Miki T, Takemoto Y, Nakura J, Endo Y, Ogihara T
Department of Geriatric Medicine, Osaka University Medical School, Japan.
Hum Cell. 1990 Dec;3(4):323-7.
For the purpose of cloning the gene of myotonic dystrophy (DM) using the technique of reverse genetics, we have introduced new methods such as microdissection, a YAC library and a Not I linking library and cloned many DNA fragments derived from the region of 19q13.2. Then we have assigned these to chromosome 19 by linkage map (CEPH families and linkage disequilibrium) and physical map (PFGE and in situ hybridization). Here we have described these methods.
为了利用反向遗传学技术克隆强直性肌营养不良(DM)基因,我们引入了诸如显微切割、YAC文库和Not I连接文库等新方法,并克隆了许多源自19q13.2区域的DNA片段。然后,我们通过连锁图谱(CEPH家系和连锁不平衡)和物理图谱(PFGE和原位杂交)将这些片段定位到19号染色体上。在此我们描述了这些方法。