MOE Key Laboratory of Protein Sciences, School of Life Sciences, Tsinghua University, Beijing, 100084, China.
Center for Structural Biology, Department of Basic Medical Sciences, School of Medicine, Tsinghua University, Beijing, 100084, China; Tsinghua-Peking Center for Life Sciences, Beijing, 100084, China.
Biochem Biophys Res Commun. 2018 Oct 20;505(1):325-332. doi: 10.1016/j.bbrc.2018.09.098. Epub 2018 Sep 21.
Spindlin1 (SPIN1), a histone modification reader protein, was enriched in the cell nucleolus and facilitated rRNA expression. However, how SPIN1 localizes to the nucleolus and its functional role in rRNA gene expression remain unresolved. Here, we identified a nucleolar localization signal in the N-terminal region of SPIN1 that is essential for its enrichment and function in the nucleolus. We also discovered that, in addition to its H3K4me3 recognizing activity, the H3R8me2a-recognizing capacity of SPIN1 is also indispensable for stimulating rRNA expression. Chromatin immunoprecipitation results indicated that SPIN1 is required for the association or assembly of selective factor 1 (SL1) complex, probably facilitating the initiation of rDNA transcription through its H3 K4me3-R8me2a reader function.
Spindlin1(SPIN1)是一种组蛋白修饰读取蛋白,在核仁中富集,并促进 rRNA 的表达。然而,SPIN1 如何定位到核仁以及其在 rRNA 基因表达中的功能作用仍未解决。在这里,我们鉴定了 SPIN1 中 N 端区域的核仁定位信号,该信号对于其在核仁中的富集和功能至关重要。我们还发现,除了其识别 H3K4me3 的活性外,SPIN1 识别 H3R8me2a 的能力对于刺激 rRNA 的表达也是必不可少的。染色质免疫沉淀结果表明,SPIN1 对于选择性因子 1(SL1)复合物的结合或组装是必需的,可能通过其 H3 K4me3-R8me2a 读取功能促进 rDNA 转录的起始。