Starr T, Howell A M, McDowall J, Peters K, Rose A M
Department of Medical Genetics, University of British Columbia, Vancouver, Canada.
Genome. 1989 Jun;32(3):365-72. doi: 10.1139/g89-456.
We have isolated probes for DNA polymorphisms across the linkage group I gene cluster in Caenorhabditis elegans, using Tc1-linkage selection. The probes detect strain polymorphism between the wild-type strains of var. Bristol and var. Bergerac. As a result of mapping the sites hP4, hP5, hP6, hP7, hP9, and sPl, more than 1000 kilobases (kb) of cloned cosmid DNA has been positioned on the genetic map. We found there is more DNA per map unit in the center of the gene cluster than expected on the basis of the genomic average. Furthermore, the amount is not constant across the entire region but reaches a peak in the hP9 unc-13 interval. To find the coding regions, we examined DNA cross-homology between two species, Caenorhabditis elegans and Caenorhabditis briggsae. Approximately one-third of the DNA in the hP5 hP9 interval was examined for coding regions and 21 sequences were identified within 318 kb of DNA.
我们利用Tc1连锁选择法,分离出了秀丽隐杆线虫连锁群I基因簇中DNA多态性的探针。这些探针可检测布里斯托变种和贝热拉克变种野生型菌株之间的菌株多态性。通过对hP4、hP5、hP6、hP7、hP9和sP1位点进行定位,超过1000千碱基(kb)的克隆黏粒DNA已被定位到遗传图谱上。我们发现,基因簇中心每个图谱单位的DNA比基于基因组平均值预期的要多。此外,该数量在整个区域并不恒定,而是在hP9 unc-13区间达到峰值。为了找到编码区域,我们检测了秀丽隐杆线虫和布里格隐杆线虫这两个物种之间的DNA交叉同源性。在hP5 hP9区间大约三分之一的DNA中检测编码区域,并在318 kb的DNA内鉴定出21个序列。