The yeast NOP4 gene product is an essential nucleolar protein required for pre-rRNA processing and accumulation of 60S ribosomal subunits.

Abstract

The Saccharomyces cerevisiae NOP4 gene was isolated by screening a lambda gt11 yeast genomic DNA library with a monoclonal antibody against a yeast nucleolar protein. NOP4 encodes a 78 kDa protein that contains two prototypical RNA recognition motifs (RRMs) flanking an imperfect RRM lacking characteristic RNP1 and RNP2 motifs. In addition, there is a fourth incomplete RRM. NOP4 is a single copy essential gene present on chromosome XVI, between RAD1 and PEP4. To examine the function of Nop4p, we constructed a conditional null allele of NOP4 by placing this gene under the control of the glucose‐repressible GAL1 promoter. When cells are shifted from galactose‐containing medium to glucose‐containing medium, NOP4 transcription is terminated, Nop4 protein is depleted and cell growth is impaired. Nop4 protein depletion results in diminished accumulation of 60S ribosomal subunits, assignable to a defect in ribosome biogenesis arising from a lack of production of mature 25S rRNA from 27S precursor rRNA.

Dbp9p, a putative ATP-dependent RNA helicase involved in 60S-ribosomal-subunit biogenesis, functionally interacts with Dbp6p

“…The results presented in this study, however, support a model where Dbp9p would act at a very early step in the formation of 60S ribosomal subunits+ First, the most pronounced pre-rRNA processing phenotype associated with the genetic depletion of Dbp9p is the reduced formation and the lower steady-state levels of all 27S precursors, especially of the 27SB pre-rRNAs, to mature 25S and 5+8S rRNA+ Similar phenotypes have been observed upon depletion of other protein trans-acting factors (Bergès et al+, 1994;Sun & Woolford, 1994;Kressler et al+, 1998;Zanchin & Goldfarb, 1999), and they are most readily explained by the instability of early pre-ribosomal particles (discussed in Kressler et al+, 1999b)+ Second, Dbp9p depletion affects 18S rRNA production more drastically than depletion of other protein trans-acting factors involved in 60S-ribosomalsubunit biogenesis does (Bergès et al+, 1994;Sun & Woolford, 1994;de la Cruz et al+, 1998;Kressler et al+, 1999c;Zanchin & Goldfarb, 1999;Burger et al+, 2000)+ Intriguingly, the block of the early cleavages at sites A 0 to A 2 , however, seems to be less pronounced, as judged by the relatively low levels of 23S rRNA accumulation, upon Dbp9p depletion+ One conceivable explanation is that the instability of early pre-ribosomal particles is masking the effect of inhibited A 0 to A 2 cleavage; delayed or blocked cleavage at these sites is generally observed in mutants affecting 60S-ribosomal-subunit biogenesis (discussed in Venema & Tollervey, 1999)+ Finally, our genetic data (synthetic lethality, dosage suppression, and weak interaction in a yeast two-hybrid assay) indicate that Dbp9p functionally interacts with Dbp6p, which has been previously suggested to be acting at an early step on the pathway to formation of 60S ribosomal subunits (Kressler et al+, 1998(Kressler et al+, , 1999a)+ The observed genetic interactions are highly specific because neither the dbp9 nor dbp6 mutant phenotypes are synthetically enhanced by, for example, the spb4-1 mutation (data not shown and Kressler et al+, 1999a)+ Moreover, the cold sensitivity of the dbp6-4 mutant cannot be suppressed by overexpression of other DEADbox proteins, such as Dbp10p and Spb4p, implicated in the biogenesis of 60S ribosomal subunits (data not shown)+ Interestingly, this is the first time that a putative RNA helicase has been shown to suppress a mutation in another helicase gene involved in ribosome biogenesis+ A similar suppression has so far only been demonstrated for the cytoplasmic Ded1p by its homolog Dbp1p (Jamieson & Beggs, 1991)+ However, in this case, overexpression of Dbp1p results in a bypass suppression, which is clearly not the case for the couple DBP6/DBP9+ Increased dosage of Dbp9p allows suppression of certain dbp6 mutant alleles indicati...…”

Why Molecular Chaperones Buffer Mutational Damage: A Case Study With a Yeast Hsp40/70 System

“…However, the molecular basis of this genetic interaction could be very special. It is probably not coincidental that rrp1 and nop4 (as well as rrp15, identified in the first screen) are mutations in genes required for maturation of the 60S ribosomal unit (Sun and Woolford 1994;Horsey et al 2004;de Marchis et al 2005), the complex to which Zuo1p is anchored. It indicates that Zuo1p participates in biogenesis of the ribosome either passively as its future constituent or actively as a working enzyme.…”

Spb4p, an essential putative RNA helicase, is required for a late step in the assembly of 60S ribosomal subunits in Saccharomyces cerevisiae

“…In many characterized mutants that are defective in synthesis of the 60S subunits, most r-proteins and the 27S pre-rRNAs are degraded rapidly+ This is seen on depletion of some 60S subunit r-proteins, e+g+, L16 (Moritz et al+, 1990), or with mutations in trans-acting factors that are believed to function at early steps in the 60S ribosomal subunit assembly pathway, e+g+, Nop4p/ Nop77p, Dbp6p or Dbp7p (Bergès et al+, 1994;Sun & Woolford, 1994;Daugeron & Linder, 1998;Kressler et al+, 1998)+ In contrast, the accumulation of the 27SB pre-rRNAs observed in the spb4-1 and GAL::SPB4 strains most resembles the phenotypes described for strains depleted of Nop2p, Nop3p, or Nip7p (Russell & Tollervey, 1992;Hong et al+, 1997;Zanchin et al+, 1997)+ We speculate that Spb4p, as well as Nop2p, Nop3p, and Nip7p, are required for a late step in the 60S ribo-FIGURE 9. HA-Spb4p localizes to the nucleolus+ Indirect immunofluorescence was performed with cells expressing HASpb4p from the SPB4 promoter (JDY8-1A YCplac111-HA-SPB4)+ A: Nop1p was detected by polyclonal rabbit anti-Nop1p antibodies, followed by decoration with a goat anti-rabbit fluorescein-conjugated antibody+ B: HA-Spb4p was detected by the monoclonal mouse anti-HA 16B12 antibody, followed by decoration with a goat anti-mouse rhodamine-conjugated antibody+ C: Chromatin DNA was stained using 49,6-diamidino-2-phenylindole dihydrochloride (DAPI)+ Pseudo-colors were assigned to the digitized micrographs (A-C) and images were merged+ Overlapping distributions are revealed in: (D) yellow for Nop1p and HA-Spb4p colocalization; (E) magenta for HA-Spb4p and chromatin DNA colocalization; and (F) cyan for Nop1p and chromatin DNA colocalization+ somal subunit assembly+ In the absence of the activity of these factors, the pre-ribosomes accumulate in a form that is relatively close to the normal structure, leading to their co-sedimentation with the normal 66S pre-ribosomes+ Some structural defects, however, prevent the processing reactions at sites C 1 and C 2 from proceeding, preventing synthesis of the 25S and 5+8S rRNAs+ In view of the presumed ATP-dependent RNA helicase activity of Spb4p, we assume that it normally functions in the restructuring of the pre-rRNA within the 66S pre-ribosome+ Ten putative ATP-dependent RNA helicases have been reported to function in ribosome biogenesis (see Introduction)+ Because most of the genes are essential for viability, we conclude that each of these proteins plays a specific, nonredundant function during ribosome biogenesis+ This interpretation is supported by the fact that overexpression of other genes encoding putative RNA helicases required for the 60S ribosomal subunit synthesis (DBP6, DBP7, and DRS1) do not suppress either the slow-growth phenotype or the coldsensitivity of the spb4-1 mutant and do not bypass the lethal phenotype of the spb4 null strain (data not shown)+ In addition, overexpression of SPB4 does not suppress the slow-growth and the temperature sensitivity of dbp6 (D+ Kressler & P+ Linder, unpubl+) or dbp7 mutants (Daugeron & Linder, 1998) and double spb4-1 dbp6 or spb4-1 dbp7 mutants are not synthetically lethal (Daugeron & Linder, 1998 and data not shown)+ During th...…”