裂殖酵母SUMO靶向泛素连接酶Slx8在功能上与核外围的聚类中心粒和沉默交配型区域相关联

Shrena Chakraborty, Joanna Strachan, Kamila Schirmeisen, Laetitia Besse, Eve Mercier, Karine Freon, Haidao Zhang, Ning Zhao, Elizabeth Bayne, Sarah AE Lambert
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摘要

SUMO靶向泛素连接酶(STUbL)家族通过多种机制参与多种细胞过程,以维持基因组的稳定性。STUbL 的进化保守功能之一是促进 DNA 病变的核定位变化,将其靶向到核外围。在Schizossacharomyces pombe中,STUbL Slx8是SUMO化蛋白的调控因子,通过抵消SUMO共轭物的毒性促进复制胁迫耐受性。为了研究 S. pombe 基因组核空间中泛素化和 SUMO 化之间的动态辩证关系,我们分析了 Slx8 的定位。意外的是,我们没有检测到复制胁迫诱导的 Slx8 病灶。然而,我们发现 Slx8 形成了一个单一的核病灶,富集在核外围,它标记了主轴极体和沉默交配型区域的集群中心点。这个单一的 Slx8 病灶的形成需要 E3 SUMO 连接酶 Pli1、多 SUMOylation 和负责异染色质组蛋白标记 H3-K9 甲基化的组蛋白甲基转移酶 Clr4。最后,我们证实 Slx8 能促进中心粒集群和异染色质结构域的基因沉默。总之,我们的数据强调了STUbL与异染色质结构域之间的进化保守和功能关系,以促进基因沉默和核组织。
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The fission yeast SUMO-targeted Ubiquitin Ligase Slx8 functionally associates with clustered centromeres and the silent mating type region at the nuclear periphery
The SUMO-targeted Ubiquitin ligase (STUbL) family is involved in multiple cellular processes via a wide range of mechanisms to maintain genome stability. One of the evolutionarily conserved functions of STUbL is to promote changes in the nuclear positioning of DNA lesions, targeting them to the nuclear periphery. In Schizossacharomyces pombe, the STUbL Slx8 is a regulator of SUMOylated proteins and promotes replication stress tolerance by counteracting the toxicity of SUMO conjugates. In order to study the dynamic dialectic between Ubiquitinylation and SUMOylation in the nuclear space of the S. pombe genome, we analyzed Slx8 localization. Unexpectedly, we did not detect replication stress-induced Slx8 foci. However, we discovered that Slx8 forms a single nuclear focus, enriched at the nuclear periphery, which marks both clustered centromeres at the spindle pole body and the silent mating type region. The formation of this single Slx8 focus requires the E3 SUMO ligase Pli1, poly-SUMOylation and the histone methyl transferase Clr4 that is responsible for the heterochromatin histone mark H3-K9 methylation. Finally, we established that Slx8 promotes centromere clustering and gene silencing at heterochromatin domains. Altogether, our data highlight evolutionarily conserved and functional relationships between STUbL and heterochromatin domains to promote gene silencing and nuclear organization.
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