Cooper D N, Niemann S C, Gosden J R, Mitchell A R, Goate A M, Rajendran G S, Miller D A, Lim L, Schmidtke J
Hum Genet. 1987 Feb;75(2):129-35. doi: 10.1007/BF00591073.
A human genomic DNA fragment, pAM37 (HGM8; D21S22), was mapped to chromosome 21q2.1-q2.21 by in situ hybridization. This segment is therefore situated on the boundary of the "pathological region" of Down syndrome. A genomic restriction map encompassing 35 kb of chromosome 21 was derived and two restriction fragment length polymorphisms (RFLPs) were mapped and characterized. A homologous sequence was detected in the mouse genome but no homologous RNA was detected in a range of human tissues. This DNA segment will contribute to the linkage mapping of chromosome 21 and will facilitate delineation of the pathological region of Down syndrome.
一个人类基因组DNA片段pAM37(HGM8;D21S22)通过原位杂交被定位到21号染色体的21q2.1 - q2.21区域。因此,该片段位于唐氏综合征“病理区域”的边界上。构建了一个包含21号染色体35 kb的基因组限制性图谱,并对两个限制性片段长度多态性(RFLP)进行了定位和特征分析。在小鼠基因组中检测到了同源序列,但在一系列人类组织中未检测到同源RNA。该DNA片段将有助于21号染色体的连锁图谱绘制,并有助于划定唐氏综合征的病理区域。