DETECTION OF SMALL, SINGLE-COPY GENES ON PROTEIN-G-BANDED CHROMOSOMES BY ELECTRON-MICROSCOPY

被引:11
|
作者
FETNI, R
LEMIEUX, N
MALFOY, B
DUTRILLAUX, B
MESSIER, PE
RICHER, CL
机构
[1] UNIV MONTREAL, FAC MED, DEPT ANAT, CP 6128, SUCC A, MONTREAL H3C 3J7, QUEBEC, CANADA
[2] UNIV MONTREAL, FAC MED, DEPT PATHOL, MONTREAL H3C 3J7, QUEBEC, CANADA
[3] INST CURIE, BIOL SECT, CNRS, URA 620, F-75231 PARIS 05, FRANCE
来源
CYTOGENETICS AND CELL GENETICS | 1992年 / 60卷 / 3-4期
关键词
D O I
10.1159/000133332
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
A method for the detection by electron microscopy of chromosome banding after in situ hybridization of small, nonradioactive DNA sequences is described. Typical high-resolution G-banding is produced by adding 5-bromodeoxyuridine (BrdU) during the last part of the S-phase and by applying a monoclonal antibody against the BrdU-substituted chromosome segments, followed by the addition of protein G, but no further treatment. A protocol for in situ hybridization of small, single-copy biotinylated DNA sequences and their detection by immunogold tagging on banded chromosomes is also described. This combined approach permits high-resolution mapping of small DNA sequences and should be useful in discriminating between neighboring DNA fragments.
引用
收藏
页码:187 / 189
页数:3
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