Sensitivity of multiple color spectral karyotyping in detecting small interchromosomal rearrangements

被引:34
作者
Fan, YS
Siu, VM
Jung, JH
Xu, J
机构
[1] London Hlth Sci Ctr, Cytogenet Div, London, ON N6A 4G5, Canada
[2] Univ Western Ontario, Dept Pathol, London, ON, Canada
[3] London Hlth Sci Ctr, Med Genet Program, London, ON N6A 4G5, Canada
[4] McMaster Univ, Med Ctr, Hamilton, ON, Canada
来源
GENETIC TESTING | 2000年 / 4卷 / 01期
关键词
D O I
10.1089/109065700316417
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Multiple color spectral karyotyping (SKY) has been proven to be a very useful tool for characterization of the complex rearrangements in cancer cells and the de novo constitutional structural abnormalities. The sensitivity of SKY in detecting interchromosomal alterations was assessed with 10 constitutional translocations involving subtelomeric regions. Among the 13 small segments tested, 9 were clearly visualized and 8 mere unambiguously identified by SKY. Fluorescence in situ hybridizations (FISH) with subtelomeric probes confirmed the reciprocity in three of the four translocations in which a small segment was not detectable by SKY. On the basis of resolution level of G-banding and the information obtained from the FISH analysis, the minimum alteration that SKY can detect is estimated to be 1,000-2,000 kbp in size with the currently available probes. This study has demonstrated the power, but also the limitations, of SKY in detecting small interchromosomal alterations, particularly those in subtelomeric regions.
引用
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页码:9 / 14
页数:6
相关论文
共 37 条
[1]   Establishment and characterization of a megakaryoblast cell line with amplification of MLL [J].
Allen, RJ ;
Smith, SD ;
Moldwin, RL ;
Lu, MM ;
Giordano, L ;
Vignon, C ;
Suto, Y ;
Harden, A ;
Tomek, R ;
Veldman, T ;
Ried, T ;
Larson, RA ;
Le Beau, MM ;
Rowley, JD ;
Zeleznik-Le, N .
LEUKEMIA, 1998, 12 (07) :1119-1127
[2]  
Anderlid B, 1999, AM J HUM GENET, V65, pA67
[3]  
Blancato JK, 1999, PRINCIPLES OF CLINICAL CYTOGENETICS, P443
[4]  
Coleman AE, 1997, CANCER RES, V57, P4585
[5]   DETECTION OF CHROMOSOME-ABERRATIONS IN METAPHASE AND INTERPHASE TUMOR-CELLS BY INSITU HYBRIDIZATION USING CHROMOSOME-SPECIFIC LIBRARY PROBES [J].
CREMER, T ;
LICHTER, P ;
BORDEN, J ;
WARD, DC ;
MANUELIDIS, L .
HUMAN GENETICS, 1988, 80 (03) :235-246
[6]  
Fan YS, 1999, AM J MED GENET, V86, P118, DOI 10.1002/(SICI)1096-8628(19990910)86:2<118::AID-AJMG6>3.0.CO
[7]  
2-S
[8]   MAPPING SMALL DNA-SEQUENCES BY FLUORESCENCE INSITU HYBRIDIZATION DIRECTLY ON BANDED METAPHASE CHROMOSOMES [J].
FAN, YS ;
DAVIS, LM ;
SHOWS, TB .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1990, 87 (16) :6223-6227
[9]  
Fan YS, 1999, CANCER GENET CYTOGEN, V112, P190
[10]   A new complex variant Philadelphia chromosome, t(1;9;22)ins(17;22), characterized by fluorescence in situ hybridization in an adult ALL [J].
Fan, YS ;
Rizkalla, K ;
Barr, RM .
LEUKEMIA RESEARCH, 1999, 23 (11) :1001-1006