Basak Anindita, Query Charles C
Department of Cell Biology, Albert Einstein College of Medicine, Bronx, NY 10461, USA.
Department of Cell Biology, Albert Einstein College of Medicine, Bronx, NY 10461, USA.
Cell Rep. 2014 Aug 21;8(4):966-73. doi: 10.1016/j.celrep.2014.07.004. Epub 2014 Aug 7.
Although pseudouridine nucleobases are abundant in tRNAs, rRNAs, and small nuclear RNAs (snRNAs), they are not known to have physiologic roles in cell differentiation. We have identified a pseudouridine residue (Ψ28) on spliceosomal U6 snRNA that is induced during filamentous growth of Saccharomyces cerevisiae. Pus1p catalyzes this modification and is upregulated during filamentation. Several U6 snRNA mutants are strongly pseudouridylated at Ψ28. Remarkably, these U6 mutants activate pseudohyphal growth, dependent upon Pus1p, arguing that U6-Ψ28 per se can initiate at least part of the filamentous growth program. We confirmed this by using a designer small nucleolar RNA (snoRNA) targeting U6-U28 pseudouridylation. Conversely, mutants that block U6-U28 pseudouridylation inhibit pseudohyphal growth. U6-U28 pseudouridylation changes the splicing efficiency of suboptimal introns; thus, Pus1p-dependent pseudouridylation of U6 snRNA contributes to the filamentation growth program.
虽然假尿嘧啶核苷碱基在转运RNA(tRNA)、核糖体RNA(rRNA)和小核RNA(snRNA)中大量存在,但它们在细胞分化中的生理作用尚不清楚。我们在酿酒酵母丝状生长过程中,在剪接体U6 snRNA上鉴定出一个假尿嘧啶残基(Ψ28)。Pus1p催化这种修饰,并且在丝状生长过程中上调。几个U6 snRNA突变体在Ψ28处强烈假尿嘧啶化。值得注意的是,这些U6突变体激活假菌丝生长,这依赖于Pus1p,表明U6-Ψ28本身可以启动至少部分丝状生长程序。我们通过使用靶向U6-U28假尿嘧啶化的设计小核仁RNA(snoRNA)证实了这一点。相反,阻断U6-U28假尿嘧啶化的突变体抑制假菌丝生长。U6-U28假尿嘧啶化改变次优内含子的剪接效率;因此,U6 snRNA的Pus1p依赖性假尿嘧啶化有助于丝状生长程序。