Literature DB >> 9195225

DNA repair characteristics and mutations in the ERCC2 DNA repair and transcription gene in a trichothiodystrophy patient.

K Takayama1, D M Danks, E P Salazar, J E Cleaver, C A Weber.   

Abstract

Patient TTD183ME is male and has typical trichothiodystrophy characteristics, including brittle hair, ichthyosis, characteristic face with receding chin and protruding ears, sun sensitivity, and mental and growth retardation. The relative amount of NER carried out by a TTD183ME fibroblast cell strain after ultraviolet (UV) exposure was approximately 65% of normal as determined by a method that converts repair patches into quantifiable DNA breaks. UV survival curves show a reduction in survival only at doses greater than 4 J/m2. Nucleotide sequence analysis of the ERCC2 (XPD) DNA repair and transcription gene cDNA revealed both a Leu461-to-Val substitution and a deletion of amino acids 716-730 in one allele and an Ala725-to-Pro substitution in the other allele. The first allele has also been reported in one xeroderma pigmentosum group D patient and two other trichothiodystrophy patients, while the second allele has not been previously reported. Comparisons suggest that the mutation of Ala725 to Pro correlates with TTD with intermediate UV sensitivity.

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Year:  1997        PMID: 9195225     DOI: 10.1002/(SICI)1098-1004(1997)9:6<519::AID-HUMU4>3.0.CO;2-X

Source DB:  PubMed          Journal:  Hum Mutat        ISSN: 1059-7794            Impact factor:   4.878


  7 in total

1.  Use of Big Data to Estimate Prevalence of Defective DNA Repair Variants in the US Population.

Authors:  Jennifer Pugh; Sikandar G Khan; Deborah Tamura; Alisa M Goldstein; Maria Teresa Landi; John J DiGiovanna; Kenneth H Kraemer
Journal:  JAMA Dermatol       Date:  2019-01-01       Impact factor: 10.282

Review 2.  Trichothiodystrophy: a systematic review of 112 published cases characterises a wide spectrum of clinical manifestations.

Authors:  S Faghri; D Tamura; K H Kraemer; J J Digiovanna
Journal:  J Med Genet       Date:  2008-06-25       Impact factor: 6.318

3.  PIBIDS syndrome in two Brazilian siblings.

Authors:  Kerstin Taniguchi Abagge; Felipe Haupenthal; Gabriella Yamashita Felber; Salmo Raskin
Journal:  BMJ Case Rep       Date:  2018-12-22

4.  Abnormal XPD-induced nuclear receptor transactivation in DNA repair disorders: trichothiodystrophy and xeroderma pigmentosum.

Authors:  Xiaolong Zhou; Sikandar G Khan; Deborah Tamura; Takahiro Ueda; Jennifer Boyle; Emmanuel Compe; Jean-Marc Egly; John J DiGiovanna; Kenneth H Kraemer
Journal:  Eur J Hum Genet       Date:  2012-12-12       Impact factor: 4.246

5.  Phenotype-specific adverse effects of XPD mutations on human prenatal development implicate impairment of TFIIH-mediated functions in placenta.

Authors:  Roxana Moslehi; Anil Kumar; James L Mills; Xavier Ambroggio; Caroline Signore; Amiran Dzutsev
Journal:  Eur J Hum Genet       Date:  2012-01-11       Impact factor: 4.246

6.  Xeroderma Pigmentosum-Trichothiodystrophy overlap patient with novel XPD/ERCC2 mutation.

Authors:  Henrik H Kralund; Lilian Ousager; Nicolaas G Jaspers; Anja Raams; Erling B Pedersen; Else Gade; Anette Bygum
Journal:  Rare Dis       Date:  2013-05-06

7.  Nucleotide excision repair/transcription gene defects in the fetus and impaired TFIIH-mediated function in transcription in placenta leading to preeclampsia.

Authors:  Roxana Moslehi; Xavier Ambroggio; Vijayaraj Nagarajan; Anil Kumar; Amiran Dzutsev
Journal:  BMC Genomics       Date:  2014-05-15       Impact factor: 3.969

  7 in total

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