a method for rapid and simultaneous mapping of genetic loci and introgression sizes in nematode species方法快速、同步映射在线虫物种基因位点和基因渗入的大小.pdfVIP
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a method for rapid and simultaneous mapping of genetic loci and introgression sizes in nematode species方法快速、同步映射在线虫物种基因位点和基因渗入的大小
A Method for Rapid and Simultaneous Mapping of
Genetic Loci and Introgression Sizes in Nematode
Species
Cheung Yan, Yu Bi, Da Yin, Zhongying Zhao*
Department of Biology, Faculty of Science, Hong Kong Baptist University, Hong Kong, China
Abstract
Caenorhabditis briggsae is emerging as an attractive model organism not only in studying comparative biology against C.
elegans, but also in developing novel experimentation avenues. In particular, recent identification of a new Caenorhabditis
species, C. sp.9 with which it can mate and produce viable progeny provides an opportunity for studying the genetics of
hybrid incompatibilities (HI) between the two. Mapping of a specific HI locus demands repeated backcrossing to get hold of
the specific genomic region underlying an observed phenotype. To facilitate mapping of HI loci between C. briggsae and C.
sp.9, an efficient mapping method and a genetic map ideally consisting of dominant markers are required for systematic
introgression of genomic fragments between the two species. We developed a fast and cost-effective method for high
throughput mapping of dominant loci with resolution up to 1 million bps in C. briggsae. The method takes advantage of the
introgression between C. briggsae and C. sp.9 followed by PCR genotyping using C. briggsae specific primers. Importantly,
the mapping results can not only serve as an effective way for estimating the chromosomal position of a genetic locus in C.
briggsae, but also provides size information for the introgression fragment in an otherwise C. sp.9 background. In addition, it
also helps generate introgression line as a side-product that is invaluable for the subsequent mapping of HI loci. The
method will greatly facilitate the construction of a genetic map consisting of dominant markers and pave the way for
systematic isolation of HI loci
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