Evidence map›Paper›PMID 31754036›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2019

Mammalian germ cells are determined after PGC colonization of the nascent gonad.

Peter K Nicholls, Hubert Schorle, Sahin Naqvi, Yueh-Chiang Hu, Yuting Fan, Michelle A Carmell, Ina Dobrinski, Adrienne L Watson, Daniel F Carlson, Scott C Fahrenkrug and 1 more

Open access · bronzeAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 75 papers.

0numbers the graph read from it
0cells of the map it votes in
75citing papers in PubMed
11.5field-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

75 citing papers in PubMed, 120 citations in OpenAlex.

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

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

11 authors at 7 institutions in 4 countries.

Peter K NichollsWhitehead Institute, Cambridge, MA 02142.ORCID 0000-0002-5540-442X
Hubert SchorleWhitehead Institute, Cambridge, MA 02142.
Sahin NaqviWhitehead Institute, Cambridge, MA 02142.
Yueh-Chiang HuWhitehead Institute, Cambridge, MA 02142.
Yuting FanWhitehead Institute, Cambridge, MA 02142.
Michelle A CarmellWhitehead Institute, Cambridge, MA 02142.
Ina DobrinskiDepartment of Comparative Biology & Experimental Medicine, Faculty of Veterinary Medicine, University of Calgary, Calgary, AB T2N 4N1, Canada.ORCID 0000-0002-0695-2606
Adrienne L WatsonRecombinetics, Inc., Saint Paul, MN 55104.
Daniel F CarlsonRecombinetics, Inc., Saint Paul, MN 55104.
Scott C FahrenkrugRecombinetics, Inc., Saint Paul, MN 55104.
David C PageWhitehead Institute, Cambridge, MA 02142; dcpage@wi.mit.edu.ORCID 0000-0001-9920-3411
Recombinetics (United States) · USWhitehead Institute for Biomedical Research · USCincinnati Children's Hospital Medical Center · USHoward Hughes Medical Institute · USSun Yat-sen University · CNUniversity of Bonn · DEUniversity of Calgary · CA

Funding

Modeling Disease in Swine by Transplantation of Gene Targeted Germ CellsR44GM108150 · NIGMS · RECOMBINETICS, INC. · PI CARLSON, DANIEL FRED · 2018 to 2019
$2.0M
Modeling disease in swine by transplantation of gene targeted germ cells.R43GM108150 · NIGMS · RECOMBINETICS, INC. · PI CARLSON, DANIEL FRED, FAHRENKRUG, SCOTT CHRISTOPHER · 2014 to 2014
$375k
Howard Hughes Medical InstituteNIGMS NIH HHS R43 GM108150NIGMS NIH HHS R44 GM108150
6 · The paper itself

Abstract

Mammalian primordial germ cells (PGCs) are induced in the embryonic epiblast, before migrating to the nascent gonads. In fish, frogs, and birds, the germline segregates even earlier, through the action of maternally inherited germ plasm. Across vertebrates, migrating PGCs retain a broad developmental potential, regardless of whether they were induced or maternally segregated. In mammals, this potential is indicated by expression of pluripotency factors, and the ability to generate teratomas and pluripotent cell lines. How the germline loses this developmental potential remains unknown. Our genome-wide analyses of embryonic human and mouse germlines reveal a conserved transcriptional program, initiated in PGCs after gonadal colonization, that differentiates germ cells from their germline precursors and from somatic lineages. Through genetic studies in mice and pigs, we demonstrate that one such gonad-induced factor, the RNA-binding protein DAZL, is necessary in vivo to restrict the developmental potential of the germline; DAZL's absence prolongs expression of a

Indexed as

Embryo, MammalianGerm CellsGonadsAnimalsCell DifferentiationFemaleGene Expression Regulation, DevelopmentalMaleMiceOvarian NeoplasmsPluripotent Stem CellsRNA-Binding ProteinsSwineTeratomaTesticular NeoplasmsDAZL protein, humanDAZL protein, mouseRNA-Binding ProteinscommitmentDazlgerm cellpluripotencyteratoma

Identifiers

PMID31754036
PMCPMC6925976
OpenAlexW2991012148

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.