Nguyen Son C, Yu Stephanie, Oberlick Elaine, Wu Chao-Ting
Department of Genetics, Harvard Medical School, Boston, Massachusetts 02115.
Department of Genetics, Harvard Medical School, Boston, Massachusetts 02115
Genetics. 2017 Feb;205(2):551-558. doi: 10.1534/genetics.116.187849. Epub 2016 Nov 23.
Polycomb group (PcG) proteins are major chromatin-bound factors that can read and modify chromatin states to maintain gene silencing throughout development. Here we focus on a close homolog of the PcG protein Posterior sex combs to better understand how these proteins affect regulation. This homolog, called Suppressor 2 of zeste [Su(z)2] is composed of two regions: the N-terminal homology region (HR), which serves as a hub for protein interactions, and the C-terminal region (CTR), which is believed to harbor the core activity of compacting chromatin. Here, we describe our classical genetic studies to dissect the structure of Su(z)2 Surprisingly, we found that the CTR is dispensable for viability. Furthermore, the core activity of Su(z)2 seems to reside in the HR instead of the CTR. Remarkably, our data also suggest a regulatory cascade between CTR and HR of Su(z)2, which, in turn, may help prioritize the myriad of PcG interactions that occur with the HR.
多梳蛋白家族(PcG)是主要的染色质结合因子,能够读取和修饰染色质状态,以在整个发育过程中维持基因沉默。在此,我们聚焦于PcG蛋白后性梳的一个紧密同源物,以更好地理解这些蛋白如何影响调控。这个同源物称为zeste抑制因子2 [Su(z)2],由两个区域组成:N端同源区域(HR),作为蛋白质相互作用的中心;以及C端区域(CTR),据信其具有压缩染色质的核心活性。在此,我们描述了剖析Su(z)2结构的经典遗传学研究。令人惊讶的是,我们发现CTR对于生存力并非必需。此外,Su(z)2的核心活性似乎存在于HR而非CTR中。值得注意的是,我们的数据还表明了Su(z)2的CTR和HR之间存在调控级联,这反过来可能有助于对与HR发生的众多PcG相互作用进行优先级排序。