Mol Cell Biol, April 1998, p. 1855-1865, Vol. 18, No. 4
0270-7306/98/$04.00+0
Copyright © 1998, American Society for Microbiology. All rights reserved.
Département de Biochimie
Médicale,
Received 31 October 1997/Returned for modification 21 November
1997/Accepted 30 December 1997
A previously uncharacterized Saccharomyces cerevisiae
open reading frame, YNR038W, was analyzed in the context of the
European Functional Analysis Network. YNR038W encodes a putative
ATP-dependent RNA helicase of the DEAD-box protein family and
was therefore named DBP6 (DEAD-box protein 6). Dbp6p is
essential for cell viability. In vivo depletion of Dbp6p results in a
deficit in 60S ribosomal subunits and the appearance of half-mer
polysomes. Pulse-chase labeling of pre-rRNA and steady-state analysis
of pre-rRNA and mature rRNA by Northern hybridization and primer
extension show that Dbp6p depletion leads to decreased production of
the 27S and 7S precursors, resulting in a depletion of the mature 25S and 5.8S rRNAs. Furthermore, hemagglutinin epitope-tagged Dbp6p is
detected exclusively within the nucleolus. We propose that Dbp6p is
required for the proper assembly of preribosomal particles during the
biogenesis of 60S ribosomal subunits, probably by acting as an rRNA
helicase.
*
Corresponding author. Mailing address:
Département de Biochimie Médicale, Centre Médical
Universitaire, Université de Genève, 1 rue Michel-Servet,
CH-1211 Geneva 4, Switzerland. Phone: 41 22 702 55 08. Fax: 41 22 702 55 02. E-mail: dieter.kressler{at}medecine.unige.ch.
This article has been cited by other articles:
| J. Bacteriol. | J. Virol. | Eukaryot. Cell |
|---|
| Microbiol. Mol. Biol. Rev. | Clin. Vaccine Immunol. | All ASM Journals |
|---|