Evidence map›Paper›PMID 29500235›Full record

ArticleGenome research2018

Intrinsic DNA binding properties demonstrated for lineage-specifying basic helix-loop-helix transcription factors.

Bradford H Casey, Rahul K Kollipara, Karine Pozo, Jane E Johnson

Open access · bronzeAbstract read
In one paragraph

Article in Genome research, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
–field-weighted citation impact
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

28 citing papers in PubMed, 47 citations in OpenAlex.

  1. Article
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  10. Insights and applications of direct neuronal reprogramming.Current opinion in genetics & development · 2023
    Review
  11. Article
  12. Article
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  15. Article
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  17. Article
  18. Mechanisms of Binding Specificity among bHLH Transcription Factors.International journal of molecular sciences · 2021
    Review
  19. Amino Acid Composition in Various Types of Nucleic Acid-Binding Proteins.International journal of molecular sciences · 2021
    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

4 authors at 1 institution in 1 country.

Bradford H CaseyDepartment of Neuroscience, UT Southwestern Medical Center, Dallas, Texas 75390, USA.
Rahul K KolliparaMcDermott Center for Human Growth and Development, UT Southwestern Medical Center, Dallas, Texas 75390, USA.
Karine PozoDepartment of Neuroscience, UT Southwestern Medical Center, Dallas, Texas 75390, USA.
Jane E JohnsonDepartment of Neuroscience, UT Southwestern Medical Center, Dallas, Texas 75390, USA.ORCID 0000-0002-8605-2746
Southwestern Medical Center · US

Funding

REGULATION OF THE NEURAL DETERMINATION GENE MASH1R01NS032817 · NINDS · UT SOUTHWESTERN MEDICAL CENTER · PI JOHNSON, JANE E · 1995 to 2016
$5.8M
NINDS NIH HHS R01 NS032817
6 · The paper itself

Abstract

During development, transcription factors select distinct gene programs, providing the necessary regulatory complexity for temporal and tissue-specific gene expression. How related factors retain specificity, especially when they recognize the same DNA motifs, is not understood. We address this paradox using basic helix-loop-helix (bHLH) transcription factors ASCL1, ASCL2, and MYOD1, crucial mediators of lineage specification. In vivo, these factors recognize the same DNA motifs, yet bind largely different genomic sites and regulate distinct transcriptional programs. This suggests that their ability to identify regulatory targets is defined either by the cellular environment of the partially defined lineages in which they are endogenously expressed, or by intrinsic properties of the factors themselves. To distinguish between these mechanisms, we directly compared the chromatin binding properties of this subset of bHLH factors when ectopically expressed in embryonic stem cells, presenting them with a common chromatin landscape and cellular components. We find that these factors retain distinct binding sites; thus, specificity of binding is an intrinsic property not requiring a restricted landscape or lineage-specific cofactors. Although the ASCL factors and MYOD1 have some distinct DNA motif preference, it is not sufficient to explain the extent of the differential binding. All three factors can bind inaccessible chromatin and induce changes in chromatin accessibility and H3K27ac. A reiterated pattern of DNA binding motifs is uniquely enriched in inaccessible chromatin at sites bound by these bHLH factors. These combined properties define a subclass of lineage-specific bHLH factors and provide context for their central roles in development and disease.

Indexed as

Amino Acid SequenceBasic Helix-Loop-Helix ProteinsBinding SitesChromatinDNA-Binding ProteinsGene Expression RegulationGenomeHumansMyoD ProteinNucleotide MotifsProtein BindingASCL1 protein, humanASCL2 protein, humanBasic Helix-Loop-Helix ProteinsChromatinDNA-Binding ProteinsMyoD1 myogenic differentiation proteinMyoD Protein

Identifiers

PMID29500235
PMCPMC5880239
OpenAlexW2793677295

What OpenQuestion holds

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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 OpenQuestion graph.