Bohnsack Markus T, Martin Roman, Granneman Sander, Ruprecht Maike, Schleiff Enrico, Tollervey David
Wellcome Trust Centre for Cell Biology, University of Edinburgh, UK.
Mol Cell. 2009 Nov 25;36(4):583-92. doi: 10.1016/j.molcel.2009.09.039.
Yeast ribosome synthesis requires 19 different RNA helicases, but none of their pre-rRNA-binding sites were previously known, making their precise functions difficult to determine. Here we identify multiple binding sites for the helicase Prp43 in the 18S and 25S rRNA regions of pre-rRNAs, using UV crosslinking. Binding in 18S was predominantly within helix 44, close to the site of 18S 3' cleavage, in which Prp43 is functionally implicated. Four major binding sites were identified in 25S, including helix 34. In strains depleted of Prp43 or expressing only catalytic point mutants, six snoRNAs that guide modifications close to helix 34 accumulated on preribosomes, implicating Prp43 in their release, whereas other snoRNAs showed reduced preribosome association. Prp43 was crosslinked to snoRNAs that target sequences close to its binding sites, indicating direct interactions. We propose that Prp43 acts on preribosomal regions surrounding each binding site, with distinct functions at different locations.
酵母核糖体的合成需要19种不同的RNA解旋酶,但此前它们的前体rRNA结合位点均不为人所知,这使得确定它们的确切功能变得困难。在此,我们利用紫外线交联技术,在pre-rRNA的18S和25S rRNA区域鉴定出解旋酶Prp43的多个结合位点。18S中的结合主要发生在螺旋44内,靠近18S 3'切割位点,Prp43在该位点具有功能相关性。在25S中鉴定出四个主要结合位点,包括螺旋34。在Prp43缺失或仅表达催化点突变体的菌株中,六种引导靠近螺旋34处修饰的snoRNA在核糖体前体上积累,这表明Prp43参与它们的释放,而其他snoRNA与核糖体前体的结合减少。Prp43与靶向靠近其结合位点序列的snoRNA发生交联,表明存在直接相互作用。我们提出,Prp43作用于每个结合位点周围的核糖体前体区域,在不同位置具有不同功能。