Identification of the Fanconi anemia complementation group I gene, FANCI

Cellular Oncology

Volumn 29, Issue 3, 2007, Pages 211-218

  Dorsman, Josephine C ^a   Levitus, Marieke ^a   Rockx, Davy ^a   Rooimans, Martin A ^a   Oostra, Anneke B ^a   Haitjema, Anneke ^a   Bakker, Sietske T ^a   Steltenpool, Jûrgen ^a   Schuler, Dezsö ^b   Mohan, Sheila ^c   Schindler, Detlev ^d   Arwert, Fré ^a   Pals, Gerard ^a   Mathew, Christopher G ^e   Waisfisz, Quinten ^a   De Winter, Johan P ^a   Joenje, Hans ^a  

^a VU UNIVERSITY MEDICAL CENTER   (Netherlands)

^b National Institute of Child Health   (Hungary)

^c APOLLO HOSPITALS   (India)

^d UNIVERSITY OF WÜRZBURG   (Germany)

^e GUY S HOSPITAL   (United Kingdom)

Author keywords

Data mining; FANCI; Fanconi anemia; Gene identification; Positional cloning

Indexed keywords

MITOMYCIN C; SMALL INTERFERING RNA;

ADOLESCENT; ADULT; ARTICLE; CHILD; CHROMOSOME 15Q; CHROMOSOME BREAKAGE; CLINICAL ARTICLE; FANCONI ANEMIA; FANCONI ANEMIA COMPLEMENTATION GROUP I GENE; GENE; GENE IDENTIFICATION; GENE LOCUS; GENE MUTATION; HELA CELL; HUMAN; HUMAN CELL; NUCLEAR LOCALIZATION SIGNAL; NUCLEOTIDE SEQUENCE; PHENOTYPE; PRIORITY JOURNAL; PROTEIN FUNCTION;

ADOLESCENT; ADULT; BASE SEQUENCE; CELL LINE; CHILD; CHROMOSOMAL INSTABILITY; FANCONI ANEMIA COMPLEMENTATION GROUP D2 PROTEIN; FANCONI ANEMIA COMPLEMENTATION GROUP PROTEINS; FEMALE; GENOME, HUMAN; HELA CELLS; HUMANS; MALE; MOLECULAR SEQUENCE DATA; MUTATION; PEDIGREE; PHENOTYPE; UBIQUITIN;

EID: 34249332276     PISSN: 15705870     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (16)

1. A. Ciccia, C. Ling, R. Coulthard, Z. Yan, Y. Xue, A.R. Meetei, H. el Laghmani, H. Joenje, N. McDonald, J.P. de Winter, W. Wang and S.C. West, Identification of FAAP24, a Fanconi anemia core complex protein that interacts with FANCM, Mol. Cell. 25 (2007), 487-490.
2. I. Garcia-Higuera, T. Taniguchi, S. Ganesan, M.S. Meyn, C. Timmers, J. Hejna, M. Grompe and A.D. D'Andrea, Interaction of the Fanconi anemia proteins and BRCA1 in a common pathway, Mol. Cell 7 (2001), 249-262.
3. J.J. Gregory Jr, J.E. Wagner, P.C. Verlander, O. Levran, S.D. Batish, C.R. Eide, A. Steffenhagen, B. Hirsch and A.D. Auerbach, Somatic mosaicism in Fanconi anemia: evidence of genotypic reversion in lymphohematopoietic stem cells, Proc. Natl. Acad. Sci. USA 98 (2001), 2532-2537.
4. M. Gross, H. Hanenberg, S. Lobitz, R. Friedl, S. Herterich, R. Dietrich, B. Gruhn, D. Schindler and H. Hoehn, Reverse mosaicism in Fanconi anemia: natural gene therapy via molecular self-correction, Cytogenet. Genome Res. 98 (2002), 126-135.
5. H. Joenje, F. Arwert, A.W. Eriksson, H. de Koning and A.B. Oostra, Oxygen-dependence of chromosomal aberrations in Fanconi's anaemia, Nature 290 (1981), 142-143.
6. H. Joenje and K.J. Patel, The emerging genetic and molecular basis of Fanconi anaemia, Nat. Rev. Genet. 2 (2001), 446-457.
7. M. Levitus, M.A. Rooimans, J. Steltenpool, N.F. Cool, A.B. Oostra, C.G. Mathew, M.E. Hoatlin, Q. Waisfisz, F. Arwert, J.P. de Winter and H. Joenje, Heterogeneity in Fanconi anemia: evidence for 2 new genetic subtypes, Blood 103 (2004), 2498-2503.
8. M. Levitus, H. Joenje and J.P. de Winter, The Fanconi anemia pathway of genomic maintenance, Cell. Oncol. 28 (2006), 3-29.
9. J.R. Lo Ten Foe, M.L. Kwee, M.A. Rooimans, A.B. Oostra, A.J. Veerman, M. van Weel, R.M. Pauli, N.T. Shahidi, I. Dokal, I. Roberts, C. Altay, E. Gluckman, R.A. Gibson, C.G. Mathew, F. Arwert and H. Joenje, Somatic mosaicism in Fanconi anemia: molecular basis and clinical significance, Eur. J. Hum. Genet. 5 (1997), 137-148.
10. A. Mankad, T. Taniguchi, B. Cox, Y. Akkari, R.K. Rathbun, L. Lucas, G. Bagby, S. Olson, A. D'Andrea and M. Grompe, Natural gene therapy in monozygotic twins with Fanconi anemia, Blood 107 (2006), 3084-3090.
11. A.R. Meetei, J.P. de Winter, A.L. Medhurst, M. Wallisch, Q. Waisfisz, H.J. van de Vrugt, A.B. Oostra, Z. Yan, C. Ling, C.E. Bishop, M.E. Hoatlin, H. Joenje and W. Wang, A novel ubiquitin ligase is deficient in Fanconi anemia, Nat. Genet. 35 (2003), 165-170.
12. S. Reid, D. Schindler, H. Hanenberg, K. Barker, S. Hanks, R. Kalb, K. Neveling, P. Kelly, S. Seal, M. Freund, M. Wurm, S.D. Batish, F.P. Lach, S. Yetgin, H. Neitzel, H. Ariffin, M. Tischkowitz, C.G. Mathew, A.D. Auerbach and N. Rahman, Biallelic mutations in PALB2 cause Fanconi anemia subtype FA-N and predispose to childhood cancer, Nat. Genet. 39 (2007), 162-164.
13. T. Taniguchi and A.D. D'Andrea, Molecular pathogenesis of Fanconi anemia: recent progress, Blood 107 (2006), 4223-4233.
14. C. Timmers, T. Taniguchi, J. Hejna, C. Reifsteck, L. Lucas, D. Bruun, M. Thayer, B. Cox, S. Olson, A.D. D'Andrea, R. Moses and M. Grompe, Positional cloning of a novel Fanconi anemia gene, FANCD2, Mol. Cell 7 (2001), 241-248.
15. Q. Waisfisz, N.V. Morgan, M. Savino, J.P. de Winter, C.G. van Berkel, M.E. Hoatlin, L. Ianzano, R.A. Gibson, F. Arwert, A. Savoia, C.G. Mathew, J.C. Pronk and H. Joenje, Spontaneous functional correction of homozygous fanconi anaemia alleles reveals novel mechanistic basis for reverse mosaicism, Nat. Genet. 22 (1999), 279-383.
16. B. Xia, J.C. Dorsman, N. Ameziane, Y. de Vries, M.A. Rooimans, Q. Sheng, G. Pals, A. Errami, E. Gluckman, J. Llera, W. Wang, D.M. Livingston, H. Joenje and J.P. de Winter, Fanconi anemia is associated with a defect in the BRCA2 partner PALB2, Nat. Genet. 39 (2007), 159-161.