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CELL BIOLOGY AND SIGNAL TRANSDUCTION

Arabidopsis Ribosomal Proteins RPL23aA and RPL23aB Are Differentially Targeted to the Nucleolus and Are Disparately Required for Normal Development^{1,[C],[W],[OA]}

Department of Biology, University of Saskatchewan, Saskatoon, Saskatchewan, Canada S7N 5E2

	ABSTRACT

TOP ABSTRACT RESULTS DISCUSSION MATERIALS AND METHODS LITERATURE CITED

 
Protein synthesis is catalyzed by the ribosome, a two-subunit enzyme comprised of four ribosomal RNAs and, in Arabidopsis (Arabidopsis thaliana), 81 ribosomal proteins (r-proteins). Plant r-protein genes exist as families of multiple expressed members, yet only one r-protein from each family is incorporated into any given ribosome, suggesting that many r-protein genes may be functionally redundant or development/tissue/stress specific. Here, we characterized the localization and gene-silencing phenotypes of a large subunit r-protein family, RPL23a, containing two expressed genes (RPL23aA and RPL23aB). Live cell imaging of RPL23aA and RPL23aB in tobacco with a C-terminal fluorescent-protein tag demonstrated that both isoforms accumulated in the nucleolus; however, only RPL23aA was targeted to the nucleolus with an N-terminal fluorescent protein tag, suggesting divergence in targeting efficiency of localization signals. Independent knockdowns of endogenous RPL23aA and RPL23aB transcript levels using RNA interference determined that an RPL23aB knockdown did not alter plant growth or development. Conversely, a knockdown of RPL23aA produced a pleiotropic phenotype characterized by growth retardation, irregular leaf and root morphology, abnormal phyllotaxy and vasculature, and loss of apical dominance. Comparison to other mutants suggests that the phenotype results from reduced ribosome biogenesis, and we postulate a link between biogenesis, microRNA-target degradation, and maintenance of auxin homeostasis. An additional RNA interference construct that coordinately silenced both RPL23aA and RPL23aB demonstrated that this family is essential for viability.

Arabidopsis RPL23a is part of a universally conserved r-protein family (Lecompte et al., 2002) that binds directly to LSU rRNA and is essential for ribosome biogenesis (El-Baradi et al., 1984, 1985, 1987; Rutgers et al., 1991). Structural studies have mapped its yeast (Saccharomyces cerevisiae) and bacterial counterparts (L25 and L23, respectively) to the LSU, adjacent to the polypeptide exit tunnel (Nissen et al., 2000; Spahn et al., 2001). This position suggests a role for RPL23a in protein translocation and secretion, and this role has been validated in both prokaryotes and eukaryotes (Beckmann et al., 1997; Morgan et al., 2002; Pool et al., 2002; Halic et al., 2004; Maier et al., 2005; Menetret et al., 2005). There are two members of the RPL23a family in Arabidopsis, RPL23aA and RPL23aB. Transcript expression profiles have shown that RPL23aA is more abundant than RPL23aB in all tissues, and that accumulation of each differs in response to cold, wounding, and copper stress (McIntosh and Bonham-Smith, 2005). Both isoforms are incorporated into the ribosome (Chang et al., 2005; Giavalisco et al., 2005; Carroll et al., 2008), and RPL23aA functionality was confirmed by its ability to complement a yeast l25 mutant (McIntosh and Bonham-Smith, 2001).

The consequences of overlapping r-protein expression in plants have yet to be fully elucidated. In yeast, 59 of 79 r-proteins are encoded by two expressed paralogs, producing identical or near-identical r-protein isoforms. Although these paralogs can be transcribed at divergent levels (Tornow and Santangelo, 1994; Planta, 1997), a high transcription rate from one paralog is compensated for by a low rate from the other, resulting in a consistent transcript level for each r-protein (Warner et al., 1985; Planta, 1997). As with yeast, most of the Arabidopsis r-protein paralogs encode very similar proteins. However, unlike yeast, there is no evidence suggesting that transcript levels among paralogs are linked in a regulated manner. For example, hormone and stress treatment of Arabidopsis seedlings leads to changes in transcript levels of single paralogs from the RPS15a and RPL23a families but has no affect on the levels of the other expressed paralogs (Hulm et al., 2005; McIntosh and Bonham-Smith, 2005). Further, despite overlapping transcript expression, phenotypic characterization of single paralog silencing or knockout lines suggest that paralogs are not functionally equivalent. In tobacco (Nicotiana tabacum), for example, silencing RPL3A led to an increase in RPL3B transcript levels, but this increase was unable to compensate for the reduced RPL3A levels, resulting in abnormal growth and development (Popescu and Tumer, 2004). In Arabidopsis, rps13b and rps18a T-DNA insertional mutants develop narrow, pointed first leaves and have stunted root growth and delayed flowering; in both cases, northern analyses confirmed that transcript levels from paralogs were unaffected (Van Lijsebettens et al., 1994; Ito et al., 2000). It remains to be determined whether these findings result from a biological shortage of r-proteins for ribosome biogenesis caused by the loss of one copy from a redundant family, or if they are indicative of specialized functions for specific paralogs.

In this work, we investigated whether the two Arabidopsis RPL23a paralogs are equivalent with respect to cellular localization and phenotypic response to gene knockdowns. Accordingly, C- and N-terminal RPL23a-fluorescent protein fusions were made, and their localization followed in vivo in a heterologous tobacco system. We found that the two isoforms have different affinities for nucleolar accumulation, with RPL23aA predominating. We then designed estrogen-inducible, RNA interference (RNAi)-mediated silencing constructs targeting RPL23aA and RPL23aB, independently and coordinately. RPL23aA silencing resulted in growth retardation and morphological abnormalities, while RPL23aB silencing had no affect. We also showed, for the first time in plants, that coordinate silencing of both RPL23aA and RPL23aB is lethal. Our results indicate that the two RPL23a isoforms are not of equivalent importance for normal plant development.

	RESULTS

TOP ABSTRACT RESULTS DISCUSSION MATERIALS AND METHODS LITERATURE CITED

 

RPL23a Isoform Comparison

RPL23aA and RPL23aB share 68.8% identity at the transcript level (83.7% between open reading frames [ORFs]) but encode proteins exhibiting 94.8% amino acid identity. They also share a high degree of primary sequence conservation with other eukaryotic orthologs (Fig. 1A ), especially within the C-terminal domain that binds LSU rRNA (Rutgers et al., 1991). The eukaryotic L23a/L25 r-proteins possess an N-terminal extension region that is absent from prokaryotic counterparts and contains the nuclear localization signal (NLS; Rutgers et al., 1990; Schaap et al., 1991; Jakel and Gorlich, 1998). Although the NLS of plant RPL23a proteins has yet to be experimentally determined, all residue differences between Arabidopsis RPL23a isoforms reside within the N-terminal region (Fig. 1A). Further, two of these differences occur within a classical monopartite NLS [Fig. 1A; consensus (K/R)₂XK/R, where X denotes any residue] that purportedly also functions as a nucleolus localization signal (NoLS; Kalderon et al., 1984; Dingwall and Laskey, 1991; Weber et al., 2000; Horke et al., 2004).

View larger version (82K): [in this window] [in a new window] [as a PowerPoint slide]   Figure 1. Alignment and localization of the Arabidopsis RPL23a isoforms. A, Clustal alignment of the two Arabidopsis RPL23a isoforms (AtRPL23aA and AtRPL23aB) with tobacco RPL23a (NtRPL23a), two rice RPL23a isoforms (OsRPL23a-1, LOC_Os01g24690; OsRPL23a-2, LOC_Os04g42270), human RPL23a (HsRPL23a), and yeast RPL25 (ScRPL25). Identical and similar residues shared by four or more orthologs are shaded black and gray, respectively, while those shared by three or fewer orthologs are shaded white. Experimentally determined domains responsible for nuclear localization in human (Jakel and Gorlich, 1998) and yeast (Schaap et al., 1991) are highlighted in yellow. The C-terminal domain, which contains rRNA-binding capacity, is highlighted red (Rutgers et al., 1991; Kooi et al., 1994). Putative monopartite NLSs [(K/R)XK/R] in Arabidopsis are delineated by green brackets. Numbering is for reference only. B to I, CLSM images of tobacco epidermal cells transiently coexpressing FIB2-EGFP and RPL23aA-mRFP (B and C) or FIB2-EGFP and RPL23aB-mRFP (D, E, and I), or expressing RPL23aB-mRFP alone (F–H). Nucleolar and nucleoplasmic signals are indicated by transparent white arrowheads and small white arrows, respectively (B–I). White arrowheads point to cajal bodies (Beven et al., 1995; B–E, left). Images of the same optical slice were merged to show signal overlap (B–E and I, right). Bars = 10 µm.

To investigate whether differences in putative RPL23a NLS/NoLS domains have any impact on localization patterns, we designed RPL23aA/B C-terminal fusions with monomeric red fluorescent protein (mRFP) separated by a glutathione S-transferase (GST) linker. The GST linker was added to increase translational fusion mass beyond the size exclusion limit of nuclear pore complexes (>60 kD) and to enable affinity purification of bound proteins (Grebenok et al., 1997; Merkle, 2003); it did not interfere with localization in any noticeable way (see also Ookata et al., 1995; Kishi et al., 1996). C-terminal fusions were investigated because it has previously been shown that attachment of a small (approximately 2 kD) FLAG-His₆ tag to the C terminus of RPL23aA did not disrupt the ability of the fusion protein to incorporate into ribosomes and form polysomes (Zanetti et al., 2005). RPL23a orthologs are known to be involved in LSU biogenesis within the nucleolus (Jeeninga et al., 1996; van Beekvelt et al., 2001), and hence we hypothesized that Arabidopsis RPL23a would accumulate to the greatest extent in the nucleolus. To enable definitive identification of nucleolar accumulation, we used a nucleolar marker, Arabidopsis FIBRILLARIN2 (FIB2), with a C-terminal enhanced GFP (EGFP) tag (Barneche et al., 2000). FIB2 specifically localizes to the nucleolus, where it directs a requisite step in rRNA processing and ribosome assembly (Tollervey et al., 1993; Barneche et al., 2000). RPL23aA/B-mRFP chimerics were transiently coexpressed with the FIB2-EGFP marker in tobacco epidermal cells via infiltration with transformed Agrobacterium tumefaciens (Sparkes et al., 2006). Cells imaged with a confocal laser scanning microscope (CLSM) 72 h postinfiltration showed strong nucleolar accumulation of FIB2-EGFP (Fig. 1, B–E and I, left) and weaker but clearly discernible nucleolar signals for RPL23aA-mRFP (Fig. 1, B and C, middle) and RPL23aB-mRFP (Fig. 1, D and E, middle). FIB2-EGFP also localized to mobile cajal bodies (Fig. 1, B–E; see Supplemental Results S1 for details on cajal bodies and nucleoli properties), which are nonmembrane-bound inclusions associated with nucleoli (Beven et al., 1995; Kim et al., 2007).

While both RPL23a isoforms were capable of localizing to the nucleolus, RPL23aB-mRFP was occasionally unable to target the core of the nucleolus (Fig. 1, F–I), instead accumulating only at the periphery of the nucleolus (13.6% of cells, n = 66; Fig. 1, F and I) or being excluded altogether (19.7% of cells, n = 66; Fig. 1, G and H). Further, although nonnucleolar targeting of RPL23aA-mRFP was observed (10.4% of cells, n = 67), it was a significantly more common occurrence with RPL23aB-mRFP (33.3% of cells, P = 0.001). Alignment of Arabidopsis RPL23a isoforms with tobacco RPL23a (Gao et al., 1994) showed that RPL23aB had two nonconservative K substitutions within putative NLS/NoLS domains (Fig. 1A, reference numbering positions 38 and 56) relative to RPL23aA and NtRPL23a. To examine whether these substitutions might confer a competitive advantage for nucleolar accumulation to RPL23aA, we coexpressed both RPL23aA and RPL23aB in the same tobacco epidermal cells. Accordingly, two additional fusion-protein constructs were made where the C-terminal mRFP tag of RPL23aA and RPL23aB was replaced with a GFP variant modified for plant expression, GFP5 (Haseloff et al., 1997). Coexpression of RPL23aA-GFP5 with RPL23aB-mRFP resulted in a high rate of coexclusion from the nucleolus (40% of cells, n = 25; data not shown). Yet in all instances where nucleolar localization was observed, RPL23aA-GFP5 successfully targeted the nucleolus (100% of cells, n = 13), whereas accumulation of RPL23aB-mRFP was inconsistent, as it was frequently excluded or peripherally localized (40 and 20% of cells, respectively, n = 13; Fig. 2, A and B ). However, when the two isoforms were coexpressed with the converse set of fluorescent protein tags, RPL23aA-mRFP and RPL23aB-GFP5 showed conucleolar accumulation (100% of cells, n = 13; Fig. 2, C and D). These contradictory findings suggest that the fluorescent protein tags may be affecting RPL23aA/B localization (discussed below) but nevertheless indicate that both isoforms accumulate in the nucleolus.

View larger version (72K): [in this window] [in a new window] [as a PowerPoint slide]   Figure 2. Nucleolar colocalization of C-terminally tagged RPL23aA and RPL23aB in tobacco epidermal cells is fluorophore dependent. A to D, CLSM images of tobacco epidermal cells transiently coexpressing RPL23aA-GFP5 and RPL23aB-mRFP (A and B) or RPL23aA-mRFP and RPL23aB-GFP5 (C and D). Solid white arrowheads point to nucleoli; transparent white arrowheads point to nucleolus exclusion zones. Images of the same optical slice were merged to show signal overlap (A–D, right). Bars = 10 µm. [See online article for color version of this figure.]

The N-terminal domain of the yeast RPL23a ortholog is necessary for both nuclear localization and LSU biogenesis (van Beekvelt et al., 2001). To determine if we could interfere with the ability of the N-terminal domain of Arabidopsis RPL23a to direct nuclear/nucleolar accumulation, the RPL23a fusion protein constructs were redesigned such that the GFP5 tag was N terminal, separated from RPL23aA and RPL23aB by the GST linker. As a control, we coexpressed GFP5-RPL23aA/B with free mRFP, which labels the cytoplasm and nucleoplasm but is actively excluded from the nucleolus (Campbell et al., 2002). Shifting the 466-residue fluorescent protein tag to the N terminus completely disrupted GFP5-RPL23aB nucleolar localization (0% of cells showed nucleolar localization, n = 50), resulting in a solely cytoplasmic and nucleoplasmic distribution (Fig. 3, C, D , and F). However, the N-terminal tag did not interfere with nucleolar targeting of RPL23aA (100% of cells showed nucleolar localization, n = 50), which accumulated within the nucleolus at levels indistinguishable from RPL23aA-GFP5 (Fig. 3, A, B, and E; compare with Fig. 2, A and B).

View larger version (72K): [in this window] [in a new window] [as a PowerPoint slide]   Figure 3. RPL23aB with an N-terminal GFP5 tag is unable to accumulate in the nucleolus in tobacco epidermal cells. A to D, CLSM images of tobacco epidermal cells transiently coexpressing GFP5-RPL23aA and free mRFP (A and B) or GFP5-RPL23aB and free mRFP (C and D). E and F, Close-up images of cells expressing GFP5-RPL23aA (E) or GFP5-RPL23aB (F). Solid white arrowheads point to nucleoli (A, B, and E) and transparent white arrowheads point to nucleolar exclusion zones (C and F). Free mRFP delineates the cytoplasm and nucleoplasm (A–D, middle). Images of the same optical slice were merged to show signal overlap (A–D, right). Bars = 10 µm. [See online article for color version of this figure.]

As our previous results suggested that the two RPL23a isoforms are differentially accumulated in the nucleolus, we wanted to investigate the resulting phenotypical consequences of paralog knockdowns in Arabidopsis. Correspondingly, we individually silenced RPL23aA and RPL23aB by engineering paralog-specific self-complementary segments of 3' untranslated regions within an estradiol-regulated vector, pER8 (Zuo et al., 2000; Guo et al., 2003). Consistent with our results from the characterization of an rpl23ab T-DNA knockout line (R. Degenhardt and P. Bonham-Smith, unpublished data), none of the three T₃ transgenic RPL23aB-silencing lines (RPL23aB-ihp-1 to RPL23aB-ihp-3) showed any abnormal phenotype when grown on inductive media (Fig. 4A ). However, T₃ transgenic RPL23aA-silencing lines (RPL23aA-ihp-1 to RPL23aA-ihp-5) showed retarded growth and developmental abnormalities when plated on inductive media, which were most severe in line RPL23aA-ihp-4. Initially, this line developed narrow, pointed first leaves on short, stubby petioles (Fig. 4, A and C). With further development, it produced leaf or leaf-like organs prolifically (Fig. 4B), with an average of 26 leaf organs at bolting (SEM = 0.88, n = 7) compared to an average of 11 (SEM = 0.24, n = 30) on the induced empty vector control pER8-ihp transgenics. RPL23aA-ihp-4 transgenics also produced irregularly shaped or fused older leaves (Fig. 4, B and D), showed delayed transition to reproductive growth when plated on inductive media (some induced seedlings had not flowered at 7 weeks of age; data not shown), and were shorter than pER8-ihp controls at maturity (15.3 cm, SEM = 1.8 cm, versus 20.4 cm, SEM = 0.9; Fig. 4F). Apical dominance was lost, with older RPL23aA-ihp-4 plants showing substantially increased rosette branching (RPL23aA-ihp-4 = 8.8 rosette reproductive shoots, SEM = 1.4; pER8-ihp-4 = 3.3, SEM = 0.6; Fig. 4F). The RPL23aA-ihp-4 line also had substantially reduced root growth and an abnormal root phenotype characterized by short root hairs and malformed lateral roots (Fig. 4D). The atypical leaf phenotype of RPL23aA-ihp-4 resembled that of pointed first leaf (pfl) mutants characterized for RPS13B and RPS18A knockouts (Van Lijsebettens et al., 1994; Ito et al., 2000), but was unique with respect to a greater delay in the transition to reproductive growth, reduced seed production (data not shown), increased leaf number, longer persistence of the pointed morphology (Fig. 4B), and abnormal root growth (Fig. 4D). Nishimura et al. (2005) have reported that an RPL24B knockout also develops a pfl phenotype, as well as additional defects in patterning of cotyledon vasculature and the gynoecium, which were attributed to a specific role for RPL24 in regulating expression of auxin polar transport and response factors. As RPL23aA-ihp-4 has aberrant phyllotaxis, apical dominance, and root development, all of which are auxin-mediated processes (Reed et al., 1998; Chatfield et al., 2000; Reinhardt, 2005), we investigated whether vascular patterning was also disrupted. Chloral hydrate-cleared RPL23aA-ihp-4 seedlings were examined and found to have venation that deviated dramatically from the closed, reticulate venation of pER8-ihp controls (Fig. 4E). Mutant leaves had substantially reduced venation, little to no tertiary or quaternary veins, open vein loops with distal segments ending freely in the lamina, and aberrant anastamosis that was most apparent in the first leaves where the midvein bifurcated close to the hypocotyl-petiole junction (Fig. 4E). Veins also exhibited reduced lateral orientation, with a predominance for base to tip alignment. We did not observe any defects in gynoecium patterning of RPL23aA-ihp-4 plants that had been transferred at bolting to fresh media augmented with estradiol. However, the inducible system we utilized was not readily amenable to analysis of reproductive organs or fertility due to the half-life of the inducer and the requirement of growing transgenics on sealed plates for both sterility and to prevent rapid oxidation of estradiol.

View larger version (85K): [in this window] [in a new window] [as a PowerPoint slide]   Figure 4. Characterization of Arabidopsis RPL23aA- and RPL23aB-silencing mutants. A, The 10-d-old seedlings grown on basal media without or with 10 to 50 µM estradiol (noninduced and induced, respectively). Images shown are representative of T3 transgenics expressing the RPL23aA- or the RPL23aB-silencing cassette (RPL23aA-ihp and RPL23aB-ihp, respectively) or the empty vector control (pER8-ihp). Misshapen leaves with a pointed morphology are indicated by arrowheads. B, The 13-, 18-, and 21-d-old pER8-ihp-2 and RPL23aA-ihp-4 grown on inductive media as above. Bar = 2 mm. C, Comparison of the first four leaves from 13-d-old pER8-ihp-2 and RPL23aA-ihp-4 T3 transgenic seedlings grown on inductive media. Leaves are ordered chronologically (oldest to youngest) left to right. Bars = 2 mm. D, Abnormal leaf and root morphology of 18-d-old RPL23aA-ihp-4 transgenics grown on inductive media. A segment of root from an 18-d-old pER8-ihp-2 transgenic seedling is shown for comparison. Roots are stained with toluidine blue. Arrowheads point to lateral roots. E, Dark-field micrographs showing leaf venation of 14- to 18-d-old pER8-ihp-2 and RPL23aA-ihp-4 T3 transgenic seedlings grown on inductive media and cleared with chloral hydrate. Shown are the first, second, and third leaves and the hypocotyl/petiole junction. Arrowhead shows bifurcation of midveins in the petiole of RPL23aA-ihp-4 transgenics. F, The 38- and 74-d-old (top and bottom, respectively) pER8-ihp-2 and RPL23aA-ihp-4 T3 transgenic seedlings grown on inductive media. Arrowheads in top segments point to rosette flowering branches in RPL23aA-ihp-4 transgenics. Bars = 2 cm. G, qRT-PCR quantification of RPL23aA and RPL23aB transcript abundance in RPL23aA-ihp-1 to -5, RPL23aB-ihp-1 to -3, and pER8-ihp-2 to -4 T3 Arabidopsis transgenic seedlings plated on inductive media. Vertical and horizontal hatched lines represent the ACT7 standardized level of RPL23aA and RPL23aB transcripts, respectively, in transgenic lines on inductive media normalized to the transcript level in noninduced wild-type seedlings (set to 1). Black bars represent SEM. Gray bar represents 100% of wild-type transcript abundance. Asterisks highlight the lines depicted in A to F. [See online article for color version of this figure.]

The RPL23a Family Is Essential for Viability

The purported involvement of RPL23a orthologs in numerous critical ribosomal functions suggests that RPL23a should be essential for plant viability. To test this hypothesis, we designed an RNAi construct that targets a highly conserved region of the ORFs. T₃ seed from six transgenic lines (RPL23a-ihp-3 to RPL23a-ihp-7) were screened on inductive media, and the majority of lines showed acute growth defects, characterized by severely retarded development, reduced root growth, atypical leaf and root morphology, accumulation of anthocyanins, prolific leaf organ development, delayed transition to reproductive growth, flower abortion, and early senescence (Fig. 5, C and D ; reproductive defects data not shown). Two lines (RPL23a-ihp-5 and -6) were nonviable on inductive media and died postgermination (Fig. 5, A and B). Line RPL23a-ihp-5 was grown for 14 d on noninductive media and transferred to inductive media; thereafter, it began to show symptoms consistent with protein synthesis inhibition (impeded growth, chlorosis, necrosis), which progressively worsened and proved lethal 14 to 21 d postinduction (data not shown). To confirm that observed phenotypes were a direct result of silencing RPL23aA and RPL23aB, we conducted qRT-PCR analyses on RNA from transgenic seedlings (10–13 d old) grown on inductive and noninductive media. Transcript levels of RPL23aA and RPL23aB were dramatically lower in induced seedlings of lines RPL23a-ihp-5 to -7 relative to wild type (Fig. 5E). Line -7, which had a survival rate of approximately 10% to 20% when plated on inductive media, had decreased levels of RPL23aA and increased levels of RPL23aB relative to line -6, which had a survival rate of <5% on inductive media. This suggests that RPL23aB may be capable of functionally compensating for RPL23aA. Overall, findings show that, consistent with its orthologs, the Arabidopsis RPL23a family is essential for viability.

View larger version (46K): [in this window] [in a new window] [as a PowerPoint slide]   Figure 5. The Arabidopsis RPL23a family is essential for viability. A to C, Representative images of 11-d-old (A) and 18-d-old (B and C) T3 transgenics expressing the RPL23a family-silencing cassette (RPL23a-ihp) germinated on basal media without or with 10 to 50 µM estradiol (noninduced and induced, respectively). Bars = 2 mm. Abnormal leaf morphology of RPL23a-ihp-5 transgenics on noninductive media, indicated by black arrowhead, suggests leaky expression. D, Aberrant leaf morphology apparent on 29-d-old RPL23a-ihp-7 transgenics grown on inductive media. Black arrowheads indicate leaves with particular anomalous form. E, qRT-PCR quantification of RPL23aA and RPL23aB transcript abundance in RPL23a-ihp-3 to -8 T3 Arabidopsis transgenic seedlings plated on inductive media. Vertical and horizontal hatched lines represent the ACT7 standardized level of RPL23aA and RPL23aB transcripts, respectively, in transgenic lines on inductive media normalized to the transcript level in noninduced wild-type seedlings (set to 1). Black bars represent SEM. Gray bar represents 100% of wild-type transcript abundance. Asterisks highlight the lines depicted in A to D. [See online article for color version of this figure.]

	DISCUSSION

TOP ABSTRACT RESULTS DISCUSSION MATERIALS AND METHODS LITERATURE CITED

We have shown that there are differences in nucleolar targeting of tagged isoforms but not of nuclear accumulation, suggesting that the nine residue differences between RPL23aA and RPL23aB disrupt one or more NoLSs or reduce efficiency of NoLS(s). One divergent region between the RPL23a isoforms occurs within a stretch of basic amino acids containing a putative NoLS/NLS (Kalderon et al., 1984; Dingwall and Laskey, 1991; Weber et al., 2000; Horke et al., 2004). In RPL23aA, this putative NoLS conforms to the core consensus sequence for nucleolin binding in mammals [(K/R)₂XK; Xue et al., 1993; Lee et al., 1998; Intine et al., 2004; Wang et al., 2005]. Nucleolin is a major nucleolar protein involved in RNA polymerase I transcription of rDNA, rRNA processing, and nucleocytoplasmic trafficking of RNA and ribonucleoprotein particles (RNPs; Bouvet et al., 1998; Ginisty et al., 1998; Roger et al., 2003; Mongelard and Bouvet, 2007). It has recently been reported that nucleolin also functions in rDNA condensation and maintaining the nucleolus's structure in plants (Pontvianne et al., 2007). A nucleolin-binding motif in RPL23aA could explain why this isoform shows greater affinity for nucleolar accumulation than RPL23aB, which lacks a consensus nucleolin-binding motif. Nucleolin could function as a nucleolar anchor for the r-protein prior to its assembly into preribosomal particles, in the same manner as nucleolin-containing U3 small nucleolar RNPs bind to rDNA to prepare for processing of nascent rRNA transcripts (Caparros-Ruiz et al., 1997). A similar mechanism may function in the monocot rice (Oryza sativa), which also has two members to its RPL23a family. Only one rice isoform has a putative nucleolin-binding motif (OsRPL23a-1; Fig. 1A), suggesting that one member of both the rice and Arabidopsis RPL23a families may have lost (or gained) its nucleolin-binding capacity following the respective duplication events that created the paralogs.

RPL23aA silencing results in development of a pleiotropic phenotype with symptoms similar to other characterized r-protein mutants: RPS5B, RPS13B, RPS18A, and RPL24B (Van Lijsebettens et al., 1994; Ito et al., 2000; Weijers et al., 2001; Nishimura et al., 2005). In each case, loss/reduction of an r-protein leads to reduced cell division, retarded growth, morphological abnormalities, and late flowering. Further, vascular patterning is disrupted in all r-protein mutants (Ito et al., 2000; Weijers et al., 2001; Nishimura et al., 2005), except possibly for RPS18A, where vasculature was not examined (Van Lijsebettens et al., 1994). This phenotype has been replicated in a recently characterized Arabidopsis nucleolin gene knockout mutant, Atnuc-l1 (Kojima et al., 2007; Petricka and Nelson, 2007; Pontvianne et al., 2007). As described above, nucleolin has an established role in rDNA transcription and rRNA processing (Ginisty et al., 1999). For the latter, it assembles with the U3 small nucleolar RNP complex that cleaves nascent rRNA at the 5' external transcribed spacer primary processing site (Caparros-Ruiz et al., 1997; Saez-Vasquez et al., 2004). In the Atnuc-l1 mutant, pre-rRNA precursor accumulation is decreased, and primary cleavage and subsequent pre-rRNA processing are disrupted (Kojima et al., 2007; Petricka and Nelson, 2007; Pontvianne et al., 2007). In yeast, the RPL23a ortholog is required for efficient pre-rRNA processing (van Beekvelt et al., 2001), and both RPS13 and RPS18 are universally conserved, core structural components of the SSU that bind 18S rRNA and are associated with the pre-rRNA processing complex (Xiang and Lee, 1989; Yusupov et al., 2001; Brodersen et al., 2002; Pontvianne et al., 2007). The striking similarity of phenotype between rpl23aa, rps5b, rps13b, rps18a, rpl24b, and Atnuc-l1 mutants may thus represent the in vivo response to decreased production of processed rRNAs and the concomitant effects on ribosome biogenesis and protein production, with the observed severity gradient being a measure of the extent of the reduction in mature rRNAs. In this scenario, r-proteins likely act indirectly on pre-rRNA processing, with their binding required to induce conformational changes that facilitate pre-rRNA processing or allow the association of other r-proteins and factors involved in processing (Mandiyan et al., 1991; Ban et al., 2000; Wimberly et al., 2000; van Beekvelt et al., 2001).

It is interesting that the phenotype obtained by silencing RPL23aA is not only similar to other r-protein and ribosome biogenesis mutants, but also to plants with disrupted auxin-responsiveness/polar auxin transport. For example, vascular patterning abnormalities similar to those resulting from impaired ribosome biogenesis have also been reported for ettin/auxin response factor3 (arf3) and monopteros/arf5, which are auxin-regulated transcription factor mutants (Przemeck et al., 1996; Sessions et al., 1997; Nemhauser et al., 2000); pin-formed1, an auxin efflux transporter mutant (Goto et al., 1991; Bennett et al., 1995; Petrasek et al., 2006); auxin resistant1, a mutant with reduced expression of a subunit of an enzyme complex that activates the auxin-regulated SCF^TIR ubiquitin-ligase (del Pozo et al., 2002; Deyholos et al., 2003); hve1/cand1, a mutant with reduced levels of a regulator of SCF^TIR assembly (Alonso-Peral et al., 2006); and lop1/tornado1 and tornado2, which are mutant in establishing/maintaining auxin homeostasis (Carland and McHale, 1996; Cnops et al., 2000, 2006). Moreover, treatment of wild-type plants with inhibitors of polar auxin transport has also been reported to disrupt vasculature, causing veins to be restricted to leaf margins and disrupting the midvein (Mattsson et al., 1999; Sieburth, 1999). Petricka and Nelson (2007) determined that auxin response maxima (detected with a synthetic reporter construct, DR5-GUS; Ulmasov et al., 1997; Sabatini et al., 1999), which predict future sites of higher order venation (primary, secondary, tertiary, etc.; Mattsson et al., 2003), were mislocalized in developing leaves of their Atnuc-l1 mutant, such that response maxima were not observed in leaf margins or at sites predicting tertiary or quaternary vein development. This reduction in marginal auxin response maxima was maintained when Atnuc-l1 leaves were treated with an inhibitor of polar auxin transport, which in wild-type plants restricts response maxima to leaf margins (Mattsson et al., 2003; Petricka and Nelson, 2007). It is suggested that the observed pointed/narrow leaf and abnormal venation phenotypes result from a lack of marginal auxin sources/response factors, causing a reduction in auxin-mediated laterally directed cell division and negating procambial differentiation at leaf margins, leading to a decrease in lateral expansion of the leaf and reduced vasculature with predominantly base to tip vein orientation (Petricka and Nelson, 2007). A more general reduction of auxin response would also explain our observation of a loss of apical dominance, as auxin/auxin-responsiveness at the shoot apex is responsible for preventing the formation of lateral buds (Lincoln et al., 1990; Cline, 1991). Thus, perhaps the simplest explanation for the observed relationship between ribosome biogenesis and auxin transport/responsiveness is that synthesis of specific response/trafficking proteins is decreased below a certain required spatiotemporal threshold, disrupting auxin-regulated development and altering patterning. However, this explanation would seem to require a very specific reduction in the translation of auxin-response/-trafficking genes.

Another possibility is that auxin homeostasis is linked to cellular translational status through microRNAs (miRNAs). miRNAs are a class of small RNAs (approximately 22 nucleotides) that originate from long single-stranded RNAs transcribed from endogenous genes by RNA polymerase II (Xie et al., 2005). The single-stranded RNAs possess internal complementarity allowing fold-back and formation of double-stranded RNA that is processed by DICER-LIKE1 (DCL1) in conjunction with the double-stranded RNA-binding protein HYL1 (for review, see Mallory and Vaucheret, 2006). The double-stranded miRNAs are subsequently methylated by HEN1 and loaded onto ARGONAUTE1 (ARG1), which facilitates miRNA maturation and directs cleavage of transcripts with near-perfect complementarity to the miRNAs. Support for a link between miRNAs and auxin homeostasis is 2-fold. First, mutants in miRNA biogenesis (dcl1, hyl1, hen1, arg1) have a range of severe pleiotropic symptoms consistent with disrupted auxin responses, including altered leaf morphology, reduced stature, aberrant gynoecium patterning, decreased apical dominance, atypical phyllotaxis, and irregular vasculature (Bohmert et al., 1998; Jacobsen et al., 1999; Lu and Fedoroff, 2000; Chen et al., 2002). Secondly, several experimentally and computationally determined targets of miRNAs are involved in the auxin response, including TIR1, a component of the SCF^TIR complex; NAC1/NAM, an auxin signal transducer; and ARF6, ARF8, ARF10, ARF16, and ARF17 (Bonnet et al., 2004; Vazquez et al., 2004; Xie et al., 2007; for review, see Eckardt, 2005; Mallory and Vaucheret, 2006). How then are miRNA-mediated processes dependent on translational status? A possible answer comes from recent experiments in fruit fly (Drosophila melanogaster), where Eulalio et al. (2007) fused the 3' untranslated region of different miRNA targets to the firefly luciferase ORF and quantified luciferase transcript levels in cell culture following incubation with or without cognate miRNAs. Transcript levels were shown to decrease significantly following incubation with miRNAs; however, treatment of cells with translation inhibitors (cycloheximide, homoharringtonine, and hippuristanol) caused the stabilization of a subset of miRNA targets. Eulalio et al. (2007) attributed the translational dependency of miRNA target degradation to the possibility that silencing of some targets is initiated after translation commences. A similar mechanism operating in plants would provide an elegant model to explain our findings. Under normal conditions, translation in mitotically active tissues is occurring at a very high rate, allowing the accurate degradation of miRNA targets (which include a large number of auxin response transcripts) and the maintenance of auxin homeostasis. However, when ribosome biogenesis and, consequently, translation are impaired, some miRNA targets are stabilized, resulting in the disruption of auxin feedback cycles, leading to an array of developmental abnormalities. This model could, for example, explain our finding of reduced apical dominance; it has previously been shown that transgenic Arabidopsis expressing an engineered miRNA-resistant version of ARF17 have increased levels of ARF17 transcript (Mallory et al., 2005). This line had a variety of auxin-related developmental defects and showed an increase in transcript levels of two auxin-conjugating enzymes, GH3.2/YDK1 and GH3.3, suggesting that ARF17 functions as a repressor of the conjugating enzymes. Overexpression of YDK1 has previously been shown to result in reduced apical dominance (Takase et al., 2004), presumably because of a reduction in free auxin acting on the meristem to inhibit the formation of lateral buds. It is clear from the phenotypes of auxin response, miRNA synthesis, and ribosome biogenesis mutants that the regulation of auxin homeostasis is very complex, but it is an intriguing possibility that a common link relates all three processes.

We observed that no phenotype was detected as a result of silencing RPL23aB or in a T-DNA insertion rpl23ab knockout line (R. Degenhardt and P. Bonham-Smith, unpublished data). This adds to the mounting body of evidence indicating that, despite often overlapping transcript accumulation patterns, disparity exists in the requirement of r-protein paralogs for normal development (Barakat et al., 2001; McIntosh and Bonham-Smith, 2006). For example, expression profiles of Arabidopsis RPS5A and RPS5B (Weijers et al., 2001), RPS18A to RPS18C (Van Lijsebettens et al., 1994; Vanderhaeghen et al., 2006), and RPL23aA and RPL23aB (McIntosh and Bonham-Smith, 2005) indicate that transcripts from all paralogs accumulate to the highest levels in mitogenic tissues (e.g. meristems and young leaves) and the lowest in nondividing tissues. In all cases, the absolute transcript level varies, but the relative contribution from each paralog remains fairly constant. This is exemplified by transcript profiling of RPS18A to RPS18C, indicating that RPS18A, RPS18B, and RPS18C represent approximately 27%, 16%, and 57%, respectively, of the total RPS18 transcript pool (Vanderhaeghen et al., 2006). Yet, for each of these families, it has been demonstrated that knockout or knockdown mutants of a single paralog triggers development of the atypical phenotype (RPS5B, RPS18A, and RPL23aA; Van Lijsebettens et al., 1994; Weijers et al., 2001; this work). These findings could easily be reconciled if the phenotype-triggering mutation disrupted the predominantly expressed gene or if a corresponding mutation in another paralog induced the same phenotypic response, but this is not supported by experimental data. For example, RPS18A represents roughly only one-quarter of the total RPS18 transcript, and yet its loss produces the pfl phenotype (Van Lijsebettens et al., 1994). Similarly, this phenotype was reproduced in a knockout of RPS13B, which also makes only a small contribution to the RPS13 transcript pool (Ito et al., 2000). It could also be the case that differential spatiotemporal expression of paralogs leads to observed knockout/knockdown phenotypes. It has been shown that RPS5B is predominately localized to cell division zones, while RPS5A is found in less mitotically active regions (Weijers et al., 2001). Yet, this too would be an oversimplified explanation given our findings of overlapping GUS-staining directed by RPL23aA and RPL23aB 5' regulatory regions (K. McIntosh, R. Degenhardt, and P. Bonham-Smith, unpublished data). Moreover, evidence to date suggests that plant r-protein paralogs are differentially required for normal development, with ancillary paralogs functioning only under exceptional conditions, perhaps mediated through spatiotemporal regulation, stimulus-induced expression, assumption of extra-ribosomal roles (for review, see Wool, 1996), or via disparity in cognate binding partners (e.g. affinity for nucleolin).

We have demonstrated that the RPL23a family is essential for viability in Arabidopsis. This is in agreement with previous findings in numerous prokaryotes, yeast, and Caenorhabditis elegans (Kamath et al., 2003; Zhang et al., 2004). Induction of the RPL23a family-silencing construct results in a range of severe pleiotropic phenotypes characterized by developmental defects, reduced shoot and root growth, flower abortion, and, in the most severe case, death upon germination. Given the established importance of RPL23a, our inducibly lethal RPL23a-silencing lines could be useful tools for the in vivo analysis of rRNA processing, LSU assembly, and protein synthesis defects. This adds RPL23a to a growing list of r-proteins from higher eukaryotes that are essential for viability, including RPS5 from Arabidopsis (Weijers et al., 2001), and RPS2, RPS3, RPS4, RPS5, RPS6, RPS13, RPS14, RPL5, RPL9, RPL14, RPL19, and RPL38 from fruit fly (for review, see Saboe-Larssen et al., 1998; Marygold et al., 2005).

Herein, we have demonstrated that the Arabidopsis RPL23a paralogs are differentially targeted to the nucleolus. Disparity within a putative NoLS appears to be responsible, but future work is necessary to determine whether this directly affects their respective abilities to bind to the nucleolus structural protein, nucleolin. We have shown by RNAi-mediated silencing that RPL23aB is phenotypically dispensable, while RPL23aA knockdown leads to a severe pfl phenotype that is possibly due to impaired pre-rRNA processing and consequential effects on miRNA target stability and auxin homeostasis. How directly r-proteins, and particularly RPL23a, are involved in pre-rRNA processing has yet to be elucidated. We have determined that the RPL23a family is essential for survival by the nonviability of transgenic lines that silence both paralogs. These lines have a normal lifecycle on noninductive media and thus may be useful tools for studying ribosome biogenesis at different developmental stages.

	MATERIALS AND METHODS

TOP ABSTRACT RESULTS DISCUSSION MATERIALS AND METHODS LITERATURE CITED

 

Plant Material

Arabidopsis (Arabidopsis thaliana) ‘Columbia-0’ and tobacco (Nicotiana tabacum) ‘Petit Havana’ were used for all experiments. Unless otherwise stated, Arabidopsis was plated on one-half-strength Murashige and Skoog media (Sigma-Aldrich) supplemented with 0.8% phytagar (Invitrogen) and 1.5% Suc (hereafter called basal media). Growth conditions are provided in Supplemental Materials and Methods S1.

Fluorescent Protein and RNAi Constructs

Standard techniques were followed for all molecular cloning (Sambrook et al., 1989). All cloning products were verified by automated sequencing (National Research Council-Plant Biotechnology Institute). The fluorescent proteins used were monomeric GFP5 modified for plants (Haseloff et al., 1997), mRFP (Campbell et al., 2002), and EGFP (ClonTech). Details of cloning methodology are available in the Supplemental Materials and Methods S1.

For RNAi-mediated gene silencing, targeted regions of RPL23aA and RPL23aB were cloned in sense and antisense orientation, separated by an intron, into the binary vector pER8 (Zuo et al., 2000), creating the estrogen-inducible, hairpin RNA-forming cassettes RPL23aA-ihp, RPL23aB-ihp, and RPL23a-ihp. The pER8 vector system is strictly regulated by estrogen and shows no nonspecific effects on plant growth or development (Zuo et al., 2000). Details of cloning methodology are available in the Supplemental Materials and Methods S1.

Transient Expression in Tobacco

Fluorescent protein constructs within binary vectors were used to transform Agrobacterium tumefaciens strain LBA4404 (Hoekema et al., 1983) via electroporation. All constructs in pGREEN were coelectroporated with pSOUP, which must be coresident in A. tumefaciens to provide the replication functions, in trans, for pGREEN (Hellens et al., 2000). Tobacco infiltrations were carried out following previously described protocols (Batoko et al., 2000; Brandizzi et al., 2002; Sparkes et al., 2006). Following infiltration, tobacco plants were returned to the growth chamber for 48 to 72 h prior to visualization with the CLSM.

Confocal Microscopy

Live cell imaging was conducted with an inverted Zeiss LSM 510 META CLSM using previously described settings (Brandizzi et al., 2002; Runions et al., 2006), with the exception that a 585- to 615-nm bandpass filter was used to detect mRFP. These settings prevented spectral bleed-through of fluorescence emission from EGFP/GFP5 + mRFP during coexpression experiments. Acquired images were processed with Zeiss LSM Image Browser software and exported to Adobe Photoshop 7.0 software for figure preparations.

Generation and Induction of Stable RNAi Transgenics

Stable transgenics carrying the inducible silencing cassettes were generated via the floral dip protocol (Clough and Bent, 1998). As a negative control, Arabidopsis was transformed with the pER8 empty vector using the same technique. T₃ transgenic lines, created by selecting each successive generation on basal media supplemented with 25 µg mL^–1 hygromycin (Invivogen) and 200 µg mL^–1 cefotaxime (Sanofi-Aventis), were used for RNAi studies. Seed from independently transformed lines was plated on basal media supplemented with 0 to 100 µM estradiol. Transgenics grown on noninductive media (0 µM estradiol) were occasionally transferred to inductive media (2–100 µM estradiol) to observe responses.

Dark-Field Microscopy

Digital images of transgenics were taken with a Zeiss Stemi 2000-C stereomicroscope. Root sections were observed following staining with toluidine blue. Vasculature was examined by fixing 14- to 18-d-old seedlings overnight in 3:1 ethanol:acetic acid. Fixed seedlings were processed through an ethanol series (80%, 90%, 95%, and 100% ethanol) and cleared by incubation overnight in saturated chloral hydrate. Images were taken at 100 to 200x zoom with a Zeiss Axioskop microscope equipped with a dark-field diaphragm. Approximately eight to 10 cleared seedlings were analyzed for each genotype (pER8-ihp-4 and RPL23aA-ihp-4).

qPCR

qPCR was performed using RNA extracted from 10- to 18-d-old whole seedlings with an iQ5 real-time PCR detection system (Bio-Rad). For each sample, amplifications of RPL23aA, RPL23aB, and ACT7 were performed in triplicate, within the same qPCR run, and only one amplicon was produced per reaction. The ACT7 gene was used as an internal control to standardize RPL23aA/B levels in induced and noninduced transgenics, and threshold cycle changes were compared to standardized levels in noninduced wild-type seedlings of equivalent age using the comparative threshold cycle method (Livak and Schmittgen, 2001). The entire procedure (RNA extraction, first-strand synthesis, qPCR) was repeated for a minimum of three biological replicates. Data was obtained using the iQ5 Optical System software (Bio-Rad) and subsequently exported to Microsoft Excel for summarizing. Detailed methodology for RNA extractions, first-strand synthesis, primer selection and validation, and qPCR optimization are available in the Supplemental Materials and Methods S1.

Accession Numbers

GenBank accession numbers for materials/sequences described in this manuscript are X65305 (pGEM4), U13855 (pGEX-4T-3), AF234306 (pCAMBIA1381z), AF234301 (pCAMBIA1380), AF309825 (pER8), X52327 (pBSKS+), U87973 (GFP5), AF506027 (mRFP), Q07761 (tobacco RPL23a), EAW51131 (human RPL23a), NP_014514 (yeast RPL25), NP_001042974 (rice RPL23a-1), CAC09511 (rice RPL23a-2), AC004218 (Arabidopsis F₁2L6 BAC), At2g39460 (Arabidopsis RPL23aA), At3g55280 (Arabidopsis RPL23aB), At4g25630 (Arabidopsis FIB2), and AT5G09810 (Arabidopsis ACT7).

Supplemental Data

The following materials are available in the online version of this article.

Supplemental Figure S1. Nucleoli of tobacco epidermal cells exhibit spatial separation.

Supplemental Figure S2. Fluorescent protein-tagged FIB2, RPL23aA, and RPL23aB accumulate outside the nucleolus in the cytoplasm and nucleoplasm.

Supplemental Results S1. Ribosome heterogeneity and properties of tobacco nucleoli.

Supplemental Materials and Methods S1.

	ACKNOWLEDGMENTS

 
We are grateful to Federica Brandizzi (Michigan State University) for the pVKH18En6 binary vector and the monomeric GFP5 and mRFP fluorescent protein constructs, Manuel Echeverría (Université de Perpignan) for the ppk100-FIB2-EGFP construct, and Nam-Hai Chua (Rockefeller University) for the pER8 binary vector and pSK-int cloning vector. We are indebted to Sally Hanton and Loren Matheson for their assistance with tobacco infiltrations and confocal microscopy. We thank Jacqueline Hulm, Donna Lindsay, and Heather Wakely for technical assistance. Special thanks to Kerri McIntosh for cloning the RPL23a paralogs and for helpful discussions.

Received October 26, 2007; accepted February 26, 2008; published March 5, 2008.

	FOOTNOTES

 
¹ This work was supported by the Natural Sciences and Engineering Research Council of Canada.

The author responsible for distribution of materials integral to the findings presented in this article in accordance with the policy described in the Instructions for Authors (www.plantphysiol.org) is: Peta C. Bonham-Smith (peta.bonhams{at}usask.ca).

^[C] Some figures in this article are displayed in color online but in black and white in the print edition.

^[W] The online version of this article contains Web-only data.

^[OA] Open Access articles can be viewed online without a subscription.

www.plantphysiol.org/cgi/doi/10.1104/pp.107.111799

^* Corresponding author; e-mail rfd014{at}mail.usask.ca.

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