Kwiatkowski D J, Henske E P, Weimer K, Ozelius L, Gusella J F, Haines J
Division of Experimental Medicine and Hematology-Oncology, Brigham and Women's Hospital, Boston, Massachusetts.
Genomics. 1992 Feb;12(2):229-40. doi: 10.1016/0888-7543(92)90370-8.
To construct a framework map of human chromosome 9 consisting of highly informative markers, we identified 36 cosmid clones from chromosome 9 that contained long GT repeat sequences. The cosmids were found to cluster on the long arm of the chromosome, particularly in the q32-34 region. Thirteen highly informative polymorphisms from 9q were identified, with median observed heterozygosity 0.75 and median calculated heterozygosity based upon allele frequencies of 0.75. These new GT repeat polymorphisms (D9S56, D9S58-67), as well as anchor GT polymorphisms for D9S15 (MCT112, 9q13), and ABL and ASS (both 9q34.1) were utilized to construct a linkage map of human 9q by the typing of the Venezuelan Reference Pedigree. Care was taken to avoid errors, including analysis of the data with CHROMLOOK and verification of all double crossover events detected within a 30 cM interval by repetition of the marker analysis. The map was generated using the MAPMAKER program. All positions in the resulting map are favored by odds of greater than 10(4):1. The map has a sex-averaged length of 90 cM (Kosambi function) with a single maximum intermarker recombination fraction of 26%. All other intermarker recombination fractions are less than 15%. As D9S15 is known to be closely linked to markers on proximal 9p, and ASS/ABL are in band 34.1, this set of GT polymorphisms spans the length of 9q and provides a useful panel for linkage analysis of disease genes to this region. The marker order was confirmed by in situ hybridization of the cosmid clones to metaphase spreads of normal human chromosomes, which indicated an excess of recombination in the telomeric region in comparison to centromeric 9q, in agreement with previous chiasmata distribution observations. Two spontaneous new mutations for these GT repeat markers were identified, giving an overall observed spontaneous mutation rate of 0.00045 per locus per gamete. Direct observation of new mutations has not been previously reported for dinucleotide polymorphisms, but the observed rate is consistent with frequencies observed for other VNTR polymorphisms.
为构建一张由高信息含量标记组成的人类9号染色体框架图,我们从9号染色体中鉴定出36个含有长GT重复序列的黏粒克隆。这些黏粒在染色体长臂上成簇分布,尤其集中在q32 - 34区域。从9q鉴定出13个高信息含量的多态性位点,观察到的杂合度中位数为0.75,基于等位基因频率计算出的杂合度中位数为0.75。利用这些新的GT重复多态性位点(D9S56、D9S58 - 67)以及D9S15(MCT112,9q13)、ABL和ASS(均位于9q34.1)的锚定GT多态性位点,通过对委内瑞拉参考家系进行分型来构建人类9q的连锁图谱。我们小心避免错误,包括使用CHROMLOOK分析数据以及通过重复标记分析来验证在30 cM区间内检测到的所有双交换事件。该图谱使用MAPMAKER程序生成。所得图谱中所有位置的优势比均大于10(4):1。该图谱的性别平均长度为90 cM(Kosambi函数),单个标记间最大重组率为26%。所有其他标记间重组率均小于15%。由于已知D9S15与9号染色体短臂近端的标记紧密连锁,且ASS/ABL位于34.1带,这组GT多态性位点跨越了9q的长度,为该区域疾病基因的连锁分析提供了一个有用的标记组。通过将黏粒克隆与正常人染色体中期铺展进行原位杂交,证实了标记顺序,这表明与9q着丝粒区域相比,端粒区域的重组过多,这与之前交叉分布的观察结果一致。鉴定出了这些GT重复标记的两个自发新突变,每个位点每个配子的总体观察到的自发突变率为0.00045。此前尚未有关于二核苷酸多态性新突变的直接观察报道,但观察到的突变率与其他VNTR多态性观察到的频率一致。