Evidence map›Paper›PMID 9649535›Full record

ArticleGenetics1998

Autoregulation of transformer-2 alternative splicing is necessary for normal male fertility in Drosophila.

M E McGuffin, D Chandler, D Somaiya, B Dauwalder, W Mattox

Open access · bronzeAbstract read
In one paragraph

Article in Genetics, 1998. 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
0.6field-weighted citation impact, top 33% 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, 38 citations in OpenAlex.

  1. Article
  2. Article
  3. Auto-regulatory feedback by RNA-binding proteins.Journal of molecular cell biology · 2019
    Review
  4. Article
  5. Genetics · 2017
    Article
  6. Article
  7. Altering the sex determination pathway in Drosophila fat body modifies sex-specific stress responses.American journal of physiology. Regulatory, integrative and comparative physiology · 2014
    Article
  8. Article
  9. Article
  10. Review
  11. Article
  12. Article
  13. Article
  14. Article
  15. Direct repression of splicing by transformer-2.Molecular and cellular biology · 2003
    Article
  16. Article
  17. Article
  18. Article
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

5 authors at 1 institution in 1 country.

M E McGuffinDepartment of Molecular Genetics, The University of Texas, M. D. Anderson Cancer Center, Houston, Texas 77030, USA.
D Chandler
D Somaiya
B Dauwalder
W Mattox
The University of Texas MD Anderson Cancer Center · US

Funding

TRAINING PROGRAM IN MOLECULAR GENETICS OF CANCERT32CA009299 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI LOZANO, GUILLERMINA · 1985 to 2014
$4.7M
REGULATING ALTERNATIVE PRE-MRNA SPLICING IN DROSOPHILAR29GM050825 · NIGMS · UNIVERSITY OF TEXAS MD ANDERSON CAN CTR · PI MATTOX, WILLIAM W · 1994 to 1998
–
NCI NIH HHS CA09299NIGMS NIH HHS GM50825
6 · The paper itself

Abstract

In the male germline of Drosophila the transformer-2 protein is required for differential splicing of pre-mRNAs from the exuperantia and att genes and autoregulates alternative splicing of its own pre-mRNA. Autoregulation of TRA-2 splicing results in production of two mRNAs that differ by the splicing/retention of the M1 intron and encode functionally distinct protein isoforms. Splicing of the intron produces an mRNA encoding TRA-2(226), which is necessary and sufficient for both male fertility and regulation of downstream target RNAs. When the intron is retained, an mRNA is produced encoding TRA-2(179), a protein with no known function. We have previously shown that repression of M1 splicing is dependent on TRA-2(226), suggesting that this protein quantitatively limits its own expression through a negative feedback mechanism at the level of splicing. Here we examine this idea, by testing the effect that variations in the level of tra-2 expression have on the splicing of M1 and on male fertility. Consistent with our hypothesis, we observe that as tra-2 gene dosage is increased, smaller proportions of TRA-2(226) mRNA are produced, limiting expression of this isoform. Feedback regulation is critical for male fertility, since it is significantly decreased by a transgene in which repression of M1 splicing cannot occur and TRA-2(226) mRNA is constitutively produced. The effect of this transgene becomes more severe as its dosage is increased, indicating that fertility is sensitive to an excess of TRA-2(226). Our results suggest that autoregulation of TRA-2(226) expression in male germ cells is necessary for normal spermatogenesis.

Indexed as

Alternative SplicingDrosophila ProteinsGene Expression RegulationAnimalsAnimals, Genetically ModifiedCrosses, GeneticDNA Transposable ElementsDrosophilaFemaleFertilityGene DosageHomeostasisMaleRibonucleoproteinsRNA, MessengerTranscription, GeneticDNA Transposable ElementsDrosophila ProteinsRibonucleoproteinsRNA, Messengertra2 protein, Drosophila

Identifiers

PMID9649535
PMCPMC1460228
OpenAlexW2155514926

What OpenQuestion holds

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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.