Arabidopsis SOG1 (suppressor of gamma response 1) is a plant‐specific transcription factor that governs the DNA damage response. Here we report that SOG1 is phosphorylated in response to DNA damage, and that this phosphorylation is mediated by the sensor kinase ataxia telangiectasia mutated (ATM). We show that SOG1 phosphorylation is crucial for the response to DNA damage, including transcriptional induction of downstream genes, transient arrest of cell division and programmed cell death. Although the amino‐acid sequences of SOG1 and the mammalian tumour suppressor p53 show no similarity, this study demonstrates that ATM‐mediated phosphorylation of a transcription factor has a pivotal role in the DNA damage response in both plants and mammals.

The asymmetric cell division of the zygote is the initial and crucial developmental step in most multicellular organisms. In flowering plants, whether zygote polarity is inherited from the preexisting organization in the egg cell or reestablished after fertilization has remained elusive. How dynamically the intracellular organization is generated during zygote polarization is also unknown. Here, we used a live-cell imaging system with Arabidopsis zygotes to visualize the dynamics of the major elements of the cytoskeleton, microtubules (MTs), and actin filaments (F-actins), during the entire process of zygote polarization. By combining image analysis and pharmacological experiments using specific inhibitors of the cytoskeleton, we found features related to zygote polarization. The preexisting alignment of MTs and F-actin in the egg cell is lost on fertilization. Then, MTs organize into a transverse ring defining the zygote subapical region and driving cell outgrowth in the apical direction. F-actin forms an apical cap and longitudinal arrays and is required to position the nucleus to the apical region of the zygote, setting the plane of the first asymmetrical division. Our findings show that, in flowering plants, the preexisting cytoskeletal patterns in the egg cell are lost on fertilization and that the zygote reorients the cytoskeletons to perform directional cell elongation and polar nuclear migration. Significance In animals and plants, the zygote divides unequally, and the daughter cells inherit different developmental fates to form a proper embryo along the body axis. The cytological events leading to zygote polarization have remained unknown in flowering plants. Here, we report that the two essential components of the cytoskeleton, microtubules and actin filaments, are both disorganized on fertilization and then, arranged to form a transverse ring leading directional cell elongation and longitudinal arrays underlying polar nuclear migration, respectively. These results provide insights into the intracellular dynamics of zygote and the specific roles of cytoskeletons on zygote polarization in flowering plants.