Kere J, Nagaraja R, Mumm S, Ciccodicola A, D'Urso M, Schlessinger D
Department of Molecular Microbiology, Washington University School of Medicine, St. Louis, Missouri.
Genomics. 1992 Oct;14(2):241-8. doi: 10.1016/s0888-7543(05)80212-5.
Sequence-tagged sites (STSs) derived from end fragments of chromosome-specific yeast artificial chromosomes (YACs) can facilitate the assembly of an overlapping YAC/STS map. Contigs form rapidly by iteratively screening YAC collections with end-fragment STSs from YACs that have not yet been detected by any previous STS. The map is rendered rapidly useful during its assembly by incorporating supplementary STSs from genes and genetic linkage probes with known locations. Methods for the systematic development and testing of the end-fragments STSs are given here, and a group of 100 STSs is presented for the X chromosome. The mapping strategy is shown to be successful in simulations with portions of the X chromosome already largely mapped into overlapping YACs by other means.
从染色体特异性酵母人工染色体(YAC)末端片段衍生而来的序列标签位点(STS)有助于构建重叠的YAC/STS图谱。通过用来自尚未被任何先前STS检测到的YAC的末端片段STS反复筛选YAC文库,重叠群迅速形成。通过纳入来自已知位置的基因和遗传连锁探针的补充STS,该图谱在构建过程中迅速变得有用。本文给出了系统开发和测试末端片段STS的方法,并展示了一组针对X染色体的100个STS。在对X染色体部分区域的模拟中,该定位策略已被证明是成功的,这些区域已经通过其他方法大致定位到重叠的YAC中。