ABSTRACT

The identifi cation of plant genes by positional cloning is a lengthy process that requires a number of steps to be performed. Firstly, a mapping population must be constructed in which the gene of interest segregates in a genetically defi ned ratio. The mapping population can then be used to identify genetic markers linked to the locus of interest, enabling construction of a local genetic map. Conversion of the genetic map into a physical map requires a large-insert genomic library that can be used for chromosome walking or, as has become possible in recent years, the availability of a complete genome sequence. Finally, candidate genes identifi ed in the interval between the genetic markers most closely fl anking the locus of interest, must be tested by complementation to identify the functional gene.