Evidence map›Paper›PMID 33473133›Full record

ArticleNature communications2021

Single-cell analysis of Schistosoma mansoni identifies a conserved genetic program controlling germline stem cell fate.

Pengyang Li, Dania Nanes Sarfati, Yuan Xue, Xi Yu, Alexander J Tarashansky, Stephen R Quake, Bo Wang

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 36 papers.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed
4.5field-weighted citation impact, top 4% 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

36 citing papers in PubMed, 65 citations in OpenAlex.

  1. Article
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  15. Article
  16. Article
  17. Schistosomiasis.Advances in experimental medicine and biology · 2024
    Review
  18. Genome-wide transcriptome analysis ofFrontiers in cellular and infection microbiology · 2024
    Article
  19. Trematode Genomics and Proteomics.Advances in experimental medicine and biology · 2024
    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

7 authors at 3 institutions in 1 country.

Pengyang LiDepartment of Bioengineering, Stanford University, Stanford, CA, 94305, USA.
Dania Nanes Sarfati *Department of Biology, Stanford University, Stanford, CA, 94305, USA.ORCID 0000-0001-5233-7906
Yuan Xue *Department of Bioengineering, Stanford University, Stanford, CA, 94305, USA.
Xi YuDepartment of Bioengineering, Stanford University, Stanford, CA, 94305, USA.
Alexander J TarashanskyDepartment of Bioengineering, Stanford University, Stanford, CA, 94305, USA.
Stephen R QuakeDepartment of Bioengineering, Stanford University, Stanford, CA, 94305, USA.ORCID 0000-0002-1613-0809
Bo WangDepartment of Bioengineering, Stanford University, Stanford, CA, 94305, USA. wangbo@stanford.edu.ORCID 0000-0001-8880-1432
Stanford University · USChan Zuckerberg Initiative (United States) · USStanford Medicine · US

Funding

NIAID NIH HHS HHSN272201000005CNIAID NIH HHS HHSN272201000005I
6 · The paper itself

Abstract

Schistosomes are parasitic flatworms causing one of the most prevalent infectious diseases from which millions of people are currently suffering. These parasites have high fecundity and their eggs are both the transmissible agents and the cause of the infection-associated pathology. Given its biomedical significance, the schistosome germline has been a research focus for more than a century. Nonetheless, molecular mechanisms that regulate its development are only now being understood. In particular, it is unknown what balances the fate of germline stem cells (GSCs) in producing daughter stem cells through mitotic divisions versus gametes through meiosis. Here, we perform single-cell RNA sequencing on juvenile schistosomes and capture GSCs during de novo gonadal development. We identify a genetic program that controls the proliferation and differentiation of GSCs. This program centers around onecut, a homeobox transcription factor, and boule, an mRNA binding protein. Their expressions are mutually dependent in the schistosome male germline, and knocking down either of them causes over-proliferation of GSCs and blocks germ cell differentiation. We further show that this germline-specific regulatory program is conserved in the planarian, schistosome's free-living evolutionary cousin, but the function of onecut has changed during evolution to support GSC maintenance.

Indexed as

AnimalsCell DifferentiationCell ProliferationFemaleGene Expression Regulation, DevelopmentalGenes, HomeoboxGerm CellsMaleMicePlanariansRNA-Binding ProteinsRNA InterferenceRNA, MessengerSchistosoma mansoniSchistosomiasis mansoniSingle-Cell AnalysisRNA-Binding ProteinsRNA, MessengerTranscription Factors

Identifiers

PMID33473133
PMCPMC7817839
OpenAlexW3122547168

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.