Gupta Ritu, Sadhale Parag P, Vijayraghavan Usha
Department of Microbiology and Cell Biology, Indian Institute of Science, Bangalore, 560012, India.
PLoS One. 2015 Jul 6;10(7):e0132350. doi: 10.1371/journal.pone.0132350. eCollection 2015.
Saccharomyces cerevisiae Sub1 is involved in several cellular processes such as, transcription initiation, elongation, mRNA processing and DNA repair. It has also been reported to provide cellular resistance during conditions of oxidative DNA damage and osmotic stress. Here, we report a novel role of SUB1 during starvation stress-induced sporulation, which leads to meiosis and spore formation in diploid yeast cells. Deletion of SUB1 gene significantly increased sporulation efficiency as compared to the wild-type cells in S288c genetic background. Whereas, the sporulation functions of the sub1(Y66A) missense mutant were similar to Sub1. SUB1 transcript and protein levels are downregulated during sporulation, in highly synchronized and sporulation proficient wild-type SK1 cells. The changes in Sub1 levels during sporulation cascade correlate with the induction of middle sporulation gene expression. Deletion of SUB1 increased middle sporulation gene transcript levels with no effect on their induction kinetics. In wild-type cells, Sub1 associates with chromatin at these loci in a temporal pattern that correlates with their enhanced gene expression seen in sub1Δ cells. We show that SUB1 genetically interacts with HOS2, which led us to speculate that Sub1 might function with Set3 repressor complex during sporulation. Positive Cofactor 4, human homolog of Sub1, complemented the sub1Δ sporulation phenotype, suggesting conservation of function. Taken together, our results suggest that SUB1 acts as a negative regulator of sporulation.
酿酒酵母的Sub1参与多种细胞过程,如转录起始、延伸、mRNA加工和DNA修复。据报道,它在氧化DNA损伤和渗透胁迫条件下还能赋予细胞抗性。在此,我们报道了SUB1在饥饿胁迫诱导的孢子形成过程中的新作用,该过程导致二倍体酵母细胞减数分裂和孢子形成。与S288c遗传背景下的野生型细胞相比,SUB1基因的缺失显著提高了孢子形成效率。而sub1(Y66A)错义突变体的孢子形成功能与Sub1相似。在高度同步化且孢子形成能力强的野生型SK1细胞中,孢子形成过程中SUB1转录本和蛋白水平下调。孢子形成级联过程中Sub1水平的变化与中期孢子形成基因表达的诱导相关。SUB1的缺失增加了中期孢子形成基因的转录水平,但对其诱导动力学没有影响。在野生型细胞中,Sub1以一种与sub1Δ细胞中增强的基因表达相关的时间模式与这些位点的染色质结合。我们发现SUB1与HOS2存在遗传相互作用,这使我们推测Sub1在孢子形成过程中可能与Set3阻遏复合物共同发挥作用。Sub1的人类同源物正向辅因子4补充了sub1Δ的孢子形成表型,表明功能保守。综上所述,我们的结果表明SUB1作为孢子形成的负调节因子发挥作用。