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大肠杆菌的Chi序列与RecBC D酶

Chi and the RecBC D enzyme of Escherichia coli.

作者信息

Myers R S, Stahl F W

机构信息

Institute of Molecular Biology, University of Oregon, Eugene 97403-1229.

出版信息

Annu Rev Genet. 1994;28:49-70. doi: 10.1146/annurev.ge.28.120194.000405.

Abstract

The products of genes recB and recC are responsible for conjugal recombination and for the repair of chromosomal double chain breaks in Escherichia coli. The product of the recD gene, which combines with the RecB and RecC proteins to comprise the RecBCD enzyme, is not required for either recombination or repair. On the contrary, RecBCD enzyme is a potent exonuclease which inhibits recombination by destroying linear DNA. The RecD Ejection model supposes that RecBCD enzyme enters DNA at a double-chain end and travels destructively along the DNA until (typically) it encounters the recombination hotspot sequence chi. Chi then alters the RecBCD enzyme by weakening the affinity of the RecD subunit for the RecBC heterodimer. With the loss of the RecD subunit from the enzyme, the resulting protein, RecBC(D-), becomes deficient for exonuclease activity and proficient as a recombinagenic helicase. Thus, the RecD Ejection model proposes that chi participates in recombination by acting as a toggle to convert RecBCD (a powerful exonuclease) to RecBC(D-) (a recombinase). We review the properties of RecBCD and its cognate site chi, including recent results that support both the RecD Ejection model and the view that chi plays only an indirect role in recombination.

摘要

recB和recC基因的产物负责大肠杆菌中的接合重组以及染色体双链断裂的修复。recD基因的产物与RecB和RecC蛋白结合形成RecBCD酶,该产物对于重组或修复并非必需。相反,RecBCD酶是一种有效的核酸外切酶,它通过破坏线性DNA来抑制重组。RecD排出模型假定RecBCD酶从双链末端进入DNA,并沿着DNA进行破坏性移动,直到(通常)遇到重组热点序列chi。然后,chi通过削弱RecD亚基与RecBC异源二聚体的亲和力来改变RecBCD酶。随着RecD亚基从酶中丢失,产生的蛋白质RecBC(D-)核酸外切酶活性不足,但作为重组解旋酶却很有效。因此,RecD排出模型提出,chi通过作为一个切换开关将RecBCD(一种强大的核酸外切酶)转化为RecBC(D-)(一种重组酶)来参与重组。我们综述了RecBCD及其同源位点chi的特性,包括支持RecD排出模型以及chi在重组中仅起间接作用观点的最新研究结果。

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