Stanyon Roscoe, Stone Gary
Dipartimento di Biologia Animale e Genetica, Florence University, Firenze, Italy.
Methods Mol Biol. 2008;422:13-29. doi: 10.1007/978-1-59745-581-7_2.
Chromosome sorting by flow cytometry is the principle source of chromosome-specific DNA not only for chromosome painting, but also for many other types of genomic analysis such as library construction, discovery and isolation of genes, chromosome specific direct DNA selection, and array painting. Chromosome sorting coupled with chromosome painting is a rapid method for global phylogenomic comparisons. These two techniques have made notable contributions to our knowledge of the evolution of the mammalian genome. The flow sorting of multiple species allows reciprocal painting and permits the delineation of subchromosomal homology and the definition of chromosomal breakpoints. Chromosomes are valuable phylogenetic makers because rearrangements that become fixed at the species level are considered rare events and apparently tightly bound to the speciation process. This chapter covers the preparation of a single chromosome suspension from cell cultures, bivariate chromosome flow sorting, preparation of chromosome paints by degenerate oligonucleotide primed-PCR and the fluorescence in-situ hybridization and detection of whole chromosome specific probes.
通过流式细胞术进行染色体分选不仅是用于染色体涂染的染色体特异性DNA的主要来源,也是用于许多其他类型基因组分析的主要来源,如文库构建、基因的发现与分离、染色体特异性直接DNA选择和阵列涂染。染色体分选与染色体涂染相结合是进行全球系统发育基因组比较的快速方法。这两种技术为我们了解哺乳动物基因组的进化做出了显著贡献。对多个物种进行流式分选可实现相互涂染,并允许描绘亚染色体同源性和定义染色体断点。染色体是有价值的系统发育标记,因为在物种水平上固定下来的重排被认为是罕见事件,并且显然与物种形成过程紧密相关。本章涵盖了从细胞培养物中制备单染色体悬液、双变量染色体流式分选、通过简并寡核苷酸引物PCR制备染色体涂染探针以及全染色体特异性探针的荧光原位杂交和检测。