Direct labelling of BAC-DNA by rolling-circle amplification

被引：21

作者：

Berr, A ^{[1
]}

Schubert, I ^{[1
]}

机构：

[1] Inst Plant Genet & Crop Plant Res, D-06466 Gatersleben, Germany

来源：

PLANT JOURNAL | 2006年 / 45卷 / 05期

关键词：

rolling-circle amplification; BAC labelling; chromosome painting; FISH;

D O I：

10.1111/j.1365-313X.2005.02637.x

中图分类号：

Q94 [植物学];

学科分类号：

071001 ;

摘要：

Efficient amplification and labelling of probes are crucial for successful sequence detection by fluorescent in situ hybridization (FISH). In particular, chromosome painting to visualize chromosome segments or entire chromosomes by FISH requires large amounts of probes derived from extended templates. There are a number of techniques for probe labelling. The most widespread is nick translation, based on the replicational incorporation of modified nucleotides. Here we demonstrate successful rolling-circle amplification (RCA) of very low amounts of long circular template sequences (single bacterial artificial chromosomes (BACs) or pools of BACs). The amplicons were suitable for labelling by nick translation and subsequent FISH. A novel achievement is the use of RCA for simultaneous amplification and labelling of single BACs or BAC pools in a labour- and cost-effective manner.

引用

页码：857 / 862

页数：6

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