| Literature DB >> 28138017 |
Yan Zhu1, Liang Rong2, Qiang Luo3, Baihui Wang3, Nana Zhou3, Yue Yang3, Chi Zhang3, Haiyang Feng3, Lina Zheng2, Wen-Hui Shen3,4, Jinbiao Ma5, Aiwu Dong1.
Abstract
NUCLEOSOME ASSEMBLY PROTEIN1 (NAP1) defines an evolutionarily conserved family of histone chaperones and loss of function of the Arabidopsis thaliana NAP1 family genes NAP1-RELATED PROTEIN1 (NRP1) and NRP2 causes abnormal root hair formation. Yet, the underlying molecular mechanisms remain unclear. Here, we show that NRP1 interacts with the transcription factor WEREWOLF (WER) in vitro and in vivo and enriches at the GLABRA2 (GL2) promoter in a WER-dependent manner. Crystallographic analysis indicates that NRP1 forms a dimer via its N-terminal α-helix. Mutants of NRP1 that either disrupt the α-helix dimerization or remove the C-terminal acidic tail, impair its binding to histones and WER and concomitantly lead to failure to activate GL2 transcription and to rescue the nrp1-1 nrp2-1 mutant phenotype. Our results further demonstrate that WER-dependent enrichment of NRP1 at the GL2 promoter is involved in local histone eviction and nucleosome loss in vivo. Biochemical competition assays imply that the association between NRP1 and histones may counteract the inhibitory effect of histones on the WER-DNA interaction. Collectively, our study provides important insight into the molecular mechanisms by which histone chaperones are recruited to target chromatin via interaction with a gene-specific transcription factor to moderate chromatin structure for proper root hair development.Entities:
Mesh:
Substances:
Year: 2017 PMID: 28138017 PMCID: PMC5354192 DOI: 10.1105/tpc.16.00719
Source DB: PubMed Journal: Plant Cell ISSN: 1040-4651 Impact factor: 11.277