Prp43 Bound at Different Sites on the Pre-rRNA Performs Distinct Functions in Ribosome Synthesis

被引:142
作者
Bohnsack, Markus T. [1 ,3 ]
Martin, Roman [3 ]
Granneman, Sander [1 ]
Ruprecht, Maike [3 ]
Schleiff, Enrico [3 ,4 ]
Tollervey, David [1 ,2 ]
机构
[1] Univ Edinburgh, Wellcome Trust Ctr Cell Biol, Edinburgh EH9 3JR, Midlothian, Scotland
[2] Univ Edinburgh, Ctr Syst Biol, Edinburgh EH9 3JR, Midlothian, Scotland
[3] Goethe Univ Frankfurt, Cluster Excellence Macromol Complexes, Inst Mol Biosci, D-60438 Frankfurt, Germany
[4] Goethe Univ Frankfurt, Ctr Membrane Prote, D-60438 Frankfurt, Germany
基金
英国生物技术与生命科学研究理事会; 英国惠康基金;
关键词
DEAD-BOX PROTEINS; COMPREHENSIVE MUTATIONAL ANALYSIS; SMALL NUCLEOLAR RNA; PRERIBOSOMAL RNA; LARIAT-INTRON; HELICASE; RELEASE; SNORNA; FAMILY; ATPASE;
D O I
10.1016/j.molcel.2009.09.039
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
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.
引用
收藏
页码:583 / 592
页数:10
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