Rok1p is a putative RNA helicase required for rRNA processing

被引:91
作者
Venema, J
BousquetAntonelli, C
Gelugne, JP
CaizerguesFerrer, M
Tollervey, D
机构
[1] EUROPEAN MOL BIOL LAB, D-69117 HEIDELBERG, GERMANY
[2] CNRS, LAB BIOL MOL EUCARYOTE, F-31062 TOULOUSE, FRANCE
关键词
D O I
10.1128/MCB.17.6.3398
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The synthesis of ribosomes involves many small nucleolar ribonucleoprotein particles (snoRNPs) as transacting factors. Yeast strains lacking the snoRNA, snR10, are viable but are impaired in growth and delayed in the early pre-rRNA cleavages at sites A(0), A(1), and A(2), which lead to the synthesis of 18S rRNA. The same cleavages are inhibited by genetic depletion of the essential snoRNP protein Gar1p. Screens for mutations showing synthetic lethality with deletion of the SNR10 gene or with a temperature-sensitive gar1 allele both identified the ROK1 gene, encoding a putative, ATP-dependent RNA helicase of the DEAD-box family. The ROK1 gene is essential for viability, and depletion of Rok1p inhibits pre-rRNA processing at sites A(0), A(1), and A(2), thereby blocking 18S rRNA synthesis. Indirect immunofluorescence by using a ProtA-Rok1p construct shows the protein to be predominantly nucleolar. These results suggest that Rok1p is required for the function of the snoRNP complex carrying out the early pre-rRNA cleavage reactions.
引用
收藏
页码:3398 / 3407
页数:10
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