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A genetic link between epigenetic repressor AS1–AS2 and DNA replication factors in establishment of adaxial–abaxial leaf polarity of Arabidopsis

机译:表观遗传阻遏物AS1-AS2与DNA复制因子在拟南芥正反叶极性建立中的遗传联系

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摘要

Balanced development of adaxial and abaxial domains in leaf primordia is critical for the formation of flat symmetric leaf lamina. Arabidopsis ASYMMETRIC LEAVES1 (AS1) and AS2 proteins form a complex (AS1–AS2), which acts as key regulators for the adaxial development by the direct repression of expression of the abaxial gene ETTIN/AUXIN RESPONSE FACTOR3 (ETT/ARF3). Many modifier mutations have been identified, which enhance the defect of as1 and as2 mutations to generate abaxialized filamentous leaves without adaxial traits, suggesting that the development of the adaxial domain is achieved by cooperative repression by AS1–AS2 and the wild-type proteins corresponding to the modifiers. Mutations of several genes for DNA replication-related chromatin remodeling factors such as Chromatin Assembly Factor-1 (CAF-1) have been also identified as modifiers. It is still unknown, however, whether mutations in genes involved in DNA replication themselves might act as modifiers. Here we report that as1 and as2 mutants grown in the presence of hydroxyurea, a known inhibitor of DNA replication, form abaxialized filamentous leaves in a concentration-dependent manner. We further show that a mutation of the INCURVATA2 (ICU2) gene, which encodes the putative catalytic subunit of DNA polymerase α, and a mutation of the Replication Factor C Subunit3 (RFC3) gene, which encodes a protein used in replication as a clamp loader, act as modifiers. In addition, as2-1 icu2-1 double mutants showed increased mRNA levels of the genes for leaf abaxialization. These results suggest a tight link between DNA replication and the function of AS1–AS2 in the development of flat leaves.
机译:叶片原基中轴突和轴突域的平衡发育对于形成平坦对称叶片至关重要。拟南芥的ASYMMETRIC LEAVES1(AS1)和AS2蛋白形成复合物(AS1-AS2),通过直接抑制背面基因ETTIN / AUXIN RESPONSE FACTOR3(ETT / ARF3)的表达,作为近端发育的关键调控因子。已经鉴定出许多修饰子突变,这些突变增强了as1和as2突变的缺陷,从而产生了无轴性的无轴丝状叶片,这表明通过AS1–AS2和与之相对应的野生型蛋白的协同抑制可以实现近轴域的发展。修饰符。与DNA复制相关的染色质重塑因子(例如,染色质装配因子1(CAF-1))的几个基因的突变也被确定为修饰子。但是,尚不清楚DNA复制本身涉及的基因突变是否可以充当修饰子。在这里我们报告说,在羟基脲(一种已知的DNA复制抑制剂)的存在下生长的as1和as2突变体,以浓度依赖的方式形成了背面的丝状叶片。我们进一步显示INCURVATA2(ICU2)基因的突变,它编码了DNA聚合酶α的推定催化亚基,而复制因子C Subunit3(RFC3)基因的突变,它编码了用于复制的蛋白质作为钳位加载器,充当修饰符。此外,as2-1 icu2-1双重突变体显示出叶片背面轴突基因的mRNA水平升高。这些结果表明,DNA复制与扁平叶发育中AS1-AS2的功能之间存在紧密联系。

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