Sanchez-Moran Eugenio, Santos Juan-Luis, Jones Gareth H, Franklin F Christopher H
School of Biosciences, University of Birmingham, Birmingham B15 2TT, United Kingdom.
Genes Dev. 2007 Sep 1;21(17):2220-33. doi: 10.1101/gad.439007.
ASY1 is an Arabidopsis protein required for synapsis and crossover formation during meiosis. The chronology of meiotic recombination has been investigated in wild type and an asy1 mutant. We observe a delay between the appearance of chromatin-associated AtSPO11-1 foci and DNA double-strand break (DSB) formation, which occurs contemporaneously with chromosome axis formation and transition of ASY1 from chromatin-associated foci to a linear axis-associated signal. DSBs are formed independently of ASY1 in an AtSPO11-1-dependent manner. They are partially restored in Atspo11-1-3 using cisplatin, but their control appears abnormal. Axis morphogenesis is independent of ASY1, but axis structure may be compromised in asy1. Localization of the strand exchange proteins AtRAD51 and AtDMC1 to the chromatin occurs asynchronously shortly after DSB formation, with AtDMC1 localizing in advance of AtRAD51. In wild-type nuclei, both recombinases form numerous foci that persist for approximately 12 h before gradually decreasing in number. In asy1, initial localization of AtDMC1 is normal, but declines abruptly such that interhomolog recombination is severely compromised. Limited ASY1-independent, DMC1-dependent interhomolog recombination remains, but appears restricted to subtelomeric sequences where the homologs are fortuitously in proximity. Thus, ASY1 plays a key role in coordinating the activity of the RecA homologs to create a bias in favor of interhomolog recombination.
ASY1是拟南芥减数分裂过程中配对和交叉形成所必需的一种蛋白质。我们已经在野生型和asy1突变体中研究了减数分裂重组的时间顺序。我们观察到染色质相关的AtSPO11-1焦点出现与DNA双链断裂(DSB)形成之间存在延迟,DSB形成与染色体轴形成以及ASY1从染色质相关焦点向线性轴相关信号的转变同时发生。DSB以依赖AtSPO11-1的方式独立于ASY1形成。在Atspo11-1-3中使用顺铂可部分恢复DSB,但对其控制似乎异常。轴形态发生独立于ASY1,但asy1中的轴结构可能受损。链交换蛋白AtRAD51和AtDMC1在DSB形成后不久异步定位于染色质,AtDMC1比AtRAD51提前定位。在野生型细胞核中,两种重组酶都形成大量焦点,这些焦点持续约12小时,然后数量逐渐减少。在asy1中,AtDMC1的初始定位正常,但会突然下降,导致同源染色体间重组严重受损。仍然存在有限的不依赖ASY1、依赖DMC1的同源染色体间重组,但似乎仅限于同源染色体偶然靠近的亚端粒序列。因此,ASY1在协调RecA同源物的活性以产生有利于同源染色体间重组的偏向中起关键作用。