Ueno Yoshihisa, Ishikawa Takaaki, Watanabe Keiro, Terakura Shinji, Iwakawa Hidekazu, Okada Kiyotaka, Machida Chiyoko, Machida Yasunori
Division of Biological Sciences, Graduate School of Science, Nagoya University, Furo-cho, Chikusa-ku, Nagoya 464-8602, Japan.
Plant Cell. 2007 Feb;19(2):445-57. doi: 10.1105/tpc.106.042325. Epub 2007 Feb 9.
We show that two Arabidopsis thaliana genes for histone deacetylases (HDACs), HDT1/HD2A and HDT2/HD2B, are required to establish leaf polarity in the presence of mutant ASYMMETRIC LEAVES2 (AS2) or AS1. Treatment of as1 or as2 plants with inhibitors of HDACs resulted in abaxialized filamentous leaves and aberrant distribution of microRNA165 and/or microRNA166 (miR165/166) in leaves. Knockdown mutations of these two HDACs by RNA interference resulted in phenotypes like those observed in the as2 background. Nuclear localization of overproduced AS2 resulted in decreased levels of mature miR165/166 in leaves. This abnormality was abolished by HDAC inhibitors, suggesting that HDACs are required for AS2 action. A loss-of-function mutation in HASTY, encoding a positive regulator of miRNA levels, and a gain-of-function mutation in PHABULOSA, encoding a determinant of adaxialization, suppressed the generation of abaxialized filamentous leaves by inhibition of HDACs in the as1 or as2 background. AS2 and AS1 were colocalized in subnuclear bodies adjacent to the nucleolus where HDT1/HD2A and HDT2/HD2B were also found. Our results suggest that these HDACs and both AS2 and AS1 act independently to control levels and/or patterns of miR165/166 distribution and the development of adaxial-abaxial leaf polarity and that there may be interactions between HDACs and AS2 (AS1) in the generation of those miRNAs.
我们发现,在存在突变型不对称叶片2(AS2)或AS1的情况下,拟南芥中两个组蛋白去乙酰化酶(HDAC)基因HDT1/HD2A和HDT2/HD2B对于建立叶片极性是必需的。用HDAC抑制剂处理as1或as2植株会导致叶片背化呈丝状,且叶片中微小RNA165和/或微小RNA166(miR165/166)分布异常。通过RNA干扰对这两个HDAC进行敲除突变,会产生与在as2背景中观察到的类似表型。过量表达的AS2的核定位导致叶片中成熟miR165/166水平降低。HDAC抑制剂消除了这种异常,表明HDAC对于AS2的作用是必需的。编码miRNA水平正向调节因子的HASTY功能缺失突变,以及编码近轴化决定因子的PHABULOSA功能获得突变,在as1或as2背景中通过抑制HDAC抑制了叶片背化呈丝状的产生。AS2和AS1共定位于靠近核仁的亚核小体中,在那里也发现了HDT1/HD2A和HDT2/HD2B。我们的结果表明,这些HDAC以及AS2和AS1独立发挥作用,以控制miR165/166的分布水平和/或模式以及叶片近轴-远轴极性的发育,并且在这些miRNA的产生过程中HDAC与AS2(AS1)之间可能存在相互作用。