Atchison L, Cannizzaro L, Caamano J, Atchison M, Comis R L
Fox Chase Cancer Center, Department of Medical Oncology, Philadelphia, Pennsylvania 19111.
Genomics. 1990 Mar;6(3):441-50. doi: 10.1016/0888-7543(90)90474-9.
Thirty-five single-copy and 17 repetitive sequence DNA probes specific for human chromosome 3 were isolated from human chromosome 3-derived genomic libraries. Seven DNA clones, including three that are polymorphic for BglII or MspI, were mapped by in situ hybridization. Four probes were mapped to 3p subregions and 3 were mapped to 3q subregions. Three of the DNA sequences map to regions overlapping a segment of chromosome 3 (3p14-23) frequently deleted in small cell lung cancer cells. By Southern blot analysis on a deletion hybrid panel, we previously mapped 6 of these probes to three distinct chromosome 3 subregions. Our in situ data support these assignments and more precisely determine the localization of each clone to the following regions: D3S34 (3p14-21), D3S35 (3p21), D3S39 (3p21), D3S40 (3p12-13), D3S37 (3q21-23), and D3S36 (3q21). Clone pL84c, a low repeat sequence clone (approximately 30 copies), was mapped to the 3q21-29 subregion. These DNA clones mapped by in situ hybridization can provide useful landmarks for the ordering and localization of other clones.
从源自人类 3 号染色体的基因组文库中分离出 35 个单拷贝和 17 个针对人类 3 号染色体的重复序列 DNA 探针。通过原位杂交对 7 个 DNA 克隆进行了定位,其中包括 3 个对 BglII 或 MspI 呈多态性的克隆。4 个探针定位于 3p 亚区域,3 个定位于 3q 亚区域。其中 3 个 DNA 序列定位于与小细胞肺癌细胞中经常缺失的 3 号染色体片段(3p14 - 23)重叠的区域。通过对缺失杂交细胞系进行 Southern 印迹分析,我们之前将其中 6 个探针定位于 3 号染色体的三个不同亚区域。我们的原位杂交数据支持这些定位,并更精确地确定了每个克隆在以下区域的定位:D3S34(3p14 - 21)、D3S35(3p21)、D3S39(3p21)、D3S40(3p12 - 13)、D3S37(3q21 - 23)和 D3S36(3q21)。克隆 pL84c 是一个低重复序列克隆(约 30 个拷贝),定位于 3q21 - 29 亚区域。通过原位杂交定位的这些 DNA 克隆可为其他克隆的排序和定位提供有用的标记。