Evidence map›Paper›PMID 12192043›Full record

ArticleMolecular and cellular biology2002

Coupling of termination, 3' processing, and mRNA export.

C M Hammell, Stefan Gross, Daniel Zenklusen, Catherine V Heath, Francoise Stutz, Claire Moore, C N Cole

Open access · greenAbstract read
In one paragraph

Article in Molecular and cellular biology, 2002. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 75 papers.

0numbers the graph read from it
0cells of the map it votes in
75citing papers in PubMed
4.9field-weighted citation impact, top 4% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

75 citing papers in PubMed, 131 citations in OpenAlex.

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15 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors at 2 institutions in 1 country.

C M HammellDepartment of Biochemistry, Dartmouth Medical School, Hanover, New Hampshire 03755, USA.
Stefan Gross
Daniel Zenklusen
Catherine V Heath
Francoise Stutz
Claire Moore
C N Cole
Dartmouth College · USTufts University · US

Funding

REGULATION OF THE METABOLISM OF EUCARYOTIC MRNAR01GM033998 · NIGMS · DARTMOUTH COLLEGE · PI COLE, CHARLES N. · 1985 to 2013
$6.1M
Molecular mechanism of mRNA 3'-end formation in yeastR01GM041752 · NIGMS · TUFTS UNIVERSITY BOSTON · PI MOORE, CLAIRE L · 1989 to 2010
$4.0M
Cancer Biology and Molecular TherapeuticsT32CA009658 · NCI · DARTMOUTH COLLEGE · PI EASTMAN, ALAN R · 1991 to 2011
$3.8M
NCI NIH HHS CA09658NCI NIH HHS T32 CA009658NIGMS NIH HHS GM33998NIGMS NIH HHS GM41752NIGMS NIH HHS R01 GM033998NIGMS NIH HHS R01 GM041752
6 · The paper itself

Abstract

In a screen to identify genes required for mRNA export in Saccharomyces cerevisiae, we isolated an allele of poly(A) polymerase (PAP1) and novel alleles encoding several other 3' processing factors. Many newly isolated and some previously described mutants (rna14-48, rna14-49, rna14-64, rna15-58, and pcf11-1 strains) are defective in polymerase II (Pol II) termination but, interestingly, retain the ability to polyadenylate these improperly processed transcripts at the nonpermissive temperature. Deletion of the cis-acting sequences required to couple 3' processing and termination also produces transcripts that fail to exit the nucleus, suggesting that all of these processes (cleavage, termination, and export) are coupled. We also find that several but not all mRNA export mutants produce improperly 3' processed transcripts at the nonpermissive temperature. 3' maturation defects in mRNA export mutants include improper Pol II termination and/or the previously characterized hyperpolyadenylation of transcripts. Importantly, not all mRNA export mutants have defects in 3' processing. The similarity of the phenotypes of some mRNA export mutants and 3' processing mutants indicates that some factors from each process may mechanistically interact to couple mRNA processing and export. Consistent with this assumption, we present evidence that Xpo1p interacts in vivo with several 3' processing factors and that the addition of recombinant Xpo1p to in vitro processing reaction mixtures stimulates 3' maturation. Of the core 3' processing factors tested (Rna14p, Rna15p, Pcf11p, Hrp1p, Fip1p, and Cft1p), only Hrp1p shuttles. Overexpression of Rat8p/Dbp5p suppresses both 3' processing and mRNA export defects found in xpo1-1 cells.

Indexed as

Receptors, Cytoplasmic and NuclearSaccharomyces cerevisiae ProteinsAllelesBiological TransportCell NucleusExportin 1 ProteinFlow CytometryFungal ProteinsGene DeletionGreen Fluorescent ProteinsKaryopherinsLuminescent ProteinsmRNA Cleavage and Polyadenylation FactorsMutationNuclear ProteinsOpen Reading FramesExportin 1 ProteinFungal ProteinsGreen Fluorescent ProteinsKaryopherinsLuminescent ProteinsmRNA Cleavage and Polyadenylation FactorsNuclear ProteinsPancreatitis-Associated ProteinsPCF11 protein, S cerevisiaePolynucleotide AdenylyltransferaseReceptors, Cytoplasmic and NuclearREG3A protein, humanRNARNA14 protein, S cerevisiaeRNA15 protein, S cerevisiaeRNA-Binding ProteinsRNA, MessengerSaccharomyces cerevisiae Proteins

Identifiers

PMID12192043
PMCPMC135649
OpenAlexW2132316587

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.