Janson M, Larsson C, Werelius B, Jones C, Glaser T, Nakamura Y, Jones C P, Nordenskjöld M
Department of Clinical Genetics, Karolinska Hospital, Stockholm, Sweden.
Proc Natl Acad Sci U S A. 1991 Dec 1;88(23):10609-13. doi: 10.1073/pnas.88.23.10609.
We have constructed a physical map of the region q12-13 on chromosome 11 by combining data generated from a panel of radiation-reduced somatic cell hybrids and pulsed-field gel electrophoresis (PFGE). Twenty different genetic markers have been sublocalized and ordered within this region and a total of 8.0 megabases has been mapped in detail using rare-cutting restriction endonucleases and PFGE. In two instances, the long-range restriction PFGE map spans the total distance between pairs of loci that have been previously mapped by genetic linkage in reference families. Comparison of this physical map with the available linkage map indicates a great variation in the recombination frequency over the region. The recombination rate is higher than expected, particularly for markers flanking the MEN1 region. Thus, for the closest pair of linked markers on the centromeric side, one centimorgan corresponds to approximately 300 kilobases, and for markers on the telomeric side, one centimorgan corresponds to approximately 350-600 kilobases.
我们通过整合来自一组辐射减少的体细胞杂种和脉冲场凝胶电泳(PFGE)产生的数据,构建了11号染色体上q12 - 13区域的物理图谱。20种不同的遗传标记已在该区域内进行了亚定位和排序,并且使用稀有切割限制性内切酶和PFGE详细绘制了总共8.0兆碱基的图谱。在两个实例中,长距离限制性PFGE图谱跨越了先前在参考家系中通过遗传连锁定位的基因座对之间的总距离。将此物理图谱与可用的连锁图谱进行比较表明,该区域的重组频率存在很大差异。重组率高于预期,特别是对于MEN1区域两侧的标记。因此,对于着丝粒侧最近的一对连锁标记,一个厘摩大约对应300千碱基,而对于端粒侧的标记,一个厘摩大约对应350 - 600千碱基。