Steinhauf Daniel, Rodriguez Alejandro, Vlachakis Dimitrios, Virgo Gordon, Maksimov Vladimir, Kristell Carolina, Olsson Ida, Linder Tomas, Kossida Sophia, Bongcam-Rudloff Erik, Bjerling Pernilla
Department of Medical Biochemistry and Microbiology, Science for Life Laboratory, University of Uppsala, Uppsala, Sweden.
Bioinformatics and Medical Informatics Laboratory, Biomedical Research Foundation of the Academy of Athens, Athens, Greece.
PLoS One. 2014 Jan 27;9(1):e86948. doi: 10.1371/journal.pone.0086948. eCollection 2014.
The fission yeast, Schizosaccharomyces pombe, is a well-established model for heterochromatin formation, but the exact sequence of events for initiation remains to be elucidated. The essential factors involved include RNA transcribed from repeated sequences together with the methyltransferase Clr4. In addition, histone deacetylases, like Clr3, found in the SHREC complex are also necessary for transcriptional silencing. Clr2 is another crucial factor required for heterochromatin formation found in the SHREC complex. The function of Clr2 has been difficult to establish due to the lack of conserved domains or homology to proteins of known molecular function. Using a bioinformatics approach, three conserved motifs in Clr2 were identified, which contained amino acids important for transcriptional repression. Analysis of clr2 mutant strains revealed a major role for Clr2 in mating-type and rDNA silencing, and weaker effects on centromeric silencing. The effect on mating-type silencing showed variegation in several of the strains with mutated versions of Clr2 indicating an establishment or maintenance defect. Moreover, the critical amino acids in Clr2 were also necessary for transcriptional repression in a minimal system, by the tethering of Clr4 upstream of a reporter gene, inserted into the euchromatic part of the genome. Finally, in silico modeling suggested that the mutations in Clr2 cause disruption of secondary structures in the Clr2 protein. Identification of these critical amino acids in the protein provides a useful tool to explore the molecular mechanism behind the role of Clr2 in heterochromatin formation.
裂殖酵母(Schizosaccharomyces pombe)是一种成熟的异染色质形成模型,但起始过程的确切事件顺序仍有待阐明。涉及的关键因素包括从重复序列转录的RNA以及甲基转移酶Clr4。此外,在SHREC复合物中发现的组蛋白脱乙酰酶,如Clr3,对于转录沉默也是必需的。Clr2是在SHREC复合物中发现的异染色质形成所需的另一个关键因素。由于缺乏保守结构域或与已知分子功能的蛋白质的同源性,Clr2的功能一直难以确定。使用生物信息学方法,在Clr2中鉴定出三个保守基序,其中包含对转录抑制重要的氨基酸。对clr2突变菌株的分析揭示了Clr2在交配型和rDNA沉默中的主要作用,对着丝粒沉默的影响较弱。对交配型沉默的影响在几个具有Clr2突变版本的菌株中表现出斑驳现象,表明存在建立或维持缺陷。此外,通过将Clr4拴系在插入基因组常染色质部分的报告基因上游,Clr2中的关键氨基酸对于最小系统中的转录抑制也是必需的。最后,计算机模拟表明Clr2中的突变会导致Clr2蛋白二级结构的破坏。鉴定该蛋白中的这些关键氨基酸为探索Clr2在异染色质形成中的作用背后的分子机制提供了有用的工具。