Division of Biology and Biological Engineering, California Institute of Technology, Pasadena, United States.
Institute of Molecular Genetics, Russian Academy of Sciences, Moscow, Russian Federation.
Elife. 2020 Nov 9;9:e52416. doi: 10.7554/eLife.52416.
Ribosomal RNAs (rRNAs) are essential components of the ribosome and are among the most abundant macromolecules in the cell. To ensure high rRNA level, eukaryotic genomes contain dozens to hundreds of rDNA genes, however, only a fraction of the rRNA genes seems to be active, while others are transcriptionally silent. We found that individual rDNA genes have high level of cell-to-cell heterogeneity in their expression in . Insertion of heterologous sequences into rDNA leads to repression associated with reduced expression in individual cells and decreased number of cells expressing rDNA with insertions. We found that SUMO (Small Ubiquitin-like Modifier) and SUMO ligase Ubc9 are required for efficient repression of interrupted rDNA units and variable expression of intact rDNA. Disruption of the SUMO pathway abolishes discrimination of interrupted and intact rDNAs and removes cell-to-cell heterogeneity leading to uniformly high expression of individual rDNA in single cells. Our results suggest that the SUMO pathway is responsible for both repression of interrupted units and control of intact rDNA expression.
核糖体 RNA(rRNA)是核糖体的重要组成部分,也是细胞中含量最丰富的大分子之一。为了确保 rRNA 的高水平,真核生物基因组包含数十到数百个 rDNA 基因,但似乎只有一小部分 rRNA 基因是活跃的,而其他基因则处于转录沉默状态。我们发现,在 中,单个 rDNA 基因的表达存在高度的细胞间异质性。异源序列插入 rDNA 会导致基因表达受到抑制,从而导致插入细胞的 rDNA 表达减少,表达 rDNA 的细胞数量减少。我们发现,SUMO(小泛素样修饰物)和 SUMO 连接酶 Ubc9 对于有效抑制中断的 rDNA 单位和完整 rDNA 的可变表达是必需的。SUMO 途径的破坏消除了对中断和完整 rDNA 的区分,并消除了细胞间异质性,从而导致单个细胞中单个 rDNA 的均匀高表达。我们的结果表明,SUMO 途径负责中断单位的抑制和完整 rDNA 表达的控制。