Brockdorff N, Fisher E M, Cavanna J S, Lyon M F, Brown S D
Department of Biochemistry, St Mary's Hospital Medical School, London, UK.
EMBO J. 1987 Nov;6(11):3291-7. doi: 10.1002/j.1460-2075.1987.tb02648.x.
A large number of microclones obtained by microdissection of the mouse X chromosome have been mapped using an interspecific Mus domesticus/Mus spretus cross. Clones displaying close linkage to a number of loci of known phenotype but unknown gene product, such as mdx (X-linked muscular dystrophy), have been obtained. Over a central 30 cM span of the mouse X chromosome, 17 clones have been mapped and ordered at a sufficient density to contemplate the complete physical mapping of this region that will aid in the isolation of a number of unidentified genes. Some of the mapped microclones detect moderately repetitive sequences that were clustered in several discrete regions of the mouse X chromosome.
通过对小鼠X染色体进行显微切割获得的大量微克隆已利用家鼠/斯氏小家鼠种间杂交进行了定位。已获得了与许多已知表型但未知基因产物的基因座紧密连锁的克隆,例如mdx(X连锁型肌营养不良症)。在小鼠X染色体的中央30厘摩跨度范围内,17个克隆已被定位并以足够的密度排序,以便考虑对该区域进行完整的物理图谱绘制,这将有助于分离一些未鉴定的基因。一些已定位的微克隆检测到中等重复序列,这些序列聚集在小鼠X染色体的几个离散区域。