Use of fluorescent sequence-specific polyamides to discriminate human chromosomes by microscopy and flow cytometry

被引:27
作者
Gygi, MP
Ferguson, MD
Mefford, HC
Lund, KP
O'Day, C
Zhou, P
Friedman, C
van den Engh, G
Stolowitz, ML
Trask, BJ
机构
[1] Fred Hutchinson Canc Res Ctr, Div Human Biol, Seattle, WA 98109 USA
[2] Univ Washington, Dept Mol Biotechnol, Seattle, WA 98195 USA
[3] Univ Washington, Dept Genet, Seattle, WA 98195 USA
[4] Prolinx Inc, Bothell, WA 98021 USA
[5] Inst Syst Biol, Seattle, WA 98103 USA
关键词
D O I
10.1093/nar/gkf406
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
In this paper, we demonstrate the use of synthetic polyamide probes to fluorescently label heterochromatic regions on human chromosomes for discrimination in cytogenetic preparations and by flow cytometry. Polyamides bind to the minor groove of DNA in a sequence-specific manner. Unlike conventional sequence-specific DNA or RNA probes, polyamides can recognize their target sequence without the need to subject chromosomes to harsh denaturing conditions. For this study, we designed and synthesized a polyamide to target the TTCCA-motif repeated in the heterochromatic regions of chromosome 9, Y and 1. We demonstrate that the fluorescently labeled polyamide binds to its target sequence in both conventional cytogenetic preparations of metaphase chromosomes and suspended chromosomes without denaturation. Chromosomes 9 and Y can be discriminated and purified by flow sorting on the basis of polyamide binding and Hoechst 33258 staining. We generate chromosome 9- and Y-specific 'paints' from the sorted fractions. We demonstrate the utility of this technology by characterizing the sequence of an olfactory receptor gene that is duplicated on multiple chromosomes. By separating chromosome 9 from chromosomes 10-12 on the basis of polyamide fluorescence, we determine and differentiate the haplotypes of the highly similar copies of this gene on chromosomes 9 and 11.
引用
收藏
页码:2790 / 2799
页数:10
相关论文
共 72 条
[1]   CHROMOSOME-SPECIFIC DNA HYBRIDIZATION IN SUSPENSION FOR FLOW CYTOMETRIC DETECTION OF CHIMERISM IN BONE-MARROW TRANSPLANTATION AND LEUKEMIA [J].
ARKESTEIJN, GJA ;
ERPELINCK, SLA ;
MARTENS, ACM ;
HAGENBEEK, A .
CYTOMETRY, 1995, 19 (04) :353-360
[2]  
Asbury CL, 1996, CYTOMETRY, V24, P234, DOI 10.1002/(SICI)1097-0320(19960701)24:3<234::AID-CYTO6>3.0.CO
[3]  
2-H
[4]   Human-specific duplication and mosaic transcripts: The recent paralogous structure of chromosome 22 [J].
Bailey, JA ;
Yavor, AM ;
Viggiano, L ;
Misceo, D ;
Horvath, JE ;
Archidiacono, N ;
Schwartz, S ;
Rocchi, M ;
Eichler, EE .
AMERICAN JOURNAL OF HUMAN GENETICS, 2002, 70 (01) :83-100
[5]   Segmental duplications: Organization and impact within the current Human Genome Project assembly [J].
Bailey, JA ;
Yavor, AM ;
Massa, HF ;
Trask, BJ ;
Eichler, EE .
GENOME RESEARCH, 2001, 11 (06) :1005-1017
[6]   Solid phase synthesis of polyamides containing imidazole and pyrrole amino acids [J].
Baird, EE ;
Dervan, PB .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1996, 118 (26) :6141-6146
[7]   MEASUREMENT AND PURIFICATION OF HUMAN-CHROMOSOMES BY FLOW CYTOMETRY AND SORTING [J].
CARRANO, AV ;
GRAY, JW ;
LANGLOIS, RG ;
BURKHARTSCHULTZ, KJ ;
VANDILLA, MA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1979, 76 (03) :1382-1384
[8]   STUDY OF X-CHROMOSOME ABNORMALITY IN XX-MALES USING BIVARIATE FLOW KARYOTYPE ANALYSIS AND FLOW SORTED DOT BLOTS [J].
CARTER, NP ;
FERGUSONSMITH, ME ;
AFFARA, NA ;
BRIGGS, H ;
FERGUSONSMITH, MA .
CYTOMETRY, 1990, 11 (01) :202-207
[9]   Unique chromosome identification and sequence-specific structural analysis with short PNA oligomers [J].
Chen, CF ;
Wu, BL ;
Wei, T ;
Egholm, M ;
Strauss, WM .
MAMMALIAN GENOME, 2000, 11 (05) :384-391
[10]   CLONING OF A REPRESENTATIVE GENOMIC LIBRARY OF THE HUMAN X-CHROMOSOME AFTER SORTING BY FLOW-CYTOMETRY [J].
DAVIES, KE ;
YOUNG, BD ;
ELLES, RG ;
HILL, ME ;
WILLIAMSON, R .
NATURE, 1981, 293 (5831) :374-376