Bumgarner Stacie L, Dowell Robin D, Grisafi Paula, Gifford David K, Fink Gerald R
Whitehead Institute for Biomedical Research, 9 Cambridge Center, Cambridge, MA 02142, USA.
Proc Natl Acad Sci U S A. 2009 Oct 27;106(43):18321-6. doi: 10.1073/pnas.0909641106. Epub 2009 Sep 30.
The identification of specific functional roles for the numerous long noncoding (nc)RNAs found in eukaryotic transcriptomes is currently a matter of intense study amid speculation that these ncRNAs have key regulatory roles. We have identified a pair of cis-interfering ncRNAs in yeast that contribute to the control of variegated gene expression at the FLO11 locus by implementing a regulatory circuit that toggles between two stable states. These capped, polyadenylated ncRNAs are transcribed across the large intergenic region upstream of the FLO11 ORF. As with mammalian long intervening (li)ncRNAs, these yeast ncRNAs (ICR1 and PWR1) are themselves regulated by transcription factors (Sfl1 and Flo8) and chromatin remodelers (Rpd3L) that are key elements in phenotypic transitions in yeast. The mechanism that we describe explains the unanticipated role of a histone deacetylase complex in activating gene expression, because Rpd3L mutants force the ncRNA circuit into a state that silences the expression of the adjacent variegating gene.
在真核生物转录组中发现的众多长链非编码(nc)RNA的特定功能作用的鉴定,目前是深入研究的课题,因为有人推测这些ncRNA具有关键的调控作用。我们在酵母中鉴定出一对顺式干扰ncRNA,它们通过实施一种在两种稳定状态之间切换的调控回路,来控制FLO11基因座处的斑驳基因表达。这些带有帽结构、多聚腺苷酸化的ncRNA转录跨越FLO11开放阅读框上游的大片基因间区域。与哺乳动物的长链居间(li)ncRNA一样,这些酵母ncRNA(ICR1和PWR1)本身受转录因子(Sfl1和Flo8)以及染色质重塑因子(Rpd3L)的调控,而这些因子是酵母表型转变中的关键要素。我们所描述的机制解释了组蛋白脱乙酰酶复合体在激活基因表达中出人意料的作用,因为Rpd3L突变体迫使ncRNA回路进入一种使相邻斑驳基因表达沉默的状态。