Distribution and linkage of repetitive clusters from the heterochromatic region of human chromosome 22

Chromosome Research

Volumn 4, Issue 4, 1996, Pages 282-287

  Müllenbach, Roman ^a   Pusch, Carsten ^b   Holzmann, Karlheinz ^b   Suijkerbuijk, Ron ^c,d   Blin, Nikolaus ^b  

^a UNIVERSITY COLLEGE LONDON   (United Kingdom)

^b UNIVERSITY OF TÜBINGEN   (Germany)

^c Cancer Center   (United States)

^d RADBOUD UNIVERSITY MEDICAL CENTER   (Netherlands)

Author keywords

48 bp motif; Centromere; Cosmid clone; Fluorescence in situ hybridization; Satellite DNA

Indexed keywords

REPETITIVE DNA;

ACROCENTRIC CHROMOSOME; ARTICLE; CHROMOSOME 22; CHROMOSOME 22P; CHROMOSOME 22Q; CONTROLLED STUDY; COSMID; DIGEORGE SYNDROME; DNA LIBRARY; FLUORESCENCE IN SITU HYBRIDIZATION; GENE CLUSTER; GENE DELETION; GENE LOCATION; GENETIC LINKAGE; HETEROCHROMATIN; HUMAN; HUMAN CELL; PRIORITY JOURNAL; PULSED FIELD GEL ELECTROPHORESIS;

CENTROMERE; CHROMOSOME MAPPING; CHROMOSOMES, HUMAN, PAIR 22; COSMIDS; ELECTROPHORESIS, GEL, PULSED-FIELD; HETEROCHROMATIN; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; LINKAGE (GENETICS); REPETITIVE SEQUENCES, NUCLEIC ACID;

EID: 0030056683     PISSN: 09673849     EISSN: None     Source Type: Journal    
DOI: 10.1007/BF02263678     Document Type: Article

References (33)

1. Alexandrov IA, Maskova TD, Akopian TA et al. (1991) Chromosome specific alpha satellites. Genomics 11: 15-23.
2. Assum G, Fink T, Steinbeisser T, Fisel KJ (1993) Analysis of human extrachromosomal DNA elements originating from different β-satellite subfamilies. Hum Genet 91: 489-495.
3. Carey A, Roach S, Williamson R et al. (1990) Localization of 27 DNA markers to the region of human chromosome 22q11-pter deleted in patients with the DiGeorge syndrome and duplicated in the der22 syndrome. Genomics 7: 299-306.
4. Cherif D, Julier C, Delattre O et al. (1990) Simultaneous localization of cosmids and chromosome R-banding by fluorescence microscopy. Proc Natl Acad Sci USA 87: 475-479.
5. Church GM, Gilbert W (1984) Genome sequencing. Proc Natl Acad Sci USA 81: 1991-1995.
6. Clarke L (1990) Centromeres of budding and fission yeast. Trends Genet 6: 150-154.
7. Cooper KF, Fisher RB, Tyler-Smith C (1992) Structure of the pericentric long arm of the human Y chromosome. J Mol Biol 228: 421-432.
8. Gravholt CH, Friedrich U, Caprani M, Jorgensen AL (1992) The organisation of repetitive DNA sequences on human chromosomes with respect to the kinetochore analysed using a combination of oligonucleotide primers and CREST anticentromere serum. Genomics 14: 924-930.
9. Herrmann BG, Barlow DP, Lehrach H (1987) A larged inverted duplication allows homologous recombination between chromosomes heterozygous for the proximal T complex inversion. Cell 48: 813-825.
10. Jackson MS, Mole SE, Ponder BAJ (1992) Characterisation of a boundary between satellite III and alphoid sequences on human chromosome 10. Nucleic Acids Res 18: 4781-4787.
11. Johnson DH, Kroisel PM, Klapper HJ, Rosenkranz W (1992) Microdissection of a human marker chromosome reveals its origin and a new family of centromeric repetitive DNA. Hum Mol Genet 1: 741-747.
12. McDermid HE, Duncan AM, Higgins MJ et al. (1986) Isolation and characterization of an α-satellite repeated sequence from human chromosome 22. Chromosoma 94: 228-234.
13. Maio JJ (1971) DNA strand reassociation and polyribonucleotide binding in the African green monkey, Cercopithecus aethiops. J Mol Biol 56: 579-595.
14. Metzdorf R, Göttert E, Blin N (1988) A novel repetitive DNA from human chromosome 22. Chromosoma 97: 154-158.
15. Moyzis, RK, Torney DC, Meyne J et al. (1989) The distribution of interspersed repetitive DNA sequences in the human genome. Genomics 4: 273-289.
16. Müllenbach R, Lutz S, Holzmann K, Dooley S, Blin N (1992) A non-alphoid repetitive DNA sequence from chromosome 21. Hum Genet 89: 519-523.
17. Nizetic D, Zehenter G, Monaco AP (1991) Construction, arraying and high-density screening of large insert libraries of human chromosomes X and 21: Their potential use as reference libraries. Proc Natl Acad Sci USA 88: 3233-3237.
18. Oakey R, Tyler-Smith C (1990) Y-chromosome DNMA haplotyping suggests that most European and Asian men are descended from one of two males. Genomics 7: 325-330.
19. Pluta AF, Cooke CA, Earnshaw WC (1990) Structure of the human centromere at metaphase. Trends Biochem Sci 15: 181-185.
20. Prosser J, Frommer J, Paul C, Vincent PC (1986) Sequence relationship of three human satellite DNAs. J Mol Biol 187: 145-155.
21. Rocchi M, Archidiacono N, Ward DC, Baldini A (1991) A human chromosome 9-specific alphoid DNA repeat spatially resolvable from satellite 3 DNA by fluoresence in situ hybridization. Genomics 9: 517-523.
22. Scherthan H, Lutz S, Metzdorf R, Blin N (1989) Interspecies relationship of a repetitive chromosome-specific DNA. Hereditas 111: 183-188.
23. Suijkerbuijk R, Matthopoulos D, Kearney L et al. (1992) Fluorescence in situ identification of human chromosomes using flow sorting and Alu element-mediated PCR. Genomics, 13: 355-362.
24. Tyler-Smith C, Brown WRA (1987) Structure of repetitive sequences in the centromeric regions. J Mol Biol 195: 457-470.
25. Tyler-Smith C, Willard H (1993) Mammalian chromosome structure. Curr Opin Genet Dev 3: 390-397.
26. Warburton PE, Willard HF (1990) Genomic analysis of sequence variations in tandemly repeated DNA. J Mol Biol 216: 3-16.
27. Waye JS, Willard H (1989) Human beta satellite DNA: genomic organization and sequence definition. Proc Natl Acad Sci USA 86: 6250-6254.
28. Wevrick R, Willard VP, Willard HF (1992) Structure of DNA near long tandem arrays of alpha satellite DNA at the centromere of human chromosome 7, Genomics 14: 912-923.
29. Willard HF (1985) Chromosome-specific organisation of human alpha satellite DNA. Am J Hum Genet 37: 524-532.
30. Willard HF (1992) Centromeres - primary constrictions are primarily complicated. Hum Mol Genet 1: 667-668.
31. Willard HF, Waye JS (1987) Hierarchical order in chromosome specific human alpha satellites. Trends Genet 3: 192-198.
32. Wullich B, Kiechle-Schwarz M, Mayfrank L, Schempp W (1989) Cytogenetic and in situ DNA-hybridization studies in intracranial tumors of a patient with central neurofibromatosis. Hum Genet 82: 31-34.
33. Yunis JJ, Yasmineh WG (1971) Heterochromatin, satellite DNA, and cell function. Science 174: 1200-1209.