Gillespie G A, Germino G G, Somlo S, Weinstat-Saslow D, Breuning M H, Reeders S T
Yale University School of Medicine, New Haven, CT.
Nucleic Acids Res. 1990 Dec 11;18(23):7071-5. doi: 10.1093/nar/18.23.7071.
The locus responsible for the most common form of autosomal dominant polycystic kidney disease (PKD1) is located on chromosome 16p13.3. Genetic mapping studies indicate that PKD1 is flanked on the proximal side by the DNA marker 26.6 (D16S125). Here we show that 26.6 has undergone a locus duplication and that the two loci are less than 150kb apart. One of the two loci contains a polymorphic TaqI site that has been used in genetic studies and represents the proximal boundary for the PKD1 locus. We demonstrate that the polymorphic locus is the more proximal of the two 26.6-hybridizing loci. Therefore, four cosmids isolated from the distal 26.6-hybridizing locus contain candidate sequences for the PKD1 gene. These cosmids were found to contain two CpG islands that are likely markers for transcribed regions. A third CpG island was detected and cloned by directional chromosome jumping.
导致最常见的常染色体显性多囊肾病(PKD1)的基因座位于16号染色体的16p13.3区域。基因图谱研究表明,PKD1基因座近端侧翼为DNA标记26.6(D16S125)。我们在此表明,26.6发生了基因座重复,且两个基因座相距不到150kb。两个基因座之一含有一个多态性TaqI位点,该位点已用于基因研究,并代表PKD1基因座的近端边界。我们证明该多态性基因座是两个与26.6杂交的基因座中更靠近近端的那个。因此,从远端与26.6杂交的基因座分离出的四个黏粒含有PKD1基因的候选序列。发现这些黏粒包含两个可能是转录区域标记的CpG岛。通过定向染色体跳跃检测并克隆到了第三个CpG岛。