Weiffenbach B, Falls K, Bricker A, Hall L, McMahon J, Wasmuth J, Funanage V, Donis-Keller H
Collaborative Research, Inc., Bedford, Massachusetts 01730.
Genomics. 1991 May;10(1):173-85. doi: 10.1016/0888-7543(91)90498-4.
A genetic map of human chromosome 5 that contains 60 restriction fragment length polymorphism (RFLP) loci in one linkage group has been constructed. Segregation data using these markers and 40 large multigenerational families supplied by the Centre d'Etude du Polymorphisme Humain have been collected. Linkage analyses were performed with the program package CRI-MAP; using odds greater than 1000:1, 30 RFLP loci could be placed on the map. This genetic map spans 289 cM sex-equal, 353 cM in females, and 244 cM in males. While the relative rate of recombination for female meioses is nearly twice that of males over much of the chromosome, several instances of statistically significant excess male recombination were observed. The order of probes on the genetic map has been confirmed by their physical order as determined by somatic cell hybrid lines containing deletions of normal chromosome 5. There is concordance between the physical positions of markers and their genetic positions. Our most distal probes on the genetic map are cytologically localized to the most distal portions of the chromosome. This suggests that our genetic map spans most of chromosome 5.
构建了人类5号染色体的遗传图谱,该图谱在一个连锁群中包含60个限制性片段长度多态性(RFLP)位点。利用这些标记以及由人类多态性研究中心提供的40个大型多代家庭的分离数据已被收集。使用CRI-MAP程序包进行连锁分析;在比值大于1000:1的情况下,30个RFLP位点可被定位到该图谱上。这个遗传图谱在性别均等时跨度为289厘摩,女性为353厘摩,男性为244厘摩。虽然在染色体的大部分区域,女性减数分裂的相对重组率几乎是男性的两倍,但也观察到了几例男性重组在统计学上显著过量的情况。遗传图谱上探针的顺序已通过含有正常5号染色体缺失的体细胞杂种系所确定的物理顺序得到证实。标记的物理位置与其遗传位置之间存在一致性。我们在遗传图谱上最远端的探针在细胞学上定位于染色体的最远端部分。这表明我们的遗传图谱覆盖了5号染色体的大部分区域。