Summary Correct chloroplast development and function require co‐ordinated expression of chloroplast and nuclear genes. This is achieved through chloroplast signals that modulate nuclear gene expression in accordance with the chloroplast's needs. Genetic evidence indicates that GUN1, a chloroplast‐localized pentatricopeptide repeat (PPR) protein with a C‐terminal Small MutS‐Related (SMR) domain, is involved in integrating multiple developmental and stress‐related signals in both young seedlings and adult leaves. Recently, GUN1 was found to interact physically with factors involved in chloroplast protein homeostasis, and with enzymes of tetrapyrrole biosynthesis in adult leaves that function in various retrograde signalling pathways. Here we show that following perturbation of chloroplast protein homeostasis: (i) by growth in lincomycin‐containing medium; or (ii) in mutants defective in either the FtsH protease complex (ftsh), plastid ribosome activity (prps21‐1 and prpl11‐1) or plastid protein import and folding (cphsc70‐1), GUN1 influences NEP‐dependent transcript accumulation during cotyledon greening and also intervenes in chloroplast protein import.

王林发) 186 • Guoping Wang (王国平) 85 • Yanxiang Wang (王雁翔) 85 • Yaqin Wang (王亚琴) 38 • Muhammad Waqas 187 • Tàiyún Wèi (魏太云) 188 • Shaohua Wen (温少华) 85 • Anna E. Whitfield 189 • John V. Williams 190 • Yuri I. Wolf 99 • Jiangxiang Wu (吴建祥) 38 • Lei Xu (徐雷) 138 • Hironobu Yanagisawa (栁澤広 宣) 191 • Caixia Yang (杨彩霞) 69 • Zuokun Yang (杨作坤) 85 • F. Murilo Zerbini 192 • Lifeng Zhai (翟立峰) 193 • Yong-Zhen Zhang (张永振) 220,221 • Song Zhang (张松) 34 • Jinguo Zhang (张靖国) 194 • Zhe Zhang (张哲) 85 • Xueping Zhou (周雪平) 195

The GENOMES UNCOUPLED 1 (GUN1) gene has been reported to encode a chloroplast-localized pentatricopeptide-repeat protein, which acts to integrate multiple indicators of plastid developmental stage and altered plastid function, as part of chloroplast-to-nucleus retrograde communication. However, the molecular mechanisms underlying signal integration by GUN1 have remained elusive, up until the recent identification of a set of GUN1-interacting proteins, by co-immunoprecipitation and mass-spectrometric analyses, as well as protein–protein interaction assays. Here, we review the molecular functions of the different GUN1 partners and propose a major role for GUN1 as coordinator of chloroplast translation, protein import, and protein degradation. This regulatory role is implemented through proteins that, in most cases, are part of multimeric protein complexes and whose precise functions vary depending on their association states. Within this framework, GUN1 may act as a platform to promote specific functions by bringing the interacting enzymes into close proximity with their substrates, or may inhibit processes by sequestering particular pools of specific interactors. Furthermore, the interactions of GUN1 with enzymes of the tetrapyrrole biosynthesis (TPB) pathway support the involvement of tetrapyrroles as signaling molecules in retrograde communication.

Plastid genes in higher plants are transcribed by at least two different RNA polymerases, the plastid-encoded RNA polymerase (PEP), a bacteria-like core enzyme whose subunits are encoded by plastid genes ( rpoA , rpoB , rpoC1 and rpoC2 ), and the nuclear-encoded plastid RNA polymerase (NEP), a monomeric bacteriophage-type RNA polymerase. Both PEP and NEP enzymes are active in non-green plastids and in chloroplasts at all developmental stages. Their transcriptional activity is affected by endogenous and exogenous factors and requires a strict coordination within the plastid and with the nuclear gene expression machinery. This review focuses on the different molecular mechanisms underlying chloroplast transcription regulation and its coordination with the photosynthesis-associated nuclear genes ( PhANGs ) expression. Particular attention is given to the link between NEP and PEP activity and the GUN1- (Genomes Uncoupled 1) mediated chloroplast-to-nucleus retrograde communication with respect to the Δrpo adaptive response, i.e. the increased accumulation of NEP-dependent transcripts upon depletion of PEP activity, and the editing-level changes observed in NEP-dependent transcripts, including rpoB and rpoC1 , in gun1 cotyledons after norflurazon or lincomycin treatment. The role of cytosolic preproteins and HSP90 chaperone as components of the GUN1-retrograde signalling pathway, when chloroplast biogenesis is inhibited in Arabidopsis cotyledons, is also discussed. This article is part of the theme issue ‘Retrograde signalling from endosymbiotic organelles’.

Although light is essential for photosynthesis, when in excess, it may damage the photosynthetic apparatus, leading to a phenomenon known as photoinhibition. photoinhibition was thought as a light-induced damage to photosystem ii; however, it is now clear that even photosystem i may become very vulnerable to light. one main characteristic of light induced damage to photosystem ii (pSii) is the increased turnover of the reaction center protein, D1: when rate of degradation exceeds the rate of synthesis, loss of pSii activity is observed. With respect to photosystem i (pSi), an excess of electrons, instead of an excess of light, may be very dangerous. plants possess a number of mechanisms able to prevent, or limit, such damages by safe thermal dissipation of light energy (non-photochemical quenching, npQ), slowing-down of electron transfer through the intersystem transport chain (photosynthesis-control, pSc) in cooperation with the proton Gradient Regulation (pGR) proteins, PGR5 and PGRL1, collectively called as short-term photoprotection mechanisms, and the redistribution of light between photosystems, called state transitions (responsible of fluorescence quenching at PSII, qt), is superimposed to these short term photoprotective mechanisms. in this manuscript we have generated a number of higher order mutants by crossing genotypes carrying defects in each of the short-term photoprotection mechanisms, with the final aim to obtain a direct comparison of their role and efficiency in photoprotection. We found that mutants carrying a defect in the ΔpH-dependent photosynthesis-control are characterized by photoinhibition of both photosystems, irrespectively of whether pSBS-dependent npQ or state transitions defects were present or not in the same individual, demonstrating the primary role of pSc in photoprotection. Moreover, mutants with a limited capability to develop a strong PSBS-dependent NPQ, were characterized by a high turnover of the D1 protein and high values of Y(NO), which might reflect energy quenching processes occurring within the PSII reaction center. Photoinhibition of photosynthesis is a long-known phenomenon 1. Due to the discovery of the high turnover D1-protein 2 and its subsequent recognition as a main component of PSII reaction center harboring most of PSII redox cofactors 3,4 , photoinhibition was thought as the increase of degradation rate for the D1 over its synthesis or, more in general, as an unbalance between damage and repair of PSII 5,6. The repair cycle of PSII is now a

Camellia japonica plants manifesting a complex and variable spectrum of viral symptoms like chlorotic ringspots, necrotic rings, yellowing with necrotic rings, yellow mottle, leaves and petals deformations, flower color-breaking were studied since 1940 essentially through electron microscopic analyses; however, a strong correlation between symptoms and one or more well characterized viruses was never verified. In this work samples collected from symptomatic plants were analyzed by NGS technique and a complex virome composed by viruses members of the Betaflexiviridae and Fimoviridae families was identified. In particular, the genomic fragments typical of the emaravirus group were organized in the genomes of two new emaraviruses species, tentatively named Camellia japonica associated emaravirus 1 and 2. They are the first emaraviruses described in camellia plants and were always found solely in symptomatic plants. On the contrary, in both symptomatic and asymptomatic plants, we detected five betaflexiviruses isolates that, based on aa identitiy

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Correct chloroplast development and function require coordinated expression of chloroplast and nuclear genes. This is achieved through chloroplast signals that modulate nuclear gene expression in accordance with the chloroplast's needs. Genetic evidence indicates that GUN1, a chloroplast-localized pentatricopeptide-repeat (PPR) protein with a C-terminal Small MutS-Related (SMR) domain, is involved in integrating multiple developmental and stress-related signals in both young seedlings and adult leaves. Recently, GUN1 was found to interact physically with factors involved in chloroplast protein homeostasis, and with enzymes of tetrapyrrole biosynthesis in adult leaves that function in various retrograde signaling pathways. Here we show that, following perturbation of chloroplast protein homeostasis i) by growth in lincomycin-containing medium, or ii) in mutants defective in either the FtsH protease complex (ftsh), plastid ribosome activity (prps21-1 and prpl11-1) or plastid protein import and folding (cphsp70-1), GUN1 influences NEP-dependent transcript accumulation during cotyledon greening and also intervenes in chloroplast protein import. import Chloroplast biogenesis is achieved through a cascade of events that include cytosolic synthesis of chloroplasttargeted proteins, followed by their import, assembly and folding, while unfolded/misfolded proteins and damaged or malformed chloroplasts are degraded (Sakamoto et al., 2008; Jarvi and López-Jauez, 2013; Izumi and Nakamura, 2018; Otegui, 2018). Most chloroplast-targeted proteins enter the chloroplasts via the protein complexes TOC ('translocon at outer envelope of chloroplast') and TIC ('translocon at inner envelope of chloroplast'). On the cytosolic side, precursor proteins are directed to the Toc34 and Toc159 receptors through the interaction of their chloroplast-targeting peptides with the chaperone heat shock protein 90 (Hsp90) and the guidance complex formed by Hsp70 and a 14-3-3 protein. Active transport through the chloroplast envelope is then mediated by an ATP-dependent import motor, consisting of Hsp70, Hsp90 and the stromal Hsp93 (ClpC2) proteins (Kessler and Schnell, 2009; Sjuts et al., 2017).On the stromal side, transcription of the plastid-encoded genes in higher plants requires two different RNA polymerases: the nuclear-encoded RNA polymerase (NEP), also termed RpoTp (located specifically in the chloroplasts and encoded by the RPOT3 gene) or RpoTmp (located both in mitochondria and plastids and encoded by the RPOT2 gene) and the plastid-encoded RNA polymerase (PEP) (Yu et al., 2014; Börner et al., 2015). NEP is a monomeric T3-T7 bacteriophage-type RNA polymerase that is mainly responsible for transcribing housekeeping genes, whereas PEP is a bacterial-type multisubunit enzyme largely tasked with transcribing photosynthesis-related genes. Chloroplast development is associated with a shift in the primary RNA polymerase from NEP to PEP. Furthermore, compensatory responses can be observed between the two RNA polymerases, as depletion of PEP activ...