Zischler H, Hinkkanen A, Studer R
Max-Planck-Institut für Psychiatrie, Martinsried, Germany.
Electrophoresis. 1991 Feb-Mar;12(2-3):141-6. doi: 10.1002/elps.1150120208.
The first topic to be treated in this paper is the nonradioactive DNA fingerprinting by means of in-gel hybridization with digoxigenated (CAC)5. Besides the fact that time-consuming Southern blotting can be avoided, the dried agarose is an excellent matrix to produce background-free nonradioactive DNA fingerprints. There is no tendency of either the oligonucleotide probe or the antibody towards unspecific binding to the dried agarose. Prehybridization and blocking steps are therefore superfluous. Furthermore, we will discuss what effect the degree of crosslinking of the antibody-enzyme conjugates has. The second topic concerns the isolation and characterization of locus-specific probes from a human (CAC)5 fingerprint. The isolation and characterization of one variable probe, by screening complete genomic libraries, is described and discussed. This probe is compared to a hypervariable single-copy probe, isolated from a size-enriched genomic library. The sequence of the repeat flanking locus-specific probe is presented and a semi-specific, adaptor-mediated polymerase chain reaction was designed to amplify (CAC)n/(GTG)n flanking sequences.
本文要探讨的第一个主题是通过与地高辛标记的(CAC)5进行凝胶内杂交来进行非放射性DNA指纹分析。除了可以避免耗时的Southern印迹法这一事实外,干燥的琼脂糖是产生无背景非放射性DNA指纹的极佳基质。寡核苷酸探针或抗体都没有与干燥琼脂糖发生非特异性结合的倾向。因此,预杂交和封闭步骤是多余的。此外,我们将讨论抗体-酶偶联物的交联程度有何影响。第二个主题涉及从人类(CAC)5指纹中分离和鉴定位点特异性探针。描述并讨论了通过筛选完整基因组文库来分离和鉴定一个可变探针的过程。将该探针与从大小富集基因组文库中分离出的高可变单拷贝探针进行了比较。给出了位点特异性探针侧翼重复序列的序列,并设计了一种半特异性的、衔接子介导的聚合酶链反应来扩增(CAC)n/(GTG)n侧翼序列。