Evidence map›Paper›PMID 12101229›Full record

ArticleMolecular and cellular biology2002

Multiple roles for SR proteins in trans splicing.

Suzanne Furuyama, James P Bruzik

Abstract 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 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
1.0field-weighted citation impact, top 24% 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

6 citing papers in PubMed, 22 citations in OpenAlex.

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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

2 authors at 1 institution in 1 country.

Suzanne FuruyamaCenter for RNA Molecular Biology, Case Western Reserve University School of Medicine, 10900 Euclid Avenue, Cleveland, OH 44106, USA.
James P Bruzik
Case Western Reserve University · US

Funding

SR PROTEINS AND TRANS SPLICINGR01GM054204 · NIGMS · CASE WESTERN RESERVE UNIVERSITY · PI BRUZIK, JAMES P · 1996 to 2006
$1.2M
NIGMS NIH HHS R01 GM 54204
6 · The paper itself

Abstract

The trans-splicing reaction involves the association of 5' and 3' splice sites contained on separate transcripts. The mechanism by which these splice sites are juxtaposed during trans-spliceosome assembly and the role of SR proteins at each stage in this process have not been determined. Utilizing a system that allows for the separation of the RNA binding and RS domains of SR proteins, we have found that SR proteins are required for at least two stages of the trans-splicing reaction. They are important both prior to and subsequent to the addition of U2 snRNP to the 3' acceptor. In addition, we have demonstrated a role for RS domain phosphorylation in both of these activities. Dephosphorylation of the RS domain led to a block in U2 snRNP binding to the substrate. In a separate experiment, RS domain phosphorylation was also determined to be necessary for trans splicing to proceed on a substrate that had U2 snRNP already bound. This newly identified role for phosphorylated SR proteins post-U2-snRNP addition coincides with the recruitment of the 5' splice site contained on the SL RNP, suggesting a role for SR proteins in splice site communication in trans splicing.

Indexed as

Capsid ProteinsAnimalsAscaris lumbricoidesCapsidCell-Free SystemCell LineMacromolecular SubstancesNuclear ProteinsNuclease Protection AssaysPhosphoproteinsPhosphorylationProtein Structure, TertiaryRecombinant Fusion ProteinsRibonucleoprotein, U2 Small NuclearRNA-Binding ProteinsRNA, Spliced LeaderCapsid ProteinsMacromolecular SubstancesNuclear ProteinsPhosphoproteinsRecombinant Fusion ProteinsRibonucleoprotein, U2 Small NuclearRNA-Binding ProteinsRNA, Spliced LeaderSerine-Arginine Splicing Factors

Identifiers

PMID12101229
PMCPMC133944
OpenAlexW2129387559

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.