Kano Shungo, Satoh Nori, Sordino Paolo
Laboratory of Biochemistry and Molecular Biology, Stazione Zoologica A. Dohrn, Naples 80121, Italy.
Zoolog Sci. 2006 Jan;23(1):31-9. doi: 10.2108/zsj.23.31.
For whole-genome analysis in a basal chordate (protochordate), we used F1 pseudo-testcross mapping strategy and amplified fragment length polymorphism (AFLP) markers to construct primary linkage maps of the ascidian tunicate Ciona intestinalis. Two genetic maps consisted of 14 linkage groups, in agreement with the haploid chromosome number, and contained 276 and 125 AFLP loci derived from crosses between British and Neapolitan individuals. The two maps covered 4218.9 and 2086.9 cM, respectively, with an average marker interval of 16.1 and 18.9 cM. We observed a high recombinant ratio, ranging from 25 to 49 kb/cM, which can explain the high degree of polymorphism in this species. Some AFLP markers were converted to sequence tagged sites (STSs) by sequence determination, in order to create anchor markers for the fragmental physical map. Our recombination tools provide basic knowledge of genetic status and whole genome organization, and genetic markers to assist positional cloning in C. intestinalis.
为了对一种基础脊索动物(原索动物)进行全基因组分析,我们采用了F1伪测交定位策略和扩增片段长度多态性(AFLP)标记来构建海鞘Ciona intestinalis的初级连锁图谱。两个遗传图谱由14个连锁群组成,与单倍体染色体数目一致,包含来自英国个体和那不勒斯个体杂交产生的276个和125个AFLP位点。这两个图谱分别覆盖4218.9和2086.9厘摩,平均标记间隔为16.1和18.9厘摩。我们观察到较高的重组率,范围为25至49千碱基/厘摩,这可以解释该物种的高度多态性。通过序列测定将一些AFLP标记转化为序列标签位点(STS),以便为片段物理图谱创建锚定标记。我们的重组工具提供了遗传状态和全基因组组织的基础知识,以及有助于C. intestinalis中定位克隆的遗传标记。