Graduate School of Bioagricultural Sciences; Nagoya University; Chikusa, Nagoya, Japan.
Plant Signal Behav. 2012 Sep 1;7(9):1079-81. doi: 10.4161/psb.21133. Epub 2012 Aug 17.
Endomitosis and endoreplication are atypical modes of cell cycle that results in genome duplication in single nucleus. Because the cell size of given cell type is generally proportional to the nuclear DNA content, endoreplication and endomitosis are effective strategy of cell growth, which are widespread in multicellular organisms, especially those in plant kingdom. We found that these processes might be differently regulated by GIGAS CELL1 (GIG1) and its paralog UV-INSENSITIVE4 (UVI4) in Arabidopsis thaliana. GIG1 and UVI4 may negatively regulate activities of anaphase-promoting complex or cyclosome (APC/C) ubiquitin ligase that acts as an important mitotic regulator. The gig1 mutation induced ectopic occurrence of endomitosis during somatic cell division, while it has been reported that uvi4 mutation resulted in premature occurrence of endoreplication during organ development. Overexpression of GIG1 and UVI4 dramatically increased the amount of mitotic cyclin, CYCB1;1, a well-known substrate of APC/C. Ectopic endomitosis in gig1 was enhanced by mutation in CYCB2;2 and suppressed by downregulation of APC10 encoding a core subunit of APC/C. Overexpression of CDC20.1, an activator protein of APC/C, further promoted the ectopic endomitosis in gig1. These findings suggest that endomitosis and endoreplication are regulated by similar molecular mechanisms, in which two related proteins, GIG1 and UVI4, may inhibit APC/C in different ways.
核内有丝分裂和核内复制是细胞周期的非典型模式,导致单个核内的基因组复制。由于给定细胞类型的细胞大小通常与核 DNA 含量成正比,因此核内复制和核内有丝分裂是细胞生长的有效策略,在多细胞生物中广泛存在,尤其是在植物界。我们发现这些过程可能在拟南芥中由 GIGAS CELL1(GIG1)及其同源物 UV-INSENSITIVE4(UVI4)以不同的方式调节。GIG1 和 UVI4 可能负调节后期促进复合物或细胞周期蛋白(APC/C)泛素连接酶的活性,APC/C 作为重要的有丝分裂调节剂。gig1 突变诱导体细胞分裂过程中核内有丝分裂的异位发生,而 uvi4 突变已被报道导致器官发育过程中核内复制的过早发生。GIG1 和 UVI4 的过表达显著增加了有丝分裂周期蛋白 CYCB1;1 的量,CYCB1;1 是 APC/C 的一个重要底物。gig1 中的异位核内有丝分裂通过突变 CYCB2;2 增强,并通过下调 APC/C 的核心亚基 APC10 抑制。APC/C 的激活蛋白 CDC20.1 的过表达进一步促进了 gig1 中的异位核内有丝分裂。这些发现表明核内有丝分裂和核内复制受相似的分子机制调节,其中两个相关蛋白 GIG1 和 UVI4 可能以不同的方式抑制 APC/C。