Conservation of aphidicolin-induced fragile sites in Papionini (Primates) species and humans

Chromosome Research

Volumn 12, Issue 7, 2004, Pages 683-690

  Ruiz Herrera, Aurora ^a   Garcia, Francisca ^a   Frönicke, Lutz ^b   Ponsà, Montserrat ^a   Egozcue, Josep ^a   Caldés, Montserrat Garcia ^a   Stanyon, Roscoe ^b  

^a UNIVERSITAT AUTÒNOMA DE BARCELONA   (Spain)

^b NATIONAL CANCER INSTITUTE   (United States)

Author keywords

Artificial chromosome; Cytogenetics; Evolution; Fluorescence in situ hybridization; Fragile site; Primate

Indexed keywords

APHIDICOLIN; ENZYME INHIBITOR;

ARTICLE; BACTERIAL ARTIFICIAL CHROMOSOME; CHROMOSOME 1; CHROMOSOME 18; CHROMOSOME 3; CHROMOSOME 5; CHROMOSOME 7; CHROMOSOME BAND; CHROMOSOME MAP; CHROMOSOME STRUCTURE; CONTROLLED STUDY; EVOLUTION; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; GENETIC CONSERVATION; HUMAN; HUMAN CELL; HUMAN CHROMOSOME; INTERSPECIFIC RELATIONSHIP; MACACA; MANDRILLUS SPHINX; MOLECULAR CLONING; NONHUMAN; PRIMATE; PRIORITY JOURNAL; PROTEIN EXPRESSION; SPECIES DIFFERENCE; STRUCTURAL HOMOLOGY; X CHROMOSOME; YEAST ARTIFICIAL CHROMOSOME; ANIMAL; CHROMOSOME; CHROMOSOME FRAGILE SITE; DRUG EFFECT; GENETIC MARKER; GENETIC RECOMBINATION; GENETICS; MANDRILLUS;

BACTERIA (MICROORGANISMS); MACACA; MACACA FASCICULARIS; MAMMALIA; MANDRILLUS SPHINX; PAPIONINI; PRIMATES;

ANIMALS; APHIDICOLIN; CHROMOSOME FRAGILE SITES; CHROMOSOME MAPPING; CHROMOSOMES; ENZYME INHIBITORS; GENETIC MARKERS; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; MACACA FASCICULARIS; MANDRILLUS; RECOMBINATION, GENETIC;

EID: 21644477348     PISSN: 09673849     EISSN: None     Source Type: Journal    
DOI: 10.1023/B:CHRO.0000045753.88789.ea     Document Type: Article

References (28)

1. Arlt MF, Miller DE, Beer DG, Glower TW (2002) Molecular characterization of FRAXB and comparative common fragile site instability in cancer cells. Genes Chromosomes Cancer 33: 82-92.
2. Arlt MF, Casper AM, Glower TW (2003) Common fragile sites. Cytogenet Genome Res 100: 92-100.
3. Borrell A, Ponsà M, Egozcue J, Rubio A, Garcia M (1998) Chromosome abnormalities in peripheral blood lymphocytes from Macaca fascicularis and Erythrocebus patas (Cercopithecidae, Catarrhini) after X-irradiation. Mutat Res 403: 185-198.
4. Casper AM, Nghiem P, Arlt MF, Glower TW (2002) ATR regulates fragility site stability. Cell 111: 779-789.
5. Clemente IC, Ponsà M, Garcia M, Egozcue J (1990) Chromosome evolution in the Cercopithecidae and its relationship to human fragile sites and neoplasia. Int J Primatol 11: 377-398.
6. Dekaban A (1965) Persisting clone of cells with an abnormal chromosome in a woman previously irradiated. J Nucl Med 6: 740-746.
7. Fang JM, Arlt MF, Burgess AC, Dagenais SL, Beer DG, Glover TW (2001) Translocation breakpoints in FHIT and FRA3B in both homologs of chromosome 3 in an esophageal adenocarcinoma. Genes Chromosomes Cancer 30: 292-298.
8. Fundia A, Gorostiaga M, Delprat A, Mudry M (1991) Fragile sites analysis and definition of chromosome landmarks, regions and bands in Alouatta caraya (ACA). In Ehara A, Kimura T, Takanaka O, Iwato M, eds., Primatology Today. Amsterdam: Elsevier, pp. 617-618.
9. Fundia A, Gorostiaga M, Mudry M (2000) Expression of common fragile sites in two Ceboidea species: Saimiri boliviensis and Alouatta caraya (Primates: Platyrrhini). Genet Sel Evol 32: 87-97.
10. Miró R, Clemente IC, Fuster C, Egozcue J (1987) Fragile sites, chromosome evolution, and human neoplasia. Hum Genet 75: 345-349.
11. Mishmar D, Rahat A, Scherer SW et al. (1998) Molecular characterization of a common fragile site (FRA7H) on human chromosome 7 by the cloning of a simian virus 40 integration site. Proc Natl Acad Sci USA 95: 8141-8146.
12. Mudry MD (1990) Cytogenetic variability within and across populations of Cebus apella in Argentina. Folia Primatol 54: 206-216.
13. Müller S, Stanyon R, Finelli P, Archidiacono N, Wienberg J (2000) Molecular cytogenetic dissection of human chromosome 3 and 21 evolution. Proc Natl Acad Sci USA 97: 206-211.
14. Müller S, Wienberg J (2001) 'Bar-coding' primate chromosomes: molecular cytogenetic screening for the ancestral hominoid karyotype. Hum Genet 109: 85-94.
15. National Cancer Institute (NCI) database (http://cgap.nci.nih.gov). Accessed 2001.
16. Nickerson E, Nelson DL (1998) Molecular definition of pericentric inversion breakpoints occurring during the evolution of humans and chimpanzees. Genomics 50: 368-372.
17. Ruiz-Herrera A, Ponsà M, García F, Egozcue J, Garcia M (2002a) Fragile sites in human and Macaca fascicularis chromosomes are breakpoints in chromosome evolution. Chromosome Res 10: 33-44.
18. Ruiz-Herrera A, García F, Azzalin C et al. (2002b) Distribution of intrachromosomal telomeric sequences (ITS) on Macaca fascicularis (Primates) chromosomes and their implication for chromosome evolution. Hum Genet 110: 578-586.
19. Ruiz-Herrera A, García F, Giulotto E et al. (2004a) Evolutionary breakpoints are correlated with fragile sites and intrachromosomal telomeric sequences in Primates. Cytogenet Genome Res (in press).
20. Ruiz-Herrera A, García F, Mora L, Egozcue J, Ponsà M, Garcia M (2004b) Evolutionary conserved chromosomal segments in the human karyotype are bounded by unstable chromosome bands. Cytogenet Genome Res (in press).
21. Schmid M, Ott G, Haaf T, Scheres JM (1985) Evolutionary conservation of fragile sites induced by 5-azacytidine and 5-azadeoxycytidine in man, gorilla, and chimpanzee. Hum Genet 71: 342-350.
22. Smeets DF, Van de Klundert FA (1990) Common fragile sites in man and three closely related primate species. Cytogenet Cell Genet 53: 8-14.
23. Stanyon R, Consigliere S, Bigoni F, Ferguson-Smith M, O'Brien PCM, Wienberg J (2001) Reciprocal chromosome painting between a New World primate, the woolly monkey, and humans. Chromosome Res 9: 97-106.
24. Sutherland GR (1979) Heritable fragile sites on human chromosomes I. Factors affecting expression in lymphocyte culture. Am J Hum Genet 31: 125-135.
25. Sutherland GR, Baker E (2000) The clinical significance of fragile sites on human chromosomes. Clin Genet 58: 157-161.
26. Telenius H, Pelmear AH, Tunnacliffe A et al. (1992) Cytogenetic analysis by chromosome painting using DOP-PCR amplified flow-sorted chromosomes. Genes Chromosomes Cancer 4: 257-263.
27. Vallente-Samonte RU, Conte RA, Verma RS (2000) Syntenic homology of human unique DNA sequences within chromosome regions 5q31, 10q22, 13q32-33 and 19q13.1 in the great apes. Genet Mol Biol 23: 527-529.
28. Wilke CM, Guo SW, Hall BK et al. (1994) Multicolor FISH mapping of YAC clones in 3p14 and identification of a YAC spanning both FRA3B and the t(3;8) associated with hereditary renal cell carcinoma. Genomics 22: 319-326.