Identification of XP complementation groups by recombinant adenovirus carrying DNA repair genes

Journal of Investigative Dermatology

Volumn 129, Issue 2, 2009, Pages 502-506

  Leite, Ricardo A ^a   Marchetto, Maria C ^b   Muotri, Alysson R ^b   De Moraes Vasconcelos, Dewton ^a   Prado De Oliveira, Zilda N ^a   Rivitti MacHado, Maria C ^a   Martins Menck, Carlos F ^a  

^a UNIVERSITY OF SÃO PAULO   (Brazil)

^b SALK INSTITUTE FOR BIOLOGICAL STUDIES   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

COMPLEMENTARY DNA;

ADENOVIRUS; DNA REPAIR; DNA SEQUENCE; EXCISION REPAIR; FIBROBLAST; GENE MUTATION; HUMAN; LETTER; PRIORITY JOURNAL; SKIN BIOPSY; SKIN CANCER; SUN EXPOSURE; XERODERMA PIGMENTOSUM;

ADENOVIRIDAE; CHILD; DNA REPAIR; DNA-BINDING PROTEINS; GENETIC SCREENING; HUMANS; RECOMBINANT FUSION PROTEINS; XERODERMA PIGMENTOSUM; XERODERMA PIGMENTOSUM GROUP A PROTEIN;

EID: 58549103698     PISSN: 0022202X     EISSN: 15231747     Source Type: Journal    
DOI: 10.1038/jid.2008.239     Document Type: Letter

References (14)

1. Armelini MG, Muotri AR, Marchetto MC, de Lima-Bessa KM, Sarasin A, Menck CF (2005) Restoring DNA repair capacity of cells from three distinct diseases by XPD gene-recombinant adenovirus. Cancer Gene Ther 12: 389-96
2. Carreau M, Eveno E, Quilliet X, Chevalier-Lagente O, Benoit A, Tanganelli B et al. (1995) Development of a new easy complementation assay for DNA repair deficient human syndromes using cloned repair genes. Carcinogenesis 16:1003-9
3. Chavanne F, Broughton BC, Pietra D, Nardo T, Browitt A, Lehmann AR et al. (2000) Mutations in the XPC gene in families with xeroderma pigmentosum and consequences at the cell, protein, and transcript levels. Cancer Res 60:1974-82
4. Cleaver JE (1968) Defective repair replication of DNA in xeroderma pigmentosum. Nature 218:652-6
5. Cleaver JE, Bootsma D, Friedberg E (1975) Human diseases with genetically altered DNA repair processes. Genetics 79(Suppl):215-25
6. Costa RM, Chigancas V, Galhardo RS, Carvalho H, Menck CF (2003) The eukaryotic nucleotide excision repair pathway. Biochimie 85:1083-99
7. Gozukara EM, Khan SG, Metin A, Emmert S, Busch DB, Shahlavi T et al. (2001) A stop codon in xeroderma pigmentosum group C families in Turkey and Italy: molecular genetic evidence for a common ancestor. J Invest Dermatol 117:197-204
8. Khan SG, Levy HL, Legerski R, Quackenbush E, Reardon JT, Emmert S et al. (1998) Xeroderma pigmentosum group C splice mutation associated with autism and hypoglycinemia. J Invest Dermatol 111:791-6
9. Khan SG, Oh KS, Shahlavi T, Ueda T, Busch DB, Inui H et al. (2006) Reduced XPC DNA repair gene mRNA levels in clinically normal parents of xeroderma pigmentosum patients. Carcinogenesis 27:84-94
10. Lehmann AR (2003) DNA repair-deficient diseases, xeroderma pigmentosum, Cockayne syndrome and trichothiodystrophy. Biochimie 85:1101-11
11. Lima-Bessa KM, Chigancas V, Stary A, Kannouche P, Sarasin A, Armelini MG et al. (2006) Adenovirus mediated transduction of the human DNA polymerase eta cDNA. DNA Repair 5:925-34
12. Muotri AR, Marchetto MC, Zerbini LF, Libermann TA, Ventura AM, Sarasin A et al. (2002) Complementation of the DNA repair deficiency in human xeroderma pigmentosum group a and C cells by recombinant adenovirus-mediated gene transfer. Hum Gene Ther 13:1833-44
13. Uchida A, Sugasawa K, Masutani C, Dohmae N, Araki M, Yokoi M et al. (2002) The carboxyterminal domain of the XPC protein plays a crucial role in nucleotide excision repair through interactions with transcription factor IIH. DNA Repair 1:449-61
14. Zeng L, Quilliet X, Chevallier-Lagente O, Eveno E, Sarasin A, Mezzina M (1997) Retrovirus-mediated gene transfer corrects DNA repair defect of xeroderma pigmentosum cells of complementation groups A, B and C. Gene Ther 4:1077-84