Uncoupled Expression of Nuclear and Plastid Photosynthesis-Associated Genes Contributes to Cell Death in a Lesion Mimic Mutant. Issue 1 (9th January 2019) - Lv, Ruiqing
Abstract : The salicylic acid-responsive regulator SIGMA FACTOR BINDING PROTEIN1 localizes in the nucleus and chloroplasts and uncouples photosynthesis-associated gene expression, contributing to the lsd1 lesion-mimic phenotype. Abstract: Chloroplast-to-nucleus retrograde signaling is essential for the coupled expression of photosynthesis-associated nuclear genes (PhANGs) and plastid genes (PhAPGs) to ensure the functional status of chloroplasts (Cp) in plants. Although various signaling components involved in the process have been identified in Arabidopsis ( Arabidopsis thaliana ), the biological relevance of such coordination remains an enigma. Here, we show that the uncoupled expression of PhANGs and PhAPGs contributes to the cell death in the lesion simulating disease1 ( lsd1 ) mutant of Arabidopsis. A daylength-dependent increase of salicylic acid (SA) appears to rapidly up-regulate a gene encoding SIGMA FACTOR BINDING PROTEIN1 (SIB1), a transcriptional coregulator, in lsd1 before the onset of cell death. The dual targeting of SIB1 to the nucleus and the Cps leads to a simultaneous up-regulation of PhANGs and down-regulation of PhAPGs. Consequently, this disrupts the stoichiometry of photosynthetic proteins, especially in PSII, resulting in the generation of the highly reactive species singlet oxygen ( 1 O2 ) in Cps. Accordingly, inactivation of the nuclear-encoded Cp protein EXECUTER1, a putative 1 O2 sensor, significantly attenuates the lsd1 -conferred cell death. Together, these results provide a pathway from the SA- to the 1 O2 -signaling pathway, which are intertwined via the uncoupled expression of PhANGs and PhAPGs, contributing to the lesion-mimicking cell death in lsd1 .