H 2 O 2 as a Feedback Signal on Dual-Located WHIRLY1 Associates with Leaf Senescence in Arabidopsis

• Published in: Cells (Basel, Switzerland) Switzerland), 2019-12, Vol.8 (12)
• Main Authors: Lin, Wenfang, Huang, Dongmei, Shi, Ximiao, Deng, Ban, Ren, Yujun, Lin, Wenxiong, Miao, Ying
• Format: Article
• Language: English
• ISSN: 2073-4409

Leaf senescence, either as a natural stage of development or as an induced process under stress conditions, incorporates multiple intricate signaling pathways. At the cellular level, retrograde signals have been considered as important players during the initiation and progression of senescence in both animals and plants. The plant-specific single-strand DNA-binding protein WHIRLY1 (WHY1), a repressor of leaf natural senescence, is dually located in both nucleus and plastids. Despite many years of studies, the myth about its dual location and the underlying functional implications remain elusive. Here, we provide further evidence in showing that alteration in WHY1 allocation between the nucleus and chloroplast causes perturbation in H O homeostasis, resulting in adverse plant senescence phenotypes. The knockout of WHY1 increased H O content at 37 days post-germination, coincident with an early leaf senescence phenotype, which can be rescued by ectopic expression of the nuclear isoform (nWHY1), but not by the plastid isoform (pWHY1). Instead, accumulated pWHY1 greatly provoked H O in cells. On the other hand, exogenous H O treatment induced a substantial plastid accumulation of WHY1 proteins and at the same time reduced the nuclear isoforms. This H O -induced loss of nucleus WHY1 isoform was accompanied by enhanced enrichments of histone H3 lysine 9 acetylation (H3K9ac) and recruitment of RNA polymerase II (RNAP II) globally, and specifically at the promoter of the senescence-related transcription factor , which in turn activated transcription and led to a senescence phenotype. Thus, the distribution of WHY1 organelle isoforms and the feedback of H O intervene in a circularly integrated regulatory network during plant senescence in .