Münke M, Cox D R, Jackson I J, Hogan B L, Francke U
Cytogenet Cell Genet. 1986;42(4):236-40. doi: 10.1159/000132284.
Two probes derived from a mouse recombinant lambda-clone (H24.1), that contains a sequence closely homologous to the Drosophila antennapedia homeo box, were mapped to mouse chromosome (MMU) 11 by filter hybridization of somatic cell hybrid DNA. This sequence is highly homologous to a human homeo box gene (HOX2) and appears to represent one of the two genes in the Hox-2 cluster previously assigned to MMU 11. To regionally map the Hox-2 cluster, we have carried out in situ hybridization of the two H24.1 probes and of an independently isolated Hox-2 probe. The autoradiographic silver grain distributions were similar in all three experiments with a peak over band 11D. This region contains the locus for the tail-short (Ts) mutation which causes skeletal abnormalities in heterozygotes and early embryonic death in homozygotes.
从一个含有与果蝇触角足同源异型框序列紧密同源的小鼠重组λ克隆(H24.1)中获得的两个探针,通过体细胞杂种DNA的滤膜杂交被定位到小鼠11号染色体(MMU)上。该序列与一个人类同源异型框基因(HOX2)高度同源,并且似乎代表了先前定位到MMU 11上的Hox - 2基因簇中的两个基因之一。为了对Hox - 2基因簇进行区域定位,我们对两个H24.1探针以及一个独立分离的Hox - 2探针进行了原位杂交。在所有三个实验中,放射自显影片上银颗粒的分布相似,在11D带上方有一个峰值。该区域包含短尾(Ts)突变的基因座,该突变在杂合子中导致骨骼异常,在纯合子中导致早期胚胎死亡。