Evidence map›Paper›PMID 32756905›Full record

ArticleThe Journal of cell biology2020

Notch2 complements Notch1 to mediate inductive signaling that initiates early T cell development.

Maile Romero-Wolf, Boyoung Shin, Wen Zhou, Maria Koizumi, Ellen V Rothenberg, Hiroyuki Hosokawa

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of cell biology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
2.3field-weighted citation impact, top 11% 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

25 citing papers in PubMed, 41 citations in OpenAlex.

  1. Animals have expanded the evolutionary legacy of unicellular ancestors in blood cells.Proceedings of the National Academy of Sciences of the United States of America · 2026
    Article
  2. Article
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  4. Article
  5. Article
  6. Article
  7. Review
  8. Transcriptional network dynamics in early T cell development.The Journal of experimental medicine · 2024
    Review
  9. Article
  10. T-cell commitment inheritance-an agent-based multi-scale model.NPJ systems biology and applications · 2024
    Article
  11. Prognostic value of CD8Frontiers in immunology · 2024
    Article
  12. Article
  13. Article
  14. Article
  15. Review
  16. Review
  17. Article
  18. Article
  19. Review
  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

6 authors at 2 institutions in 2 countries.

Maile Romero-WolfDivision of Biology & Biological Engineering, California Institute of Technology, Pasadena, CA.
Boyoung ShinDivision of Biology & Biological Engineering, California Institute of Technology, Pasadena, CA.
Wen ZhouDivision of Biology & Biological Engineering, California Institute of Technology, Pasadena, CA.
Maria KoizumiDepartment of Immunology, Tokai University School of Medicine, Isehara, Kanagawa, Japan.
Ellen V RothenbergDivision of Biology & Biological Engineering, California Institute of Technology, Pasadena, CA.
Hiroyuki HosokawaDivision of Biology & Biological Engineering, California Institute of Technology, Pasadena, CA.
California Institute of Technology · USTokai University · JP

Funding

FUNCTIONAL GENOMICS AND MECHANISM OF BCL11B ACTION IN LYMPHOCYTE COMMITMENTR01AI135200 · NIAID · CALIFORNIA INSTITUTE OF TECHNOLOGY · PI ROTHENBERG, ELLEN V. · 2018 to 2022
$3.2M
Genomic site binding rules and regulatory factor function in developing T cellsR01HD076915 · NICHD · CALIFORNIA INSTITUTE OF TECHNOLOGY · PI ROTHENBERG, ELLEN V. · 2013 to 2017
$2.5M
Bcl11b in early T cell developmentR01AI083514 · NIAID · CALIFORNIA INSTITUTE OF TECHNOLOGY · PI ROTHENBERG, ELLEN V. · 2011 to 2015
$1.8M
NIAID NIH HHS R01 AI083514NIAID NIH HHS R01 AI135200NICHD NIH HHS R01 HD076915
6 · The paper itself

Abstract

Notch signaling is the dominant intercellular signaling input during the earliest stages of T cell development in the thymus. Although Notch1 is known to be indispensable, we show that it does not mediate all Notch signaling in precommitment stages: Notch2 initially works in parallel to promote early murine T cell development and antagonize other fates. Notch-regulated target genes before and after T lineage commitment change dynamically, and we show that this partially reflects shifts in genome-wide DNA binding by RBPJ, the transcription factor activated by complex formation with the Notch intracellular domain. Although Notch signaling and transcription factor PU.1 can activate some common targets in precommitment T progenitors, Notch signaling and PU.1 activity have functionally antagonistic effects on multiple targets, delineating separation of pro-T cells from alternative PU.1-dependent fates. These results define a distinct mechanism of Notch signal response that distinguishes the initial stages of murine T cell development.

Indexed as

AnimalsCell DifferentiationGene Expression Regulation, DevelopmentalHumansMiceProto-Oncogene ProteinsProto-Oncogene Protein Spi-1Receptor, Notch1Receptor, Notch2Signal TransductionT-LymphocytesTrans-ActivatorsNotch1 protein, mouseNotch2 protein, mouseProto-Oncogene ProteinsProto-Oncogene Protein Spi-1Receptor, Notch1Receptor, Notch2Trans-Activators

Identifiers

PMID32756905
PMCPMC7659720
OpenAlexW3047130367

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.