Plant Diversity ›› 2026, Vol. 48 ›› Issue (03): 529-543.DOI: 10.1016/j.pld.2025.10.004
• Articles • Previous Articles Next Articles
Qing Wua,b, Ruoruo Wangc, Yawen Maoa,b, Liling Yanga, Weiyue Zhaoa, Liangliang Hea,b, Shaoli Zhoua, Jia Luoa,b, Hailong Zhanga, Hanyan Fengd, Yuqi Fangd, Mingli Liue, Yu Liua, Jianghua Chena,b,d, Baolin Zhaoa,b
Received:2025-07-21
Revised:2025-10-03
Online:2026-06-10
Published:2026-05-25
Contact:
Qing Wu,E-mail:wuqing18@mails.ucas.ac.cn;Ruoruo Wang,E-mail:ruozhu_w@163.com;Yawen Mao,E-mail:maoyawen16@mails.ucas.ac.cn;Liling Yang,E-mail:llyang1211@163.com;Weiyue Zhao,E-mail:zhaoweiyue@xtbg.ac.cn;Liangliang He,E-mail:heliangliang@xtbg.ac.cn;Shaoli Zhou,E-mail:zhoushaoli@xtbg.ac.cn;Jia Luo,E-mail:luojia@xtbg.ac.cn;Hailong Zhang,E-mail:zhanghailong0311@163.com;Hanyan Feng,E-mail:fenghanyan0923@163.com;Yuqi Fang,E-mail:fangyuqi@xtbg.ac.cn;Mingli Liu,E-mail:liumingli08@163.com;Yu Liu,E-mail:oklahomaliu@163.com;Jianghua Chen,E-mail:jhchen@xtbg.ac.cn;Baolin Zhao,E-mail:zhaobaolin@xtbg.ac.cn
Supported by:Qing Wua,b, Ruoruo Wangc, Yawen Maoa,b, Liling Yanga, Weiyue Zhaoa, Liangliang Hea,b, Shaoli Zhoua, Jia Luoa,b, Hailong Zhanga, Hanyan Fengd, Yuqi Fangd, Mingli Liue, Yu Liua, Jianghua Chena,b,d, Baolin Zhaoa,b
通讯作者:
Qing Wu,E-mail:wuqing18@mails.ucas.ac.cn;Ruoruo Wang,E-mail:ruozhu_w@163.com;Yawen Mao,E-mail:maoyawen16@mails.ucas.ac.cn;Liling Yang,E-mail:llyang1211@163.com;Weiyue Zhao,E-mail:zhaoweiyue@xtbg.ac.cn;Liangliang He,E-mail:heliangliang@xtbg.ac.cn;Shaoli Zhou,E-mail:zhoushaoli@xtbg.ac.cn;Jia Luo,E-mail:luojia@xtbg.ac.cn;Hailong Zhang,E-mail:zhanghailong0311@163.com;Hanyan Feng,E-mail:fenghanyan0923@163.com;Yuqi Fang,E-mail:fangyuqi@xtbg.ac.cn;Mingli Liu,E-mail:liumingli08@163.com;Yu Liu,E-mail:oklahomaliu@163.com;Jianghua Chen,E-mail:jhchen@xtbg.ac.cn;Baolin Zhao,E-mail:zhaobaolin@xtbg.ac.cn
基金资助:Qing Wu, Ruoruo Wang, Yawen Mao, Liling Yang, Weiyue Zhao, Liangliang He, Shaoli Zhou, Jia Luo, Hailong Zhang, Hanyan Feng, Yuqi Fang, Mingli Liu, Yu Liu, Jianghua Chen, Baolin Zhao. The mitochondrial DnaJA protein LMA1 regulates reactive oxygen species homeostasis and anthocyanin biosynthesis in Medicago truncatula[J]. Plant Diversity, 2026, 48(03): 529-543.
Qing Wu, Ruoruo Wang, Yawen Mao, Liling Yang, Weiyue Zhao, Liangliang He, Shaoli Zhou, Jia Luo, Hailong Zhang, Hanyan Feng, Yuqi Fang, Mingli Liu, Yu Liu, Jianghua Chen, Baolin Zhao. The mitochondrial DnaJA protein LMA1 regulates reactive oxygen species homeostasis and anthocyanin biosynthesis in Medicago truncatula[J]. Plant Diversity, 2026, 48(03): 529-543.
| [1] Albertos, P., Tatematsu, K., Mateos, I., et al., 2021. Redox feedback regulation of ANAC089 signaling alters seed germination and stress response. Cell Rep. 35, 109263. [2] Almagro Armenteros, J.J., Salvatore, M., Emanuelsson, O., et al., 2019. Detecting sequence signals in targeting peptides using deep learning. Life Sci. Alliance 2, e201900429. [3] Altangerel, N., Ariunbold, G.O., Gorman, C., et al., 2017. In vivo diagnostics of early abiotic plant stress response via Raman spectroscopy. Proc. Natl. Acad. Sci. U.S.A. 114, 3393-3396. [4] Bi, X.L., Zhang, J.L., Chen, C.S., et al., 2014. Anthocyanin contributes more to hydrogen peroxide scavenging than other phenolics in apple peel. Food Chem. 152, 205-209. [5] Blum, T., Briesemeister, S., Kohlbacher, O., 2009. MultiLoc2: integrating phylogeny and gene ontology terms improves subcellular protein localization prediction. BMC Bioinformatics 10, 274. [6] Bolger, A.M., Lohse, M., Usadel, B., 2014. Trimmomatic: a flexible trimmer for illumina sequence data. Bioinformatics (Edam) 30, 2114-2120. [7] Buckley, T., Kaundal, R., Loaiza, C.D., et al., 2020. Plant-mSubP: a computational framework for the prediction of single- and multi-target protein subcellular localization using integrated machine-learning approaches. AoB Plants 12, plz068. [8] Buhrman, K., Aravena-Calvo, J., Zaulich, C.R., et al., 2022. Anthocyanic vacuolar inclusions: from biosynthesis to storage and possible applications. Front. Chem. 10, 913324. [9] Cai, G., Xu, Y., Zhang, S., et al., 2022. A tomato chloroplast-targeted DnaJ protein, SlDnaJ20 maintains the stability of photosystem I/II under chilling stress. Plant Signal. Behav. 17, 2139116. [10] Capella-Gutierrez, S., Silla-Martinez, J.M., Gabaldon, T., 2009. trimAl: a tool for automated alignment trimming in large-scale phylogenetic analyses. Bioinformatics (Edam) 25, 1972-1973. [11] Castro, B., Citterico, M., Kimura, S., et al., 2021. Stress-induced reactive oxygen species compartmentalization, perception and signalling. Nat. Plants 7, 403-412. [12] Catalá, R., Medina, J., Salinas, J., 2011. Integration of low temperature and light signaling during cold acclimation response in Arabidopsis. Proc. Natl. Acad. Sci. U.S.A. 108, 16475-16480. [13] Chalker-Scott, L., 1999. Environmental significance of anthocyanins in plant stress responses. Photochem. Photobiol. 70, 1-9. [14] Chen, C.J., Wu, Y., Li, J.W., et al., 2023. TBtools-II: a ""one for all, all for one""bioinformatics platform for biological big-data mining. Mol. Plant 16, 1733-1742. [15] Chen, K.M., Holmström, M., Raksajit, W., et al., 2010. Small chloroplast-targeted DnaJ proteins are involved in optimization of photosynthetic reactions in Arabidopsis thaliana. BMC Plant Biol. 10, 43. [16] Chiu, C.C., Chen, L.J., Su, P.H., et al., 2013. Evolution of chloroplast J proteins. PLoS One 8, e70384. [17] Corpas, F.J., González-Gordo, S., Palma, J.M., 2020. Plant peroxisomes: a factory of reactive species. Front. Plant Sci. 11, 853. [18] Cosson, V., Eschstruth, A., Ratet, P., 2015. Medicago truncatula Transformation Using Leaf Explants, in: Wang, K (ed), Agrobacterium Protocols, Vol 1, 3rd Edition, pp. 43-56. [19] Davies, K.M., Albert, N.W., Zhou, Y., et al., 2018. Functions of flavonoid and betalain pigments in abiotic stress tolerance in plants. Ann. Plant Rev. Online 1, 21-61. [20] Davies, K.M., Andre, C.M., Kulshrestha, S., et al., 2024. The evolution of flavonoid biosynthesis. Philos. Trans. R. Soc. B-Biol. Sci. 379, 20230361. [21] Dietz, K.-J., Vogelsang, L., 2024. A general concept of quantitative abiotic stress sensing. Trends Plant Sci. 29, 319-328. [22] Dixon, R.A., Sumner, L.W., 2003. Legume natural products: understanding and manipulating complex pathways for human and animal health. Plant Physiol. 131, 878-885. [23] Duchniewicz, M., Germaniuk, A., Westermann, B., et al., 1999. Dual role of the mitochondrial chaperone Mdj1p in inheritance of mitochondrial DNA in yeast. Mol. Cell Biol. 19, 8201-8210. [24] Feng, Z., Zhang, B., Ding, W., et al., 2013. Efficient genome editing in plants using a CRISPR/Cas system. Cell Res. 23, 1229-1232. [25] Fu, Z.Q., Dong, X., 2013. Systemic Acquired Resistance: Turning Local Infection into Global Defense, in: Merchant, SS (ed), Ann. Rev. Plant Biol. Vol 64, pp. 839-863. [26] Georgopoulos, C.P., Lundquistheil, A., Yochem, J., et al., 1980. Identification of the escherichia-coli DNA-J gene-product. Mol. Gen. Genet. 178, 583-588. [27] Gholami, A., De Geyter, N., Pollier, J., et al., 2014. Natural product biosynthesis in Medicago species. Nat. Prod. Rep. 31, 356-380. [28] Giesguth, M., Sahm, A., Simon, S., et al., 2015. Redox-dependent translocation of the heat shock transcription factor AtHSFA8 from the cytosol to the nucleus in Arabidopsis thaliana. FEBS Lett. 589, 718-725. [29] Gleason, C., Huang, S., Thatcher, L.F., et al., 2011. Mitochondrial complex II has a key role in mitochondrial-derived reactive oxygen species influence on plant stress gene regulation and defense. Proc. Natl. Acad. Sci. U.S.A. 108, 10768-10773. [30] Goffin, L., Georgopoulos, C., 1998. Genetic and biochemical characterization of mutations affecting the carboxy-terminal domain of the Escherichia coli molecular chaperone DnaJ. Mol. Microbiol. 30, 329-340. [31] Gould, K.S., McKelvie, J., Markham, K.R., 2002. Do anthocyanins function as antioxidants in leaves?: imaging of H2O2 in red and green leaves after mechanical injury. Plant Cell Environ. 25, 1261-1269. [32] Hageman, J., Kampinga, H.H., 2009. Computational analysis of the human HSPH/HSPA/DNAJ family and cloning of a human HSPH/HSPA/DNAJ expression library. Cell Stress Chaperones 14, 1-21. [33] Hasanuzzaman, M., Bhuyan, M.H.M., Zulfiqar, F., et al., 2020. Reactive oxygen species and antioxidant defense in plants under abiotic stress: revisiting the crucial role of a universal defense regulator. Antioxidants 9, 681. [34] Jaakola, L., 2013. New insights into the regulation of anthocyanin biosynthesis in fruits. Trends Plant Sci. 18, 477-483. [35] Jia, N., Lv, T.T., Li, M.X., et al., 2016. The J-protein AtDjB1 is required for mitochondrial complex I activity and regulates growth and development through ROS-mediated auxin signalling. J. Exp. Bot. 67, 3481-3496. [36] Jiang, C., Chen, C., Huang, Z., et al., 2015. ITIS, a bioinformatics tool for accurate identification of transposon insertion sites using next-generation sequencing data. BMC Bioinformatics 16, 72. [37] Jiang, T.T., He, Y.X., Wu, Z., et al., 2023. Enhancing stimulation of cyaniding, GhLDOX3 activates reactive oxygen species to regulate tolerance of alkalinity negatively in cotton. Ecotoxicol. Environ. Saf. 267, 115655. [38] Jin, Y., Jia, J., Yang, Y., et al., 2024. DNAJ protein gene expansion mechanism in Panicoideae and PgDNAJ functional identification in pearl millet. Theor. Appl. Genet. 137, 149. [39] Kampinga, H.H., Craig, E.A., 2010. The HSP70 chaperone machinery: j proteins as drivers of functional specificity. Nat. Rev. Mol. Cell Biol. 11, 579-592. [40] Karami, M., Rafiei, F., Shiran, B., et al., 2015. Comparative response of annual Medicago spp. to salinity. Russ. J. Plant Physiol. 62, 617-624. [41] Katoh, K., Standley, D.M., 2013. MAFFT multiple sequence alignment software version 7: improvements in performance and usability. Mol. Biol. Evol. 30, 772-780. [42] Khan, K., Tran, H.C., Mansuroglu, B., et al., 2024. Mitochondria-derived reactive oxygen species are the likely primary trigger of mitochondrial retrograde signaling in Arabidopsis. Curr. Biol. 34, 327-342.e324. [43] Kim, D., Paggi, J.M., Park, C., et al., 2019. Graph-based genome alignment and genotyping with HISAT2 and HISAT-genotype. Nat. Biotechnol. 37, 907. [44] Koes, R., Verweij, W., Quattrocchio, F., 2005. Flavonoids: a colorful model for the regulation and evolution of biochemical pathways. Trends Plant Sci. 10, 236-242. [45] Kong, F., Deng, Y., Wang, G., et al., 2014a. LeCDJ1, a chloroplast DnaJ protein, facilitates heat tolerance in transgenic tomatoes. J. Integr. Plant Biol. 56, 63-74. [46] Kong, F., Deng, Y., Zhou, B., et al., 2014b. A chloroplast-targeted DnaJ protein contributes to maintenance of photosystem II under chilling stress. J. Exp. Bot. 65, 143-158. [47] Landi, M., Tattini, M., Gould, K.S., 2015. Multiple functional roles of anthocyanins in plant-environment interactions. Environ. Exp. Bot. 119, 4-17. [48] Lanfear, R., von Haeseler, A., Woodhams, M.D., et al., 2020. IQ-TREE 2: new models and efficient methods for phylogenetic inference in the genomic era. Mol. Biol. Evol. 37, 1530-1534. [49] Lee, D.W., Gould, K.S., 2002. Why leaves turn red - pigments called anthocyanins probably protect leaves from light damage by direct shielding and by scavenging free radicals. Am. Sci. 90, 524-531. [50] Lee, E.S., Park, J.H., Wi, S.D., et al., 2021. Redox-dependent structural switch and CBF activation confer freezing tolerance in plants. Nat. Plants 7, 914-922. [51] Lenaz, G., 2001. The mitochondrial production of reactive oxygen species: mechanisms and implications in human pathology. IUBMB Life 52, 159-164. [52] Li, G., Li, Z., Yang, Z., et al., 2021. Mitochondrial heat-shock cognate protein 70 contributes to auxin-mediated embryo development. Plant Physiol. 186, 1101-1121. [53] Li, G., Zhao, J., Qin, B., et al., 2019. ABA mediates development-dependent anthocyanin biosynthesis and fruit coloration in Lycium plants. BMC Plant Biol. 19, 317. [54] Li, J.Z., Oian, X.G., Sha, B., 2003. The crystal structure of the yeast Hsp40 Ydj1 complexed with its peptide substrate. Structure 11, 1475-1483. [55] Liao, Y., Smyth, G.K., Shi, W., 2014. featureCounts: an efficient general purpose program for assigning sequence reads to genomic features. Bioinformatics (Edam) 30, 923-930. [56] Liu, H., Ding, Y., Zhou, Y., et al., 2017. CRISPR-P 2.0: an improved CRISPR-Cas9 tool for genome editing in plants. Mol. Plant 10, 530-532. [57] Liu, Y.B., Fiskum, G., Schubert, D., 2002. Generation of reactive oxygen species by the mitochondrial electron transport chain. J. Neur. 80, 780-787. [58] Love, M.I., Huber, W., Anders, S., 2014. Moderated estimation of fold change and dispersion for RNA-seq data with DESeq2. Genome Biol. 15, 550. [59] Lu, S., Van Eck, J., Zhou, X., et al., 2006. The cauliflower or gene encodes a DnaJ cysteine-rich domain-containing protein that mediates high levels of β-carotene accumulation. Plant Cell 18, 3594-3605. [60] Lu, Z., Cyr, D.M., 1998. The conserved carboxyl terminus and zinc finger-like domain of the co-chaperone Ydj1 assist Hsp70 in protein folding. J. Biol. Chem. 273, 5970-5978. [61] Ma, X., Zhang, Q., Zhu, Q., et al., 2015. A Robust CRISPR/Cas9 system for convenient, high-efficiency multiplex genome editing in monocot and dicot plants. Mol. Plant 8, 1274-1284. [62] Mahmoud, L.M., Killiny, N., Dutt, M., 2024. Physiological and molecular responses of 'Hamlin' sweet orange trees expressing the VvmybA1 gene under cold stress conditions. Planta 260, 67. [63] May, G.D., Dixon, R.A., 2004. Medicago truncatula. Curr. Biol. 14, R180-R181. [64] Meng, X., Li, L., De Clercq, I., et al., 2019. ANAC017 coordinates organellar functions and stress responses by reprogramming retrograde signaling. Plant Physiol. 180, 634-653. [65] Meng, Y., Hou, Y., Wang, H., et al., 2017. Targeted mutagenesis by CRISPR/Cas9 system in the model legume Medicago truncatula. Plant Cell Rep. 36, 371-374. [66] Miernyk, J.A., 2001. The J-domain proteins of Arabidopsis thaliana:: an unexpectedly large and diverse family of chaperones. Cell Stress Chaperones 6, 209-218. [67] Mittler, R., 2017. ROS are good. Trends Plant Sci. 22, 11-19. [68] Mittler, R., Zandalinas, S.I., Fichman, Y., et al., 2022. Reactive oxygen species signalling in plant stress responses. Nat. Rev. Mol. Cell Biol. 23, 663-679. [69] Nakabayashi, R., Yonekura-Sakakibara, K., Urano, K., et al., 2014. Enhancement of oxidative and drought tolerance in Arabidopsis by overaccumulation of antioxidant flavonoids. Plant J. 77, 367-379. [70] Neill, S.O., Gould, K.S., Kilmartin, P.A., et al., 2002. Antioxidant activities of red versus green leaves in Elatostema rugosum. Plant Cell Environ. 25, 539-547. [71] Noctor, G., Reichheld, J.P., Foyer, C.H., 2018. ROS-related redox regulation and signaling in plants. Semin. Cell Dev. Biol. 80, 3-12. [72] Ødum, M.T., Teufel, F., Thumuluri, V., et al., 2024. DeepLoc 2.1: multi-label membrane protein type prediction using protein language models. NAR 52, W215-W220. [73] Ohta, M., Takaiwa, F., 2014. Emerging features of ER resident J-proteins in plants. Plant Signal. Behav. 9, e28194. [74] Page, M., Sultana, N., Paszkiewicz, K., et al., 2012. The influence of ascorbate on anthocyanin accumulation during high light acclimation in Arabidopsis thaliana: further evidence for redox control of anthocyanin synthesis. Plant Cell Environ. 35, 388-404. [75] Park, M.Y., Kim, S.Y., 2014. The Arabidopsis J protein AtJ1 is essential for seedling growth, flowering time control and ABA response. Plant Cell Physiol. 55, 2152-2163. [76] Petsalaki, E.I., Bagos, P.G., Litou, Z.I., et al., 2006. PredSL: a tool for the N-Terminal sequence-based prediction of protein subcellular localization. Genom. Proteom. Bioinform. 4, 48-55. [77] Previtali, P., Dokoozlian, N.K., Pan, B.S., et al., 2021. Crop load and plant water status influence the ripening rate and aroma development in berries of grapevine (Vitis vinifera L.) cv. Cabernet Sauvignon. J. Agric. Food Chem. 69, 7709-7724. [78] Qin, L., Sun, L., Wei, L., et al., 2021. Maize SRO1e represses anthocyanin synthesis through regulating the MBW complex in response to abiotic stress. Plant J. 105, 1010-1025. [79] Qiu, T., Zhao, X., Feng, H., et al., 2021. OsNBL3, a mitochondrion-localized pentatricopeptide repeat protein, is involved in splicing nad5 intron 4 and its disruption causes lesion mimic phenotype with enhanced resistance to biotic and abiotic stresses. Plant Biotechnol. J. 19, 2277-2290. [80] Raghavendra, A.S., Gonugunta, V.K., Christmann, A., et al., 2010. ABA perception and signalling. Trends Plant Sci. 15, 395-401. [81] Rowley, N., Pripbuus, C., Westermann, B., et al., 1994. MDJ1P, a novel chaperone of the DNAJ family, IS involved in mitochondrial biogenesIS and protein-folding. Cell 77, 249-259. [82] Sahi, C., Craig, E.A., 2007. Network of general and specialty J protein chaperones of the yeast cytosol. Proc. Natl. Acad. Sci. U.S.A. 104, 7163-7168. [83] Sarkar, N.K., Thapar, U., Kundnani, P., et al., 2013. Functional relevance of J-protein family of rice (Oryza sativa). Cell Stress Chaperones 18, 321-331. [84] Savojardo, C., Martelli, P.L., Fariselli, P., et al., 2015. TPpred3 detects and discriminates mitochondrial and chloroplastic targeting peptides in eukaryotic proteins. Bioinformatics (Edam) 31, 3269-3275. [85] Shi, H., Liu, G., Wei, Y., et al., 2018. The zinc-finger transcription factor ZAT6 is essential for hydrogen peroxide induction of anthocyanin synthesis in Arabidopsis. Plant Mol. Biol. 97, 165-176. [86] Small, I., Peeters, N., Legeai, F., et al., 2004. Predotar: a tool for rapidly screening proteomes for N-terminal targeting sequences. Proteomics 4, 1581-1590. [87] Song, R.-F., Hu, X.-Y., Liu, W.-C., et al., 2024. ABA functions in low phosphate-induced anthocyanin accumulation through the transcription factor ABI5 in Arabidopsis. Plant Cell Rep. 43, 55. [88] Sperschneider, J., Catanzariti, A.-M., DeBoer, K., et al., 2017. LOCALIZER: subcellular localization prediction of both plant and effector proteins in the plant cell. Sci. Rep. 7, 44598. [89] Springob, K., Nakajima, J., Yamazaki, M., et al., 2003. Recent advances in the biosynthesis and accumulation of anthocyanins. Nat. Prod. Rep. 20, 288-303. [90] Steyn, W.J., Wand, S.J.E., Holcroft, D.M., et al., 2002. Anthocyanins in vegetative tissues: a proposed unified function in photoprotection. New Phytol. 155, 349-361. [91] Sun, P., Jiao, B., Yang, Y., et al., 2022. WGDI: a user-friendly toolkit for evolutionary analyses of whole-genome duplications and ancestral karyotypes. Mol. Plant 15, 1841-1851. [92] Sun, T., Wang, P., Rao, S., et al., 2023. Co-chaperoning of chlorophyll and carotenoid biosynthesis by ORANGE family proteins in plants. Mol. Plant 16, 1048-1065. [93] Sun, T., Zhou, F., Huang, X.-Q., et al., 2019. ORANGE represses chloroplast biogenesis in etiolated arabidopsis cotyledons via interaction with TCP14. Plant Cell 31, 2996-3014. [94] Tadege, M., Wen, J.Q., He, J., et al., 2008. Large-scale insertional mutagenesis using the Tnt1 retrotransposon in the model legume Medicago truncatula. Plant J. 54, 335-347. [95] Unal, D., García-Caparrós, P., Kumar, V., et al., 2020. Chloroplast-associated molecular patterns as concept for fine-tuned operational retrograde signalling. Philos. Trans. R. Soc. B-Biol. Sci. 375, 20190443. [96] Verma, A.K., Diwan, D., Raut, S., et al., 2017. Evolutionary conservation and emerging functional diversity of the cytosolic Hsp70: j protein chaperone network of Arabidopsis thaliana. G3-Genes Genom. Genet. 7, 1941-1954. [97] Verma, A.K., Tamadaddi, C., Tak, Y., et al., 2019. The expanding world of plant J-domain proteins. Crit. Rev. Plant Sci. 38, 382-400. [98] Wang, G., Kong, F., Zhang, S., et al., 2015. A tomato chloroplast-targeted DnaJ protein protects Rubisco activity under heat stress. J. Exp. Bot. 66, 3027-3040. [99] Wang, P., Liu, W.C., Han, C., et al., 2024. Reactive oxygen species: multidimensional regulators of plant adaptation to abiotic stress and development. J. Integr. Plant Biol. 66, 330-367. [100] Wang, R., Lu, N., Liu, C., et al., 2022. MtGSTF7, a TT19-like GST gene, is essential for accumulation of anthocyanins, but not proanthocyanins in Medicago truncatula. J. Exp. Bot. 73, 4129-4146. [101] Wei, S.-S., Niu, W.-T., Zhai, X.-T., et al., 2019. Arabidopsis mtHSC70-1 plays important roles in the establishment of COX-dependent respiration and redox homeostasis. J. Exp. Bot. 70, 5575-5590. [102] Welsch, R., Zhou, X.J., Yuan, H., et al., 2018. Clp protease and OR directly control the proteostasis of phytoene synthase, the crucial enzyme for Carotenoid biosynthesis in Arabidopsis. Mol. Plant 11, 149-162. [103] Westermann, B., Gaume, B., Herrmann, J.M., et al., 1996. Role of the mitochondrial DnaJ homolog Ndj1p as a chaperone for mitochondrially synthesized and imported proteins. Mol. Cell Biol. 16, 7063-7071. [104] Xu, G., Zhong, X., Shi, Y., et al., 2020. A fungal effector targets a heat shock-dynamin protein complex to modulate mitochondrial dynamics and reduce plant immunity. Sci. Adv. 6, eabb7719. [105] Xu, Z.H., Mahmood, K., Rothstein, S.J., 2017. ROS induces anthocyanin production via late biosynthetic genes and anthocyanin deficiency confers the hypersensitivity to ROS-generating stresses in arabidopsis. Plant Cell Physiol. 58, 1364-1377. [106] Yang, Y., Zhao, Y., Zhang, Y., et al., 2022. A mitochondrial RNA processing protein mediates plant immunity to a broad spectrum of pathogens by modulating the mitochondrial oxidative burst. Plant Cell 34, 2343-2363. [107] Yang, Z., 2007. PAML 4: phylogenetic analysis by maximum likelihood. Mol. Biol. Evol. 24, 1586-1591. [108] Yoo, S.D., Cho, Y.-H., Sheen, J., 2007. Arabidopsis mesophyll protoplasts: a versatile cell system for transient gene expression analysis. Nat. Protoc. 2, 1565-1572. [109] Yu, C.S., Chen, Y.C., Lu, C.H., et al., 2006. Prediction of protein subcellular localization. Proteins: Struct., Funct., Bioinf. 64, 643-651. [110] Yuan, H., Owsiany, K., Sheeja, T.E., et al., 2015. A single amino acid substitution in an ORANGE protein promotes carotenoid overaccumulation in arabidopsis. Plant Physiol. 169, 421-431. [111] Zhang, J., Bai, Z., Ouyang, M., et al., 2021. The DnaJ proteins DJA6 and DJA5 are essential for chloroplast iron-sulfur cluster biogenesis. EMBO (Eur. Mol. Biol. Organ.) J. 40, e106742. [112] Zhang, L., Wang, L., Fang, Y., et al., 2024. Phosphorylated transcription factor PuHB40 mediates ROS-dependent anthocyanin biosynthesis in pear exposed to high light. Plant Cell 36, 3562-3583. [113] Zhang, R., Malinverni, D., Cyr, D.M., et al., 2023. J-domain protein chaperone circuits in proteostasis and disease. Trends Cell Biol. 33, 30-47. [114] Zhou, W., Zhou, T., Li, M.X., et al., 2012. The Arabidopsis J-protein AtDjB1 facilitates thermotolerance by protecting cells against heat-induced oxidative damage. New Phytol. 194, 364-378. [115] Zhou, X., Hua, D., Chen, Z., et al., 2009. Elongator mediates ABA responses, oxidative stress resistance and anthocyanin biosynthesis in Arabidopsis. Plant J. 60, 79-90. [116] Zhou, X., Welsch, R., Yang, Y., et al., 2015. Arabidopsis OR proteins are the major posttranscriptional regulators of phytoene synthase in controlling carotenoid biosynthesis. Proc. Natl. Acad. Sci. U.S.A. 112, 3558-3563. [117] Zhu, J.K., 2016. Abiotic stress signaling and responses in plants. Cell 167, 313-324. [118] Zhu, N., Duan, B., Zheng, H., et al., 2023. An R2R3 MYB gene GhMYB3 functions in drought stress by negatively regulating stomata movement and ROS accumulation. Plant Physiol. Biochem. 197, 107648. [119] Zhu, X.B., Liang, S.H., Yin, J.J., et al., 2015. The DnaJ OsDjA7/8 is essential for chloroplast development in rice (Oryza sativa). Gene 574, 11-19. |
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