RNA Therapeutics Institute, UMass Medical School, 368 Plantation Street, Worcester, MA 01605, USA; Howard Hughes Medical Institute.
RNA Therapeutics Institute, UMass Medical School, 368 Plantation Street, Worcester, MA 01605, USA.
Cell Rep. 2018 Feb 27;22(9):2254-2264. doi: 10.1016/j.celrep.2018.02.009. Epub 2018 Feb 15.
Protein-coding genes undergo a wide array of regulatory interactions with factors that engage non-coding regions. Open reading frames (ORFs), in contrast, are thought to be constrained by coding function, precluding a major role in gene regulation. Here, we explore Piwi-interacting (pi)RNA-mediated transgene silencing in C. elegans and show that marked differences in the sensitivity to piRNA silencing map to the endogenous sequences within transgene ORFs. Artificially increasing piRNA targeting within the ORF of a resistant transgene can lead to a partial yet stable reduction in expression, revealing that piRNAs not only silence but can also "tune" gene expression. Our findings support a model that involves a temporal element to mRNA regulation by germline Argonautes, likely prior to translation, and suggest that piRNAs afford incremental control of germline mRNA expression by targeting the body of the mRNA, including the coding region.
蛋白质编码基因与参与非编码区域的因子之间存在广泛的调控相互作用。相比之下,开放阅读框(ORF)被认为受到编码功能的限制,排除了其在基因调控中的主要作用。在这里,我们探索了 Piwi 相互作用(pi)RNA 在秀丽隐杆线虫中的转基因沉默,并表明对 piRNA 沉默的敏感性的显著差异映射到转基因 ORF 内的内源性序列。在抗性转基因的 ORF 内人为地增加 piRNA 的靶向性可以导致表达的部分但稳定的降低,这表明 piRNAs 不仅可以沉默,还可以“调节”基因表达。我们的研究结果支持了一种模型,该模型涉及生殖系 Argonautes 对 mRNA 调控的时间因素,可能在翻译之前,并表明 piRNAs 通过靶向 mRNA 的主体,包括编码区,为生殖系 mRNA 表达提供了增量控制。