Evidence map›Paper›PMID 25220236›Full record

ArticleBiochimica et biophysica acta2014

SRSF2 promotes splicing and transcription of exon 11 included isoform in Ron proto-oncogene.

Heegyum Moon, Sunghee Cho, Tiing Jen Loh, Hyun Kyung Oh, Ha Na Jang, Jianhua Zhou, Young-Soo Kwon, D Joshua Liao, Youngsoo Jun, Soohyun Eom and 5 more

Open access · greenAbstract read
In one paragraph

Article in Biochimica et biophysica acta, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
1.7field-weighted citation impact, top 16% 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

18 citing papers in PubMed, 26 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Review
  5. Review
  6. Article
  7. Article
  8. Splicing factor SRSF2-centric gene regulation.International journal of biological sciences · 2021
    Review
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Review
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

15 authors at 6 institutions in 4 countries.

Heegyum MoonSchool of Life Sciences, Gwangju Institute of Science and Technology, Gwangju 500-712, Republic of Korea.
Sunghee ChoSchool of Life Sciences, Gwangju Institute of Science and Technology, Gwangju 500-712, Republic of Korea.
Tiing Jen LohSchool of Life Sciences, Gwangju Institute of Science and Technology, Gwangju 500-712, Republic of Korea.
Hyun Kyung OhSchool of Life Sciences, Gwangju Institute of Science and Technology, Gwangju 500-712, Republic of Korea.
Ha Na JangSchool of Life Sciences, Gwangju Institute of Science and Technology, Gwangju 500-712, Republic of Korea.
Jianhua ZhouJiangSu Key Laboratory of Neuroregeneration, Nantong University, Nantong, China.
Young-Soo KwonDepartment of Bioscience & Biotechnology, Sejong University, Seoul 143-747, Republic of Korea.
D Joshua LiaoHormel Institute, University of Minnesota, Austin, MN, USA.
Youngsoo JunSchool of Life Sciences, Gwangju Institute of Science and Technology, Gwangju 500-712, Republic of Korea.
Soohyun EomSchool of Life Sciences, Gwangju Institute of Science and Technology, Gwangju 500-712, Republic of Korea.
Claudia GhignaIstituto di Genetica Molecolare, Consiglio Nazionale delle Ricerche, via Abbiategrasso 207, 27100 Pavia, Italy.
Giuseppe BiamontiIstituto di Genetica Molecolare, Consiglio Nazionale delle Ricerche, via Abbiategrasso 207, 27100 Pavia, Italy.
Michael R GreenHoward Hughes Medical Institute and Programs in Gene Function and Expression and Molecular Medicine, University of Massachusetts Medical School, Worcester, MA 01605, USA.
Xuexiu ZhengSchool of Life Sciences, Gwangju Institute of Science and Technology, Gwangju 500-712, Republic of Korea.
Haihong ShenSchool of Life Sciences, Gwangju Institute of Science and Technology, Gwangju 500-712, Republic of Korea. Electronic address: haihongshen@gist.ac.kr.
Gwangju Institute of Science and Technology · KRIstituto di Genetica Molecolare · ITHoward Hughes Medical Institute · USNantong University · CNSejong University · KRUniversity of Minnesota · US

Funding

SPLICING OF MRNA PRECURSORSR01GM035490 · NIGMS · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI GREEN, MICHAEL R · 1985 to 2021
$4.7M
Howard Hughes Medical InstituteNIGMS NIH HHS R01 GM035490
6 · The paper itself

Abstract

The product of proto-oncogene Ron is a human receptor for the macrophage-stimulating protein (MSP). Upon activation, Ron is able to induce cell dissociation, migration and matrix invasion. Exon 11 skipping of Ron pre-mRNA produces Ron△165 protein that is constitutively active even in the absence of its ligand. Here we show that knockdown of SRSF2 promotes the decrease of exon 11 inclusion, whereas overexpression of SRSF2 promotes exon 11 inclusion. We demonstrate that SRSF2 promotes exon 11 inclusion through splicing and transcription procedure. We also present evidence that reduced expression of SRSF2 induces a decrease in the splicing of both introns 10 and 11; by contrast, overexpression of SRSF2 induces an increase in the splicing of introns 10 and 11. Through mutation analysis, we show that SRSF2 functionally targets and physically interacts with CGAG sequence on exon 11. In addition, we reveal that the weak strength of splice sites of exon 11 is not required for the function of SRSF2 on the splicing of Ron exon 11. Our results indicate that SRSF2 promotes exon 11 inclusion of Ron proto-oncogene through targeting exon 11. Our study provides a novel mechanism by which Ron is expressed.

Indexed as

RNA SplicingTranscription, GeneticCells, CulturedExonsHeLa CellsHumansIsoenzymesNuclear ProteinsProto-Oncogene MasProto-OncogenesReceptor Protein-Tyrosine KinasesRibonucleoproteinsSerine-Arginine Splicing FactorsIsoenzymesMAS1 protein, humanNuclear ProteinsProto-Oncogene MasReceptor Protein-Tyrosine KinasesRibonucleoproteinsRON proteinSerine-Arginine Splicing FactorsSRSF2 protein, humanExon 11 inclusionPre-mRNA splicingProto-oncogeneRonSRSF2Transcription

Identifiers

PMID25220236
PMCPMC4535357
OpenAlexW2007501783

What OpenQuestion holds

Textmetadata
LicenceTDM
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.