT, which facilitates RNAPII elongation through chromatin, to induce nucleosome disassembly at transcribing regions during RNAPII transcription. Mutants, resulting in reduced nucleosome-barrier, such as deletion mutants of histones H3/H4 themselves and the genes encoding components of histone deacetylase Clr6 complex II suppress the defects in growth and RNAPII occupancy of cells lacking Fun30 Fft3 . These data suggest that RNAPII utilizes the chromatin remodeller, Fun30 Fft3 , to overcome the nucleosome barrier to transcription elongation.