Evidence map›Paper›PMID 26391952›Full record

ArticleMolecular and cellular biology2015

An Organizational Hub of Developmentally Regulated Chromatin Loops in the Drosophila Antennapedia Complex.

Mo Li, Zhibo Ma, Jiayang K Liu, Sharmila Roy, Sapna K Patel, Derrick C Lane, Haini N Cai

Open access · bronzeAbstract read
In one paragraph

Article in Molecular and cellular biology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
0.9field-weighted citation impact, top 25% 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

12 citing papers in PubMed, 18 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Mechanisms of Interaction between Enhancers and Promoters in ThreeInternational journal of molecular sciences · 2023
    Review
  5. Article
  6. Homeotic Genes: Clustering, Modularity, and Diversity.Frontiers in cell and developmental biology · 2021
    Review
  7. Article
  8. Article
  9. Review
  10. Sex combs reduced (Scr) regulatory region of Drosophila revisited.Molecular genetics and genomics : MGG · 2017
    Article
  11. Review
  12. 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

7 authors at 1 institution in 1 country.

Mo LiDepartment of Cellular Biology, University of Georgia, Athens, Georgia, USA.
Zhibo MaDepartment of Cellular Biology, University of Georgia, Athens, Georgia, USA.
Jiayang K LiuDepartment of Cellular Biology, University of Georgia, Athens, Georgia, USA.
Sharmila RoyDepartment of Cellular Biology, University of Georgia, Athens, Georgia, USA.
Sapna K PatelDepartment of Cellular Biology, University of Georgia, Athens, Georgia, USA.
Derrick C LaneDepartment of Cellular Biology, University of Georgia, Athens, Georgia, USA.
Haini N CaiDepartment of Cellular Biology, University of Georgia, Athens, Georgia, USA hcai@uga.edu.
University of Georgia · US

Funding

STUDY OF INSULATOR FUNCTION IN DROSOPHILAR01GM058458 · NIGMS · UNIVERSITY OF GEORGIA (UGA) · PI CAI, HAINI N · 1999 to 2005
$816k
NIGMS NIH HHS R01 GM058458
6 · The paper itself

Abstract

Chromatin boundary elements (CBEs) are widely distributed in the genome and mediate formation of chromatin loops, but their roles in gene regulation remain poorly understood. The complex expression pattern of the Drosophila homeotic gene Sex combs reduced (Scr) is directed by an unusually long regulatory sequence harboring diverse cis elements and an intervening neighbor gene fushi tarazu (ftz). Here we report the presence of a multitude of CBEs in the Scr regulatory region. Selective and dynamic pairing among these CBEs mediates developmentally regulated chromatin loops. In particular, the SF1 boundary plays a central role in organizing two subsets of chromatin loops: one subset encloses ftz, limiting its access by the surrounding Scr enhancers and compartmentalizing distinct histone modifications, and the other subset subdivides the Scr regulatory sequences into independent enhancer access domains. We show that these CBEs exhibit diverse enhancer-blocking activities that vary in strength and tissue distribution. Tandem pairing of SF1 and SF2, two strong CBEs that flank the ftz domain, allows the distal enhancers to bypass their block in transgenic Drosophila, providing a mechanism for the endogenous Scr enhancer to circumvent the ftz domain. Our study demonstrates how an endogenous CBE network, centrally orchestrated by SF1, could remodel the genomic environment to facilitate gene regulation during development.

Indexed as

Gene Expression Regulation, DevelopmentalAnimalsAnimals, Genetically ModifiedAntennapedia Homeodomain ProteinChromatinDNA-Binding ProteinsDrosophilaDrosophila melanogasterDrosophila ProteinsEnhancer Elements, GeneticFushi Tarazu Transcription FactorsGenes, InsectInsulator ElementsPromoter Regions, GeneticRNA-Binding ProteinsRNA Splicing FactorsAntennapedia Homeodomain ProteinAntp protein, DrosophilaChromatinDNA-Binding ProteinsDrosophila Proteinsftz protein, DrosophilaFushi Tarazu Transcription FactorsRNA-Binding ProteinsRNA Splicing FactorsScr protein, DrosophilaSF1 protein, DrosophilaSF2 protein, DrosophilaTranscription Factors

Identifiers

PMID26391952
PMCPMC4628056
OpenAlexW2173938341

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.