Evidence map›Paper›PMID 31607207›Full record

ArticleJournal of biological rhythms2019

The E3 Ligases Spsb1 and Spsb4 Regulate RevErbα Degradation and Circadian Period.

Tsedey Mekbib, Ting-Chung Suen, Aisha Rollins-Hairston, Jason P DeBruyne

Open access · bronzeAbstract read
In one paragraph

Article in Journal of biological rhythms, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.5field-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

2 citing papers in PubMed, 10 citations in OpenAlex.

  1. Review
  2. 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 1 institution in 1 country.

Tsedey MekbibNeuroscience Institute, Department of Pharmacology and Toxicology, Morehouse School of Medicine, Atlanta, Georgia.
Ting-Chung SuenNeuroscience Institute, Department of Pharmacology and Toxicology, Morehouse School of Medicine, Atlanta, Georgia.
Aisha Rollins-HairstonNeuroscience Institute, Department of Pharmacology and Toxicology, Morehouse School of Medicine, Atlanta, Georgia.
Jason P DeBruyneNeuroscience Institute, Department of Pharmacology and Toxicology, Morehouse School of Medicine, Atlanta, Georgia.ORCID 0000-0001-9803-9568
Morehouse School of Medicine · US

Funding

Morehouse School of Medicine Center of Excellence Research Endowment ProgramS21MD000101 · NIMHD · MOREHOUSE SCHOOL OF MEDICINE · PI MONTGOMERY-RICE, VALERIE C. · 2001 to 2015
$74.3M
TRANSCRIPTION FACTORS AND PROSTATE CANCERG12RR003034 · NCRR · MOREHOUSE SCHOOL OF MEDICINE · PI ZHAO, XUEYING · 1986 to 2011
$32.4M
TRANSPLANTATION OF EXOSOMES FROM HYPOXIA-PRECONDITIONED ADIPOSE-DERIVED STEM CELLS PROMOTES ANGIOGENESIS IN ISCHEMIC HEARTG12MD007602 · NIMHD · MOREHOUSE SCHOOL OF MEDICINE · PI BOND, VINCENT C · 2012 to 2017
$18.4M
Morehouse School of Medicine MEB2 Renovation and Research Core ConsolidationG20RR031196 · NCRR · MOREHOUSE SCHOOL OF MEDICINE · PI MONTGOMERY-RICE, VALERIE C. · 2010 to 2010
$9.9M
Program Evaluation - Internal & External U54NS083932 · NINDS · MOREHOUSE SCHOOL OF MEDICINE · PI MACLEISH, PETER RAYMOND · 2013 to 2017
$7.7M
Roles of protein degradation in the circadian clockR35GM127044 · NIGMS · MOREHOUSE SCHOOL OF MEDICINE · PI JASON P DEBRUYNE · 2018 to 2026
$3.2M
Degradation Mechanisms of Mammalian Circadian Clock ProteinsSC1GM109861 · NIGMS · MOREHOUSE SCHOOL OF MEDICINE · PI DEBRUYNE, JASON P · 2014 to 2017
$1.4M
RENOV OF MEDICAL SCI &EDUCATION BLDGS: RETINAL CELLSC06RR018386 · NCRR · MOREHOUSE SCHOOL OF MEDICINE · PI SULLIVAN, LOUIS W. · 2002 to 2002
$1.3M
NCRR NIH HHS C06 RR018386NCRR NIH HHS G12 RR003034NCRR NIH HHS G20 RR031196NIGMS NIH HHS R35 GM127044NIGMS NIH HHS SC1 GM109861NIMHD NIH HHS G12 MD007602NIMHD NIH HHS S21 MD000101NINDS NIH HHS U54 NS083932
6 · The paper itself

Abstract

The time-dependent degradation of core circadian clock proteins is essential for the proper functioning of circadian timekeeping mechanisms that drive daily rhythms in gene expression and, ultimately, an organism's physiology. The ubiquitin proteasome system plays a critical role in regulating the stability of most proteins, including the core clock components. Our laboratory developed a cell-based functional screen to identify ubiquitin ligases that degrade any protein of interest and have started screening for those ligases that degrade circadian clock proteins. This screen identified Spsb4 as a putative novel E3 ligase for RevErbα. In this article, we further investigate the role of Spsb4 and its paralogs in RevErbα stability and circadian rhythmicity. Our results indicate that the paralogs Spsb1 and Spsb4, but not Spsb2 and Spsb3, can interact with and facilitate RevErbα ubiquitination and degradation and regulate circadian clock periodicity.

Indexed as

Gene Expression RegulationCell LineCircadian ClocksCircadian RhythmCLOCK ProteinsHumansIntracellular Signaling Peptides and ProteinsNuclear Receptor Subfamily 1, Group D, Member 1Suppressor of Cytokine Signaling ProteinsUbiquitinationUbiquitin-Protein LigasesCLOCK ProteinsIntracellular Signaling Peptides and ProteinsNR1D1 protein, humanNuclear Receptor Subfamily 1, Group D, Member 1SPSB1 protein, humanSPSB4 protein, humanSuppressor of Cytokine Signaling ProteinsUbiquitin-Protein Ligasescircadian clockdegradationE3 ligaseRevErbαSpsb1Spsb4

Identifiers

PMID31607207
PMCPMC7953592
OpenAlexW2980831567

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.