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10.1091/mbc.E16-04-0244 http://scihub22266oqcxt.onion/10.1091/mbc.E16-04-0244 C5007094!5007094 !27385342     free     free     free Warning: file_get_contents(https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&id=27385342 &cmd=llinks): Failed to open stream: HTTP request failed! 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Altered RNA processing and export lead to retention of mRNAs near transcription sites and nuclear pore complexes or within the nucleolus |pdf=|usr=}}{{27385342 }} gab.com Text Altered RNA processing and export lead to retention of mRNAs near transcription sites and nuclear pore complexes or within the nucleolus JO: Mol Biol Cell http://www.kidney.de/pget.php?&tw=1&pmid=27385342 #FOAvip Many protein factors are required for mRNA biogenesis and nuclear export, which are central to the eukaryotic gene expression program. It is unclear, however, whether all factors have been identified. Here we report on a screen of >1000 essential gene mutants in Saccharomyces cerevisiae for defects in mRNA processing and export, identifying 26 mutants with defects in this process. Single-molecule FISH data showed that the majority of these mutants accumulated mRNA within specific regions of the nucleus, which included 1) mRNAs within the nucleolus when nucleocytoplasmic transport, rRNA biogenesis, or RNA processing and surveillance was disrupted, 2) the buildup of mRNAs near transcription sites in 3'-end processing and chromosome segregation mutants, and 3) transcripts being enriched near nuclear pore complexes when components of the mRNA export machinery were mutated. These data show that alterations to various nuclear processes lead to the retention of mRNAs at discrete locations within the nucleus. Twit Text FOAVip Altered RNA processing and export lead to retention of mRNAs near transcription sites and nuclear pore complexes or within the nucleolus ????Mol Biol Cell http://www.kidney.de/pget.php?&tw=1&pmid=27385342 #FOAvip Twit Text # Free Paper on # # # # # LINK http://www.kidney.de/pget.php?&tw=1&pmid=27385342 #FOAvip English Wikipedia <ref>{{Cite pmid|27385342 }}</ref> Altered RNA processing and export lead to retention of mRNAs near transcription sites and nuclear pore complexes or within the nucleolus #MMPMID27385342 Paul B ; Montpetit B Mol Biol Cell 2016[Sep]; 27 (17 ): 2742-56 PMID27385342 show ga Many protein factors are required for mRNA biogenesis and nuclear export, which are central to the eukaryotic gene expression program. It is unclear, however, whether all factors have been identified. Here we report on a screen of >1000 essential gene mutants in Saccharomyces cerevisiae for defects in mRNA processing and export, identifying 26 mutants with defects in this process. Single-molecule FISH data showed that the majority of these mutants accumulated mRNA within specific regions of the nucleus, which included 1) mRNAs within the nucleolus when nucleocytoplasmic transport, rRNA biogenesis, or RNA processing and surveillance was disrupted, 2) the buildup of mRNAs near transcription sites in 3'-end processing and chromosome segregation mutants, and 3) transcripts being enriched near nuclear pore complexes when components of the mRNA export machinery were mutated. These data show that alterations to various nuclear processes lead to the retention of mRNAs at discrete locations within the nucleus. |Active Transport, Cell Nucleus/genetics/physiology [MESH] |Cell Nucleolus/metabolism [MESH] |Cell Nucleus/metabolism [MESH] |Nuclear Pore/metabolism [MESH] |Nuclear Proteins/metabolism [MESH] |RNA Transport/*physiology [MESH] |RNA, Fungal/genetics/metabolism [MESH] |RNA, Messenger/biosynthesis/*genetics/*metabolism [MESH] |RNA-Binding Proteins/metabolism [MESH] |Saccharomyces cerevisiae Proteins/metabolism [MESH] |Saccharomyces cerevisiae/genetics/metabolism [MESH]Altered RNA processing and export lead to retention of mRNAs near tran(epmc).pdf DeepDyve Pubget Overpricing