Evidence map›Paper›PMID 31433867›Full record

ArticleJournal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research2019

Hop2 Interacts with ATF4 to Promote Osteoblast Differentiation.

Yang Zhang, Tonghui Lin, Na Lian, Huan Tao, Cong Li, Lingzhen Li, Xiangli Yang

Open access · bronzeAbstract read
In one paragraph

Article in Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
0.7field-weighted citation impact, top 31% 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

10 citing papers in PubMed, 17 citations in OpenAlex.

  1. Article
  2. Transcriptional Readthrough atbioRxiv : the preprint server for biology · 2025
    Article
  3. Article
  4. Review
  5. The Arabidopsis HOP2 gene has a role in preventing illegitimate connections between nonhomologous chromosome regions.Chromosome research : an international journal on the molecular, supramolecular and evolutionary aspects of chromosome biology · 2022
    Article
  6. Article
  7. Review
  8. Review
  9. Article
  10. 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 4 institutions in 2 countries.

Yang ZhangPediatric Research Center, Department of Pediatrics, UTHealth McGovern Medical School, Houston, TX, USA.
Tonghui LinPediatric Research Center, Department of Pediatrics, UTHealth McGovern Medical School, Houston, TX, USA.
Na LianPediatric Research Center, Department of Pediatrics, UTHealth McGovern Medical School, Houston, TX, USA.
Huan TaoDepartment of Medicine, Division of Cardiovascular Medicine, Vanderbilt University Medical Center, Nashville, TX, USA.
Cong LiPediatric Research Center, Department of Pediatrics, UTHealth McGovern Medical School, Houston, TX, USA.
Lingzhen LiDepartment of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, USA.
Xiangli YangPediatric Research Center, Department of Pediatrics, UTHealth McGovern Medical School, Houston, TX, USA.ORCID 0000-0002-2333-8747
The University of Texas Health Science Center · USBaylor College of Medicine · USNanfang Hospital · CNVanderbilt University Medical Center · US

Funding

ATF4 in Chondrocytes Regulates Cartilage to Bone TransitionR01AR067303 · NIAMS · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI YANG, XIANGLI · 2015 to 2020
$1.7M
Transcriptional Regulation of Indian Hedgehog Expression in ChondrocytesR01AR055972 · NIAMS · VANDERBILT UNIVERSITY · PI YANG, XIANGLI · 2008 to 2012
$1.7M
NIAMS NIH HHS R01 AR055972NIAMS NIH HHS R01 AR067303NIH HHS R01AR067303
6 · The paper itself

Abstract

Activating transcription factor 4 (ATF4) is a member of the basic leucine zipper (bZip) transcription factor family required for the terminal differentiation of osteoblasts. Despite its critical importance as one of the three main osteoblast differentiation transcription factors, regulators of osteoblast terminal maturation remain poorly defined. Here we report the identification of homologous pairing protein 2 (Hop2) as a dimerization partner of ATF4 in osteoblasts via the yeast two-hybrid system. Deletional mapping revealed that the Zip domain of Hop2 is necessary and sufficient to bind ATF4 and to enhance ATF4-dependent transcription. Ectopic Hop2 expression in preosteoblasts increased endogenous ATF4 protein content and accelerated osteoblast differentiation. Mice lacking Hop2 (Hop2

Indexed as

Cell DifferentiationActivating Transcription Factor 4AnimalsBone Diseases, MetabolicCell Cycle ProteinsCell LineEpistasis, GeneticMiceModels, BiologicalOsteoblastsPhenotypeProtein BindingTranscription, GeneticActivating Transcription Factor 4Cell Cycle ProteinsHop2 protein, mouseATF4DIFFERENTIATIONHOP2OSTEOBLASTTRANSCRIPTION FACTOR

Identifiers

PMID31433867
PMCPMC7422940
OpenAlexW2969870070

What OpenQuestion holds

Textmetadata
LicenceTDM
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.