Evidence map›Paper›PMID 30305648›Full record

ArticleScientific reports2018

The role of acetyltransferases for the temporal-specific accessibility of β-catenin to the myogenic gene locus.

Akiko Suzuki, Ryohei Minamide, Junichi Iwata

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing 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

9 citing papers in PubMed, 11 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Article
  5. Article
  6. Animals : an open access journal from MDPI · 2022
    Article
  7. Article
  8. ExcessiveFrontiers in cell and developmental biology · 2021
    Article
  9. 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

3 authors at 2 institutions in 1 country.

Akiko SuzukiDepartment of Diagnostic & Biomedical Sciences, The University of Texas Health Science Center at Houston (UTHealth) School of Dentistry, Houston, TX, 77054, USA.
Ryohei MinamideDepartment of Diagnostic & Biomedical Sciences, The University of Texas Health Science Center at Houston (UTHealth) School of Dentistry, Houston, TX, 77054, USA.
Junichi IwataDepartment of Diagnostic & Biomedical Sciences, The University of Texas Health Science Center at Houston (UTHealth) School of Dentistry, Houston, TX, 77054, USA. Junichi.Iwata@uth.tmc.edu.
The University of Texas Health Science Center at Houston · USInternational Craniofacial Institute · US

Funding

Molecular Regulatory Mechanism of Calvaria Bone Development and HomeostasisR01DE026767 · NIDCR · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI IWATA, JUNICHI · 2017 to 2021
$1.8M
Transcripts and Functions Targeted by Non-coding RNAs in Palate DevelopmentR03DE026208 · NIDCR · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI IWATA, JUNICHI · 2016 to 2017
$462k
Identification of microRNAs associated with cleft lipR03DE026509 · NIDCR · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI IWATA, JUNICHI · 2017 to 2018
$462k
Role of WNT Signaling in Craniofacial Muscle DevelopmentR03DE024759 · NIDCR · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI IWATA, JUNICHI · 2015 to 2016
$231k
NIDCR NIH HHS R01 DE026767NIDCR NIH HHS R03 DE024759NIDCR NIH HHS R03 DE026208NIDCR NIH HHS R03 DE026509U.S. Department of Health & Human Services | NIH | National Institute of Dental and Craniofacial Research (NIDCR) DE024759U.S. Department of Health & Human Services | NIH | National Institute of Dental and Craniofacial Research (NIDCR) DE026208U.S. Department of Health & Human Services | NIH | National Institute of Dental and Craniofacial Research (NIDCR) DE026509U.S. Department of Health & Human Services | NIH | National Institute of Dental and Craniofacial Research (NIDCR) DE026767
6 · The paper itself

Abstract

Molecules involved in WNT/β-catenin signaling show spatiotemporal-specific expression and play vital roles in muscle development. Our previous study showed that WNT/β-catenin signaling promotes myoblast proliferation and differentiation through the regulation of the cyclin A2 (Ccna2)/cell division cycle 25C (Cdc25c) and Fermitin family homolog 2 (Fermt2) genes, respectively. However, it remains unclear how β-catenin targets different genes from stage to stage during myogenesis. Here, we show that the accessibility of β-catenin to the promoter region of its target genes is regulated by developmental stage-specific histone acetyltransferases (HATs), lysine acetyltransferase 2B (KAT2B), and cAMP-response element-binding protein (CREB)-binding protein (CBP). We found that KAT2B was specifically expressed at the myoblast proliferation stage and formed a complex with β-catenin to induce Ccna2/Cdc25c expression. On the other hand, CBP was specifically expressed during myoblast differentiation and formed a complex with β-catenin to induce Fermt2 expression. Our findings indicate that β-catenin efficiently accesses to its target gene's promoters by forming a complex with developmental stage-specific acetyltransferases during myogenesis.

Indexed as

Gene Expression RegulationQuantitative Trait LociAcetyltransferasesAnimalsbeta CateninBiomarkersCell DifferentiationCell LineCell ProliferationEpigenesis, GeneticMiceMuscle DevelopmentMyoblastsPromoter Regions, GeneticProtein BindingRNA InterferenceAcetyltransferasesbeta CateninBiomarkersRNA, Small Interfering

Identifiers

PMID30305648
PMCPMC6180044
OpenAlexW2895060420

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.