Evidence map›Paper›PMID 27633993›Full record

ArticleDevelopment (Cambridge, England)2016

Notch signaling promotes nephrogenesis by downregulating Six2.

Eunah Chung, Patrick Deacon, Sierra Marable, Juhyun Shin, Joo-Seop Park

Open access · hybridAbstract read
In one paragraph

Article in Development (Cambridge, England), 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 41 papers.

0numbers the graph read from it
0cells of the map it votes in
41citing papers in PubMed
4.7field-weighted citation impact, top 5% 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

41 citing papers in PubMed, 72 citations in OpenAlex.

  1. A knock inbioRxiv : the preprint server for biology · 2026
    Article
  2. Article
  3. Article
  4. Measurement of adhesion and traction of cells at high yield reveals an energetic ratchet operating during nephron condensation.Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Review
  10. Article
  11. Principles of human and mouse nephron development.Nature reviews. Nephrology · 2022
    Review
  12. Article
  13. Article
  14. LGR6 marks nephron progenitor cells.Developmental dynamics : an official publication of the American Association of Anatomists · 2021
    Article
  15. Article
  16. Article
  17. Review
  18. Article
  19. 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

5 authors at 1 institution in 1 country.

Eunah ChungDivision of Pediatric Urology and Division of Developmental Biology, Cincinnati Children's Hospital Medical Center, 3333 Burnet Avenue, Cincinnati, OH 45229, USA.
Patrick DeaconDivision of Pediatric Urology and Division of Developmental Biology, Cincinnati Children's Hospital Medical Center, 3333 Burnet Avenue, Cincinnati, OH 45229, USA.
Sierra MarableDivision of Pediatric Urology and Division of Developmental Biology, Cincinnati Children's Hospital Medical Center, 3333 Burnet Avenue, Cincinnati, OH 45229, USA.
Juhyun ShinDivision of Pediatric Urology and Division of Developmental Biology, Cincinnati Children's Hospital Medical Center, 3333 Burnet Avenue, Cincinnati, OH 45229, USA.
Joo-Seop ParkDivision of Pediatric Urology and Division of Developmental Biology, Cincinnati Children's Hospital Medical Center, 3333 Burnet Avenue, Cincinnati, OH 45229, USA joo-seop.park@cchmc.org.ORCID 0000-0002-4190-4386
Cincinnati Children's Hospital Medical Center · US

Funding

Pulmonary Development and Disease Pathogenesis Training ProgramT32HL007752 · NHLBI · CINCINNATI CHILDRENS HOSP MED CTR · PI Francis Xavier McCormack, Anne-Karina Theresia Perl · 1994 to 2026
$6.3M
Cell Fate Regulation of Nephron ProgenitorsR01DK100315 · NIDDK · CINCINNATI CHILDRENS HOSP MED CTR · PI PARK, JOO-SEOP · 2014 to 2018
$1.7M
NHLBI NIH HHS T32 HL007752NIDDK NIH HHS R01 DK100315
6 · The paper itself

Abstract

During nephrogenesis, multipotent mesenchymal nephron progenitors develop into distinct epithelial segments. Each nephron segment has distinct cell types and physiological function. In the current model of kidney development, Notch signaling promotes the formation of proximal tubules and represses the formation of distal tubules. Here, we present a novel role of Notch in nephrogenesis. We show in mice that differentiation of nephron progenitors requires downregulation of Six2, a transcription factor required for progenitor maintenance, and that Notch signaling is necessary and sufficient for Six2 downregulation. Furthermore, we find that nephron progenitors lacking Notch signaling fail to differentiate into any nephron segments, not just proximal tubules. Our results demonstrate how cell fates of progenitors are regulated by a transcription factor governing progenitor status and by a differentiation signal in nephrogenesis.

Indexed as

AnimalsAnimals, NewbornCell DifferentiationDown-RegulationEmbryo, MammalianGene Expression Regulation, DevelopmentalHomeodomain ProteinsMiceMice, TransgenicNephronsOrganogenesisReceptors, NotchSignal TransductionTranscription FactorsHomeodomain ProteinsReceptors, NotchSix2 protein, mouseTranscription FactorsKidneyMouseNephrogenesisNephron progenitorsNephron segmentationNotchSix2

Identifiers

PMID27633993
PMCPMC5117151
OpenAlexW2519197521

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.