Fine mapping of distal 1p loci reveals TP73 at D1S468

Cytogenetics and Cell Genetics

Volumn 84, Issue 1-2, 1999, Pages 111-114

  Perri, P ^a   Praml, C ^a   Savelyeva, L ^a   Pillmann, A ^a   Schwab, Manfred ^a  

^a GERMAN CANCER RESEARCH CENTER DKFZ   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; BREAST CANCER; CANCER; CHROMOSOME 1; COLON CANCER; COSMID; FLUORESCENCE IN SITU HYBRIDIZATION; GENE DELETION; GENE LOCUS; GENE MAPPING; GENE MUTATION; GENE SEQUENCE; HETEROZYGOSITY LOSS; HUMAN; HUMAN CELL; MOLECULAR CLONING; NEUROBLASTOMA; PRIORITY JOURNAL; TUMOR SUPPRESSOR GENE;

EID: 0032919028     PISSN: 03010171     EISSN: None     Source Type: Journal    
DOI: 10.1159/000015233     Document Type: Article

References (16)

1. Buroker N, Bestwick R, Haight G, Magenis RE, Litt MA: Hypervariable repeated sequence on human chromosome 1p36. Hum Genet 77:175-181 (1987).
2. Jost CA, Marin MC, Kaelin WC: TP73 is a human p53-relaled protein that can induce apoptosis. Nature 389:191-194 (1997).
3. Kaghad M, Bonnet H, Yang A, Creancier L, Biscan J-C, Valent A, Minty A, Chalon P, Lelias J-M, Dumount X, Ferrara P, Mckeon F, Caput D: Monoallelically expressed gene related to p53 at 1p36, a region frequently deleted in neuroblastoma and other human cancers. Cell 90:809-819 (1997).
4. Lahti JM, Valentine M, Xiang J, Jones B, Amann J, Grenet J, Richmond G, Look AT, Kidd VJ: Alterations in the PITSLRE protein kinase gene complex on chromosome 1p36 in childhood neuroblastoma. Nature Genet 7:370-375 (1994).
5. Martinsson T, Sjöberg R-M, Hedborg F, Kogner P: Deletion of chromosome 1p loci and microsatellite instability in neuroblastomas analyzed with shorttandem repeat polymorphisms. Cancer Res 55: 5681-5686 (1995).
6. Martinsson T, Weith A, Cziepluch C, Schwab M: Chromosome 1 deletions in human neuroblastomas: generation and fine mapping of microclones from the distal 1p region. Genes Chrom Cancer 1:67-78 (1989).
7. Munn KE, Walker RA, Varley JM: Frequent alterations of chromosome 1 in ductal carcinoma in situ of the breast. Oncogene 10:1653-1657 (1995).
8. Nagai H, Negrini M, Carter SL, Gillum DR, Rosenberg AL, Schwartz GF, Croce CM: Detection and cloning of a common region of loss of heterozygosity at chromosome 1p in breast cancer. Cancer Res 55:1752-1757 (1995).
9. NIH and IMM collaboration. Ning Y, Roschke A, Smith ACM, Macha M, Precht K, Riethman H, Ledbetter DH (Group 1); Flint J, Horsley S, Regan R, Kearney L, Knight S, Kvaloy K, Brown WRA (Group 2): A complete set of human telomeric probes and their clinical application. Nature Genet 14:86-89 (1996).
10. Nomoto S, Haruki N, Kondo M, Konishi H, Takahashi T, Takahashi T, Takahashi T: Search for mutations and examination of allelic expression imbalance of TP73 gene at 1p36.33 in human lung cancers. Cancer Res 58:1380-1383 (1998).
11. Perri P, Pession AL, Mazzocco K, Scaruffi P, Strigini P, Iolascon A, Albergoni MP, Basso G, Tonini GP: Restriction fragment length polymorphism analysis reveals different allele frequency and a linkage disequilibrium at locus D1S94 in neuroblastoma patients. Eur J Cancer 33:1949-1952 (1997).
12. Perri P, Pession AL, Mazzocco K, Strigini P, Iolascon A, Basso G, Tonini GP: Peculiar allelotype associated with susceptibility to neuroblastoma. Genes Chrom Cancer 17:60-63 (1996).
13. Praml C, Finke LH, Herfarrth C, Schlag P, Schwab M, Amler LC: Deletion mapping defines different regions in 1p34.2 → pter that may harbor genetic information related to human colorectal cancer. Oncogene 11:1357-1362 (1995).
14. Savelyeva L, Claas A, Gier S, Schlag P, Finke L, Mangion J, Stratton MR, Schwab M: An interstitial tandem duplication of 9p23 → p24 coexists with a mutation in the BRCA2 gene in the germ line of three brothers with breast cancer. Cancer Res 58:863-866 (1998).
15. Schwab M, Praml C, Amler LC: Genomic instability in 1p and human malignancies. Genes Chrom Cancer 16:211-229 (1996).
16. White PS, Maris JM, Beltinger C, Sulman E, Marshall HN, Fujimori M, Kaufman BA, Biegel JA, Allen C, Hillard C, Valentine MB, Look AT, Enomoto H, Sakiyama S, Brodeur, GM: A region of consistent deletion in neuroblastoma within human chromosome 1p36.2 → p36.3. Proc natl Acad Sci, USA 92:5520-5524 (1995).