<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>16(11)</volume><submitter>Palancade B</submitter><pubmed_abstract>Using a genetic screen, we have identified a previously uncharacterized Saccharomyces cerevisiae open reading frame (renamed PML39) that displays a specific interaction with nucleoporins of the Nup84 complex. Localization of a Pml39-green fluorescent protein (GFP) fusion and two-hybrid studies revealed that Pml39 is mainly docked to a subset of nuclear pore complexes opposite to the nucleolus through interactions with Mlp1 and Mlp2. The absence of Pml39 leads to a specific leakage of unspliced mRNAs that is not enhanced upon MLP1 deletion. In addition, overexpression of PML39-GFP induces a specific trapping of mRNAs transcribed from an intron-containing reporter and of the heterogenous nuclear ribonucleoprotein Nab2 within discrete nuclear domains. In a nup60delta mutant, Pml39 is mislocal</pubmed_abstract><journal>Molecular biology of the cell</journal><pagination>5258-68</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC1266424</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Pml39, a novel protein of the nuclear periphery required for nuclear retention of improper messenger ribonucleoparticles.</pubmed_title><pmcid>PMC1266424</pmcid><pubmed_authors>Loeillet S</pubmed_authors><pubmed_authors>Doye V</pubmed_authors><pubmed_authors>Zuccolo M</pubmed_authors><pubmed_authors>Palancade B</pubmed_authors><pubmed_authors>Nicolas A</pubmed_authors></additional><is_claimable>false</is_claimable><name>Pml39, a novel protein of the nuclear periphery required for nuclear retention of improper messenger ribonucleoparticles.</name><description>Using a genetic screen, we have identified a previously uncharacterized Saccharomyces cerevisiae open reading frame (renamed PML39) that displays a specific interaction with nucleoporins of the Nup84 complex. Localization of a Pml39-green fluorescent protein (GFP) fusion and two-hybrid studies revealed that Pml39 is mainly docked to a subset of nuclear pore complexes opposite to the nucleolus through interactions with Mlp1 and Mlp2. The absence of Pml39 leads to a specific leakage of unspliced mRNAs that is not enhanced upon MLP1 deletion. In addition, overexpression of PML39-GFP induces a specific trapping of mRNAs transcribed from an intron-containing reporter and of the heterogenous nuclear ribonucleoprotein Nab2 within discrete nuclear domains. In a nup60delta mutant, Pml39 is mislocal</description><dates><release>2005-01-01T00:00:00Z</release><publication>2005 Nov</publication><modification>2025-04-18T16:10:38.096Z</modification><creation>2019-03-27T01:25:22Z</creation></dates><accession>S-EPMC1266424</accession><cross_references><pubmed>16162818</pubmed><doi>10.1091/mbc.e05-06-0527</doi></cross_references></HashMap>