Evidence map›Paper›PMID 21383317›Full record

ArticleGenome research2011

High resolution mapping of Twist to DNA in Drosophila embryos: Efficient functional analysis and evolutionary conservation.

Anil Ozdemir, Katherine I Fisher-Aylor, Shirley Pepke, Manoj Samanta, Leslie Dunipace, Kenneth McCue, Lucy Zeng, Nobuo Ogawa, Barbara J Wold, Angelike Stathopoulos

Open access · bronzeAbstract read
In one paragraph

Article in Genome research, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 43 papers.

0numbers the graph read from it
0cells of the map it votes in
43citing 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

43 citing papers in PubMed, 58 citations in OpenAlex.

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  8. Sequence reliance of abioRxiv : the preprint server for biology · 2023
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  12. Mechanisms of Binding Specificity among bHLH Transcription Factors.International journal of molecular sciences · 2021
    Review
  13. Review
  14. Article
  15. Article
  16. Article
  17. Spatiotemporal control of gene expression boundaries using a feedforward loop.Developmental dynamics : an official publication of the American Association of Anatomists · 2020
    Article
  18. Article
  19. Article
  20. Broadly expressed repressors integrate patterning across orthogonal axes in embryos.Proceedings of the National Academy of Sciences of the United States of America · 2017
    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

10 authors at 2 institutions in 1 country.

Anil OzdemirDivision of Biology, California Institute of Technology, Pasadena, CA 91125, USA.
Katherine I Fisher-Aylor
Shirley Pepke
Manoj Samanta
Leslie Dunipace
Kenneth McCue
Lucy Zeng
Nobuo Ogawa
Barbara J Wold
Angelike Stathopoulos
California Institute of Technology · USLawrence Berkeley National Laboratory · US

Funding

Global Annotation of Regulatory Elements in the Human GenomeU54HG004576 · NHGRI · STANFORD UNIVERSITY · PI MYERS, RICHARD M · 2007 to 2011
$21.8M
Patterning of Drosphila Embryos by the Dorsal-dependent Gene NetworkR01GM077668 · NIGMS · CALIFORNIA INSTITUTE OF TECHNOLOGY · PI STATHOPOULOS, ANGELIKE · 2007 to 2016
$3.0M
NHGRI NIH HHS U54 HG004576NHGRI NIH HHS U54HG004576NIGMS NIH HHS R01 GM077668NIGMS NIH HHS R01GM077668
6 · The paper itself

Abstract

Cis-regulatory modules (CRMs) function by binding sequence specific transcription factors, but the relationship between in vivo physical binding and the regulatory capacity of factor-bound DNA elements remains uncertain. We investigate this relationship for the well-studied Twist factor in Drosophila melanogaster embryos by analyzing genome-wide factor occupancy and testing the functional significance of Twist occupied regions and motifs within regions. Twist ChIP-seq data efficiently identified previously studied Twist-dependent CRMs and robustly predicted new CRM activity in transgenesis, with newly identified Twist-occupied regions supporting diverse spatiotemporal patterns (>74% positive, n = 31). Some, but not all, candidate CRMs require Twist for proper expression in the embryo. The Twist motifs most favored in genome ChIP data (in vivo) differed from those most favored by Systematic Evolution of Ligands by EXponential enrichment (SELEX) (in vitro). Furthermore, the majority of ChIP-seq signals could be parsimoniously explained by a CABVTG motif located within 50 bp of the ChIP summit and, of these, CACATG was most prevalent. Mutagenesis experiments demonstrated that different Twist E-box motif types are not fully interchangeable, suggesting that the ChIP-derived consensus (CABVTG) includes sites having distinct regulatory outputs. Further analysis of position, frequency of occurrence, and sequence conservation revealed significant enrichment and conservation of CABVTG E-box motifs near Twist ChIP-seq signal summits, preferential conservation of ±150 bp surrounding Twist occupied summits, and enrichment of GA- and CA-repeat sequences near Twist occupied summits. Our results show that high resolution in vivo occupancy data can be used to drive efficient discovery and dissection of global and local cis-regulatory logic.

Indexed as

Evolution, MolecularAnimalsBase CompositionBase SequenceBinding SitesComputational BiologyConsensus SequenceConserved SequenceDNADrosophilaGene Expression Regulation, DevelopmentalMolecular Sequence DataRegulatory Elements, TranscriptionalTwist-Related Protein 1DNATwist-Related Protein 1

Identifiers

PMID21383317
PMCPMC3065704
OpenAlexW2171255932

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.