Evidence map›Paper›PMID 38115153›Full record

ArticleBMC research notes2023

Centriolin interacts with HectD1 in a cell cycle dependent manner.

Jesus Salas, Alexander Garcia, Vancy Zora, Sean Dornbush, Fady Mousa-Ibrahim, Hanna Fogg, Zeynep Gromley, Adam Gromley

Open access · goldAbstract read
In one paragraph

Article in BMC research notes, 2023. 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
0.8field-weighted citation impact, top 26% 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, 4 citations in OpenAlex.

  1. The multifaceted roles of E3 ubiquitin ligases in osteoarthritis.Frontiers in cell and developmental biology · 2025
    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

8 authors at 1 institution in 1 country.

Jesus SalasDeBusk College of Osteopathic Medicine, Lincoln Memorial University, Harrogate, TN, USA.
Alexander GarciaDeBusk College of Osteopathic Medicine, Lincoln Memorial University, Harrogate, TN, USA.
Vancy ZoraDeBusk College of Osteopathic Medicine, Lincoln Memorial University, Harrogate, TN, USA.
Sean DornbushDeBusk College of Osteopathic Medicine, Lincoln Memorial University, Harrogate, TN, USA.
Fady Mousa-IbrahimDeBusk College of Osteopathic Medicine, Lincoln Memorial University, Harrogate, TN, USA.
Hanna FoggDeBusk College of Osteopathic Medicine, Lincoln Memorial University, Harrogate, TN, USA.
Zeynep GromleyDeBusk College of Osteopathic Medicine, Lincoln Memorial University, Harrogate, TN, USA.
Adam GromleyDeBusk College of Osteopathic Medicine, Lincoln Memorial University, Harrogate, TN, USA. adam.gromley@lmunet.edu.
Lincoln Memorial University · US

Funding

Lincoln Memorial University-DeBusk College of Osteopathic Medicine Intramural Grant
6 · The paper itself

Abstract

objectiveThe centrosome is universally recognized as the microtubule organizing center of animal cells, but emerging evidence suggests that it has other important functions including primary cilia formation, DNA damage checkpoints, and cell cycle progression. Despite this, the role of individual components of the centrosome remains unclear. Previous studies suggest that one component, centriolin, has an important function in cytokinesis and cell cycle progression, although its exact role in these processes is not known. To determine how centriolin influences the progression through the cell cycle, we sought to identify interacting partners that may be involved in regulating its function.

resultsThis study provides evidence that the ubiquitin E3 ligase HectD1 binds to centriolin and that this association likely accounts for our observation that HectD1 co-localizes with centriolin at the centrosome during mitosis. In addition to its centrosomal localization, we also show that the expression of HectD1 fluctuates throughout the cell cycle, with the highest levels during mitosis, coinciding with a marked reduction in centriolin expression. We propose that the interaction between HectD1 and centriolin may be necessary for normal cell cycle progression and we speculate that this function may involve HectD1-mediated degradation of centriolin.

Indexed as

Ubiquitin-Protein LigasesAnimalsCell CycleUbiquitin-Protein LigasesCentriolinCentrosomeHECTD1Mitosis

Identifiers

PMID38115153
PMCPMC10731774
OpenAlexW4389955014

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.