A new multicolor-FISH approach for the characterization of marker chromosomes: centromere-specific multicolor-FISH (cenM-FISH)

被引:119
作者
Nietzel, A
Rocchi, M
Starke, H
Heller, A
Fiedler, W
Wlodarska, I
Loncarevic, IF
Beensen, V
Claussen, U
Liehr, T [1 ]
机构
[1] Inst Human Genet & Anthropol, D-07740 Jena, Germany
[2] Inst Genet, Bari, Italy
[3] Catholic Univ Louvain, Ctr Human Genet, B-3000 Louvain, Belgium
关键词
D O I
10.1007/s004390100459
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Centromere-specific multi-color FISH (cenM-FISH) is a new multicolor FISH technique that allows the simultaneous characterization of all human centromeres by using labeled centromeric satellite DNA as probes. This approach allows the rapid identification of all human centromeres by their individual pseudo-coloring in one single step and is therefore a powerful tool in molecular cytogenetics. CenM-FISH fills a gap in multicolor karyotyping using WCP probes and distinguishes all centromeric regions apart from the evolutionary highly conserved regions on the chromosomes 13 and 21. The usefulness of the cenM- FISH technique for the characterization of small supernumerary marker chromosomes with no (or nearly no) euchromatin and restricted amounts of available sample material is demonstrated in prenatal, postnatal, and tumor cytogenetic cases. In addition, rarely described markers with the involvement of heterochromatic material inserted into homogeneously staining regions could be identified and characterized by using the cenM-FISH technique.
引用
收藏
页码:199 / 204
页数:6
相关论文
共 29 条
[1]   50 PROBANDS WITH EXTRA STRUCTURALLY ABNORMAL CHROMOSOMES CHARACTERIZED BY FLUORESCENCE IN-SITU HYBRIDIZATION [J].
BLENNOW, E ;
NIELSEN, KB ;
TELENIUS, H ;
CARTER, NP ;
KRISTOFFERSSON, U ;
HOLMBERG, E ;
GILLBERG, C ;
NORDENSKJOLD, M .
AMERICAN JOURNAL OF MEDICAL GENETICS, 1995, 55 (01) :85-94
[2]   High resolution multicolor-banding:: a new technique for refined FISH analysis of human chromosomes [J].
Chudoba, I ;
Plesch, A ;
Lörch, T ;
Lemke, J ;
Claussen, U ;
Senger, G .
CYTOGENETICS AND CELL GENETICS, 1999, 84 (3-4) :156-160
[3]   Maternal UPD 20 in a hyperactive child with severe growth retardation [J].
Chudoba, I ;
Franke, Y ;
Senger, G ;
Sauerbrei, G ;
Demuth, S ;
Beensen, V ;
Neumann, A ;
Hansmann, I ;
Claussen, U .
EUROPEAN JOURNAL OF HUMAN GENETICS, 1999, 7 (05) :533-540
[4]  
Crolla JA, 1998, AM J MED GENET, V75, P367, DOI 10.1002/(SICI)1096-8628(19980203)75:4<367::AID-AJMG5>3.0.CO
[5]  
2-N
[6]   Microdissection and FISH investigations in acute myeloid leukemia: A step forward to full identification of complex karyotypic changes [J].
Falzetti, D ;
Vermeesch, JR ;
Matteucci, C ;
Ciolli, S ;
Martelli, MF ;
Marynen, P ;
Mecucci, C .
CANCER GENETICS AND CYTOGENETICS, 2000, 118 (01) :28-34
[7]   Multipaint FISH: a rapid and reliable way to define cryptic and complex abnormalities [J].
Joyce, CA ;
Ross, FM ;
Dennis, NR ;
Wyre, ND ;
Barber, JCK .
CLINICAL GENETICS, 1999, 56 (03) :192-199
[8]   Neocentromeres and alpha satellite: a proposed structural code for functional human centromere DNA [J].
Koch, J .
HUMAN MOLECULAR GENETICS, 2000, 9 (02) :149-154
[9]   ENZYMATIC-SYNTHESIS OF BIOTIN-LABELED POLYNUCLEOTIDES - NOVEL NUCLEIC-ACID AFFINITY PROBES [J].
LANGER, PR ;
WALDROP, AA ;
WARD, DC .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES, 1981, 78 (11) :6633-6637
[10]   DELINEATION OF INDIVIDUAL HUMAN-CHROMOSOMES IN METAPHASE AND INTERPHASE CELLS BY INSITU SUPPRESSION HYBRIDIZATION USING RECOMBINANT DNA LIBRARIES [J].
LICHTER, P ;
CREMER, T ;
BORDEN, J ;
MANUELIDIS, L ;
WARD, DC .
HUMAN GENETICS, 1988, 80 (03) :224-234