Gardiner K, Horisberger M, Kraus J, Tantravahi U, Korenberg J, Rao V, Reddy S, Patterson D
Eleanor Roosevelt Institute for Cancer Research, Denver, CO.
EMBO J. 1990 Jan;9(1):25-34. doi: 10.1002/j.1460-2075.1990.tb08076.x.
Human chromosome 21 has been analyzed by pulsed-field gel electrophoresis using somatic cell hybrids containing limited regions of the chromosome and greater than 60 unique sequence probes. Thirty-three independent NotI fragments have been identified, totalling 43 million bp. This must account for essentially the entire long arm, and therefore gaps remaining in the map must be small. The extent of the pulsed-field map has allowed the direct correlation of the physical map with the cytogenetic map: translocation breakpoints can be unambiguously positioned along the long arm and the distances between them measured in base pairs. Three breakpoints have been identified, providing physical confirmation of cytogenetic landmarks. Information on sequence organization has been obtained: (i) 60% of the unique sequence probes are located within 11 physical linkage groups which can be contained in only 20% of the long arm; (ii) 9/21 genes are clustered within 4%; (iii) translocation breakpoints appear to occur within CpG island regions, making their identification difficult by pulsed-field techniques. This analysis contributes to the human genome mapping effort, and provides information to guide the rapid investigation of the biology of chromosome 21.
利用含有该染色体有限区域的体细胞杂种和60多个独特序列探针,通过脉冲场凝胶电泳对人类21号染色体进行了分析。已鉴定出33个独立的NotI片段,总计4300万碱基对。这必定基本上涵盖了整个长臂,因此图谱中剩余的缺口必定很小。脉冲场图谱的范围使得物理图谱与细胞遗传学图谱能够直接关联:易位断点可沿长臂明确定位,并且可以测量它们之间以碱基对为单位的距离。已鉴定出三个断点,为细胞遗传学标记提供了物理验证。已获得有关序列组织的信息:(i)60%的独特序列探针位于11个物理连锁群内,这些连锁群仅占长臂的20%;(ii)21个基因中的9个聚集在4%的范围内;(iii)易位断点似乎出现在CpG岛区域内,这使得通过脉冲场技术对其进行鉴定变得困难。该分析有助于人类基因组图谱绘制工作,并为指导对21号染色体生物学的快速研究提供信息。