Neurospora WC-1 Recruits SWI/SNF to Remodel frequency and Initiate a Circadian Cycle
Author(s) -
Bin Wang,
Arminja N. Kettenbach,
Scott A. Gerber,
Jennifer Loros,
Jay Dunlap
Publication year - 2014
Publication title -
plos genetics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.587
H-Index - 233
eISSN - 1553-7404
pISSN - 1553-7390
DOI - 10.1371/journal.pgen.1004599
Subject(s) - biology , circadian rhythm , circadian clock , swi/snf , neurospora , microbiology and biotechnology , genetics , nucleosome , transcription factor , fungal protein , chromatin , neurospora crassa , gene , endocrinology , saccharomyces cerevisiae , mutant
In the negative feedback loop comprising the Neurospora circadian oscillator, the White Collar Complex (WCC) formed from White Collar-1 (WC-1) and White Collar-2 (WC-2) drives transcription of the circadian pacemaker gene frequency ( frq ). Although FRQ-dependent repression of WCC has been extensively studied, the mechanism by which the WCC initiates a circadian cycle remains elusive. Structure/function analysis of WC-1 eliminated domains previously thought to transactivate frq expression but instead identified amino acids 100–200 as essential for frq circadian expression. A proteomics-based search for coactivators with WCC uncovered the SWI/SNF (SWItch/Sucrose NonFermentable) complex: SWI/SNF interacts with WCC in vivo and in vitro, binds to the Clock box in the frq promoter, and is required both for circadian remodeling of nucleosomes at frq and for rhythmic frq expression; interestingly, SWI/SNF is not required for light-induced frq expression. These data suggest a model in which WC-1 recruits SWI/SNF to remodel and loop chromatin at frq , thereby activating frq expression to initiate the circadian cycle.
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