Evidence map›Paper›PMID 20007774›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2009

The DM domain protein DMRT1 is a dose-sensitive regulator of fetal germ cell proliferation and pluripotency.

Anthony D Krentz, Mark W Murphy, Shinseog Kim, Matthew S Cook, Blanche Capel, Rui Zhu, Angabin Matin, Aaron L Sarver, Keith L Parker, Michael D Griswold and 3 more

Open access · greenAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 102 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
102citing papers in PubMed, 2 pooled it
10.2field-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

102 citing papers in PubMed, 2 syntheses or guidelines pooled it, 179 citations in OpenAlex.

  1. Guideline
  2. Pooled it
  3. Overlapping genetic etiology of pediatric and adult germ cell tumors.Journal of the National Cancer Institute · 2026
    Article
  4. Article
  5. Article
  6. Article
  7. Gonocytes in Transition: Establishing the Male Germline Identity.Advances in experimental medicine and biology · 2026
    Review
  8. Review
  9. Article
  10. Genes · 2024
    Article
  11. Article
  12. Article
  13. Review
  14. eLife · 2023
    Article
  15. Article
  16. Article
  17. Transcription factorZoological research · 2023
    Article
  18. Identification and functional analysis ofFrontiers in genetics · 2023
    Article
  19. Development of an odorant sensor with a cell-free synthesized olfactory receptor and a graphene field-effect transistor.Analytical sciences : the international journal of the Japan Society for Analytical Chemistry · 2022
    Article
  20. Article

42 more citing papers are in PubMed but not listed here.

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

13 authors at 8 institutions in 3 countries.

Anthony D KrentzDepartment of Genetics, Developmental Biology Center, and Masonic Cancer Center, University of Minnesota, Minneapolis, MN 55455, USA.
Mark W Murphy
Shinseog Kim
Matthew S Cook
Blanche Capel
Rui Zhu
Angabin Matin
Aaron L Sarver
Keith L Parker
Michael D Griswold
Leendert H J Looijenga
Vivian J Bardwell
David Zarkower
Masonic Cancer CenterDuke University · USThe University of Texas MD Anderson Cancer Center · USUniversity of Minnesota · USErasmus MC · NLThe University of Texas Southwestern Medical Center · USUniversity of Cambridge · GBWashington State University · US

Funding

DMRT1 IN MAMMALIAN SEXUAL DEVELOPMENTR01GM059152 · NIGMS · UNIVERSITY OF MINNESOTA TWIN CITIES · PI BARDWELL, VIVIAN J, ZARKOWER, DAVID A. · 1999 to 2019
$8.8M
Testicular Cancer Susceptibility Genes on Mouse Chr 19.R01CA093754 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI MATIN, ANGABIN · 2003 to 2009
$1.4M
DEVELOPMENTAL BIOLOGY TRAINING PROGRAMT32HD007480 · NICHD · UNIVERSITY OF MINNESOTA TWIN CITIES · PI O'CONNOR, MICHAEL BRENDAN · 1995 to 2011
$1.2M
Regulation of Germ Cell Pluripotency Through The RNA-Binding Protein, DND1R01GM087500 · NIGMS · DUKE UNIVERSITY · PI CAPEL, BLANCHE · 2010 to 2013
$1.2M
NCI NIH HHS CA093754NCI NIH HHS R01 CA093754NICHD NIH HHS T32 HD007480NICHD NIH HHS T32HD007480NIGMS NIH HHS GM59152NIGMS NIH HHS R01 GM059152NIGMS NIH HHS R01 GM087500
6 · The paper itself

Abstract

Dmrt1 (doublesex and mab-3 related transcription factor 1) is a conserved transcriptional regulator of male differentiation required for testicular development in vertebrates. Here, we show that in mice of the 129Sv strain, loss of Dmrt1 causes a high incidence of teratomas, whereas these tumors do not form in Dmrt1 mutant C57BL/6J mice. Conditional gene targeting indicates that Dmrt1 is required in fetal germ cells but not in Sertoli cells to prevent teratoma formation. Mutant 129Sv germ cells undergo apparently normal differentiation up to embryonic day 13.5 (E13.5), but some cells fail to arrest mitosis and ectopically express pluripotency markers. Expression analysis and chromatin immunoprecipitation identified DMRT1 target genes, whose missexpression may underlie teratoma formation. DMRT1 indirectly activates the GDNF coreceptor Ret, and it directly represses the pluripotency regulator Sox2. Analysis of human germ cell tumors reveals similar gene expression changes correlated to DMRT1 levels. Dmrt1 behaves genetically as a dose-sensitive tumor suppressor gene in 129Sv mice, and natural variation in Dmrt1 activity can confer teratoma susceptibility. This work reveals a genetic link between testicular dysgenesis, pluripotency regulation, and teratoma susceptibility that is highly sensitive to genetic background and to gene dosage.

Indexed as

AnimalsCell DifferentiationCell ProliferationFetal Stem CellsGene DosageGene ExpressionGenes, Tumor SuppressorHumansMaleMiceMice, Inbred C57BLMice, KnockoutMutationNeoplasm ProteinsNeoplasms, Germ Cell and EmbryonalPhenotypeDMRT1 proteinDnd1 protein, mouseNeoplasm ProteinsProto-Oncogene Proteins c-retPTEN PhosphohydrolasePten protein, mouseRet protein, mouseTranscription Factors

Identifiers

PMID20007774
PMCPMC2799724
OpenAlexW2099418523

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.