Thomsen R~Jensen TH, 2008

Pubmed ID 18258809
Title General, rapid, and transcription-dependent fragmentation of nucleolar antigens in S. cerevisiae mRNA export mutants.
Authors Rune Thomsen, Cyril Saguez, Tommy Nasser, Torben Heick Jensen
Abstract In the yeast Saccharomyces cerevisiae, mutation of some effectors of mRNA nuclear export leads to the rapid accumulation of HSP104 RNA in transcription site-associated foci. We have screened the S. cerevisiae complement of viable gene deletion mutants for their inability to export HSP104 RNA. The 15 strains identified comprise deletions of components of the THO, Thp1p/Sac3p, and nuclear pore complexes. In all three mutant classes, retained RNA overlaps the HSP104 transcription site. Thus, an early block to HSP104 RNA export is general. Incubation of the identified deletion strains, as well as seven additional mutants, under conditions where mRNA export is blocked results in rapid dissipation of nucleolar protein and RNA constituents. Time course experiments show that dissipation of nucleolar antigens succeeds mRNA retention and is reversed when the load of nuclear mRNA ceases. Consistent with a causal role of excess nuclear mRNA, nucleolar morphology in an mRNA export mutant environment remains intact when transcription by RNA polymerase II is inhibited.
Citation RNA 2008; 14:706-16


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Papers Phenotype Conditions Collection Tested mutants Data Details
Thomsen R~Jensen TH, 2008 RNA localization temperature [25ºC], temperature [42ºC], time [20 min] hap a 4,751 Discrete

Curation history

Oct. 19, 2016 Tested strains to request.
Oct. 19, 2016 Data waiting for tested.
May 7, 2017 Tested strains requested.
May 8, 2017 Tested strains to load.
May 8, 2017 Data to load.
May 11, 2017 Tested strains loaded.
May 11, 2017 Data loaded.