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ASC1 and RPS3: new actors in 18S nonfunctional rRNA decay.


ABSTRACT: In budding yeast, inactivating mutations within the 40S ribosomal subunit decoding center lead to 18S rRNA clearance by a quality control mechanism known as nonfunctional 18S rRNA decay (18S NRD). We previously showed that 18S NRD is functionally related to No-Go mRNA Decay (NGD), a pathway for clearing translation complexes stalled on aberrant mRNAs. Whereas the NGD factors Dom34p and Hbs1p contribute to 18S NRD, their genetic deletion (either singly or in combination) only partially stabilizes mutant 18S rRNA. Here we identify Asc1p (aka RACK1) and Rps3p, both stable 40S subunit components, as additional 18S NRD factors. Complete stabilization of mutant 18S rRNA in dom34?;asc1? and hbs1?;asc1? strains indicates the existence of two genetically separable 18S NRD pathways. A small region of the Rps3p C-terminal tail known to be subject to post-translational modification is also crucial for 18S NRD. We combine these findings with the effects of mutations in the 5' ? 3' and 3' ? 5' decay machinery to propose a model wherein multiple targeting and decay pathways kinetically contribute to 18S NRD.

SUBMITTER: Limoncelli KA 

PROVIDER: S-EPMC5689013 | biostudies-literature | 2017 Dec

REPOSITORIES: biostudies-literature

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<i>ASC1</i> and <i>RPS3</i>: new actors in 18S nonfunctional rRNA decay.

Limoncelli Kelly A KA   Merrikh Christopher N CN   Moore Melissa J MJ  

RNA (New York, N.Y.) 20170927 12


In budding yeast, inactivating mutations within the 40S ribosomal subunit decoding center lead to 18S rRNA clearance by a quality control mechanism known as nonfunctional 18S rRNA decay (18S NRD). We previously showed that 18S NRD is functionally related to No-Go mRNA Decay (NGD), a pathway for clearing translation complexes stalled on aberrant mRNAs. Whereas the NGD factors Dom34p and Hbs1p contribute to 18S NRD, their genetic deletion (either singly or in combination) only partially stabilizes  ...[more]

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