Gusella J, Varsanyi-Breiner A, Kao F T, Jones C, Puck T T, Keys C, Orkin S, Housman D
Proc Natl Acad Sci U S A. 1979 Oct;76(10):5239-42. doi: 10.1073/pnas.76.10.5239.
Cloned DNA probes were used in combination with a panel of five hybrid cell clones containing a series of different terminal deletions in human chromosome 11 to map precisely the human hemoglobin beta and delta chain structural genes contained on this chromosome. The region of deletion in each clone of the panel has been defined by biochemical, immunologic, and cytogenetic markers. DNA from clones containing successively larger terminal deletions was tested with appropriate DNA probes to determine the point on the chromosome at which DNA for these two closely linked hemoglobin genes is deleted. These genes, and by inference the closely linked G gamma and A gamma globin genes as well, have been assigned to the intraband region 11p1205 leads to 11p1208 on the short arm of chromosome 11, an interval containing approximately 4500 kilobases of DNA. The approach appears to have potential for even greater resolution and reasonably wide applicability for gene mapping.
克隆的DNA探针与一组五个杂交细胞克隆相结合使用,这些克隆包含人类11号染色体上一系列不同的末端缺失,以精确绘制该染色体上包含的人类血红蛋白β和δ链结构基因图谱。该组中每个克隆的缺失区域已通过生化、免疫和细胞遗传学标记进行了定义。用适当的DNA探针检测含有连续更大末端缺失的克隆的DNA,以确定染色体上这两个紧密连锁的血红蛋白基因的DNA被缺失的点。这些基因,以及由此推断出的紧密连锁的Gγ和Aγ珠蛋白基因,已被定位到11号染色体短臂上的带内区域11p1205至11p1208,该区间包含约4500千碱基的DNA。这种方法似乎具有实现更高分辨率的潜力,并且在基因图谱绘制方面具有相当广泛的适用性。