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Degradation of Normal mRNA in the Nucleus of Saccharomyces cerevisiae
A nuclear mRNA degradation (DRN) system was identified from analysis of mRNA turnover rates in nup116-Δ strains of Saccharomyces cerevisiae lacking the ability to export all RNAs, including poly(A) mRNAs, at the restrictive temperature. Northern blotting, in situ hybridization, and blocking transcri...
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American Society for Microbiology
2003
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| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC166345/ https://ncbi.nlm.nih.gov/pubmed/12897126 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1128/MCB.23.16.5502-5515.2003 |
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pubmed-1663452003-10-21 Degradation of Normal mRNA in the Nucleus of Saccharomyces cerevisiae Das, Biswadip Butler, J. Scott Sherman, Fred Mol Cell Biol Gene Expression A nuclear mRNA degradation (DRN) system was identified from analysis of mRNA turnover rates in nup116-Δ strains of Saccharomyces cerevisiae lacking the ability to export all RNAs, including poly(A) mRNAs, at the restrictive temperature. Northern blotting, in situ hybridization, and blocking transcription with thiolutin in nup116-Δ strains revealed a rapid degradation of mRNAs in the nucleus that was suppressed by the rrp6-Δ, rai1-Δ, and cbc1-Δ deletions, but not by the upf1-Δ deletion, suggesting that DRN requires Rrp6p, a 3′-to-5′ nuclear exonuclease, the Rat1p, a 5′-to-3′ nuclear exonuclease, and Cbc1p, a component of CBC, the nuclear cap binding complex, which may direct the mRNAs to the site of degradation. We propose that certain normal mRNAs retained in the nucleus are degraded by the DRN system, similar to degradation of transcripts with 3′ end formation defects in certain mutants. American Society for Microbiology 2003-08 /pmc/articles/PMC166345/ /pubmed/12897126 http://dx.doi.org/10.1128/MCB.23.16.5502-5515.2003 Text en Copyright © 2003, American Society for Microbiology |
| institution |
US National Library of Medicine |
| collection |
PubMed Central |
| language |
en |
| format |
Article |
| topic |
Gene Expression |
| spellingShingle |
Gene Expression Das, Biswadip Butler, J. Scott Sherman, Fred Degradation of Normal mRNA in the Nucleus of Saccharomyces cerevisiae |
| description |
A nuclear mRNA degradation (DRN) system was identified from analysis of mRNA turnover rates in nup116-Δ strains of Saccharomyces cerevisiae lacking the ability to export all RNAs, including poly(A) mRNAs, at the restrictive temperature. Northern blotting, in situ hybridization, and blocking transcription with thiolutin in nup116-Δ strains revealed a rapid degradation of mRNAs in the nucleus that was suppressed by the rrp6-Δ, rai1-Δ, and cbc1-Δ deletions, but not by the upf1-Δ deletion, suggesting that DRN requires Rrp6p, a 3′-to-5′ nuclear exonuclease, the Rat1p, a 5′-to-3′ nuclear exonuclease, and Cbc1p, a component of CBC, the nuclear cap binding complex, which may direct the mRNAs to the site of degradation. We propose that certain normal mRNAs retained in the nucleus are degraded by the DRN system, similar to degradation of transcripts with 3′ end formation defects in certain mutants. |
| author |
Das, Biswadip Butler, J. Scott Sherman, Fred |
| author_facet |
Das, Biswadip Butler, J. Scott Sherman, Fred |
| author_sort |
Das, Biswadip |
| title |
Degradation of Normal mRNA in the Nucleus of Saccharomyces cerevisiae |
| title_short |
Degradation of Normal mRNA in the Nucleus of Saccharomyces cerevisiae |
| title_full |
Degradation of Normal mRNA in the Nucleus of Saccharomyces cerevisiae |
| title_fullStr |
Degradation of Normal mRNA in the Nucleus of Saccharomyces cerevisiae |
| title_full_unstemmed |
Degradation of Normal mRNA in the Nucleus of Saccharomyces cerevisiae |
| title_sort |
degradation of normal mrna in the nucleus of saccharomyces cerevisiae |
| publisher |
American Society for Microbiology |
| publisher_facet |
American Society for Microbiology |
| publishDate |
2003 |
| url |
https://ncbi.nlm.nih.gov/pmc/articles/PMC166345/ https://ncbi.nlm.nih.gov/pubmed/12897126 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1128/MCB.23.16.5502-5515.2003 |
| _version_ |
1759038191772368896 |