Evidence map›Paper›PMID 9275202›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America1997

smg mutants affect the expression of alternatively spliced SR protein mRNAs in Caenorhabditis elegans.

M Morrison, K S Harris, M B Roth

Open access · greenAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 1997. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 48 papers.

0numbers the graph read from it
0cells of the map it votes in
48citing papers in PubMed
2.0field-weighted citation impact, top 13% 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

48 citing papers in PubMed, 91 citations in OpenAlex.

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  11. Physiological and pathophysiological role of nonsense-mediated mRNA decay.Pflugers Archiv : European journal of physiology · 2016
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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

3 authors at 1 institution in 1 country.

M MorrisonMolecular and Cellular Biology Program, Fred Hutchinson Cancer Research Center, 1100 Fairview Avenue, Seattle, WA 98105, USA.
K S Harris
M B Roth
Fred Hutch Cancer Center · US

Funding

INTERDISCIPLINARY TRAINING IN DEVELOPMENTAL BIOLOGYT32HD007183 · NICHD · UNIVERSITY OF WASHINGTON · PI RAIBLE, DAVID W · 1985 to 2015
$5.7M
STRUCTURE AND FUNCTION IN THE NUCLEUSR01GM048435 · NIGMS · FRED HUTCHINSON CANCER RESEARCH CENTER · PI ROTH, MARK B · 1994 to 2006
$3.0M
NICHD NIH HHS T32 HD007183NICHD NIH HHS T32HD07183-16NIGMS NIH HHS GM1659-03NIGMS NIH HHS GM48435-01A2NIGMS NIH HHS R01 GM048435
6 · The paper itself

Abstract

The expression of alternatively spliced mRNAs from genes is an ubiquitous phenomenon in metazoa. A screen for trans-acting factors that alter the expression of alternatively spliced mRNAs reveals that the smg genes of Caenorhabditis elegans participate in this process. smg genes have been proposed to function in degradation of nonsense mutant mRNAs. Here we show that smg genes affect normal gene expression by modulating the levels of alternatively spliced SRp20 and SRp30b mRNAs. These SR genes contain alternatively spliced exons that introduce upstream stop codons. The effect of smg genes on SR transcripts is specific, because the gene encoding the catalytic subunit of the cAMP-dependent protein kinase, which also contains an alternatively spliced exon that introduces upstream stop codon, is not effected in a smg background. These results suggest that the levels of alternatively spliced mRNAs may, in part, be regulated by alternative mRNA stability.

Indexed as

Alternative SplicingAnimalsCaenorhabditis elegansGene Expression RegulationNuclear ProteinsPhosphoproteinsRNA-Binding ProteinsRNA, MessengerSerine-Arginine Splicing FactorsNuclear ProteinsPhosphoproteinsRNA-Binding ProteinsRNA, MessengerSerine-Arginine Splicing Factors

Identifiers

PMID9275202
PMCPMC23268
OpenAlexW2047404710

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.