Evidence map›Paper›PMID 37800682›Full record

ArticleEMBO molecular medicine2023

Trichothiodystrophy-associated MPLKIP maintains DBR1 levels for proper lariat debranching and ectodermal differentiation.

Arjan F Theil, Alex Pines, Tuğba Kalayci, José M Heredia-Genestar, Anja Raams, Marion H Rietveld, Sriram Sridharan, Sabine Ej Tanis, Klaas W Mulder, Nesimi Büyükbabani and 10 more

Open access · goldAbstract read
In one paragraph

Article in EMBO molecular medicine, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
1.7field-weighted citation impact, top 16% 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

7 citing papers in PubMed, 11 citations in OpenAlex.

  1. RNA regulation in plants.Science China. Life sciences · 2026
    Review
  2. Review
  3. Article
  4. Review
  5. Review
  6. Article
  7. 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

20 authors at 8 institutions in 4 countries.

Arjan F TheilDepartment of Molecular Genetics, Erasmus MC Cancer Institute, Rotterdam, The Netherlands.ORCID 0000-0001-5779-1681
Alex Pines *Department of Molecular Genetics, Erasmus MC Cancer Institute, Rotterdam, The Netherlands.ORCID 0000-0001-7990-910X
Tuğba Kalayci *Department of Medical Genetics, Istanbul Faculty of Medicine, Istanbul University, Istanbul, Turkey.ORCID 0000-0002-9963-5916
José M Heredia-Genestar *Department of Molecular Genetics, Erasmus MC Cancer Institute, Rotterdam, The Netherlands.
Anja RaamsDepartment of Molecular Genetics, Erasmus MC Cancer Institute, Rotterdam, The Netherlands.
Marion H RietveldDepartment of Dermatology, Leiden University Medical Center (LUMC), Leiden, The Netherlands.
Sriram SridharanCancer Science Institute of Singapore, National University of Singapore, Singapore, Singapore.
Sabine Ej TanisDepartment of Molecular Developmental Biology, Faculty of Science, Radboud Institute for Molecular Life Sciences, Radboud University, Nijmegen, The Netherlands.
Klaas W MulderDepartment of Molecular Developmental Biology, Faculty of Science, Radboud Institute for Molecular Life Sciences, Radboud University, Nijmegen, The Netherlands.
Nesimi BüyükbabaniDepartment of Pathology, Istanbul Faculty of Medicine, Istanbul University, Istanbul, Turkey.ORCID 0000-0003-0472-4826
Birsen KaramanDepartment of Medical Genetics, Istanbul Faculty of Medicine, Istanbul University, Istanbul, Turkey.ORCID 0000-0001-8640-0176
Zehra O UygunerDepartment of Medical Genetics, Istanbul Faculty of Medicine, Istanbul University, Istanbul, Turkey.
Hülya KayseriliDepartment of Medical Genetics, Istanbul Faculty of Medicine, Istanbul University, Istanbul, Turkey.
Jan Hj HoeijmakersDepartment of Molecular Genetics, Erasmus MC Cancer Institute, Rotterdam, The Netherlands.
Hannes LansDepartment of Molecular Genetics, Erasmus MC Cancer Institute, Rotterdam, The Netherlands.ORCID 0000-0003-4417-5358
Jeroen Aa DemmersDepartment of Proteomics, Erasmus MC, Rotterdam, The Netherlands.
Joris PothofDepartment of Molecular Genetics, Erasmus MC Cancer Institute, Rotterdam, The Netherlands.
Umut AltunogluDepartment of Medical Genetics, Istanbul Faculty of Medicine, Istanbul University, Istanbul, Turkey.
Abdoelwaheb El GhalbzouriDepartment of Dermatology, Leiden University Medical Center (LUMC), Leiden, The Netherlands.ORCID 0000-0001-8351-7715
Wim VermeulenDepartment of Molecular Genetics, Erasmus MC Cancer Institute, Rotterdam, The Netherlands.ORCID 0000-0003-3616-734X
Erasmus MC Cancer Institute · NLIstanbul University · TRKoç University · TRLeiden University Medical Center · NLRadboud University Nijmegen · NLErasmus MC · NLNational University of Singapore · SGPrincess Máxima Center · NL

Funding

THE IMPACT OF CELLULAR DEFENSE ON THE ROLE OF Ku80 IN GENOME MAINTENANCE AND LONGP01AG017242 · NIA · UNIVERSITY OF TEXAS HLTH SCI CTR SAN ANT · PI VIJG, JAN · 1999 to 2023
$46.1M
NIA NIH HHS P01 AG017242
6 · The paper itself

Abstract

The brittle hair syndrome Trichothiodystrophy (TTD) is characterized by variable clinical features, including photosensitivity, ichthyosis, growth retardation, microcephaly, intellectual disability, hypogonadism, and anaemia. TTD-associated mutations typically cause unstable mutant proteins involved in various steps of gene expression, severely reducing steady-state mutant protein levels. However, to date, no such link to instability of gene-expression factors for TTD-associated mutations in MPLKIP/TTDN1 has been established. Here, we present seven additional TTD individuals with MPLKIP mutations from five consanguineous families, with a newly identified MPLKIP variant in one family. By mass spectrometry-based interaction proteomics, we demonstrate that MPLKIP interacts with core splicing factors and the lariat debranching protein DBR1. MPLKIP-deficient primary fibroblasts have reduced steady-state DBR1 protein levels. Using Human Skin Equivalents (HSEs), we observed impaired keratinocyte differentiation associated with compromised splicing and eventually, an imbalanced proteome affecting skin development and, interestingly, also the immune system. Our data show that MPLKIP, through its DBR1 stabilizing role, is implicated in mRNA splicing, which is of particular importance in highly differentiated tissue.

Indexed as

Trichothiodystrophy SyndromesAdaptor Proteins, Signal TransducingConsanguinityHumansMutationPhenotypeRNA NucleotidyltransferasesRNA SplicingAdaptor Proteins, Signal TransducingDbr1 protein, humanMPLKIP protein, humanRNA Nucleotidyltransferasesbrittle hair phenotypeepithelial barrier functionmRNA splicingskin differentiationTTDN1

Identifiers

PMID37800682
PMCPMC10630875
OpenAlexW4387392030

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.