Speleman F, Van Camp G, Van Roy N
Department of Medical Genetics, University Hospital, Gent, Belgium.
Cytogenet Cell Genet. 1996;72(2-3):189-90. doi: 10.1159/000134185.
MYCL1 has been previously mapped to 1p32. This position was in contradiction with our mapping data of 1p deletions in neuroblastoma cell lines. Using FISH on high resolution R-banded chromosomes with a YAC clone for MYCL1 we were able to reassign the gene to subband 1p34.3. This new map position is of importance for the establishment of an integrated map for chromosome 1 and the search for disease genes in this region.
MYCL1基因先前被定位到1p32。这一位置与我们在神经母细胞瘤细胞系中对1p缺失的定位数据相矛盾。我们使用一个针对MYCL1的YAC克隆,在高分辨率R带染色体上进行荧光原位杂交(FISH),从而能够将该基因重新定位到1p34.3亚带。这个新的图谱位置对于构建1号染色体的整合图谱以及在该区域寻找疾病基因具有重要意义。