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The use of synthetic oligonucleotides as hybridization probes. II. Hybridization of oligonucleotides of mixed sequence to rabbit beta-globin DNA.

机译:合成寡核苷酸作为杂交探针的用途。二。混合序列的寡核苷酸与兔β-珠蛋白DNA的杂交。

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摘要

Two oligonucleotides 14-bases long were synthesized, one complementary to rabbit beta-globin DNA (R beta G14A) and the other with the same sequence except for a single base change (T for C) (R beta G14B). Hybridization conditions were established such that R beta G14A would hybridize to globin DNA while R beta G14B would not. We also synthesized a mixture of 13-base long oligonucleotides (R beta G13Mix), representing eight of the possible coding sequences for amino acids 15-19 of rabbit beta-globin. One of the eight is complementary to globin DNA. R beta G13Mix was found to hybridize specifically to globin DNA under conditions where oligonucleotides forming single base pair mismatches do not. Furthermore, R beta G13Mix was shown to hybridize specifically to colonies containing a plasmid with a globin DNA insert. These results are discussed with respect to a general procedure for screening recombinant clones for those containing DNA coding for a protein of known amino acid sequence.
机译:合成了两个长14个碱基的寡核苷酸,一个与兔β-珠蛋白DNA(R beta G14A)互补,另一个具有相同的序列,只是一个碱基的改变(对于C为T)(R beta G14B)。建立了杂交条件,使得R beta G14A将与球蛋白DNA杂交,而R beta G14B不会。我们还合成了13个碱基长的寡核苷酸(R beta G13Mix)的混合物,代表了兔β-珠蛋白的氨基酸15-19的八个可能的编码序列。八分之一与球蛋白DNA互补。发现R beta G13Mix在形成单碱基对错配的寡核苷酸不会发生杂交的条件下与球蛋白DNA特异性杂交。此外,显示R beta G13Mix与含有带有珠蛋白DNA插入物的质粒的菌落特异性杂交。关于筛选重组克隆以寻找含有编码已知氨基酸序列的蛋白质的DNA的通用克隆的一般程序,讨论了这些结果。

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