Berardi Andrea, Quilici Giacomo, Spiliotopoulos Dimitrios, Corral-Rodriguez Maria Angeles, Martin-Garcia Fernando, Degano Massimo, Tonon Giovanni, Ghitti Michela, Musco Giovanna
Biomolecular NMR Unit, Division of Genetics and Cell Biology, IRCCS S. Raffaele Scientific Institute, Milan 20132, Italy Università degli Studi di Milano, Italy.
Biomolecular NMR Unit, Division of Genetics and Cell Biology, IRCCS S. Raffaele Scientific Institute, Milan 20132, Italy.
Nucleic Acids Res. 2016 Apr 20;44(7):3448-63. doi: 10.1093/nar/gkw103. Epub 2016 Feb 20.
Sotos syndrome is an overgrowth syndrome caused by mutations within the functional domains ofNSD1 gene coding for NSD1, a multidomain protein regulating chromatin structure and gene expression. In particular, PHDVC5HCHNSD1 tandem domain, composed by a classical (PHDV) and an atypical (C5HCH) plant homeo-domain (PHD) finger, is target of several pathological missense-mutations. PHDVC5HCHNSD1 is also crucial for NSD1-dependent transcriptional regulation and interacts with the C2HR domain of transcriptional repressor Nizp1 (C2HRNizp1)in vitro To get molecular insights into the mechanisms dictating the patho-physiological relevance of the PHD finger tandem domain, we solved its solution structure and provided a structural rationale for the effects of seven Sotos syndrome point-mutations. To investigate PHDVC5HCHNSD1 role as structural platform for multiple interactions, we characterized its binding to histone H3 peptides and to C2HRNizp1 by ITC and NMR. We observed only very weak electrostatic interactions with histone H3 N-terminal tails, conversely we proved specific binding to C2HRNizp1 We solved C2HRNizp1 solution structure and generated a 3D model of the complex, corroborated by site-directed mutagenesis. We suggest a mechanistic scenario where NSD1 interactions with cofactors such as Nizp1 are impaired by PHDVC5HCHNSD1 pathological mutations, thus impacting on the repression of growth-promoting genes, leading to overgrowth conditions.
索托斯综合征是一种过度生长综合征,由编码NSD1的NSD1基因突变引起,NSD1是一种调节染色质结构和基因表达的多结构域蛋白。特别是,由一个经典(PHDV)和一个非典型(C5HCH)植物同源结构域(PHD)指组成的PHDVC5HCHNSD1串联结构域是几种病理性错义突变的靶点。PHDVC5HCHNSD1对NSD1依赖的转录调控也至关重要,并且在体外与转录抑制因子Nizp1的C2HR结构域(C2HRNizp1)相互作用。为了从分子层面深入了解决定PHD指串联结构域病理生理相关性的机制,我们解析了其溶液结构,并为七个索托斯综合征点突变的影响提供了结构依据。为了研究PHDVC5HCHNSD1作为多种相互作用的结构平台的作用,我们通过等温滴定量热法(ITC)和核磁共振(NMR)对其与组蛋白H3肽和C2HRNizp1的结合进行了表征。我们观察到与组蛋白H3 N端尾巴只有非常微弱的静电相互作用,相反,我们证明了其与C2HRNizp1的特异性结合。我们解析了C2HRNizp1的溶液结构,并生成了复合物的三维模型,定点诱变证实了该模型。我们提出了一种机制设想,即PHDVC5HCHNSD1的病理突变会损害NSD1与诸如Nizp1等辅因子的相互作用,从而影响对促进生长基因的抑制,导致过度生长状况。