van den Engh G, Sachs R, Trask B J
Human Genome Center, Lawrence Livermore National Laboratory, Livermore, CA 94550.
Science. 1992 Sep 4;257(5075):1410-2. doi: 10.1126/science.1388286.
The folding of chromatin in interphase cell nuclei was studied by fluorescent in situ sequences chromatin according to a random walk model. This model provides the basis for calculating the spacing of sequences along the linear DNA molecule from interphase distance measurements. An interphase mapping strategy based on this model was tested with 13 probes from a 4-megabase pair (Mbp) region of chromosome 4 containing the Huntington disease locus. The results confirmed the locations of the probes and showed that the remaining gap in the published maps of this region is negligible in size. Interphase distance measurements should facilitate construction of chromosome maps with an average marker density of one per 100 kbp, approximately ten times greater than that achieved by hybridization to metaphase chromosome. achieved by hybridization to metaphase chromosomes.
通过荧光原位序列染色质,依据随机游走模型研究了间期细胞核中染色质的折叠。该模型为根据间期距离测量计算沿线性DNA分子的序列间距提供了基础。基于此模型的间期作图策略,用来自包含亨廷顿病基因座的4号染色体400万碱基对(Mbp)区域的13个探针进行了测试。结果证实了探针的位置,并表明该区域已发表图谱中剩余的缺口在大小上可忽略不计。间期距离测量应有助于构建平均标记密度为每100千碱基对一个的染色体图谱,这大约是与中期染色体杂交所达到密度的十倍。通过与中期染色体杂交实现。