Efficient splicing requires a balance between high-fidelity splice-site (SS) selection and speed. In Saccharomyces cerevisiae, Pre-mRNA processing factor 8 (Prp8) helps to balance precise SS selection and rapid, efficient intron excision and exon joining. argonaute1-52 (ago1-52) and incurvata13 (icu13) are hypomorphic alleles of the Arabidopsis thaliana genes ARGONAUTE1 (AGO1) and AUXIN RESISTANT6 (AXR6) that harbor point mutations creating a novel 3′SS and 5′SS, respectively. The spliceosome recognizes these novel SSs, as well as the intact genuine SSs, producing a mixture of wild-type and aberrant mature mRNAs. Here, we characterized five novel mutant alleles of PRP8 (one of the two Arabidopsis co-orthologs of yeast Prp8), naming these alleles morphology of ago1-52 suppressed5 (mas5). In the mas5-1 background, the spliceosome preferentially recognizes the intact genuine 3′SS of ago1-52 and 5′SS of icu13. Since point mutations that damage genuine SSs make the spliceosome prone to recognizing cryptic SSs, we also tested alleles of four genes carrying damaged genuine SSs, finding that mas5-1 did not suppress their missplicing. The mas5-1 and mas5-3 mutations represent a novel class of missplicing suppressors that increase splicing fidelity by hampering the use of novel SSs, but do not alter general pre-mRNA splicing.
All 81 ribosomal proteins (RPs) that form the Arabidopsis (Arabidopsis thaliana) 80S ribosome are encoded by several paralogous genes. For example, the nearly identical RPS24A and RPS24B proteins are encoded by RPS24A and RPS24B, respectively. Here we explored the functions of RPS24A and RPS24B in Arabidopsis. Their encoding genes exhibit combined haploinsufficiency, as at least two wild-type copies of either RPS24A or RPS24B are required for plant viability and at least three are required for normal plant development. Loss-of-function of either gene caused a pointed-leaf phenotype, a typical phenotype of null or hypomorphic recessive alleles of genes encoding ribosome biogenesis factors (RBFs) or RPs. We also found that RPS24A and RPS24B act as RBFs during early stages of 18S ribosomal RNA (rRNA) maturation, as loss of RPS24A or RPS24B function reduced the 18S/25S rRNA ratio. An RPS24B-GFP fusion protein predominantly localized to the nucleolus, as expected. The rps24b-2 mutation strengthened the phenotypes of the RBF mutants mRNA transporter4-2 and small organ4-3, which are defective in 5.8S rRNA maturation. This synergistic interaction might be an effect of increased 45S rDNA transcription, which we also observed in the rps24 mutants. Therefore, the Arabidopsis RPS24 proteins act as RBFs during 18S rRNA maturation, like their human and yeast putative orthologs. Only two plant RPs were previously shown to act not only as structural components of the ribosome but also as RBFs. We provide evidence that RPS24 proteins also regulate 45S rDNA transcription, which has not been described for their yeast or human orthologs.
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