Evidence map›Paper›PMID 26577869›Full record

ArticleDevelopmental biology2016

Cell cycle features of C. elegans germline stem/progenitor cells vary temporally and spatially.

Debasmita Roy, David Michaelson, Tsivia Hochman, Anthony Santella, Zhirong Bao, Judith D Goldberg, E Jane Albert Hubbard

Open access · greenAbstract read
In one paragraph

Article in Developmental biology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed
0.9field-weighted citation impact, top 29% 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

32 citing papers in PubMed, 49 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. Non-autonomy of age-related morphological changes in thebioRxiv : the preprint server for biology · 2025
    Article
  8. Article
  9. Review
  10. Article
  11. Article
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  14. Article
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  16. Article
  17. A male pheromone that improves the quality of the oogenic germline.Proceedings of the National Academy of Sciences of the United States of America · 2022
    Article
  18. Molecular basis of reproductive senescence: insights from model organisms.Journal of assisted reproduction and genetics · 2021
    Review
  19. Germline Stem and Progenitor Cell Aging inFrontiers in cell and developmental biology · 2021
    Review
  20. 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

7 authors at 2 institutions in 1 country.

Debasmita RoySkirball Institute of Biomolecular Medicine, Helen L. and Martin S. Kimmel Center for Stem Cell Biology, Departments of Cell Biology and Pathology, New York University School of Medicine, 540 First Avenue, New York, NY 10016, USA.
David MichaelsonSkirball Institute of Biomolecular Medicine, Helen L. and Martin S. Kimmel Center for Stem Cell Biology, Departments of Cell Biology and Pathology, New York University School of Medicine, 540 First Avenue, New York, NY 10016, USA.
Tsivia HochmanDepartments of Population Health and Environmental Medicine, Division of Biostatistics, New York University School of Medicine, 540 First Avenue, New York, NY, 10016, USA.
Anthony SantellaDevelopmental Biology Program, Sloan-Kettering Institute, 1275 York Avenue, New York, NY, 10065, USA.
Zhirong BaoDevelopmental Biology Program, Sloan-Kettering Institute, 1275 York Avenue, New York, NY, 10065, USA.
Judith D GoldbergDepartments of Population Health and Environmental Medicine, Division of Biostatistics, New York University School of Medicine, 540 First Avenue, New York, NY, 10016, USA.
E Jane Albert HubbardSkirball Institute of Biomolecular Medicine, Helen L. and Martin S. Kimmel Center for Stem Cell Biology, Departments of Cell Biology and Pathology, New York University School of Medicine, 540 First Avenue, New York, NY 10016, USA. Electronic address: jane.hubbard@med.nyu.edu.
New York University · USKettering University · US

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI Hongbiao Carl Lekaye · 1985 to 2026
$347.4M
Project-005UL1TR001445 · NCATS · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI BREDELLA, MIRIAM ANTOINETTE, HOCHMAN, JUDITH S · 2015 to 2025
$103.5M
Vaccine FacilityP30CA016087 · NCI · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI ANIRBAN MAITRA · 1985 to 2026
$83.1M
Institutional Clinical and Translational Science AwardUL1TR000038 · NCATS · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI CRONSTEIN, BRUCE NEIL, HOCHMAN, JUDITH S · 2012 to 2014
$16.8M
Enhancing and expanding the CGC Strain CollectionP40OD010440 · OD · UNIVERSITY OF MINNESOTA · PI Aric L Daul, Ann E. Rougvie · 2012 to 2026
$7.5M
CONTROL ONSET OF MEIOSIS IN C. ELEGANSR01GM061706 · NIGMS · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI HUBBARD, E. JANE ALBERT · 2000 to 2018
$5.4M
The Ubiquitin-Proteasome System in Metazoan EmbryogenesisR01GM097576 · NIGMS · SLOAN-KETTERING INST CAN RESEARCH · PI BAO, ZHIRONG · 2011 to 2020
$3.3M
An integrated system to monitor complex tissues at single-cell resolutionU01HD075602 · NICHD · SLOAN-KETTERING INST CAN RESEARCH · PI BAO, ZHIRONG · 2012 to 2016
$3.1M
NCATS NIH HHS UL1 TR000038NCATS NIH HHS UL1TR000038NCATS NIH HHS UL1 TR001445NCI NIH HHS P30 CA008748NCI NIH HHS P30 CA016087NICHD NIH HHS HD075602NICHD NIH HHS U01 HD075602NIGMS NIH HHS GM097576NIGMS NIH HHS NIHR01GM061706NIGMS NIH HHS R01 GM061706NIGMS NIH HHS R01 GM097576NIH HHS P40 OD010440
6 · The paper itself

Abstract

Many organisms accumulate a pool of germline stem cells during development that is maintained in later life. The dynamics of establishment, expansion and homeostatic maintenance of this pool are subject to both developmental and physiological influences including the availability of a suitable niche microenvironment, nutritional status, and age. Here, we investigated the dynamics of germline proliferation during stages of expansion and homeostasis, using the C. elegans germ line as a model. The vast majority of germ cells in the proliferative zone are in interphase stages of mitosis (G1, S, G2) rather than in the active mitotic (M) phase. We examined mitotic index and DNA content, comparing different life stages, mutants, and physiological conditions. We found that germ cells in larval stages cycle faster than in adult stages, but that this difference could not be attributed to sexual fate of the germ cells. We also found that larval germ cells exhibit a lower average DNA content compared to adult germ cells. We extended our analysis to consider the effects of distance from the niche and further found that the spatial pattern of DNA content differs between larval and adult stages in the wild type and among mutants in pathways that interfere with cell cycle progression, cell fate, or both. Finally, we characterized expansion of the proliferative pool of germ cells during adulthood, using a regeneration paradigm (ARD recovery) in which animals are starved and re-fed. We compared adult stage regeneration and larval stage expansion, and found that the adult germ line is capable of rapid accumulation but does not sustain a larval-level mitotic index nor does it recapitulate the larval pattern of DNA content. The regenerated germ line does not reach the number of proliferative zone nuclei seen in the continuously fed adult. Taken together, our results suggest that cell cycle dynamics are under multiple influences including distance from the niche, age and/or maturation of the germ line, nutrition and, possibly, latitude for physical expansion.

Indexed as

Cell CycleAgingAnimalsCaenorhabditis elegansCell LineageCell ProliferationDNAGerm CellsLarvaMitotic IndexMutationRegenerationStem CellsTime FactorsDNAAdult reproductive diapauseCell fateInsulinIrisesNotchS6 Kinase

Identifiers

PMID26577869
PMCPMC4827254
OpenAlexW2105368596

What OpenQuestion holds

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Registered trials

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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.