Barker D F, Fain P R
Department of Physiology, University of Utah Medical School, Salt Lake City 84108.
Genomics. 1993 Dec;18(3):712-6. doi: 10.1016/s0888-7543(05)80381-7.
New primer pair sequences specific for 25 loci in the Xp11-q22.1 region are described. Eighteen of the pairs span segments containing significant CA dinucleotide repeats, with 9 of these revealing polymorphisms of greater than 50% heterozygosity. Four of the CA-containing segments occur in probes previously reported to detect RFLPs, while the remaining 14 are from newly isolated clones. STSs were also developed for 7 other RFLP-only loci. All of these 25 STSs plus 11 other published STR markers have been fine-mapped with respect to chromosomal breakpoints, defining 15 subintervals in Xp11-Xq22. This map of 36 STSs, nearly all of which are associated with markers that are genetically mapped and/or highly polymorphic, will significantly aid efforts to construct a complete physical map of this region and to correlate it with the high-density genetic map.
本文描述了针对Xp11-q22.1区域中25个位点的新引物对序列。其中18对引物跨越含有显著CA二核苷酸重复序列的片段,其中9对显示出杂合度大于50%的多态性。4个含CA的片段出现在先前报道用于检测RFLP的探针中,其余14个来自新分离的克隆。还针对其他7个仅RFLP位点开发了STS。这25个STS以及其他11个已发表的STR标记均已根据染色体断点进行了精细定位,在Xp11-Xq22中定义了15个亚区间。这张包含36个STS的图谱,几乎所有STS都与经过遗传定位和/或高度多态的标记相关联,将极大地有助于构建该区域的完整物理图谱,并使其与高密度遗传图谱相关联。