Evidence map›Paper›PMID 24658126›Full record

ArticlePloS one2014

Piwi is required in multiple cell types to control germline stem cell lineage development in the Drosophila ovary.

Xing Ma, Su Wang, Trieu Do, Xiaoqing Song, Mayu Inaba, Yoshiya Nishimoto, Lu-ping Liu, Yuan Gao, Ying Mao, Hui Li and 12 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 55 papers.

0numbers the graph read from it
0cells of the map it votes in
55citing papers in PubMed
14.0field-weighted citation impact, top 1% 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

55 citing papers in PubMed, 85 citations in OpenAlex.

  1. Article
  2. Article
  3. Stem cell competition.Current topics in developmental biology · 2026
    Review
  4. Review
  5. Review
  6. Article
  7. Review
  8. Science advances · 2024
    Article
  9. Review
  10. Gap junction-transported cAMP from the niche controls stem cell progeny differentiation.Proceedings of the National Academy of Sciences of the United States of America · 2023
    Article
  11. Review
  12. Review
  13. Article
  14. Article
  15. Article
  16. Primordial Germ Cell Development in the Poeciliid,Frontiers in cell and developmental biology · 2022
    Article
  17. Article
  18. Article
  19. Article
  20. 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

22 authors at 6 institutions in 2 countries.

Xing MaStowers Institute for Medical Research, Kansas City, Missouri, United States of America; Department of Anatomy and Cell Biology, University of Kansas School of Medicine, Kansas City, Kansas, United States of America.
Su WangStowers Institute for Medical Research, Kansas City, Missouri, United States of America; Department of Anatomy and Cell Biology, University of Kansas School of Medicine, Kansas City, Kansas, United States of America.
Trieu DoStowers Institute for Medical Research, Kansas City, Missouri, United States of America.
Xiaoqing SongStowers Institute for Medical Research, Kansas City, Missouri, United States of America.
Mayu InabaLife Sciences Institute, Center for Stem Cell Biology, University of Michigan, Ann Arbor, Michigan, United States of America.
Yoshiya NishimotoStowers Institute for Medical Research, Kansas City, Missouri, United States of America.
Lu-ping LiuSchool of Medicine, Tsinghua University, Beijing, China.
Yuan GaoSchool of Medicine, Tsinghua University, Beijing, China.
Ying MaoSchool of Medicine, Tsinghua University, Beijing, China.
Hui LiSchool of Medicine, Tsinghua University, Beijing, China.
William McDowellStowers Institute for Medical Research, Kansas City, Missouri, United States of America.
Jungeun ParkStowers Institute for Medical Research, Kansas City, Missouri, United States of America.
Kate MalanowskiStowers Institute for Medical Research, Kansas City, Missouri, United States of America.
Allison PeakStowers Institute for Medical Research, Kansas City, Missouri, United States of America.
Anoja PereraStowers Institute for Medical Research, Kansas City, Missouri, United States of America.
Hua LiStowers Institute for Medical Research, Kansas City, Missouri, United States of America.
Karin GaudenzStowers Institute for Medical Research, Kansas City, Missouri, United States of America.
Jeff HaugStowers Institute for Medical Research, Kansas City, Missouri, United States of America.
Yukiko YamashitaLife Sciences Institute, Center for Stem Cell Biology, University of Michigan, Ann Arbor, Michigan, United States of America.
Haifan LinYale Stem Cell Center, Yale University School of Medicine, New Haven, Connecticut, United Sates of America.
Jian-quan NiSchool of Medicine, Tsinghua University, Beijing, China.
Ting XieStowers Institute for Medical Research, Kansas City, Missouri, United States of America; Department of Anatomy and Cell Biology, University of Kansas School of Medicine, Kansas City, Kansas, United States of America.
Stowers Institute for Medical Research · USTsinghua University · CNUniversity of Kansas · USMichigan United · USUniversity of Michigan–Ann Arbor · USYale University · US

Funding

Molecular Mechanisms Regulating Drosophila Ovarian Germline Stem CellsR01GM064428 · NIGMS · STOWERS INSTITUTE FOR MEDICAL RESEARCH · PI XIE, TING · 2002 to 2010
$2.2M
NIGMS NIH HHS 2R01 GM64428NIGMS NIH HHS R01 GM064428
6 · The paper itself

Abstract

The piRNA pathway plays an important role in maintaining genome stability in the germ line by silencing transposable elements (TEs) from fly to mammals. As a highly conserved piRNA pathway component, Piwi is widely expressed in both germ cells and somatic cells in the Drosophila ovary and is required for piRNA production in both cell types. In addition to its known role in somatic cap cells to maintain germline stem cells (GSCs), this study has demonstrated that Piwi has novel functions in somatic cells and germ cells of the Drosophila ovary to promote germ cell differentiation. Piwi knockdown in escort cells causes a reduction in escort cell (EC) number and accumulation of undifferentiated germ cells, some of which show active BMP signaling, indicating that Piwi is required to maintain ECs and promote germ cell differentiation. Simultaneous knockdown of dpp, encoding a BMP, in ECs can partially rescue the germ cell differentiation defect, indicating that Piwi is required in ECs to repress dpp. Consistent with its key role in piRNA production, TE transcripts increase significantly and DNA damage is also elevated in the piwi knockdown somatic cells. Germ cell-specific knockdown of piwi surprisingly causes depletion of germ cells before adulthood, suggesting that Piwi might control primordial germ cell maintenance or GSC establishment. Finally, Piwi inactivation in the germ line of the adult ovary leads to gradual GSC loss and germ cell differentiation defects, indicating the intrinsic role of Piwi in adult GSC maintenance and differentiation. This study has revealed new germline requirement of Piwi in controlling GSC maintenance and lineage differentiation as well as its new somatic function in promoting germ cell differentiation. Therefore, Piwi is required in multiple cell types to control GSC lineage development in the Drosophila ovary.

Indexed as

AnimalsArgonaute ProteinsCell DifferentiationCell LineageDNA DamageDrosophilaDrosophila ProteinsFemaleOvarySignal TransductionArgonaute ProteinsDrosophila Proteinspiwi protein, Drosophila

Identifiers

PMID24658126
PMCPMC3962343
OpenAlexW2055891675

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.