Kirkilionis A J, Gregory C A, Hamerton J L
Department of Human Genetics, University of Manitoba, Winnipeg, Canada.
Genomics. 1991 Mar;9(3):524-35. doi: 10.1016/0888-7543(91)90420-j.
In an attempt to elucidate the relationship between genetic alterations at chromosomal bands 15q11.2-12 and the Prader-Willi syndrome (PWS), we have constructed a long-range restriction map of this region using a combination of pulsed-field gel techniques and the infrequently cutting restriction enzymes NotI, MluI, SalI, SfiI, NruI, SacII, and BssHII. Four previously reported probes mapping to 15q11.2-12 and known to be deleted in PWS patients were used to construct the physical map of this region. The loci recognized by these four probes have been localized to a 2600-kb partial SalI restriction fragment and a 3200-kb partial EcoRI restriction fragment. Linkage studies were performed on nine families to estimate the recombination rates between these loci. The calculated lod scores did not indicate significant linkage between any of the four loci. The contrast between the physical distance and the observed recombination frequency suggests that these four loci are located in a recombinational "hot spot."
为了阐明染色体带15q11.2 - 12处的基因改变与普拉德 - 威利综合征(PWS)之间的关系,我们使用脉冲场凝胶技术以及稀有切割限制酶NotI、MluI、SalI、SfiI、NruI、SacII和BssHII构建了该区域的长程限制酶切图谱。使用四个先前报道的定位于15q11.2 - 12且已知在PWS患者中缺失的探针来构建该区域的物理图谱。这四个探针识别的基因座已定位到一个2600 kb的部分SalI限制片段和一个3200 kb的部分EcoRI限制片段。对九个家系进行了连锁研究,以估计这些基因座之间的重组率。计算得到的连锁对数并未表明这四个基因座中的任何一个之间存在显著连锁。物理距离与观察到的重组频率之间的差异表明这四个基因座位于一个重组“热点”区域。