Department of Biomedical and Chemical Engineering and Sciences, Florida Institute of Technology, Melbourne, FL 32901, USA.
Genetics. 2022 May 5;221(1). doi: 10.1093/genetics/iyac046.
During proteotoxic stress, a pathway known as the heat shock response is induced to maintain protein-folding homeostasis or proteostasis. Previously, we identified the Caenorhabditis elegans GATAD2 ortholog, dcp-66, as a novel regulator of the heat shock response. Here, we extend these findings to show that dcp-66 positively regulates the heat shock response at the cellular, molecular, and organismal levels. As GATAD2 is a subunit of the nucleosome remodeling and deacetylase chromatin remodeling complex, we examined other nucleosome remodeling and deacetylase subunits and found that the let-418 (CHD4) nucleosome repositioning core also regulates the heat shock response. However, let-418 acts as a negative regulator of the heat shock response, in contrast to positive regulation by dcp-66. The divergent effects of these two nucleosome remodeling and deacetylase subunits extend to the regulation of other stress responses including oxidative, genotoxic, and endoplasmic reticulum stress. Furthermore, a transcriptomic approach reveals additional divergently regulated pathways, including innate immunity and embryogenesis. Taken together, this work establishes new insights into the role of nucleosome remodeling and deacetylase subunits in organismal physiology. We incorporate these findings into a molecular model whereby different mechanisms of recruitment to promoters can result in the divergent effects of nucleosome remodeling and deacetylase subunits.
在蛋白毒性应激期间,会诱导一种称为热休克反应的途径来维持蛋白质折叠的平衡或蛋白质稳态。之前,我们鉴定了秀丽隐杆线虫 GATAD2 同源物 dcp-66,作为热休克反应的新型调节剂。在这里,我们扩展了这些发现,表明 dcp-66 在细胞、分子和机体水平上均正向调节热休克反应。由于 GATAD2 是核小体重塑和去乙酰化酶染色质重塑复合物的一个亚基,我们检查了其他核小体重塑和去乙酰化酶亚基,发现 let-418(CHD4)核小体重定位核心也调节热休克反应。然而,与 dcp-66 的正向调节相反,let-418 作为热休克反应的负调节剂发挥作用。这两个核小体重塑和去乙酰化酶亚基的不同作用扩展到其他应激反应的调节,包括氧化应激、遗传毒性和内质网应激。此外,转录组学方法揭示了其他差异调节的途径,包括先天免疫和胚胎发生。总之,这项工作为核小体重塑和去乙酰化酶亚基在机体生理学中的作用提供了新的见解。我们将这些发现纳入一个分子模型中,其中不同的募集到启动子的机制可以导致核小体重塑和去乙酰化酶亚基的不同作用。