Wintle R F, Nygaard T G, Herbrick J A, Kvaløy K, Cox D W
Research Institute, The Hospital For Sick Children, Toronto, Ontario, Canada.
Genomics. 1997 Mar 15;40(3):409-14. doi: 10.1006/geno.1996.4572.
Subtelomeric regions of human chromosomes are the sites of increased meiotic recombination and have a male-to-female recombination ratio that is higher than elsewhere in the genome. We isolated two novel, polymorphic CA repeat markers from the distal part of the immunoglobulin heavy chain gene cluster, approximately 90 and 200 kb from the telomere of chromosome 14q. The 14q telomere was unambiguously located by physical mapping of telomeric YACs and Bal31 exonuclease digestion of genomic DNA. We then constructed haplotypes using genotype data from these markers and data from sCAW1 (D14S826) for use as a highly polymorphic genetic marker. Linkage analysis using the 40 pedigree CEPH reference panel and genotype data from these and other loci physically mapped to the terminal 1.5 Mb of chromosome 14q revealed an apparent increase in meiotic recombination within this region, relative to the average rate for the genome. Further, we found that recombination was higher in females than in males, indicating that the subtelomeric region of 14q differs from other human subtelomeric regions.
人类染色体的亚端粒区域是减数分裂重组增加的位点,其雄性与雌性的重组比率高于基因组中的其他区域。我们从免疫球蛋白重链基因簇的远端分离出两个新的多态性CA重复标记,距离14号染色体q臂端粒约90和200 kb。通过端粒YAC的物理图谱和基因组DNA的Bal31核酸外切酶消化,明确了14q端粒的位置。然后,我们利用这些标记的基因型数据以及sCAW1(D14S826)的数据构建单倍型,将其用作高度多态的遗传标记。使用40个家系的CEPH参考面板以及这些位点和其他物理定位到14号染色体q臂末端1.5 Mb区域的位点的基因型数据进行连锁分析,结果显示该区域内减数分裂重组相对于基因组平均速率明显增加。此外,我们发现雌性的重组率高于雄性,这表明14q的亚端粒区域与其他人类亚端粒区域不同。