Evidence map›Paper›PMID 31874114›Full record

ArticleThe Journal of cell biology2020

WBP11 is required for splicing the TUBGCP6 pre-mRNA to promote centriole duplication.

Elizabeth M Park, Phillip M Scott, Kevin Clutario, Katelyn B Cassidy, Kevin Zhan, Scott A Gerber, Andrew J Holland

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of cell biology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.0field-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

14 citing papers in PubMed, 20 citations in OpenAlex.

  1. Review
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  9. Consistent DNA Hypomethylations in Prostate Cancer.International journal of molecular sciences · 2022
    Article
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  13. Review
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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 2 institutions in 1 country.

Elizabeth M ParkDepartment of Molecular Biology and Genetics, Johns Hopkins University School of Medicine, Baltimore, MD.
Phillip M ScottDepartment of Molecular Biology and Genetics, Johns Hopkins University School of Medicine, Baltimore, MD.
Kevin ClutarioDepartment of Molecular Biology and Genetics, Johns Hopkins University School of Medicine, Baltimore, MD.
Katelyn B CassidyDepartment of Biochemistry and Cell Biology, Geisel School of Medicine at Dartmouth, Lebanon, NH.
Kevin ZhanDepartment of Molecular Biology and Genetics, Johns Hopkins University School of Medicine, Baltimore, MD.
Scott A GerberDepartment of Biochemistry and Cell Biology, Geisel School of Medicine at Dartmouth, Lebanon, NH.
Andrew J HollandDepartment of Molecular Biology and Genetics, Johns Hopkins University School of Medicine, Baltimore, MD.
Johns Hopkins University · USDartmouth College · US

Funding

BIOCHEMISTRY, CELLULAR AND MOLECULAR BIOLOGY PROGRAMT32GM007445 · NIGMS · JOHNS HOPKINS UNIVERSITY · PI GREEN, RACHEL · 1985 to 2021
$24.1M
Training Program In Cellular and Molecular MedicineT32GM135457 · NIGMS · JOHNS HOPKINS UNIVERSITY · PI RAJINI RAO · 2020 to 2026
$5.4M
Centrosome biogenesis and copy number controlR01GM114119 · NIGMS · JOHNS HOPKINS UNIVERSITY · PI CORMACK, BRENDAN · 2015 to 2023
$3.3M
Molecular mechanism that suppresses the proliferation of cells with supernumerary centriolesR01GM133897 · NIGMS · JOHNS HOPKINS UNIVERSITY · PI CORMACK, BRENDAN · 2019 to 2022
$1.9M
Defining human kinase-substrate networks and their dynamic regulationR01GM122846 · NIGMS · DARTMOUTH COLLEGE · PI GERBER, SCOTT A. · 2017 to 2020
$1.5M
NIGMS NIH HHS R01 GM114119NIGMS NIH HHS R01 GM122846NIGMS NIH HHS R01 GM133897NIGMS NIH HHS T32 GM007445NIGMS NIH HHS T32 GM135457
6 · The paper itself

Abstract

Centriole duplication occurs once in each cell cycle to maintain centrosome number. A previous genome-wide screen revealed that depletion of 14 RNA splicing factors leads to a specific defect in centriole duplication, but the cause of this deficit remains unknown. Here, we identified an additional pre-mRNA splicing factor, WBP11, as a novel protein required for centriole duplication. Loss of WBP11 results in the retention of ∼200 introns, including multiple introns in TUBGCP6, a central component of the γ-TuRC. WBP11 depletion causes centriole duplication defects, in part by causing a rapid decline in the level of TUBGCP6. Several additional splicing factors that are required for centriole duplication interact with WBP11 and are required for TUBGCP6 expression. These findings provide insight into how the loss of a subset of splicing factors leads to a failure of centriole duplication. This may have clinical implications because mutations in some spliceosome proteins cause microcephaly and/or growth retardation, phenotypes that are strongly linked to centriole defects.

Indexed as

Cell CycleCentriolesCentrosomeColonic NeoplasmsDNA-Binding ProteinsHCT116 CellsHeLa CellsHumansIntronsMicrotubule-Associated ProteinsMitosisNuclear Receptor CoactivatorsRNA, MessengerRNA PrecursorsRNA SplicingRNA Splicing FactorsDNA-Binding ProteinsMicrotubule-Associated ProteinsNuclear Receptor CoactivatorsRNA, MessengerRNA PrecursorsRNA Splicing FactorsSNW1 protein, humanTUBGCP6 protein, humanWBP11 protein, human

Identifiers

PMID31874114
PMCPMC7039186
OpenAlexW2997591043

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.