Evidence map›Paper›PMID 28146118›Full record

ArticleInternational journal of molecular sciences2017

Jun Dimerization Protein 2 Activates Mc2r Transcriptional Activity: Role of Phosphorylation and SUMOylation.

Chiung-Min Wang, Raymond X Wang, Runhua Liu, Wei-Hsiung Yang

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.3field-weighted citation impact, top 41% 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

4 citing papers in PubMed, 7 citations in OpenAlex.

  1. Review
  2. Article
  3. Thyroid cancer prognostic biomarker ARL4A and its relationship with immune infiltration.International journal of clinical and experimental pathology · 2024
    Article
  4. 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

4 authors at 2 institutions in 1 country.

Chiung-Min WangDepartment of Biomedical Sciences, Mercer University School of Medicine, Savannah, GA 31404, USA. meowy200@yahoo.com.
Raymond X WangDepartment of Biomedical Sciences, Mercer University School of Medicine, Savannah, GA 31404, USA. xw98@cornell.edu.
Runhua LiuDepartment of Genetics and Comprehensive Cancer Center, University of Alabama at Birmingham, Birmingham, AL 35294, USA. runhua@uab.edu.
Wei-Hsiung YangDepartment of Biomedical Sciences, Mercer University School of Medicine, Savannah, GA 31404, USA. yang_w@mercer.edu.
Mercer University · USUniversity of Alabama at Birmingham · US

Funding

TRAINING AND CAREER DEVELOPMENTU54CA118948 · NCI · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI UPENDER MANNE · 2005 to 2026
$26.6M
MicroRNAs for monitoring tumor progression and predicting response to therapyR21CA179282 · NCI · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI WANG, LIZHONG · 2014 to 2015
$352k
Roles of Semaphorin Signaling in Breast Cancer Racial DisparitiesR21CA199586 · NCI · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI JIAO, KAI, WANG, LIZHONG · 2015 to 2016
$352k
NCI NIH HHS R21 CA179282NCI NIH HHS R21 CA199586NCI NIH HHS U54 CA118948
6 · The paper itself

Abstract

Jun dimerization protein 2 (JDP2), a basic leucine zipper transcription factor, is involved in numerous biological and cellular processes such as cancer development and regulation, cell-cycle regulation, skeletal muscle and osteoclast differentiation, progesterone receptor signaling, and antibacterial immunity. Though JDP2 is widely expressed in mammalian tissues, its function in gonads and adrenals (such as regulation of steroidogenesis and adrenal development) is largely unknown. Herein, we find that JDP2 mRNA and proteins are expressed in mouse adrenal gland tissues. Moreover, overexpression of JDP2 in Y1 mouse adrenocortical cancer cells increases the level of melanocortin 2 receptor (MC2R) protein. Notably, Mc2r promoter activity is activated by JDP2 in a dose-dependent manner. Next, by mapping the Mc2r promoter, we show that cAMP response elements (between -1320 and -720-bp) are mainly required for Mc2r activation by JDP2 and demonstrate that -830-bp is the major JDP2 binding site by real-time chromatin immunoprecipitation (ChIP) analysis. Mutations of cAMP response elements on Mc2r promoter disrupts JDP2 effect. Furthermore, we demonstrate that removal of phosphorylation of JDP2 results in attenuated transcriptional activity of Mc2r. Finally, we show that JDP2 is a candidate for SUMOylation and SUMOylation affects JDP2-mediated Mc2r transcriptional activity. Taken together, JDP2 acts as a novel transcriptional activator of the mouse Mc2r gene, suggesting that JDP2 may have physiological functions as a novel player in MC2R-mediated steroidogenesis as well as cell signaling in adrenal glands.

Indexed as

Transcriptional ActivationAdrenal GlandsAnimalsGene ExpressionMembrane ProteinsMicePhosphorylationPromoter Regions, GeneticProtein BindingRepressor ProteinsSumoylationJundp2 protein, mouseMembrane ProteinsMRAP protein, mouseRepressor ProteinsJun dimerization protein 2 (JDP2)melanocortin 2 receptor (MC2R)phosphorylationSUMOylationtranscriptional activity

Identifiers

PMID28146118
PMCPMC5343840
OpenAlexW2584376012

What OpenQuestion holds

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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.