Cassar Paul A, Carpenedo Richard L, Samavarchi-Tehrani Payman, Olsen Jonathan B, Park Chang Jun, Chang Wing Y, Chen Zhaoyi, Choey Chandarong, Delaney Sean, Guo Huishan, Guo Hongbo, Tanner R Matthew, Perkins Theodore J, Tenenbaum Scott A, Emili Andrew, Wrana Jeffrey L, Gibbings Derrick, Stanford William L
Institute of Medical Science University of Toronto, Toronto, ON, Canada Collaborative Program in Genome Biology and Bioinformatics, University of Toronto, Toronto, ON, Canada.
Sprott Centre for Stem Cell Research, Ottawa Hospital Research Institute, Ottawa, ON, Canada.
EMBO Rep. 2015 Oct;16(10):1334-57. doi: 10.15252/embr.201540974. Epub 2015 Aug 11.
In embryonic stem cells (ESCs), gene regulatory networks (GRNs) coordinate gene expression to maintain ESC identity; however, the complete repertoire of factors regulating the ESC state is not fully understood. Our previous temporal microarray analysis of ESC commitment identified the E3 ubiquitin ligase protein Makorin-1 (MKRN1) as a potential novel component of the ESC GRN. Here, using multilayered systems-level analyses, we compiled a MKRN1-centered interactome in undifferentiated ESCs at the proteomic and ribonomic level. Proteomic analyses in undifferentiated ESCs revealed that MKRN1 associates with RNA-binding proteins, and ensuing RIP-chip analysis determined that MKRN1 associates with mRNAs encoding functionally related proteins including proteins that function during cellular stress. Subsequent biological validation identified MKRN1 as a novel stress granule-resident protein, although MKRN1 is not required for stress granule formation, or survival of unstressed ESCs. Thus, our unbiased systems-level analyses support a role for the E3 ligase MKRN1 as a ribonucleoprotein within the ESC GRN.
在胚胎干细胞(ESC)中,基因调控网络(GRN)协调基因表达以维持ESC特性;然而,调节ESC状态的完整因子组合尚未完全明确。我们之前对ESC分化的时间微阵列分析确定E3泛素连接酶蛋白Makorin-1(MKRN1)是ESC GRN的一个潜在新组分。在此,我们使用多层系统水平分析,在蛋白质组学和核糖组学水平上,构建了一个以未分化ESC中的MKRN1为中心的相互作用组。对未分化ESC的蛋白质组学分析表明,MKRN1与RNA结合蛋白相关,随后的RNA免疫沉淀芯片分析确定MKRN1与编码功能相关蛋白(包括在细胞应激期间发挥作用的蛋白)的mRNA相关。随后的生物学验证确定MKRN1是一种新的应激颗粒驻留蛋白,尽管应激颗粒形成或未受应激的ESC存活不需要MKRN1。因此,我们的无偏系统水平分析支持E3连接酶MKRN1在ESC GRN中作为核糖核蛋白发挥作用。