Evidence map›Paper›PMID 17296729›Full record

ArticleMolecular and cellular biology2007

Proneural basic helix-loop-helix proteins and epidermal growth factor receptor signaling coordinately regulate cell type specification and cdk inhibitor expression during development.

Madina J Sukhanova, Dilip K Deb, Gabriel M Gordon, Miho Tanaka Matakatsu, Wei Du

Open access · greenAbstract read
In one paragraph

Article in Molecular and cellular biology, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
1.5field-weighted citation impact, top 19% 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

18 citing papers in PubMed, 21 citations in OpenAlex.

  1. Article
  2. Developmental control of transcriptional and proliferative potency during the evolutionary emergence of animals.Developmental dynamics : an official publication of the American Association of Anatomists · 2015
    Article
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  8. In vivo neuronal subtype-specific targets of Atoh1 (Math1) in dorsal spinal cord.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2011
    Article
  9. Article
  10. Article
  11. Article
  12. Distinct effects of Hedgehog signaling on neuronal fate specification and cell cycle progression in the embryonic mouse retina.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2009
    Article
  13. Article
  14. Article
  15. Context dependence of proneural bHLH proteins.Current opinion in genetics & development · 2008
    Review
  16. Article
  17. Review
  18. 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.

Madina J SukhanovaBen May Department for Cancer Research, The University of Chicago, 924 E. 57th Street, Chicago, IL 60637, USA.
Dilip K Deb
Gabriel M Gordon
Miho Tanaka Matakatsu
Wei Du
University of Chicago · US

Funding

Control of Cell Proliferation and Differentiation in the Developing RetinaR01GM074197 · NIGMS · UNIVERSITY OF CHICAGO · PI DU, WEI · 2006 to 2013
$2.4M
NIGMS NIH HHS R01 GM074197
6 · The paper itself

Abstract

Cell differentiation and cell cycle exit are coordinately regulated during development; however, the molecular logic underlying this regulation is not known. The Drosophila cdk inhibitor Dacapo (Dap) is one of the key cell cycle regulators that exhibit dynamic expression during development and contribute to the developmental regulation of the cell cycle. In this study, regulation of Dap expression during cell type specification was investigated. The expression of Dap in the R2 and R5 precursors of the developing eye and in the newly recruited leg disc femoral sense organ precursors was found to be controlled by the epidermal growth factor receptor signaling-regulated transcription factor Pointed (Pnt) and the proneural basic helix-loop-helix proteins Atonal (Ato) and Daughterless (Da). We show that Pnt, Ato, and Da regulate Dap expression directly through their respective binding sites precisely at the time when these transcription factors function to specify neural fates. These results show that Dap expression is directly regulated by developmental mechanisms that simultaneously control cell type specification. This is potentially a general mechanism by which the expression of key cell cycle regulators is coordinated with differentiation during normal development. The direct regulation of key cell cycle regulators by the differentiation factors ensures coordinated regulation of cell cycle and differentiation.

Indexed as

Cell LineageSignal TransductionAnimalsBasic Helix-Loop-Helix ProteinsBinding SitesDNA-Binding ProteinsDrosophila melanogasterDrosophila ProteinsEnhancer Elements, GeneticErbB ReceptorsExtremitiesEyeGene Expression Regulation, DevelopmentalGreen Fluorescent ProteinsNerve Tissue ProteinsNuclear Proteinsato protein, DrosophilaBasic Helix-Loop-Helix Proteinsdap protein, DrosophilaDa protein, DrosophilaDNA-Binding ProteinsDrosophila ProteinsErbB ReceptorsGreen Fluorescent ProteinsNerve Tissue ProteinsNuclear Proteinspnt protein, DrosophilaProto-Oncogene ProteinsTranscription Factors

Identifiers

PMID17296729
PMCPMC1899942
OpenAlexW2098925349

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.