Evidence map›Paper›PMID 14704180›Full record

ArticleGenetics2003

Screens for piwi suppressors in Drosophila identify dosage-dependent regulators of germline stem cell division.

Tora K Smulders-Srinivasan, Haifan Lin

Open access · bronzeAbstract readComparative Study
In one paragraph

Article in Genetics, 2003. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
3.3field-weighted citation impact, top 8% 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

15 citing papers in PubMed, 25 citations in OpenAlex.

  1. Review
  2. PIWI proteins and piRNAs: key regulators of stem cell biology.Frontiers in cell and developmental biology · 2025
    Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Separation of stem cell maintenance and transposon silencing functions of Piwi protein.Proceedings of the National Academy of Sciences of the United States of America · 2011
    Article
  9. Small noncoding RNAs in the germline.Cold Spring Harbor perspectives in biology · 2011
    Review
  10. Article
  11. Article
  12. The biogenesis and function of PIWI proteins and piRNAs: progress and prospect.Annual review of cell and developmental biology · 2009
    Review
  13. Regulation of telomere length in Drosophila.Cytogenetic and genome research · 2008
    Review
  14. Article
  15. Stem cell aging in the Drosophila ovary.Age (Dordrecht, Netherlands) · 2005
    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

2 authors at 2 institutions in 1 country.

Tora K Smulders-SrinivasanDepartment of Cell Biology, Duke University Medical Center, Durham, North Carolina 27710, USA.
Haifan Lin
Duke Medical Center · USDuke University Hospital · US

Funding

REGULATION OF GERMLINE STEM CELL DIVISION IN DROSOPHILAR01HD033760 · NICHD · YALE UNIVERSITY · PI LIN, HAIFAN · 1996 to 2010
$3.6M
NICHD NIH HHS HD-33760
6 · The paper itself

Abstract

The Drosophila piwi gene is the founding member of the only known family of genes whose function in stem cell maintenance is highly conserved in both animal and plant kingdoms. piwi mutants fail to maintain germline stem cells in both male and female gonads. The identification of piwi-interacting genes is essential for understanding how stem cell divisions are regulated by piwi-mediated mechanisms. To search for such genes, we screened the Drosophila third chromosome ( approximately 36% of the euchromatic genome) for suppressor mutations of piwi2 and identified six strong and three weak piwi suppressor genes/sequences. These genes/sequences interact negatively with piwi in a dosage-sensitive manner. Two of the strong suppressors represent known genes--serendipity-delta and similar, both encoding transcription factors. These findings reveal that the genetic regulation of germline stem cell division involves dosage-sensitive mechanisms and that such mechanisms exist at the transcriptional level. In addition, we identified three other types of piwi interactors. The first type consists of deficiencies that dominantly interact with piwi2 to cause male sterility, implying that dosage-sensitive regulation also exists in the male germline. The other two types are deficiencies that cause lethality and female-specific lethality in a piwi2 mutant background, revealing the zygotic function of piwi in somatic development.

Indexed as

Gene Expression Regulation, DevelopmentalAnimalsAnimals, Genetically ModifiedArgonaute ProteinsCell DivisionChromosomesDrosophilaDrosophila ProteinsFemaleGene DosageGenes, LethalGerm CellsInfertility, MaleMaleProteinsRNA-Induced Silencing ComplexArgonaute ProteinsDrosophila Proteinspiwi protein, DrosophilaProteinsRNA-Induced Silencing Complex

Identifiers

PMID14704180
PMCPMC1462913
OpenAlexW1944356630

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.