Phenotypic screening of seed retention and histological analysis of the abscission zone in Festuca pratensis and Lolium perenne.

Fodder grasses Microscopy Plant genetic resources Seed shattering

Journal

BMC plant biology
ISSN: 1471-2229
Titre abrégé: BMC Plant Biol
Pays: England
ID NLM: 100967807

Informations de publication

Date de publication:
18 Jun 2024
Historique:
received: 13 02 2024
accepted: 31 05 2024
medline: 19 6 2024
pubmed: 19 6 2024
entrez: 18 6 2024
Statut: epublish

Résumé

Seed retention is the basic prerequisite for seed harvest. However, only little breeding progress has been achieved for this trait in the major forage grasses. The aim of this study was to evaluate the potential of plant genetic resources of the important fodder grasses Festuca pratensis Huds. and Lolium perenne L. as source for seed retention in the breeding process. Furthermore, the morphology of the abscission zone, where shattering occurs, was studied on the cell tissue level in different developmental stages of contrasting accessions. 150 and 286 accessions of Festuca pratensis and Lolium perenne were screened for seed retention, respectively. Contrasting accessions were selected to be tested in a second year. We found a great variation in seed retention in Festuca pratensis and Lolium perenne, ranging from 13 to 71% (average: 35%) and 12 to 94% (average: 49%), respectively, in the first year. Seed retention was generally lower in the second year. Cultivars were within the accessions with highest seed retention in Festuca pratensis, but had lower seed retention than ecotypes in Lolium perenne. Field-shattered seeds had a lower thousand grain weight than retained seeds. Cell layers of the abscission zone appeared already in early seed stages and were nested within each other in accessions with high seed retention, while there were two to three superimposed layers in accessions with low seed retention. Plant genetic resources of Lolium perenne might be a valuable source for breeding varieties with high seed retention. However, simultaneous selection for high seed weight is necessary for developing successful commercial cultivars.

Sections du résumé

BACKGROUND BACKGROUND
Seed retention is the basic prerequisite for seed harvest. However, only little breeding progress has been achieved for this trait in the major forage grasses. The aim of this study was to evaluate the potential of plant genetic resources of the important fodder grasses Festuca pratensis Huds. and Lolium perenne L. as source for seed retention in the breeding process. Furthermore, the morphology of the abscission zone, where shattering occurs, was studied on the cell tissue level in different developmental stages of contrasting accessions.
RESULTS RESULTS
150 and 286 accessions of Festuca pratensis and Lolium perenne were screened for seed retention, respectively. Contrasting accessions were selected to be tested in a second year. We found a great variation in seed retention in Festuca pratensis and Lolium perenne, ranging from 13 to 71% (average: 35%) and 12 to 94% (average: 49%), respectively, in the first year. Seed retention was generally lower in the second year. Cultivars were within the accessions with highest seed retention in Festuca pratensis, but had lower seed retention than ecotypes in Lolium perenne. Field-shattered seeds had a lower thousand grain weight than retained seeds. Cell layers of the abscission zone appeared already in early seed stages and were nested within each other in accessions with high seed retention, while there were two to three superimposed layers in accessions with low seed retention.
CONCLUSIONS CONCLUSIONS
Plant genetic resources of Lolium perenne might be a valuable source for breeding varieties with high seed retention. However, simultaneous selection for high seed weight is necessary for developing successful commercial cultivars.

Identifiants

pubmed: 38890560
doi: 10.1186/s12870-024-05231-0
pii: 10.1186/s12870-024-05231-0
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

577

Informations de copyright

© 2024. The Author(s).

Références

Spengler RN. Anthropogenic seed dispersal. Rethinking the Origins of Plant Domestication. Trends Plant Sci. 2020;25(4):340–8. https://doi.org/10.1016/j.tplants.2020.01.005 .
doi: 10.1016/j.tplants.2020.01.005 pubmed: 32191870
Walsh MJ, Broster JC, Aves C, Powles SB. Influence of crop competition and harvest weed seed control on rigid ryegrass (Lolium rigidum) seed retention height in wheat crop canopies. Weed Sci. 2018;66:627–33.
doi: 10.1017/wsc.2018.28
Humphreys M, Feuerstein U, Vandewalle M, Baert J. Ryegrasses. In: Boller B, Posselt UK, Veronesi F, editors. Fodder crops and amenity grasses. Volume 5. New York, NY: Springer; 2010. pp. 211–60.
doi: 10.1007/978-1-4419-0760-8_10
Falcinelli M. Backcross breeding to increase seed retention in cocksfoot (Dactylis glomerata L.). Euphytica. 1991;56:133–135. https://doi.org/10.1007/BF00042055 .
Simon U. Alko the first seed-shattering resistant cultivar of meadow foxtail (Alopecurus pratensis L). Acta Hort. 1994;355:143–6. https://doi.org/10.17660/ActaHortic.1994.355.14 .
doi: 10.17660/ActaHortic.1994.355.14
Simon U. Breeding for resistance to seed-shattering in forage grasses. Proceedings of the Third International Herbage Seed Conference, Halle (Saale), Germany, June 18–23. 1995, 119–123.
Bundessortenamt L. 2022; https://www.bundessortenamt.de/bsa/media/Files/BSL/bsl_futtergraeser_2022.pdf . Accessed 07 January 2024.
Estornell LH, Agustí J, Merelo P, Talón M, Tadeo FR. Elucidating mechanisms underlying organ abscission. Plant Sci. 2013;199–200:48–60. https://doi.org/10.1016/j.plantsci.2012.10.008 .
doi: 10.1016/j.plantsci.2012.10.008 pubmed: 23265318
Yu Y, Hu H, Doust AN, Kellogg EA. Divergent gene expression networks underlie morphological diversity of abscission zones in grasses. New Phytol. 2020a;225(4):1799–815. https://doi.org/10.1111/nph.16087 .
doi: 10.1111/nph.16087 pubmed: 31372996
Yu Y, Leyva P, Tavares RL, Kellogg EA. The anatomy of abscission zones is diverse among grass species. Am J Bot. 2020b;107(4):549–61. https://doi.org/10.1002/ajb2.1454 .
doi: 10.1002/ajb2.1454 pubmed: 32207156 pmcid: 7217018
Doust AN, Mauro-Herrera M, Francis AD, Shand LC. Morphological diversity and genetic regulation of inflorescence abscission zones in grasses. Am J Bot. 2014;101(10):1759–69. https://doi.org/10.3732/ajb.1400186 .
doi: 10.3732/ajb.1400186 pubmed: 25326618
Zhao W, Xie W, Zhang J, Zhang Z. Histological characteristics, cell wall hydrolytic enzymes activity and candidate genes expression associated with seed shattering of Elymus sibiricus accessions. Front Plant Sci. 2017;19:8606. https://doi.org/10.3389/fpls.2017.00606 .
doi: 10.3389/fpls.2017.00606
Xie W, Zhang J, Zhao X, Zhang Z, Wang Y. Transcriptome profiling of Elymus sibiricus, an important forage grass in Qinghai-Tibet plateau, reveals novel insights into candidate genes that potentially connected to seed shattering. BMC Plant Biol. 2017;21(1):78. https://doi.org/10.1186/s12870-017-1026-2 .
doi: 10.1186/s12870-017-1026-2
Hodge JG, Kellogg EA. Abscission Zone development in Setaria viridis and its domesticated relative, Setaria italica. Am J Bot. 2016;103(6):998–1005. https://doi.org/10.3732/ajb.1500499 .
doi: 10.3732/ajb.1500499 pubmed: 27257006
Wójtowicz T, Zieliński A. Variability of selected traits in Meadow Fescue (Festuca pratensis huds.) Plants with different susceptibility to seed shattering. Biology Life Sci Forum. 2021;3(1):23. https://doi.org/10.3390/IECAG2021-09910 .
doi: 10.3390/IECAG2021-09910
Elgersma A, Leeuwangh JE, Wilms HJ. Abscission and seed shattering in perennial ryegrass (Lolium perenne L). Euphytica. 1988;39(3):51–7. https://doi.org/10.1007/BF00043367 .
doi: 10.1007/BF00043367
Fu Z, Song J, Zhao J, Jameson PE. Identification and expression of genes associated with the abscission layer controlling seed shattering in Lolium perenne. AoB Plants. 2019;11(1). https://doi.org/10.1093/aobpla/ply076 .
Maity A, Lamichaney A, Joshi DC, Bajwa A, Subramanian N, Walsh M, Bagavathiannan M. Seed shattering. A trait of evolutionary importance in plants. Front Plant Sci. 2021;12:657773. https://doi.org/10.3389/fpls.2021.657773 .
doi: 10.3389/fpls.2021.657773 pubmed: 34220883 pmcid: 8248667
Maity A, Singh V, Martins MB, Ferreira PJ, Smith GR, Bagavathiannan M. Species identification and morphological trait diversity assessment in ryegrass (Lolium spp.) populations from the Texas Blackland Prairies. Weed Sci. 2021b;69(3):379–92. https://doi.org/10.1017/wsc.2021.18 .
doi: 10.1017/wsc.2021.18
Tubbs TB, Chastain TG. Genetic variation for seed retention in accessions and genotypic lines of perennial ryegrass (Lolium perenne L). Crop Sci. 2023;63(1):306–19. https://doi.org/10.1002/csc2.20837 .
doi: 10.1002/csc2.20837
Keep T, Sampoux J-P, Barre P, Blanco-Pastor J-L, Dehmer KJ, Durand J-L, Hegarty M, Ledauphin T, Muylle H, Roldán-Ruiz I, Ruttink T, Surault F, Willner E, Volaire F. To grow or survive: which are the strategies of a perennial grass to face severe seasonal stress? Funct Ecol. 2021;35:1145–58. https://doi.org/10.1111/1365-2435.13770 .
doi: 10.1111/1365-2435.13770
R Core Team. R: A language and environment for statistical computing. R Foundation for Statistical Computing, Vienna, Austria. 2022. URL https://www.R-project.org/ .
Bates D, Maechler M, Bolker B, Walker S. Fitting linear mixed-effects models using lme4. J Stat Softw. 2015;67(1):1–48. https://doi.org/10.18637/jss.v067.i01 .
doi: 10.18637/jss.v067.i01
Kuznetsova A, Brockhoff PB, Christensen RHB. lmerTest package: tests in linear mixed effects models. J Stat Softw. 2017;82(13):1–26. https://doi.org/10.18637/jss.v082.i13 .
doi: 10.18637/jss.v082.i13
Wickham H. ggplot2: elegant graphics for data analysis. New York: Springer-; 2016.
doi: 10.1007/978-3-319-24277-4
Mitra PP, Loqué D. Histochemical staining of Arabidopsis thaliana secondary cell wall elements. J Vis Exp. 2014;13(87):51381. https://doi.org/10.3791/51381 .
doi: 10.3791/51381
Müller D, Graetz J, Balles A, Stier S, Hanke R, FellaC. Laboratory-based nano-computed tomography and examples of its application in the field of materials research. Crystals. 2021;11(6):677. https://doi.org/10.3390/cryst11060677 .
doi: 10.3390/cryst11060677
Graetz J, Müller D, Balles A, Fella C. Lenseless X-ray nano-tomography down to 150 nm resolution: on the quantification of modulation transfer and focal spot of the lab-based ntCT system. JINST. 2021;16(1):P01034. https://doi.org/10.1088/1748-0221/16/01/P01034 .
doi: 10.1088/1748-0221/16/01/P01034
Paganin D, Mayo SC, Gureyev TE, Miller PR, Wilkins SW. Simultaneous phase and amplitude extraction from a single defocused image of a homogeneous object. J Microsc. 2002;206(1):33. https://doi.org/10.1046/j.1365-2818.2002.01010.x .
doi: 10.1046/j.1365-2818.2002.01010.x pubmed: 12000561
Boelt B, Studer B. Breeding for grass seed yield. In: Boller B, Posselt UK, Veronesi F, editors. Fodder crops and amenity grasses. Volume 5. New York, NY: Springer; 2010. pp. 161–74.
doi: 10.1007/978-1-4419-0760-8_7
Scotton M. Wild seed harvesting at Mountainous species-Rich Grassland in Calcareous Italian Alps. Rangel Ecol Manage. 2018;71(6):762–9. https://doi.org/10.1016/j.rama.2018.04.005 .
doi: 10.1016/j.rama.2018.04.005
San Martín C, Thorne ME, Gourlie JA, Lyon DJ, Barroso J. Seed retention of grass weeds at wheat harvest in the Pacific Northwest. Weed Sci. 2021;69:238–46. https://doi.org/10.1017/wsc.2020.91 .
doi: 10.1017/wsc.2020.91
Warringa JW, Struik PC, de Visser R, Kreuzer ADH. The pattern of flowering, seed set, seed growth and ripening along the ear of Lolium perenne. Funct Plant Biol. 1998;25(2):213. https://doi.org/10.1071/PP96084 .
doi: 10.1071/PP96084
Patterson SE. Cutting loose. Abscission and dehiscence in Arabidopsis. Plant Physiol. 2001;126(2):494–500. https://doi.org/10.1104/pp.126.2.494 .
doi: 10.1104/pp.126.2.494 pubmed: 11402180 pmcid: 1540116
Brown HS, Addicott FT. The anatomy of experimental leaflet abscission in Phaseolus vulgaris. Am J Bot. 1950;37(8):650–6. https://doi.org/10.2307/2437877 .
doi: 10.2307/2437877
Li L-F, Olsen KM. To have and to hold: selection for seed and fruit retention during crop domestication. Curr Top Dev Biol. 2016;119:63–109. https://doi.org/10.1016/bs.ctdb.2016.02.002 .
doi: 10.1016/bs.ctdb.2016.02.002 pubmed: 27282024
Child RD, Summers JE, Babij J, Farrent JW, Bruce DM. Increased resistance to pod shatter is associated with changes in the vascular structure in pods of a resynthesized Brassica napus line. J Exp Bot. 2003;54(389):1919–30. https://doi.org/10.1093/jxb/erg209 .
doi: 10.1093/jxb/erg209 pubmed: 12837816
Kiesbauer J, Grieder C, Studer B, Kölliker R. Perspectives for reducing seed shattering in ryegrasses. Grass Forage Sci. 2023;78(4):425–37. https://doi.org/10.1111/gfs.12635 .
doi: 10.1111/gfs.12635

Auteurs

Mareike Kavka (M)

Genebank, Satellite Collections North, Leibniz Institute of Plant Genetics and Crop Plant Research (IPK), Inselstraße 9, 23999, Malchow/Poel, Germany. kavka@ipk-gatersleben.de.

Andreas Balles (A)

Development Center X-Ray Technology, Magnetic Resonance and X-Ray Imaging, Fraunhofer IIS, Josef- Martin-Weg 63, 97074, Würzburg, Germany.

Christof Böhm (C)

Saatzucht Steinach GmbH und Co. KG, Wittelsbacherstraße 15, 94377, Steinach, Germany.

Klaus J Dehmer (KJ)

Genebank, Satellite Collections North, Leibniz Institute of Plant Genetics and Crop Plant Research (IPK), Inselstraße 9, 23999, Malchow/Poel, Germany.

Christian Fella (C)

Development Center X-Ray Technology, Magnetic Resonance and X-Ray Imaging, Fraunhofer IIS, Josef- Martin-Weg 63, 97074, Würzburg, Germany.

Felix Rose (F)

Physiology and Cell Biology, Structural Cell Biology, Leibniz Institute of Plant Genetics and Crop Plant Research (IPK), Corrensstraße 3, 06466, Gatersleben, Germany.

Bernhard Saal (B)

PlantaServ GmbH, Erdinger Straße 82a, 85356, Freising, Germany.

Sabine Schulze (S)

Saatzucht Steinach GmbH und Co. KG, Klockower Straße 1, 17219, Ankershagen, Germany.

Evelin Willner (E)

Genebank, Satellite Collections North, Leibniz Institute of Plant Genetics and Crop Plant Research (IPK), Inselstraße 9, 23999, Malchow/Poel, Germany.

Michael Melzer (M)

Physiology and Cell Biology, Structural Cell Biology, Leibniz Institute of Plant Genetics and Crop Plant Research (IPK), Corrensstraße 3, 06466, Gatersleben, Germany.

Articles similaires

Animals Natural Killer T-Cells Mice Adipose Tissue Lipid Metabolism
Rhizosphere Glycine max Seeds Soybean Oil Soil Microbiology
Humans Mendelian Randomization Analysis Graves Disease Aging Genome-Wide Association Study

Classifications MeSH