Evidence map›Paper›PMID 8289812›Full record

ArticleMolecular and cellular biology1994

Polypurine sequences within a downstream exon function as a splicing enhancer.

K Tanaka, A Watakabe, Y Shimura

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In one paragraph

Article in Molecular and cellular biology, 1994. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 105 papers.

0numbers the graph read from it
0cells of the map it votes in
105citing papers in PubMed
8.5field-weighted citation impact, top 1% of its field
1 · What the graph read from it

What it found

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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

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3 · Its place in the literature

Who cites it

105 citing papers in PubMed, 220 citations in OpenAlex.

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

4 · The record

Corrections and comments

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5 · Who and what money

Authors and funding

3 authors at 1 institution in 1 country.

K TanakaDepartment of Biophysics, Faculty of Science, Kyoto University, Japan.
A Watakabe
Y Shimura
Kyoto University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

We have previously shown that a purine-rich sequence located within exon M2 of the mouse immunoglobulin mu gene functions as a splicing enhancer, as judged by its ability to stimulate splicing of a distant upstream intron. This sequence element has been designated ERS (exon recognition sequence). In this study, we investigated the stimulatory effects of various ERS-like sequences, using the in vitro splicing system with HeLa cell nuclear extracts. Here, we show that purine-rich sequences of several natural exons that have previously been shown to be required for splicing function as a splicing enhancer like the ERS of the immunoglobulin mu gene. Moreover, even synthetic polypurine sequences had stimulatory effects on the upstream splicing. Evaluation of the data obtained from the analyses of both natural and synthetic purine-rich sequences shows that (i) alternating purine sequences can stimulate splicing, while poly(A) or poly(G) sequences cannot, and (ii) the presence of U residues within the polypurine sequence greatly reduces the level of stimulation. Competition experiments strongly suggest that the stimulatory effects of various purine-rich sequences are mediated by the same trans-acting factor(s). We conclude from these results that the purine-rich sequences that we examined in this study also represent examples of ERS. Thus, ERS is considered a general splicing element that is present in various exons and plays an important role in splice site selection.

Indexed as

Enhancer Elements, GeneticExonsGenes, ImmunoglobulinRNA SplicingAnimalsBase SequenceDeoxyribonuclease HindIIIDeoxyribonucleases, Type II Site-SpecificImmunoglobulin mu-ChainsMiceMolecular Sequence DataMutagenesis, InsertionalOligodeoxyribonucleotidesPoly APoly UPurinesDeoxyribonuclease HindIIIDeoxyribonucleases, Type II Site-Specificendodeoxyribonuclease XBAIImmunoglobulin mu-ChainsOligodeoxyribonucleotidesPoly APoly UPurines

Identifiers

PMID8289812
PMCPMC358489
OpenAlexW2151008927

What OpenQuestion holds

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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.