Wu Kenneth, Dhillon Namrita, Bajor Antone, Abrahamson Sara, Kamakaka Rohinton T
Department of MCD Biology, 1156 High Street, University of California, Santa Cruz, CA 95064 USA.
Electrical Engineering Department, Baskin School of Engineering, 1156 High Street, University of California, Santa Cruz, CA 95064 USA.
bioRxiv. 2023 Oct 5:2023.10.05.561072. doi: 10.1101/2023.10.05.561072.
The interplay between nucleosomes and transcription factors leads to programs of gene expression. Transcriptional silencing involves the generation of a chromatin state that represses transcription and is faithfully propagated through DNA replication and cell division. Using multiple reporter assays, including directly visualizing transcription in single cells, we investigated a diverse set of UAS enhancers and core promoters for their susceptibility to heterochromatic gene silencing. These results show that heterochromatin only stably silences weak and stress induced regulatory elements but is unable to stably repress housekeeping gene regulatory elements and the partial repression did not result in bistable expression states. Permutation analysis of different UAS enhancers and core promoters indicate that both elements function together to determine the susceptibility of regulatory sequences to repression. Specific histone modifiers and chromatin remodellers function in an enhancer specific manner to aid these elements to resist repression suggesting that Sir proteins likely function in part by reducing nucleosome mobility. We also show that the strong housekeeping regulatory elements can be repressed if silencer bound Sir1 is increased, suggesting that Sir1 is a limiting component in silencing. Together, our data suggest that the heterochromatic locus has been optimized to stably silence the weak mating type gene regulatory elements but not strong housekeeping gene regulatory sequences which could help explain why these genes are often found at the boundaries of silenced domains.
核小体与转录因子之间的相互作用导致了基因表达程序。转录沉默涉及一种染色质状态的产生,这种状态会抑制转录,并通过DNA复制和细胞分裂忠实地传递下去。我们使用多种报告基因检测方法,包括直接观察单细胞中的转录情况,研究了一系列不同的上游激活序列(UAS)增强子和核心启动子对异染色质基因沉默的敏感性。这些结果表明,异染色质仅能稳定沉默弱的和应激诱导的调控元件,但无法稳定抑制管家基因调控元件,且部分抑制不会导致双稳态表达状态。对不同UAS增强子和核心启动子的置换分析表明,这两种元件共同作用以确定调控序列对抑制的敏感性。特定的组蛋白修饰因子和染色质重塑因子以增强子特异性的方式发挥作用,帮助这些元件抵抗抑制,这表明Sir蛋白可能部分通过降低核小体的移动性来发挥作用。我们还表明,如果与沉默子结合的Sir1增加,强大的管家调控元件也可以被抑制,这表明Sir1是沉默过程中的一个限制因素。总之,我们的数据表明,异染色质位点已被优化,以稳定沉默弱的交配型基因调控元件,而不是强大的管家基因调控序列,这有助于解释为什么这些基因经常出现在沉默结构域的边界。