Evidence map›Paper›PMID 23242134›Full record

ArticleBioarchitecture

Akirin: a context-dependent link between transcription and chromatin remodeling.

Scott J Nowak, Mary K Baylies

Open access · bronzeAbstract readComment
In one paragraph

Article in Bioarchitecture. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
0.4field-weighted citation impact, top 39% 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

13 citing papers in PubMed, 17 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Functional Evolution of Subolesin/Akirin.Frontiers in physiology · 2018
    Review
  10. Dual roles of Akirin2 protein duringThe Journal of biological chemistry · 2017
    Article
  11. Article
  12. Article
  13. Specification of the somatic musculature in Drosophila.Wiley interdisciplinary reviews. Developmental biology
    Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

2 authors at 2 institutions in 2 countries.

Scott J NowakDepartment of Biology and Physics, Kennesaw State University, GA, USA.
Mary K Baylies
Kennesaw State University · USNew York Proton Center · US

Funding

CELL FATE DETERMINATION IN THE MESODERM OF DROSOPHILAR01GM056989 · NIGMS · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI BAYLIES, MARY K · 1999 to 2008
$2.6M
Mechanisms Regulating Myoblast Fusion in DrosophilaR01GM078318 · NIGMS · SLOAN-KETTERING INST CAN RESEARCH · PI BAYLIES, MARY K · 2007 to 2010
$2.0M
NIGMS NIH HHS GM56989NIGMS NIH HHS GM78318NIGMS NIH HHS R01 GM056989NIGMS NIH HHS R01 GM078318
6 · The paper itself

Abstract

Embryonic patterning relies upon an exquisitely timed program of gene regulation. While the regulation of this process via the action of transcription factor networks is well understood, new lines of study have highlighted the importance of a concurrently regulated program of chromatin remodeling during development. Chromatin remodeling refers to the manipulation of the chromatin architecture through rearrangement, repositioning, or restructuring of nucleosomes to either favor or hinder the expression of associated genes. While the role of chromatin remodeling pathways during tumor development and cancer progression are beginning to be clarified, the roles of these pathways in the course of tissue specification, morphogenesis and patterning remains relatively unknown. Further, relatively little is understood as to the mechanism whereby developmentally critical transcription factors coordinate with chromatin remodeling factors to optimize target gene loci for gene expression. Such a mechanism might involve direct transcription factor/chromatin remodeling factor interactions, or could likely be mediated via an unknown intermediary. Our group has identified the relatively unknown protein Akirin as a putative member of this latter group: a secondary cofactor that serves as an interface between a developmentally critical transcription factor and the chromatin remodeling machinery. This role for the Akirin protein suggests a novel regulatory mode for regulating gene expression during development.

Indexed as

Drosophila melanogasterEmbryonic DevelopmentMusclesAnimalsCell Cycle ProteinsDrosophila ProteinsTrans-ActivatorsTwist-Related Protein 1Cell Cycle ProteinsDrosophila ProteinsTrans-ActivatorsTwist-Related Protein 1

Identifiers

PMID23242134
PMCPMC3527315
OpenAlexW2008777701

What OpenQuestion holds

Textmetadata
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.