Sublimiting concentration of TFIIH transcription/DNA repair factor causes TTD-A trichothiodystrophy disorder (Q28142934)

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object named as

J H Hoeijmakers

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author name string

W Vermeulen

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E Bergmann

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J Auriol

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S Rademakers

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P Frit

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E Appeldoorn

Molecular mechanism of nucleotide excision repair.

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language of work or name

English

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publication date

November 2000

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published in

Nature Genetics

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volume

26

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issue

3

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page(s)

307-13

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cites work

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DNA repair. The bases for Cockayne syndrome.

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DNA repair helicase: a component of BTF2 (TFIIH) basic transcription factor

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Reconstitution of TFIIH and requirement of its DNA helicase subunits, Rad3 and Rad25, in the incision step of nucleotide excision repair

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Dual roles of a multiprotein complex from S. cerevisiae in transcription and DNA repair

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Dual role of TFIIH in DNA excision repair and in transcription by RNA polymerase II

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Xeroderma pigmentosum and trichothiodystrophy are associated with different mutations in the XPD (ERCC2) repair/transcription gene.

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Nucleotide excision repair and human syndromes

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DNA repair. Engagement with transcription

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Isolation of a cDNA encoding a UV-damaged DNA binding factor defective in xeroderma pigmentosum group E cells

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Mutations in the XPD helicase gene result in XP and TTD phenotypes, preventing interaction between XPD and the p44 subunit of TFIIH

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Mutations in XPB and XPD helicases found in xeroderma pigmentosum patients impair the transcription function of TFIIH.

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Distinct roles for the helicases of TFIIH in transcript initiation and promoter escape

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A Role for the TFIIH XPB DNA Helicase in Promoter Escape by RNA Polymerase II

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Three Unusual Repair Deficiencies Associated with Transcription Factor BTF2(TFIIH): Evidence for the Existence of a Transcription Syndrome

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Cloning and characterization of p52, the fifth subunit of the core of the transcription/DNA repair factor TFIIH

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Reconstitution of the transcription factor TFIIH: assignment of functions for the three enzymatic subunits, XPB, XPD, and cdk7

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TFIIH with inactive XPD helicase functions in transcription initiation but is defective in DNA repair.

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7 January 2021

Open complex formation around a lesion during nucleotide excision repair provides a structure for cleavage by human XPG protein

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Mutational analysis of the human nucleotide excision repair gene ERCC1

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The C terminus of Ku80 activates the DNA-dependent protein kinase catalytic subunit

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A physical complex of the Fanconi anemia proteins FANCG/XRCC9 and FANCA

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Affinity Purification of Human DNA Repair/Transcription Factor TFIIH Using Epitope-tagged Xeroderma Pigmentosum B Protein

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7 January 2021

The XPB subunit of repair/transcription factor TFIIH directly interacts with SUG1, a subunit of the 26S proteasome and putative transcription factor

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7 January 2021

Lack of transcription-coupled repair of acetylaminofluorene DNA adducts in human fibroblasts contrasts their efficient inhibition of transcription

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7 January 2021

Different forms of TFIIH for transcription and DNA repair: holo-TFIIH and a nucleotide excision repairosome

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7 January 2021

Competent transcription initiation by RNA polymerase II in cell-free extracts from xeroderma pigmentosum groups B and D in an optimized RNA transcription assay

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7 January 2021

TFIIH-mediated nucleotide excision repair and initiation of mRNA transcription in an optimized cell-free DNA repair and RNA transcription assay

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Action of DNA repair endonuclease ERCC1/XPF in living cells

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7 January 2021