Polyamine depletion enhances oil body mobilization through possible regulation of oleosin degradation and aquaporin abundance on its membrane

References

• Adeleke BS, Babalola OO. Oilseed crop sunflower (Helianthus annuus) as a source of food: nutritional and health benefits. Food Sci Nutr. 2020;8(9):4666–8. doi:10.1002/fsn3.1783.
   PubMed Web of Science ®Google Scholar
• Shimada TL, Hayashi M, Hara-Nishimura I. Membrane dynamics and multiple functions of oil bodies in seeds and leaves. Plant Physiol. 2018;176(1):199–207. doi:10.1104/pp.17.01522.
   PubMed Web of Science ®Google Scholar
• Zienkiewicz K, Zienkiewicz A. Degradation of lipid droplets in plants and algae—right time, many paths, one goal. Front Plant Sci. 2020;11:579019. doi:10.3389/fpls.2020.579019.
   PubMed Web of Science ®Google Scholar
• Le Moigne D, Guéguen N, Salvaing J. Lipid droplets in plants: more than simple fat storage. Adv Bot Res. 2022;101:191–223. doi:10.1016/bs.abr.2021.07.004.
   Google Scholar
• Zienkiewicz A, Saldat M, Zienkiewicz K. Here, there and everywhere–the importance of neutral lipids in plant growth and development. Postępy Biochemii. 2022;68:46–56. doi:10.18388/pb.2021_409.
   PubMedGoogle Scholar
• Graham IA. Seed storage oil mobilization. Annu Rev Plant Biol. 2008;59(1):115–142. doi:10.1146/annurev.arplant.59.032607.092938.
   PubMedGoogle Scholar
• Sadeghipour HR, Bhatla SC. Differential sensitivity of oleosins to proteolysis during oil body mobilization in sunflower seedlings. Plant Cell Physiol. 2002;43(10):1117–1126. doi:10.1093/pcp/pcf142.
   PubMed Web of Science ®Google Scholar
• Gupta A, Bhatla S. Spatial and temporal changes in lipase activity sites during oil body mobilization in protoplasts from sunflower seedling cotyledons. Plant Growth Regul. 2005;46(1):11–17. doi:10.1007/s10725-005-5231-x.
   Web of Science ®Google Scholar
• Yadav MK, Bhatla SC. Localization of lipoxygenase activity on the oil bodies and protoplasts using a novel fluorescence imaging method. Plant Physiol Biochem. 2011;49(2):230–234. doi:10.1016/j.plaphy.2010.11.012.
   PubMed Web of Science ®Google Scholar
• Eastmond PJ. SUGAR-DEPENDENT1 encodes a patatin domain triacylglycerol lipase that initiates storage oil breakdown in germinating Arabidopsis seeds. Plant Cell. 2006;18(3):665–675. doi:10.1105/tpc.105.040543.
   PubMed Web of Science ®Google Scholar
• Kelly AA, Quettier AL, Shaw E, Eastmond PJ. Seed storage oil mobilization is important but not essential for germination or seedling establishment in Arabidopsis. Plant Physiol. 2011;157(2):866–875. doi:10.1104/pp.111.181784.
   PubMed Web of Science ®Google Scholar
• Thazar-Poulot N, Miquel M, Fobis-Loisy I, Gaude T. Peroxisome extensions deliver the Arabidopsis SDP1 lipase to oil bodies. Proc Natl Acad Sci U S A. 2015;112(13):4158–4163. doi:10.1073/pnas.1403322112.
   PubMed Web of Science ®Google Scholar
• Xu C, Fan J. Links between autophagy and lipid droplet dynamics. J Exp Bot. 2022;73(9):2848–2858. doi:10.1093/jxb/erac003.
   PubMed Web of Science ®Google Scholar
• Vandana S, Bhatla SC. Evidence for the probable oil body association of a thiol-protease, leading to oleosin degradation in sunflower seedling cotyledons. Plant Physiol Biochem. 2006;44(11–12):714–723. doi:10.1016/j.plaphy.2006.09.022.
   PubMed Web of Science ®Google Scholar
• van der Schoot C, Paul LK, Paul SB, Rinne PL. Plant lipid bodies and cell-cell signaling: a new role for an old organelle? Plant Signal Behav. 2011;6(11):1732–1738. doi:10.4161/psb.6.11.17639.
   PubMedGoogle Scholar
• Deruyffelaere C, Bouchez I, Morin H, Guillot A, Miquel M, Froissard M, Chardot T, d’Andréa S. Ubiquitin-mediated proteasomal degradation of oleosins is involved in oil body mobilization during post-germinative seedling growth in Arabidopsis. Plant Cell Physiol. 2015;56(7):1374–1387. doi:10.1093/pcp/pcv056.
   PubMed Web of Science ®Google Scholar
• Deruyffelaere C, Purkrtova Z, Bouchez I, Collet B, Cacas JL, Chardot T, Gallois JL, D’Andrea S. PUX10 is a CDC48A adaptor protein that regulates the extraction of ubiquitinated oleosins from seed lipid droplets in arabidopsis. Plant Cell. 2018;30(9):2116–2136. doi:10.1105/tpc.18.00275.
   PubMed Web of Science ®Google Scholar
• Kretzschmar FK, Mengel LA, Müller AO, Schmitt K, Blersch KF, Valerius O, Braus GH, Ischebeck T. PUX10 is a lipid droplet-localized scaffold protein that interacts with CELL DIVISION CYCLE48 and is involved in the degradation of lipid droplet proteins. Plant Cell. 2018;30(9):2137–2160. doi:10.1105/tpc.18.00276.
   PubMed Web of Science ®Google Scholar
• Hanano A, Bessoule JJ, Heitz T, Blee E. Involvement of the caleosin/peroxygenase RD20 in the control of cell death during Arabidopsis responses to pathogens. Plant Signal Behav. 2015;10(4):e991574. doi:10.4161/15592324.2014.991574.
   PubMed Web of Science ®Google Scholar
• Hanano A, Blée E, Murphy DJ. Caleosin/Peroxygenases: multifunctional proteins in plants. Ann Bot. 2023;131(3):387–409. doi:10.1093/aob/mcad001.
   PubMed Web of Science ®Google Scholar
• Fernández-Santos R, Izquierdo Y, López A, Muñiz L, Martínez M, Cascón T, Hamberg M, Castresana C. Protein profiles of lipid droplets during the hypersensitive defense response of Arabidopsis against Pseudomonas infection. Plant Cell Physiol. 2020;61(6):1144–1157. doi:10.1093/pcp/pcaa041.
   PubMed Web of Science ®Google Scholar
• Jolivet P, Roux E, D’Andrea S, Davanture M, Negroni L, Zivy M, Chardot T. Protein composition of oil bodies in Arabidopsis thaliana ecotype WS. Plant Physiol Biochem. 2004;42(6):501–509. doi:10.1016/j.plaphy.2004.04.006.
   PubMed Web of Science ®Google Scholar
• Jolivet P, Acevedo F, Boulard C, d’Andréa S, Faure JD, Kohli A, Nesi N, Valot B, Chardot T. Crop seed oil bodies: from challenges in protein identification to an emerging picture of the oil body proteome. Proteomics. 2013;13(12–13):1836–1849. doi:10.1002/pmic.201200431.
   PubMed Web of Science ®Google Scholar
• Gattolin S, Sorieul M, Frigerio L. Mapping of tonoplast intrinsic proteins in maturing and germinating Arabidopsis seeds reveals dual localization of embryonic TIPs to the tonoplast and plasma membrane. Mol Plant. 2011;4(1):180–189. doi:10.1093/mp/ssq051.
   PubMed Web of Science ®Google Scholar
• Acevedo F, Rubilar M, Shene C, Navarrete P, Romero F, Rabert C, Jolivet P, Valot B, Chardot T. Seed oil bodies from Gevuina avellana and Madia sativa. J Agric Food Chem. 2012;60(28):6994–7004. doi:10.1021/jf301390d.
   PubMed Web of Science ®Google Scholar
• Zhi Y, Taylor MC, Campbell PM, Warden AC, Shrestha P, El Tahchy A, Rolland V, Vanhercke T, Petrie JR, White RG. et al. Comparative lipidomics and proteomics of lipid droplets in the mesocarp and seed tissues of Chinese Tallow (Triadica sebifera). Front Plant Sci. 2017;8:1339. doi:10.3389/fpls.2017.01339.
   PubMed Web of Science ®Google Scholar
• Poxleitner M, Rogers SW, Lacey Samuels A, Browse J, Rogers JC. A role for caleosin in degradation of oil-body storage lipid during seed germination. Plant J. 2006;47(6):917–933. doi:10.1111/j.1365-313X.2006.02845.x.
   PubMed Web of Science ®Google Scholar
• Veerabagu M, Paul LK, PL R, van der Schoot C. Plant lipid bodies traffic on actin to plasmodesmata motorized by Myosin XIs. Int J Mol Sci. 2020;21(4):1422. doi:10.3390/ijms21041422.
   PubMed Web of Science ®Google Scholar
• Veerabagu M, Rinne PLH, Skaugen M, Paul LK, van der Schoot C. Lipid body dynamics in shoot meristems: production, enlargement, and putative organellar interactions and plasmodesmal targeting. Front Plant Sci. 2021;12:674031. doi:10.3389/fpls.2021.674031.
   PubMed Web of Science ®Google Scholar
• Scholz P, Chapman KD, Mullen RT, Ischebeck T. Finding new friends and revisiting old ones – how plant lipid droplets connect with other subcellular structures. New Phytol. 2022;236(3):833–838. doi:10.1111/nph.18390.
   PubMed Web of Science ®Google Scholar
• Frandsen GI, Mundy J, Tzen JT. Oil bodies and their associated proteins, oleosin and caleosin. Physiol Plant. 2001;112(3):301–307. doi:10.1034/j.1399–3054.2001.1120301.x.
   PubMed Web of Science ®Google Scholar
• Munns R, Tester M. Mechanisms of salinity tolerance. Annu Rev Plant Biol. 2008;59(1):651–681. doi:10.1146/annurev.arplant.59.032607.092911.
   PubMed Web of Science ®Google Scholar
• David A, Yadav S, Bhatla SC. Sodium chloride stress induces nitric oxide accumulation in root tips and oil body surface accompanying slower oleosin degradation in sunflower seedlings. Physiol Plant. 2010;140(4):342–8354. doi:10.1111/j.1399-3054.2010.01408.x.
   PubMed Web of Science ®Google Scholar
• Mukherjee S, David A, Yadav S, Baluška F, Bhatla SC. Salt stress-induced seedling growth inhibition coincides with differential distribution of serotonin and melatonin in sunflower seedling roots and cotyledons. Physiol Plant. 2014;152(4):714–728. doi:10.1111/ppl.12218.
   PubMed Web of Science ®Google Scholar
• Alencar NLM, Gadelha CG, Gallão MI, Dolder MAH, Prisco JT, Gomes-Filho E. Ultrastructural and biochemical changes induced by salt stress in Jatropha curcas seeds during germination and seedling development. Funct Plant Biol. 2015;42(9):865–874. doi:10.1071/FP15019.
   PubMed Web of Science ®Google Scholar
• Tailor A, Tandon R, Bhatla SC. Nitric oxide modulates polyamine homeostasis in sunflower seedling cotyledons under salt stress. Plant Signal Behav. 2019;14(11):1667730. doi:10.1080/15592324.2019.1667730.
   PubMed Web of Science ®Google Scholar
• Alcázar R, Bueno M, Tiburcio AF. Polyamines: small amines with large effects on plant abiotic stress tolerance. Cells. 2020;9(11):2373. doi:10.3390/cells9112373.
   PubMed Web of Science ®Google Scholar
• Gill SS, Tuteja N. Polyamines and abiotic stress tolerance in plants. Plant Signal Behav. 2010;5(1):26–33. doi:10.4161/psb.5.1.10291.
   PubMedGoogle Scholar
• Naka Y, Watanabe K, Sagor GH, Niitsu M, Pillai MA, Kusano T, Takahashi Y. Quantitative analysis of plant polyamines including thermospermine during growth and salinity stress. Plant Physiol Biochem. 2010;48(7):527–533. doi:10.1016/j.plaphy.2010.01.013.
   PubMed Web of Science ®Google Scholar
• Tailor A, Bhatla SC. Polyamine homeostasis modulates plasma membrane- and tonoplast-associated aquaporin expression in etiolated salt-stressed sunflower (Helianthus annuus L.) seedlings. Protoplasma. 2021;258(3):661–672. doi:10.1007/s00709-020-01589-8.
   PubMed Web of Science ®Google Scholar
• Hummel I, Couée I, El Amrani A, Martin-Tanguy J, Hennion F. Involvement of polyamines in root development at low temperature in the subantarctic cruciferous species Pringlea antiscorbutica. J Exp Bot. 2002;53(373):1463–1473. doi:10.1093/jexbot/53.373.1463.
   PubMed Web of Science ®Google Scholar
• Hashem AM, Moore S, Chen S, Hu C, Zhao Q, Elesawi IE, Feng Y, Topping JF, Liu J, Lindsey K. et al. Putrescine depletion affects Arabidopsis root meristem size by modulating auxin and cytokinin signaling and ROS accumulation. Int J Mol Sci. 2021;22(8):4094. doi:10.3390/ijms22084094.
   PubMed Web of Science ®Google Scholar
• Jamdar SC, Cao WF, Samaniego E. Relationship between adipose polyamine concentrations and triacylglycerol synthetic enzymes in lean and obese Zucker rats. Enzyme Protein. 1996;49(4):222–230. doi:10.1159/000468632.
   PubMedGoogle Scholar
• Büyükushu N, Ӧztürk RI. Polyamine metabolism and obesity: polyamine metabolic enzymes involved in obesity. Acta Pharm Sci. 2018;56(2):85–91. doi:10.23893/1307-2080.APS.05613.
   Google Scholar
• Tsujita T, Takaichi H, Takaku T, Sawai T, Yoshida N, Hiraki J. Inhibition of lipase activities by basic polysaccharide. J Lipid Res. 2007;48(2):358–365. doi:10.1194/jlr.M600258-JLR200.
   PubMed Web of Science ®Google Scholar