Affiliation:
1. Département de Biochimie Médicale, Centre Médical Universitaire, 1 and
2. Département de Biochimie, Sciences II, 2 Universitéde Genève, 1211 Geneva 4, Switzerland
Abstract
ABSTRACT
Dbp6p is an essential putative ATP-dependent RNA helicase that is required for 60S-ribosomal-subunit assembly in the yeast
Saccharomyces cerevisiae
(D. Kressler, J. de la Cruz, M. Rojo, and P. Linder, Mol. Cell. Biol. 18:1855–1865, 1998). To identify factors that are functionally interacting with Dbp6p, we have performed a synthetic lethal screen with conditional
dbp6
mutants. Here, we describe the cloning and the phenotypic analysis of the previously uncharacterized open reading frame YPL193W, which we renamed
RSA1
(ribosome assembly 1). Rsa1p is not essential for cell viability; however,
rsa1
null mutant strains display a slow-growth phenotype, which is exacerbated at elevated temperatures. The
rsa1
null allele synthetically enhances the mild growth defect of weak
dbp6
alleles and confers synthetic lethality when combined with stronger
dbp6
alleles. Polysome profile analysis shows that the absence of Rsa1p results in the accumulation of half-mer polysomes. However, the pool of free 60S ribosomal subunits is only moderately decreased; this is reminiscent of polysome profiles from mutants defective in 60S-to-40S subunit joining. Pulse-chase labeling of pre-rRNA in the
rsa1
null mutant strain indicates that formation of the mature 25S rRNA is decreased at the nonpermissive temperature. Interestingly, free 60S ribosomal subunits of a
rsa1
null mutant strain that was grown for two generations at 37°C are practically devoid of the 60S-ribosomal-subunit protein Qsr1p/Rpl10p, which is required for joining of 60S and 40S subunits (D. P. Eisinger, F. A. Dick, and B. L. Trumpower, Mol. Cell. Biol. 17:5136–5145, 1997). Moreover, the combination of the Δ
rsa1
and
qsr1-1
mutations leads to a strong synthetic growth inhibition. Finally, a hemagglutinin epitope-tagged Rsa1p localizes predominantly to the nucleoplasm. Together, these results point towards a function for Rsa1p in a late nucleoplasmic step of 60S-ribosomal-subunit assembly.
Publisher
American Society for Microbiology
Subject
Cell Biology,Molecular Biology
Cited by
45 articles.
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