Department of Biological Sciences, Columbia University, New York, New York 10027, USA.
Genes Dev. 2010 Jun 15;24(12):1242-52. doi: 10.1101/gad.1917910. Epub 2010 May 26.
Transcription factors represent one of the largest groups of proteins regulated by SUMO (small ubiquitin-like modifier) modification, and their sumoylation is usually associated with transcriptional repression. To investigate whether sumoylation plays a general role in regulating transcription in yeast, we determined the occupancy of sumoylated proteins at a variety of genes by chromatin immunoprecipitation (ChIP) using an antibody that recognizes the yeast SUMO peptide. Surprisingly, we detected sumoylated proteins at all constitutively transcribed genes tested but not at repressed genes. Ubc9, the SUMO conjugation enzyme, was not present on these genes, but its inactivation reduced SUMO at the constitutive promoters and modestly decreased RNA polymerase II levels. In contrast, activation of the inducible GAL1, STL1, and ARG1 genes caused not only a striking accumulation of SUMO at all three promoter regions, but also recruitment of Ubc9, indicating that gene activation involves sumoylation of promoter-bound factors. However, Ubc9 inactivation, while reducing sumoylation at the induced promoters, paradoxically resulted in increased transcription. Providing an explanation for this, the reduced sumoylation impaired the cell's ability to appropriately shut off transcription of the induced ARG1 gene, indicating that SUMO can facilitate transcriptional silencing. Our findings thus establish unexpected roles for sumoylation in both constitutive and activated transcription, and provide a novel mechanism for regulating gene expression.
转录因子是受 SUMO(小泛素样修饰物)修饰调控的最大蛋白质家族之一,其 SUMO 化通常与转录抑制有关。为了研究 SUMO 化是否在酵母转录调控中普遍起作用,我们通过染色质免疫沉淀(ChIP)使用识别酵母 SUMO 肽的抗体,确定了 SUMO 化蛋白在各种基因上的占有率。令人惊讶的是,我们在所有被测试的组成型转录基因上都检测到了 SUMO 化蛋白,但在被抑制的基因上却没有。SUMO 连接酶 Ubc9 不在这些基因上,但它的失活减少了组成型启动子上的 SUMO 化,并适度降低了 RNA 聚合酶 II 的水平。相比之下,诱导型 GAL1、STL1 和 ARG1 基因的激活不仅导致这三个启动子区域 SUMO 的显著积累,还导致 Ubc9 的募集,表明基因激活涉及启动子结合因子的 SUMO 化。然而,Ubc9 的失活虽然减少了诱导型启动子上的 SUMO 化,但却导致转录增加。这一现象提供了一个解释,减少的 SUMO 化损害了细胞适当关闭诱导型 ARG1 基因转录的能力,表明 SUMO 可以促进转录沉默。我们的发现因此确立了 SUMO 化在组成型和激活型转录中的意外作用,并为调节基因表达提供了一种新的机制。