Evidence map›Paper›PMID 40757642›Full record

ArticleNucleic acids research2025

Trichothiodystrophy-causative pathogenic variants impair a cooperative action of TFIIH and DDX1 in R-loop processing.

Debora Ferri, Giulia Branca, Manuela Lanzafame, Erica Gandolfi, Valentina Riva, Giovanni Maga, Tiziana Nardo, Claudia Landi, Luca Bini, Lavinia Arseni and 3 more

Abstract read
In one paragraph

Article in Nucleic acids research, 2025. 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
–field-weighted citation impact
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.

  1. Review
  2. Review
  3. Review
  4. Review
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

13 authors.

Debora FerriIstituto di Genetica Molecolare (IGM) L.L. Cavalli Sforza, CNR, 27100 Pavia, Italy.
Giulia BrancaIstituto di Genetica Molecolare (IGM) L.L. Cavalli Sforza, CNR, 27100 Pavia, Italy.
Manuela LanzafameIstituto di Genetica Molecolare (IGM) L.L. Cavalli Sforza, CNR, 27100 Pavia, Italy.ORCID 0000-0002-0456-1134
Erica GandolfiIstituto di Genetica Molecolare (IGM) L.L. Cavalli Sforza, CNR, 27100 Pavia, Italy.
Valentina RivaIstituto di Genetica Molecolare (IGM) L.L. Cavalli Sforza, CNR, 27100 Pavia, Italy.ORCID 0000-0002-7686-4230
Giovanni MagaIstituto di Genetica Molecolare (IGM) L.L. Cavalli Sforza, CNR, 27100 Pavia, Italy.ORCID 0000-0001-8092-1552
Tiziana NardoIstituto di Genetica Molecolare (IGM) L.L. Cavalli Sforza, CNR, 27100 Pavia, Italy.
Claudia LandiDepartment of Life Sciences, University of Siena, 53100 Siena, Italy.ORCID 0000-0003-0410-8038
Luca BiniDepartment of Life Sciences, University of Siena, 53100 Siena, Italy.
Lavinia ArseniIstituto di Genetica Molecolare (IGM) L.L. Cavalli Sforza, CNR, 27100 Pavia, Italy.
Fiorenzo A PeveraliIstituto di Genetica Molecolare (IGM) L.L. Cavalli Sforza, CNR, 27100 Pavia, Italy.
Emmanuel CompeInstitut de Génétique et de Biologie Moléculaire et Cellulaire (IGBMC), Illkirch Cedex 67404 Strasbourg, France.
Donata OrioliIstituto di Genetica Molecolare (IGM) L.L. Cavalli Sforza, CNR, 27100 Pavia, Italy.ORCID 0000-0002-3830-3408

Funding

Agence Nationale de la RecherchesANR MITORARE TFIIH-2021Fondazione AIRC ID 21737Fondazione AIRC ID 29412Fondazione AIRC IG 2018Fondazione AIRC IG 2023University of Pavia
6 · The paper itself

Abstract

The transcription factor IIH (TFIIH) is a key player in transcription and DNA repair by nucleotide excision repair. It is made of 10 subunits organized in core-TFIIH and CAK sub-complexes bridged by XPD. Pathogenic variants in the ERCC2/XPD gene give rise to xeroderma pigmentosum (XP) or trichothiodystrophy (TTD), two distinct clinical entities with opposite skin cancer proneness. Here, we show that TTD variants cause a partial dissociation of the CAK from the chromatin and from the core-TFIIH. Mass spectrometry analysis reveals that the chromatin-bound CAK, as a component of the entire TFIIH, participates in a protein assembly containing the RNA-binding proteins DDX1, SFPQ, NONO as well as RNA polymerase II (Pol II). Gene silencing experiments demonstrate that the protein assembly is required to process the DNA:RNA hybrids formed during Pol II extension and to protect the cell from transcriptional stress. TTD-specific variants in ERCC2/XPD result in TFIIH instability, altered interaction of the CAK with DDX1-SFPQ-NONO, and R-loop accumulation. Therefore, the limited amount of TFIIH that distinguishes TTD from XP gives rise to transcriptional stress and extensive gene expression deregulations, thus accounting for the wide spectrum of TTD clinical features.

Indexed as

DEAD-box RNA HelicasesR-Loop StructuresTranscription Factor TFIIHTrichothiodystrophy SyndromesXeroderma Pigmentosum Group D ProteinChromatinDNA RepairHumansRNA Polymerase IIXeroderma PigmentosumChromatinDDX1 protein, humanDEAD-box RNA HelicasesERCC2 protein, humanRNA Polymerase IITranscription Factor TFIIHXeroderma Pigmentosum Group D Protein

Identifiers

PMID40757642
PMCPMC12319539

What Socratic holds

Textmetadata
LicenceCC BY-NC
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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 Socratic graph.