Kotani H, Germann M W, Andrus A, Vinayak R, Mullah B, Kmiec E B
Department of Pharmacology, Jefferson Cancer Center, Thomas Jefferson University, Philadelphia, Pennsylvania 19107, USA.
Mol Gen Genet. 1996 Mar 20;250(5):626-34. doi: 10.1007/BF02174450.
The RecA protein of Escherichia coli catalyzes homologous pairing and strand exchange between a wide range of molecules showing nucleotide sequence complementarity, including a linear duplex and a single-stranded DNA molecule. We demonstrate that RecA can promote formation of joint molecules when the duplex contains an RNA/DNA hairpin and a single-stranded circle serves as the pairing partner. A chimeric RNA/DNA hairpin can be used to form stable joint molecules with as little as 15 bases of shared homology as long as the RNA stretch contains complementarity to the circle. The joint molecule bears some resemblance to a triple helical structure composed of RNA residues surrounded by two DNA strands which are in a parallel orientation. Evidence is presented that supports the notion that short stretches of RNA can be used in homologous pairing reactions at lengths below that required for DNA-DNA heteroduplex formation.
大肠杆菌的RecA蛋白催化多种具有核苷酸序列互补性的分子之间的同源配对和链交换,包括线性双链体和单链DNA分子。我们证明,当双链体包含RNA/DNA发夹且单链环作为配对伙伴时,RecA可以促进接头分子的形成。嵌合的RNA/DNA发夹可用于形成稳定的接头分子,只要RNA片段与环具有互补性,共享同源性低至15个碱基即可。接头分子与由两条平行取向的DNA链包围的RNA残基组成的三螺旋结构有些相似。有证据支持这样的观点,即短片段的RNA可用于同源配对反应,其长度低于DNA-DNA异源双链体形成所需的长度。