Heyer W D
Institute of General Microbiology, Bern, Switzerland.
Experientia. 1994 Mar 15;50(3):223-33. doi: 10.1007/BF01924005.
Finding the right partner is a central problem in homologous recombination. Common to all models for general recombination is a homologous pairing and DNA strand exchange step. In prokaryotes this process has mainly been studied with the RecA protein of Escherichia coli. Two approaches have been used to find homologous pairing and DNA strand exchange proteins in eukaryotes. A biochemical approach has resulted in numerous proteins from various organisms. Almost all of these proteins are biochemically fundamentally different from RecA. The in vivo role of these proteins is largely not understood. A molecular-genetical approach has identified structural homologs to the E. coli RecA protein in the yeast Saccharomyces cerevisiae and subsequently in other organisms including other fungi, mammals, birds, and plants. The biochemistry of the eukaryotic RecA homologs is largely unsolved. For the fungal RecA homologs (S. cerevisiae RAD51, RAD55, RAD57, DMC1; Schizosaccharomyces pombe rad51; Neurospora crassa mei3) a role in homologous recombination and recombinational repair is evident. Besides recombination, homologous pairing proteins might be involved in other cellular processes like chromosome pairing or gene inactivation.
寻找合适的配对分子是同源重组中的核心问题。所有通用重组模型的共同之处在于同源配对和DNA链交换步骤。在原核生物中,这一过程主要是通过大肠杆菌的RecA蛋白进行研究的。在真核生物中,人们采用了两种方法来寻找同源配对和DNA链交换蛋白。生化方法已从各种生物体中鉴定出了众多蛋白质。几乎所有这些蛋白质在生化性质上都与RecA有根本差异。这些蛋白质在体内的作用在很大程度上尚不明确。分子遗传学方法已在酿酒酵母中鉴定出了与大肠杆菌RecA蛋白结构同源的分子,随后在包括其他真菌、哺乳动物、鸟类和植物在内的其他生物体中也有发现。真核生物RecA同源物的生物化学性质在很大程度上尚未得到解决。对于真菌RecA同源物(酿酒酵母RAD51、RAD55、RAD57、DMC1;粟酒裂殖酵母rad51;粗糙脉孢菌mei3),其在同源重组和重组修复中的作用是显而易见的。除了重组之外,同源配对蛋白可能还参与其他细胞过程,如染色体配对或基因失活。