Kitayama Kumiko, Kamo Mariko, Oma Yukako, Matsuda Ryo, Uchida Takafumi, Ikura Tsuyoshi, Tashiro Satoshi, Ohyama Takashi, Winsor Barbara, Harata Masahiko
Laboratory of Molecular Biology, Graduate School of Agricultural Science, Tohoku University, Tsutsumidori-Amamiyamachi 1-1, Aoba-ku, Sendai 981-8555, Japan.
Exp Cell Res. 2009 Jan 15;315(2):206-17. doi: 10.1016/j.yexcr.2008.10.028. Epub 2008 Nov 5.
Certain actin-related proteins (Arps) of budding yeast are localized in the nucleus, and have essential roles as stoichiometric components of histone acetyltransferase (HAT) and chromatin remodeling complexes. On the other hand, identification of vertebrate nuclear Arps and their functional analyses are just beginning. We show that human Arp5 (hArp5) proteins are localized in the nucleus, and that arp5Delta yeast cells are partially complemented by hArp5. Thus, hArp5 is a novel member of the nuclear Arps of vertebrates, which possess evolutionarily conserved functions from yeast to humans. We show here that hArp5 shuttles between the nucleus and the cytoplasm. Furthermore, after the induction of DNA double strand breaks (DSB), cell growth and the accumulation of phosphorylated histone H2AX (gamma-H2AX) are impaired by hArp5 depletion. Association of hArp5 with the hIno80 chromatin remodeling enzyme and decrease of chromatin-bound hIno80 by hArp5-depletion indicate that hArp5 may have a role in the recruitment of the hINO80 complex to chromatin. Overexpression of hArp5 and hIno80 enhanced gamma-H2AX accumulation. These observations suggest that hArp5 is involved in the process of DSB repair through the regulation of the chromatin remodelling machinery.
芽殖酵母的某些肌动蛋白相关蛋白(Arps)定位于细胞核,作为组蛋白乙酰转移酶(HAT)和染色质重塑复合物的化学计量组分发挥重要作用。另一方面,脊椎动物核Arps的鉴定及其功能分析才刚刚开始。我们发现人类Arp5(hArp5)蛋白定位于细胞核,并且arp5Delta酵母细胞可被hArp5部分互补。因此,hArp5是脊椎动物核Arps的一个新成员,其具有从酵母到人类进化上保守的功能。我们在此表明hArp5在细胞核和细胞质之间穿梭。此外,在诱导DNA双链断裂(DSB)后,hArp5缺失会损害细胞生长和磷酸化组蛋白H2AX(γ-H2AX)的积累。hArp5与hIno80染色质重塑酶的结合以及hArp5缺失导致染色质结合的hIno80减少,表明hArp5可能在将hINO80复合物募集到染色质中发挥作用。hArp5和hIno80的过表达增强了γ-H2AX的积累。这些观察结果表明,hArp5通过调节染色质重塑机制参与DSB修复过程。