Evidence map›Paper›PMID 35297982›Full record

ArticleHuman reproduction update2022

Transcriptional control of human gametogenesis.

Fang Fang, Phillip J Iaquinta, Ninuo Xia, Lei Liu, Lei Diao, Renee A Reijo Pera

Open access · bronzeAbstract read
In one paragraph

Article in Human reproduction update, 2022. 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
2.8field-weighted citation impact, top 10% 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, 18 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Double jeopardy: howFrontiers in cell and developmental biology · 2026
    Review
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  7. Article
  8. Article
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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

6 authors at 2 institutions in 2 countries.

Fang FangThe First Affiliated Hospital of USTC, Division of Life Sciences and Medicine, University of Science and Technology of China, Hefei, Anhui, China.
Phillip J IaquintaDivision of Research, Economic Development, and Graduate Education, California Polytechnic State University, San Luis Obispo, CA, USA.
Ninuo XiaThe First Affiliated Hospital of USTC, Division of Life Sciences and Medicine, University of Science and Technology of China, Hefei, Anhui, China.
Lei LiuThe First Affiliated Hospital of USTC, Division of Life Sciences and Medicine, University of Science and Technology of China, Hefei, Anhui, China.
Lei DiaoThe First Affiliated Hospital of USTC, Division of Life Sciences and Medicine, University of Science and Technology of China, Hefei, Anhui, China.
Renee A Reijo PeraDivision of Research, Economic Development, and Graduate Education, California Polytechnic State University, San Luis Obispo, CA, USA.ORCID 0000-0002-6487-1329
University of Science and Technology of China · CNCalifornia Polytechnic State University · US

Funding

Dissection of the transcriptional network of human primordial germ cellsR01HD096026 · NICHD · MONTANA STATE UNIVERSITY - BOZEMAN · PI REIJO PERA, RENEE A · 2018 to 2022
$1.6M
NICHD NIH HHS R01 HD096026
6 · The paper itself

Abstract

The pathways of gametogenesis encompass elaborate cellular specialization accompanied by precise partitioning of the genome content in order to produce fully matured spermatozoa and oocytes. Transcription factors are an important class of molecules that function in gametogenesis to regulate intrinsic gene expression programs, play essential roles in specifying (or determining) germ cell fate and assist in guiding full maturation of germ cells and maintenance of their populations. Moreover, in order to reinforce or redirect cell fate in vitro, it is transcription factors that are most frequently induced, over-expressed or activated. Many reviews have focused on the molecular development and genetics of gametogenesis, in vivo and in vitro, in model organisms and in humans, including several recent comprehensive reviews: here, we focus specifically on the role of transcription factors. Recent advances in stem cell biology and multi-omic studies have enabled deeper investigation into the unique transcriptional mechanisms of human reproductive development. Moreover, as methods continually improve, in vitro differentiation of germ cells can provide the platform for robust gain- and loss-of-function genetic analyses. These analyses are delineating unique and shared human germ cell transcriptional network components that, together with somatic lineage specifiers and pluripotency transcription factors, function in transitions from pluripotent stem cells to gametes. This grand theme review offers additional insight into human infertility and reproductive disorders that are linked predominantly to defects in the transcription factor networks and thus may potentially contribute to the development of novel treatments for infertility.

Indexed as

GametogenesisGene Expression RegulationTranscription FactorsCell DifferentiationGerm CellsHumansInfertilityMalePluripotent Stem CellsTranscription, GeneticTranscription Factorsgametogenesisgene mutationsgerm cellgerm cell tumorsinfertilityin vitro differentiationpluripotent stem cellssingle-cell RNA-sequencingtranscriptional profilingtranscription factors

Identifiers

PMID35297982
PMCPMC9071081
OpenAlexW4210335132

What Socratic holds

Textmetadata
LicenceCC BY-NC
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 Socratic graph.