Concerted genomic targeting of H3K27 demethylase REF6 and chromatin-remodeling ATPase BRM in <i>Arabidopsis</i>

Li, Chenlong; Gu, Lianfeng; Gao, Lei; Chen, Chen; Wei, Chuang-Qi; Qiu, Qi; Chien, Chih-Wei; Wang, Suikang; Jiang, Lihua; Ai, Lian-Feng; Chen, Chia-Yang; Yang, Songguang; Nguyen, Vi; Qi, Yanhua; Snyder, Michael P.; Burlingame, Alma L.; Kohalmi, Susanne E.; Huang, Shangzhi; Cao, Xiaofeng; Wang, Zhi-Yong; Wu, Keqiang; Chen, Xuemei; Cui, Yuhai
2016
NATURE GENETICS
DOI
10.1038/ng.3555
SWI/SNF-type chromatin remodelers, such as BRAHMA (BRM), and H3K27 demethylases both have active roles in regulating gene expression at the chromatin level(1-5), but how they are recruited to specific genomic sites remains largely unknown. Here we show that RELATIVE OF EARLY FLOWERING 6 (REF6), a plant-unique H3K27 demethylase(6), targets genomic loci containing a CTCTGYTY motif via its zinc-finger (ZnF) domains and facilitates the recruitment of BRM. Genome-wide analyses showed that REF6 colocalizes with BRM at many genomic sites with the CTCTGYTY motif. Loss of REF6 results in decreased BRM occupancy at BRM-REF6 co-targets. Furthermore, REF6 directly binds to the CTCTGYTY motif in vitro, and deletion of the motif from a target gene renders it inaccessible to REF6 in vivo. Finally, we show that, when its ZnF domains are deleted, REF6 loses its genomic targeting ability. Thus, our work identifies a new genomic targeting mechanism for an H3K27 demethylase and demonstrates its key role in recruiting the BRM chromatin remodeler.