A 3.1-Mb YAC contig within the Werner syndrome region, on the short arm of human chromosome 8

Cytogenetics and Cell Genetics

Volumn 72, Issue 1, 1996, Pages 63-68

  Chaffanet, M ^a,b   Imbert, A ^a   Adelaide J ^b   Le Pastier, D ^c   Wagner, M J ^d   Wells, D E ^d   Birnbaum, D ^a,b   Pebusque M J ^a  

^a INSERM   (France)

^b INSTITUT PAOLI CALMETTES   (France)

^c FONDATION JEAN DAUSSET CEPH   (France)

^d UNIVERSITY OF TEXAS MD ANDERSON CANCER CENTER   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; CHROMOSOME 8P; GENE LOCATION; HUMAN; HUMAN CELL; PRIORITY JOURNAL; WERNER SYNDROME; YEAST ARTIFICIAL CHROMOSOME;

CHROMOSOME MAPPING; CHROMOSOMES, ARTIFICIAL, YEAST; CHROMOSOMES, HUMAN, PAIR 8; GENETIC MARKERS; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; RESTRICTION MAPPING; WERNER SYNDROME;

EID: 0030057689     PISSN: 03010171     EISSN: 1424859X     Source Type: Journal    
DOI: 10.1159/000134164     Document Type: Article

References (33)

1. Albertson HM, Abderrahim H, Cann HM, Dausset J, Le Paslier D, Cohen D: Construction and characterization of a yeast artificial chromosome library containing seven haploid human genome equivalents, Proc natl Acad Sci, USA 87:4256-4260 (1990).
2. Anand R, Villasantc A, Tyler-Smith C: Construction of yeast artificial chromosome libraries with large inserts using fractionation by pulsed-field gel electrophoresis, Nucl Acids Res 17:3425-3433 (1989).
3. Bellanné-Chantelot C, Lacroix B, Ougcn P, Billault A, Beaufils S, Bertrand S, Georges I, Glibcrt F, Gros I, Lucotte G, Susini L, Codani J-J, Gesnouin P, Pook S, Waysscix G, Lu-Kuo J, Ricd T, Ward D, Chumakov I, Le Paslier D, Barillot E, Cohen D: Mapping the whole human genome by fingerprinting yeast artificial chromosomes, Cell 70:1059-1068 (1992).
4. Brownstein BH, Silverman GA, Little RD, Burke DT, Korsmeyer SJ, Schlessinger D, Olson MV: Isolation of single-copy human genes from a library of yeast artificial chromosomes clones, Science 244:1348-1351 (1989).
5. Buelow KH, Weber JL, Ludwigsen S, Scherpbicr-Hed-dema T, Duyk GM, Sheffield VC, WangZ, Murray JC: Integrated human genome-wide maps constructed using the CEPH reference panel, Nature Genet 6:391-393 (1994).
6. ChalTanet M, Baens M, Aersscns J, Schoenmakers E, Cassiman J-J, Marynen P: Mapping of an ordered set of 14 cosmids to human chromosome I2p by two-color in situ hybridization, Cytogenet Cell Genet 69:27-32 (1995).
7. Cox Matise T, Perlin M, Chakravarti A: Automated construction of genetic linkage maps using an expert system (MulliMap): a human genome linkage map Nature Genet 6:384-390 (1994).
8. Dib A, Adelaide J, Chaffanet M, Imbert A, Le Paslier D, Jacquemicr J, Gaudray P, Thcillet C, Bimbaum D, Pebusque M-J: Characterization of the region of the short arm of chromosome 8 amplified in breast carcinoma, Oncogene 10:995-1001 (1995).
9. Emi M, Fujiwara Y, Nakamura Y: A primary genetic linkage map of 14 polymorphic loci for the short arm of human chromosome 8, Genomics 15:530-534 (1993).
10. Faragher RGA, Kill IR, Hunter JAA, Pope FM, Tan-nock C, Shall S: The gene responsible for the Werner syndrome may be a cell division "counting" gene, Proc natl Acad Sci, USA 90:12030-12034 (1993).
11. Goto M, Rubenstein M, Weber J, Woods K, Drayna D: Genetic linkage of Werner’s syndrome to five markers on chromosome 8, Nature 355:735-738 (1992).
12. Green ED, Olson MV: Systematic screening of yeast artificial chromosomes libraries by use of the polymerase chain reaction, Proc natl Acad Sci, USA 87:1213-1217 (1990).
13. Gyapay G, Morissette J, Vignal A, Dib C, Fizames C, Millasseau P, Marc S, Bernardi G, Lathrop G, Weissenbach J: The 1993-94 Généthon human genetic linkage map, Nature Genet 7:246-339 (1994).
14. Imbert A, Rosnet O, Marchctto S, Ollendorff V, Birnbaum D, Pebusque M-J: Characterization of a yeast artificial chromosome from human chromosome band I3qI2 containing the FLT1 and FLT3 receptor-type tyrosine kinase genes, Cytogenet Cell Genet 67:175-177 (1994).
15. Kluck PMC, Wiegant J, Raap AK, Vrolijk H, Tanke HJ, WiUemzc R, Landergent J: Order of human hematopoietic growth factor and receptor genes on the long arm of chromosome 5, as determined by fluorescence in situ hybrization, Ann Hematol 66:15-20 (1993).
16. Lafage M, Pedeutour F, Marchetto S, Simonen IJ, Prosperi M-T, Gaudray P, Birnbaum D: Fusion and amplification of two originally non-syntenic chromosomal regions in a mammary carcinoma cell line, Genes Chrom Cancer 5:40-49 (1992).
17. Mitelman F, Kaneko Y, Trent J: Report of the committee on chromosome changes in neoplasia, Eleventh International Workshop on Human Gene Mapping, Cytogenet Cell Genet 58:1053-1079 (1991).
18. Nakura J, Wijsman EM, Miki T, Kamino K, Yu C-E, Oshima J, Fukuchi K-I, Weber JL, Piussan C, Melaragno MI, Epstein CJ, Scappaticci S, Fraccaro M, Matsumura T, Murano S, Yoshida S, Fujiwara Y, Saida T, Ogihara T, Martin GM, Schellenberg GD: Homozygosity mapping of the Werner syndrome locus (WRN), Genomics 23:600-608 (1994).
19. Oshima J, Yu C-E, Boehnke M, Weber JL, Edelhot TS, Wagner MJ, Wells DE, Wood S, Disteche CM, Martin GM, Schellenberg GD: Integrated mapping analysis of the Werner syndrome region of chromosome 8, Genomics 23:100-113 (1994).
20. Pebusque M-J, Lafage-Pochitalof T M, Galland F, Si-monetti J, Armstrong E, Rimokh R, Bimbaum D: Localization of two tyrosine kinase receptor genes with respect to the 5q35 chromosomal breakpoint of Ki-1 lymphoma cell lines, Genes Chrom Cancer 8:119-126 (1993).
21. Riley J, Butler R, Ogilvie D, Finniear R, Jenner D, Powell S, Anand R, Smith JC, Markham AF: A novel, rapid method for the isolation of terminal sequences from yeast artificial chromosome (YAC) clones, Nucl Acids Res 18:2887-2890 (1990).
22. Ruta M, Howk R, Ricca G, Drohan W, Zabelhanskv M, Laurcys G, Barton D, Franckc U, Schlessinger J, Givol D: A novel protein tyrosine kinase gene whose expression is modulated during endothelial cell differentiation, Oncogene 3:9-15 (1988).
23. Schellenberg GD, Martin GM, Wijsman EM, Nakura J, Miki T, Ogihara T: Homozygosity mapping and Werner's syndrome, Lancet 339:1002 (1992).
24. Spurr NK, Blanton S, Bookstein R, Clarke R, Cotting-ham R, Daiger S, Drayna D, Faber P, Horrigan S, Kas K, Kirchgcssner C, Kumar S, Leach RJ, Liied-ecke H-J, Nakamura Y, Pebusque M-J, Ranta S, Sim E, Sullivan LS, Taklc L, Vance J, Wagner M, Wells D, Westbrook C, Yaremko L, Zaletayev D, Zuflardi O, Wood S: Report of the second international workshop on human chromosome 8 mapping, 1994, Cvtogenet Cell Genet 68:148-164 (1995).
25. Theillet C, Adélaïde J, Louason G, Bonnet-Dorion F, Jacqucmier J, Adnanc J, Longy M, Katsaros D, Sismond P, Gaudray P, Bimbaum D: FGFRI and PLAT genes and DNA amplification at 8pl2 in breast and ovarian cancers, Genes Chrom Cancer 7:219-226 (1993).
26. Thomas W, Drayna D: A polymorphic dinuclcotide repeat at the D8S339 locus, Hum molec Genet 2:828 (1993).
27. Thomas W, Rubenstein M, Goto M, Drayna D: A genetic analysis of the Wemer syndrome region on human chromosome 8p, Genomics 16:685-690 (1993).
28. Tutic M, Lu X, Schirmer RH, Wemer D: Cloning and sequencing of mammalian glutathione reductase cDNA, Eur J Biochem 188:523-528 (1990).
29. Wagner M J, Ge Y, Siciliano M, Wells DE: A hybrid cell mapping panel for regional localization of probes to human chromosome 8, Genomics 10:114-125 (1991).
30. Weissenbach J, Gyapay G, Dib C, Vignal A, Morissctte J, Millasseau G, Vaysseix G, Lathrop M: A second-generation linkage map of the human genome, Nature 359:794-801 (1992).
31. Wiegant J, Galjart NJ, Raap AK, D'azzo A: The gene encoding human protective protein (PPGB) is on the chromosome 20, Genomics 10:345-349 (1991).
32. Wood S, Othmanc KB, Bergerheim USR, Blanton SH, Bookstein R, Clarke RA, Daiger SP, Donis-Kcller H, Drayna D, Kumar S, Leach RJ, Lüdccke H-J, Oshima J, Sadler LA, Spurr NK, Steinbmeck T, Trapman J, Wagner M, Wang Z, Wells D, Westbrook CA: Report of the first international workshop on human chromosome 8 mapping, Cytogenet Cell Genet 64:134-146 (1993).
33. Yu C-E, Oshima J, Goddard KAB, Miki T, Nakura J, Ogihara T, Poot M, Hoehn H, Fraccaro M, Piussan C, Martin GM, Schellenberg GD, Wijsman EM: Linkage disequilibrium and haplotype studies of chromosome 8pl 1.1→21.1 markers and Wemer syndrome, Am J hum Genet 55:356-364 (1994).