Gilliam T C, Healey S T, MacDonald M E, Stewart G D, Wasmuth J J, Tanzi R E, Roy J C, Gusella J F
Nucleic Acids Res. 1987 Feb 25;15(4):1445-58. doi: 10.1093/nar/15.4.1445.
We have identified and characterized 40 DNA probes detecting restriction fragment length polymorphism (RFLP) on human chromosome 4. Single copy human clones were isolated from a bacteriophage library enriched for chromosome 4 sequences. Each clone was hybridized to somatic cell hybrid DNAs for verification of its species and chromosomal origin and for regional localization. Sequences specific for chromosome 4 were tested for their ability to detect RFLPs in human DNA and their potential utility as genetic markers was assessed. Approximately 263,000 base pairs or 0.13% of the chromosome was screened for sequence variation. The estimate of heterozygosity calculated from this large body of data, H = 0.0021, indicates that the degree of sequence variation on chromosome 4 is comparable to other autosomes. The characterization of these 40 markers has tripled the number of polymorphic loci available for linkage studies on chromosome 4, making it feasible to begin construction of a detailed linkage map that will span the entire chromosome.
我们已经鉴定并表征了40种可检测人类4号染色体上限制性片段长度多态性(RFLP)的DNA探针。从富含4号染色体序列的噬菌体文库中分离出单拷贝人类克隆。每个克隆都与体细胞杂种DNA杂交,以验证其物种和染色体来源以及进行区域定位。测试了4号染色体特异性序列检测人类DNA中RFLP的能力,并评估了它们作为遗传标记的潜在用途。对约263,000个碱基对或该染色体的0.13%进行了序列变异筛选。根据大量数据计算出的杂合度估计值H = 0.0021,表明4号染色体上的序列变异程度与其他常染色体相当。这40个标记的表征使可用于4号染色体连锁研究的多态性位点数量增加了两倍,从而使得开始构建覆盖整个染色体的详细连锁图谱成为可能。