The Seed and the Metabolism Regulation
Abstract
:Simple Summary
Abstract
1. Introduction
2. Dry Seed: Well-Organized to Resist
2.1. The Seed, a Special New Individual
2.2. Water, “Matrix of Life”
2.3. Respiration Resumption
2.4. Plasma Membrane Potential
3. Seed Dormancy: Higher Level of Resistance
3.1. Seed Metabolism and Dormancy
3.2. Internal Determinants of Dormancy
3.3. Environmental Impact on Dormancy
4. Seeds: The Ability to Recover from Ageing
4.1. Seed Ageing
4.2. Seed Priming
5. Conclusions
Funding
Institutional Review Board Statement
Informed Consent Statement
Data Availability Statement
Conflicts of Interest
References
- Meimoun, P.; Mordret, E.; Langlade, N.B.; Balzergue, S.; Arribat, S.; Bailly, C.; El-Maarouf-Bouteau, H. Is Gene Transcription Involved in Seed Dry After-Ripening? PLoS ONE 2014, 9, e86442. [Google Scholar] [CrossRef]
- Roberts, E.H. Predicting the Storage Life of Seeds. Seed Sci. Technol. 1973, 1, 499–514. [Google Scholar]
- Ellis, R.H.; Hong, T.D.; Roberts, E.H. An Intermediate Category of Seed Storage Behaviour? I. Coffee. J. Exp. Bot. 1990, 41, 1167–1174. [Google Scholar] [CrossRef]
- Benner, S.A. Defining Life. Astrobiology 2010, 10, 1021–1030. [Google Scholar] [CrossRef] [Green Version]
- Vitas, M.; Dobovišek, A. In the Beginning Was a Mutualism—On the Origin of Translation. Orig. Life Evol. Biospheres 2018, 48, 223–243. [Google Scholar] [CrossRef]
- Belmonte, M.F.; Kirkbride, R.C.; Stone, S.L.; Pelletier, J.M.; Bui, A.Q.; Yeung, E.C.; Hashimoto, M.; Fei, J.; Harada, C.M.; Munoz, M.D.; et al. Comprehensive Developmental Profiles of Gene Activity in Regions and Subregions of the Arabidopsis Seed. Proc. Natl. Acad. Sci. USA 2013, 110, E435–E444. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- Ingram, G.C. Family Life at Close Quarters: Communication and Constraint in Angiosperm Seed Development. Protoplasma 2010, 247, 195–214. [Google Scholar] [CrossRef]
- Ballesteros, D.; Walters, C. Detailed Characterization of Mechanical Properties and Molecular Mobility within Dry Seed Glasses: Relevance to the Physiology of Dry Biological Systems: Molecular Mobility within the Glass of Dry Seed. Plant J. 2011, 68, 607–619. [Google Scholar] [CrossRef] [PubMed]
- Vertucci, C.W.; Leopold, A.C. Bound Water in Soybean Seed and Its Relation to Respiration and Imbibitional Damage. Plant Physiol. 1984, 75, 114–117. [Google Scholar] [CrossRef] [PubMed]
- Paszkiewicz, G.; Gualberto, J.M.; Benamar, A.; Macherel, D.; Logan, D.C. Arabidopsis Seed Mitochondria Are Bioenergetically Active Immediately upon Imbibition and Specialize via Biogenesis in Preparation for Autotrophic Growth. Plant Cell 2017, 29, 109–128. [Google Scholar] [CrossRef]
- Sallon, S.; Solowey, E.; Cohen, Y.; Korchinsky, R.; Egli, M.; Woodhatch, I.; Simchoni, O.; Kislev, M. Germination, Genetics, and Growth of an Ancient Date Seed. Science 2008, 320, 1464. [Google Scholar] [CrossRef]
- Leprince, O.; Pellizzaro, A.; Berriri, S.; Buitink, J. Late Seed Maturation: Drying without Dying. J. Exp. Bot. 2017, 68, 827–841. [Google Scholar] [CrossRef] [Green Version]
- Angelovici, R.; Galili, G.; Fernie, A.R.; Fait, A. Seed Desiccation: A Bridge between Maturation and Germination. Trends Plant Sci. 2010, 15, 211–218. [Google Scholar] [CrossRef] [PubMed]
- Han, C.; Zhen, S.; Zhu, G.; Bian, Y.; Yan, Y. Comparative Metabolome Analysis of Wheat Embryo and Endosperm Reveals the Dynamic Changes of Metabolites during Seed Germination. Plant Physiol. Biochem. 2017, 115, 320–327. [Google Scholar] [CrossRef] [PubMed]
- Howell, K.A.; Narsai, R.; Carroll, A.; Ivanova, A.; Lohse, M.; Usadel, B.; Millar, A.H.; Whelan, J. Map** Metabolic and Transcript Temporal Switches during Germination in Rice Highlights Specific Transcription Factors and the Role of RNA Instability in the Germination Process. Plant Physiol. 2009, 149, 961–980. [Google Scholar] [CrossRef] [Green Version]
- ** Seed: Tansley Review. New Phytol. 2009, 182, 17–30. [Google Scholar] [CrossRef]
- Logan, D.C.; Millar, A.H.; Sweetlove, L.J.; Hill, S.A.; Leaver, C.J. Mitochondrial Biogenesis during Germination in Maize Embryos. Plant Physiol. 2001, 125, 662–672. [Google Scholar] [CrossRef] [Green Version]
- Howell, K.A.; Millar, A.H.; Whelan, J. Ordered Assembly of Mitochondria During Rice Germination Begins with Promitochondrial Structures Rich in Components of the Protein Import Apparatus. Plant Mol. Biol. 2006, 60, 201–223. [Google Scholar] [CrossRef]
- Nawa, Y.; Asahi, T. Rapid Development of Mitochondria in Pea Cotyledons during the Early Stage of Germination. Plant Physiol. 1971, 48, 671–674. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- Morohashi, Y.; Bewley, J.D. Development of Mitochondrial Activities in Pea Cotyledons: Influence of desiccation during and following germination of the axis. Plant Physiol. 1980, 66, 637–640. [Google Scholar] [CrossRef] [Green Version]
- Morohashi, Y.; Bewley, J.D.; Yeung, E.C. Biogenesis of Mitochondria in Imbibed Peanut Cotyledons: II. Development of light and heavy mitochondria. Plant Physiol. 1981, 68, 318–323. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- Ehrenshaft, M.; Brambl, R. Respiration and Mitochondrial Biogenesis in Germinating Embryos of Maize. Plant Physiol. 1990, 93, 295–304. [Google Scholar] [CrossRef] [Green Version]
- Law, S.R.; Narsai, R.; Whelan, J. Mitochondrial Biogenesis in Plants during Seed Germination. Mitochondrion 2014, 19, 214–221. [Google Scholar] [CrossRef]
- Czarna, M.; Kolodziejczak, M.; Janska, H. Mitochondrial Proteome Studies in Seeds during Germination. Proteomes 2016, 4, 19. [Google Scholar] [CrossRef]
- Benamar, A.; Rolletschek, H.; Borisjuk, L.; Avelange-Macherel, M.-H.; Curien, G.; Mostefai, H.A.; Andriantsitohaina, R.; Macherel, D. Nitrite–Nitric Oxide Control of Mitochondrial Respiration at the Frontier of Anoxia. Biochim. Biophys. Acta BBA—Bioenerg. 2008, 1777, 1268–1275. [Google Scholar] [CrossRef]
- Attucci, S.; Carde, J.P.; Raymond, P.; Saint-Gès, V.; Spiteri, A.; Pradet, A. Oxidative Phosphorylation by Mitochondria Extracted from Dry Sunflower Seeds. Plant Physiol. 1991, 95, 390–398. [Google Scholar] [CrossRef] [PubMed]
- Nietzel, T.; Mostertz, J.; Ruberti, C.; Née, G.; Fuchs, P.; Wagner, S.; Moseler, A.; Müller-Schüssele, S.J.; Benamar, A.; Poschet, G.; et al. Redox-Mediated Kick-Start of Mitochondrial Energy Metabolism Drives Resource-Efficient Seed Germination. Proc. Natl. Acad. Sci. USA 2020, 117, 741–751. [Google Scholar] [CrossRef]
- Buchanan, B.B. The Path to Thioredoxin and Redox Regulation Beyond Chloroplasts. Plant Cell Physiol. 2017, 58, 1826–1832. [Google Scholar] [CrossRef] [PubMed]
- Simon, E.W. Phospholipids and plant membrane permeability. New Phytol. 1974, 73, 377–420. [Google Scholar] [CrossRef]
- Yu, X.; Li, A.; Li, W. How Membranes Organize during Seed Germination: Three Patterns of Dynamic Lipid Remodelling Define Chilling Resistance and Affect Plastid Biogenesis: Remodelling of Membrane Lipids during Germination. Plant Cell Environ. 2015, 38, 1391–1403. [Google Scholar] [CrossRef] [PubMed]
- Lin, Y.; ** ATPases: Regulation and Biosynthesis. Plant Cell 1999, 11, 677–689. [Google Scholar] [CrossRef] [Green Version]
- Haruta, M.; Burch, H.L.; Nelson, R.B.; Barrett-Wilt, G.; Kline, K.G.; Mohsin, S.B.; Young, J.C.; Otegui, M.S.; Sussman, M.R. Molecular Characterization of Mutant Arabidopsis Plants with Reduced Plasma Membrane Proton Pump Activity. J. Biol. Chem. 2010, 285, 17918–17929. [Google Scholar] [CrossRef] [Green Version]
- Falhof, J.; Pedersen, J.T.; Fuglsang, A.T.; Palmgren, M. Plasma Membrane H+-ATPase Regulation in the Center of Plant Physiology. Mol. Plant 2016, 9, 323–337. [Google Scholar] [CrossRef] [Green Version]
- Lang, V.; Pertl-Obermeyer, H.; Safiarian, M.J.; Obermeyer, G. Pump up the Volume—A Central Role for the Plasma Membrane H+ Pump in Pollen Germination and Tube Growth. Protoplasma 2014, 251, 477–488. [Google Scholar] [CrossRef]
- Pedersen, J.T.; Falhof, J.; Ekberg, K.; Buch-Pedersen, M.J.; Palmgren, M. Metal Fluoride Inhibition of a P-Type H+ Pump: Stabilization of the phosphoenzyme intermediate contributes to post-translational pump activation. J. Biol. Chem. 2015, 290, 20396–20406. [Google Scholar] [CrossRef] [Green Version]
- Pedersen, J.T.; Kanashova, T.; Dittmar, G.; Palmgren, M. Isolation of Native Plasma Membrane H+-ATP Ase (Pma1p) in Both the Active and Basal Activation States. FEBS Open Bio 2018, 8, 774–783. [Google Scholar] [CrossRef] [Green Version]
- De Bont, L.; Naim, E.; Arbelet-Bonnin, D.; ** of Pea Seed Ageing Reveals a Pivotal Role for Genes Related to Oxidative Stress and Programmed Cell Death. PLoS ONE 2013, 8, e78471. [Google Scholar] [CrossRef] [Green Version]
- Wang, Y.; Li, Y.; Xue, H.; Pritchard, H.W.; Wang, X. Reactive Oxygen Species-Provoked Mitochondria-Dependent Cell Death during Ageing of Elm (Ulmus pumila L.) Seeds. Plant J. 2015, 81, 438–452. [Google Scholar] [CrossRef]
- Fleming, M.B.; Richards, C.M.; Walters, C. Decline in RNA Integrity of Dry-Stored Soybean Seeds Correlates with Loss of Germination Potential. J. Exp. Bot. 2017, 68, 2219–2230. [Google Scholar] [CrossRef] [Green Version]
- Fleming, M.B.; Patterson, E.L.; Reeves, P.A.; Richards, C.M.; Gaines, T.A.; Walters, C. Exploring the Fate of MRNA in Aging Seeds: Protection, Destruction, or Slow Decay? J. Exp. Bot. 2018, 69, 4309–4321. [Google Scholar] [CrossRef]
- Kranner, I.; Birtić, S.; Anderson, K.M.; Pritchard, H.W. Glutathione Half-Cell Reduction Potential: A Universal Stress Marker and Modulator of Programmed Cell Death? Free Radic. Biol. Med. 2006, 40, 2155–2165. [Google Scholar] [CrossRef]
- Clerkx, E.J.M.; El-Lithy, M.E.; Vierling, E.; Ruys, G.J.; Blankestijn-De Vries, H.; Groot, S.P.C.; Vreugdenhil, D.; Koornneef, M. Analysis of Natural Allelic Variation of Arabidopsis Seed Germination and Seed Longevity Traits between the Accessions Landsberg Erecta and Shakdara, Using a New Recombinant Inbred Line Population. Plant Physiol. 2004, 135, 432–443. [Google Scholar] [CrossRef] [Green Version]
- Long, R.L.; Kranner, I.; Panetta, F.D.; Birtic, S.; Adkins, S.W.; Steadman, K.J. Wet-Dry Cycling Extends Seed Persistence by Re-Instating Antioxidant Capacity. Plant Soil 2011, 338, 511–519. [Google Scholar] [CrossRef]
- Kibinza, S.; Vinel, D.; Côme, D.; Bailly, C.; Corbineau, F. Sunflower Seed Deterioration as Related to Moisture Content during Ageing, Energy Metabolism and Active Oxygen Species Scavenging. Physiol. Plant. 2006, 128, 496–506. [Google Scholar] [CrossRef]
- Châtelain, E.; Satour, P.; Laugier, E.; Ly Vu, B.; Payet, N.; Rey, P.; Montrichard, F. Evidence for Participation of the Methionine Sulfoxide Reductase Repair System in Plant Seed Longevity. Proc. Natl. Acad. Sci. USA 2013, 110, 3633–3638. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- Ogé, L.; Bourdais, G.; Bove, J.; Collet, B.; Godin, B.; Granier, F.; Boutin, J.-P.; Job, D.; Jullien, M.; Grappin, P. Protein Repair L -Isoaspartyl Methyltransferase1 Is Involved in Both Seed Longevity and Germination Vigor in Arabidopsis. Plant Cell 2008, 20, 3022–3037. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- Paparella, S.; Araújo, S.S.; Rossi, G.; Wijayasinghe, M.; Carbonera, D.; Balestrazzi, A. Seed Priming: State of the Art and New Perspectives. Plant Cell Rep. 2015, 34, 1281–1293. [Google Scholar] [CrossRef] [PubMed]
- Lutts, S.; Benincasa, P.; Wojtyla, L.; Kubala, S.; Pace, R.; Lechowska, K.; Quinet, M.; Garnczarska, M. Seed Priming: New Comprehensive Approaches for an Old Empirical Technique. In New Challenges in Seed Biology—Basic and Translational Research Driving Seed Technology; Araujo, S., Balestrazzi, A., Eds.; InTech Open Book Series; InTech: Rijeka, Croatia, 2016; pp. 1–46. ISBN 978-953-51-2658-4. [Google Scholar] [CrossRef] [Green Version]
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El-Maarouf-Bouteau, H. The Seed and the Metabolism Regulation. Biology 2022, 11, 168. https://doi.org/10.3390/biology11020168
El-Maarouf-Bouteau H. The Seed and the Metabolism Regulation. Biology. 2022; 11(2):168. https://doi.org/10.3390/biology11020168
Chicago/Turabian StyleEl-Maarouf-Bouteau, Hayat. 2022. "The Seed and the Metabolism Regulation" Biology 11, no. 2: 168. https://doi.org/10.3390/biology11020168