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Examination of an inverted repeat within the F factor origin of transfer: context dependence of F TraL relaxase DNA specificity

机译:F因子转移起点内反向重复序列的检查:F TraL松弛酶DNA特异性的背景依赖性

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Prior to conjugative transfer of plasmids, one plasmid strand is cleaved in a site- and strand-specific manner by an enzyme called a relaxase or nickase. In F and related plasmids, an inverted repeat is located near the plasmid strand cleavage site, and others have proposed that the ability of this sequence to form a hairpin when in single-stranded form is important for transfer. Substitutions were introduced into a cloned F oriT region and their effects on plasmid transfer were assessed. For those substitutions that substantially reduced transfer, the results generally correlated with effects on in vitro binding of oligonucleotides to the F TraI relaxase domain rather than with predicted effects on hairpin formation. One substitution shown previously to dramatically reduce both plasmid transfer and in vitro binding to a 17-base oligonucleotide had little apparent effect on binding to a 30-base oligonucleotide that contained the hairpin region. Results from subsequent experiments strongly suggest that the relaxase domain can bind to hairpin oligonucleotides in two distinct manners with different sequence specificities, and that the protein binds the oligonucleotides at the same or overlapping sites.
机译:在共轭转移质粒之前,一条质粒链被一种称为松弛酶或切口酶的酶以位点和链特异性方式切割。在F和相关质粒中,反向重复位于质粒链切割位点附近,并且其他人提出,当以单链形式存在时,该序列形成发夹的能力对于转移很重要。将取代基引入克隆的F oriT区,并评估其对质粒转移的影响。对于那些显着减少转移的取代,结果通常与寡核苷酸与F TraI松弛酶结构域的体外结合作用有关,而不与对发夹形成的预期作用有关。先前显示的一种取代可显着减少质粒转移和与17个碱基的寡核苷酸的体外结合,对与包含发夹区的30个碱基的寡核苷酸的结合几乎没有明显的影响。后续实验的结果强烈表明,松弛酶结构域可以以两种不同的方式以不同的序列特异性与发夹寡核苷酸结合,并且该蛋白质在相同或重叠的位点结合寡核苷酸。

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