Bancroft I, Westphal L, Schmidt R, Dean C
AFRC, IPSR, Cambridge Laboratory, John Innes Centre, Colney, Norwich, UK.
Nucleic Acids Res. 1992 Dec 11;20(23):6201-7. doi: 10.1093/nar/20.23.6201.
The cleavage patterns of 23 rare-cutting restriction endonucleases (rcREs) on high molecular weight DNA, isolated from leaves of Arabidopsis thaliana (Arabidopsis), have been analysed using pulsed field gel electrophoresis (PFGE). The DNA digested with rcREs can be used for restriction fragment length polymorphism (RFLP) analysis. We show that RFLPs are more readily identified in restriction fragments that require resolution by PFGE than in smaller restriction fragments. Taking advantage of the low dispersed repetitive DNA content of the Arabidopsis genome, whole yeast artificial chromosomes (YACs) were used as probes to PFGE resolved genomic DNA. This enabled whole YAC clones to be used as RFLP markers and long range restriction maps to be constructed. These techniques should enhance the analysis of regions of the genome of Arabidopsis (and other organisms with low levels of dispersed repetitive DNA) that are the subject of chromosome walking strategies to isolate particular loci.
利用脉冲场凝胶电泳(PFGE)分析了从拟南芥叶片中分离出的高分子量DNA上23种稀有切割限制内切酶(rcREs)的切割模式。用rcREs消化的DNA可用于限制性片段长度多态性(RFLP)分析。我们发现,与较小的限制性片段相比,在需要通过PFGE进行分辨率分析的限制性片段中更容易鉴定出RFLP。利用拟南芥基因组中低分散重复DNA的含量,将完整的酵母人工染色体(YACs)用作PFGE解析基因组DNA的探针。这使得完整的YAC克隆能够用作RFLP标记,并构建长程限制图谱。这些技术应能加强对拟南芥(以及其他具有低水平分散重复DNA的生物)基因组区域的分析,这些区域是通过染色体步移策略分离特定基因座的研究对象。