Tamari M, Hamaguchi M, Shimizu M, Oshimura M, Takayama H, Kohno T, Yamaguchi N, Sugimura T, Terada M, Yokota J
National Cancer Center Research Institute, Tokyo, Japan.
Genomics. 1992 Jul;13(3):705-12. doi: 10.1016/0888-7543(92)90145-i.
To construct a panel of radiation hybrids (RHs) for human chromosome 3p mapping, mouse microcell hybrid cells, A9(neo3/t)-5, containing a single copy of human chromosome 3p with pSV2neo plasmid DNA integrated at 3p21-p22 were irradiated and fused to mouse A9 cells. A panel of 96 RHs that retain several sizes and portions of human chromosome 3p segments was used to map 25 DNA markers for chromosome 3p. Eight of them, H28, H29, H32, H33, H35, H38, H48, and H64, were cloned from Alu-primed PCR products using A9(neo3/t)-5 cell DNA as a template. The most likely order of the 24 markers, except for H28, based on the statistical ordering method proposed by Falk, was cen-D3S4-D3S3-D3S30-H29-D3S13-D3S2-+ ++H48-D3F15S2-D3S32-D3S23-CCK-H35-H33- D3S11-D3S12-RARB-THRB(ERBA2-pBH302)- H64-H38-RAF1-D3S18-H32-D3S22-pter. The order and location of these markers were in good agreement with those previously determined by other mapping methods, suggesting that a panel of these 96 RHs is a valuable source for a rapid mapping of human chromosome 3p markers.
为构建用于人类3号染色体短臂(3p)图谱绘制的辐射杂种细胞(RH)面板,对含有整合于3p21 - p22处的pSV2neo质粒DNA的单拷贝人类3号染色体短臂的小鼠微细胞杂种细胞A9(neo3/t)-5进行照射,并将其与小鼠A9细胞融合。使用保留了人类3号染色体短臂片段的多种大小和部分片段的96个RH细胞面板来对25个3号染色体短臂的DNA标记进行图谱绘制。其中8个标记,即H28、H29、H32、H33、H35、H38、H48和H64,是以A9(neo3/t)-5细胞DNA为模板从Alu引物PCR产物中克隆得到的。基于Falk提出的统计排序方法,除H28外的24个标记的最可能顺序为:着丝粒 - D3S4 - D3S3 - D3S30 - H29 - D3S13 - D3S2 - +++H48 - D3F15S2 - D3S32 - D3S23 - CCK - H35 - H33 - D3S11 - D3S12 - RARB - THRB(ERBA2 - pBH302) - H64 - H38 - RAF1 - D3S18 - H32 - D3S22 - 末端。这些标记的顺序和位置与先前通过其他图谱绘制方法确定的结果高度一致,表明这96个RH细胞面板是快速绘制人类3号染色体短臂标记图谱的宝贵资源。