Chen Xiaofan, Wang Hua, Li Jiqin, Huang Hai, Xu Lin
National Laboratory of Plant Molecular Genetics, Shanghai Institute of Plant Physiology and Ecology, Shanghai Institutes for Biological Sciences, Chinese Academy of Sciences, 300 Fenglin Road, Shanghai 200032, China.
J Exp Bot. 2013 Nov;64(16):4895-905. doi: 10.1093/jxb/ert278. Epub 2013 Sep 4.
ASYMMETRIC LEAVES2 (AS2) is one of the key genes required for specifying leaf adaxial identity during leaf adaxial-abaxial polarity establishment. Previous data have shown that, in leaf development, AS2 is directly repressed by an abaxially located transcription factor KANADI1 (KAN1), so that the AS2 transcripts are restricted only in the adaxial leaf domain. It is shown here that, different from the spatial repression by KAN1, the quantitative repression of AS2 in the adaxial domain is also critical for ensuring normal leaf pattern formation. By analysing two gain-of-function as2 mutants, as2-5D and isoginchaku-2D (iso-2D), it is shown that the similar AS2-over-expressed phenotypes of these mutants reflect two different kinds of AS2 misexpression patterns. While as2-5D causes disruption of a KAN1-binding site at the AS2 promoter leading to derepression of AS2 in the abaxial side but without changing its expression level of a leaf, iso-2D results in over-expression of AS2 but without altering its adaxial expression pattern. In addition, it was found that, in iso-2D, levels of histone H3 lysine 27 trimethylation (H3K27me3) and H3K4me3 at the AS2 locus are significantly reduced and increased, respectively, compared with those in the wild type and as2-5D. These results suggest that during leaf patterning, quantitative control of the AS2 expression level might involve epigenetic regulations.
不对称叶片2(AS2)是在叶片近轴-远轴极性建立过程中确定叶片近轴特性所需的关键基因之一。先前的数据表明,在叶片发育过程中,AS2被位于远轴的转录因子KANADI1(KAN1)直接抑制,因此AS2转录本仅局限于叶片近轴区域。本文表明,与KAN1的空间抑制不同,AS2在近轴区域的定量抑制对于确保正常叶片模式形成也至关重要。通过分析两个功能获得型as2突变体as2-5D和福寿草-2D(iso-2D),发现这些突变体相似的AS2过表达表型反映了两种不同的AS2错误表达模式。虽然as2-5D导致AS2启动子处的KAN1结合位点被破坏,导致AS2在远轴侧去抑制,但不改变其在叶片中的表达水平,而iso-2D导致AS2过表达,但不改变其近轴表达模式。此外,研究发现,与野生型和as2-5D相比,在iso-2D中,AS2基因座处的组蛋白H3赖氨酸27三甲基化(H3K27me3)水平显著降低,而H3K4me3水平显著升高。这些结果表明,在叶片模式形成过程中,AS2表达水平的定量控制可能涉及表观遗传调控。