The different response of Brassica napus genotypes to microspore embryogenesis induced by heat shock and trichostatin A is not determined by changes in cell wall structure and composition but by different stress tolerance.

Autor: Camacho-Fernández C; Cell Biology Group, COMAV, Universitat Politècnica de València, Valencia, Spain., Corral-Martínez P; Cell Biology Group, COMAV, Universitat Politècnica de València, Valencia, Spain., Calabuig-Serna A; Cell Biology Group, COMAV, Universitat Politècnica de València, Valencia, Spain., Arjona-Mudarra P; Cell Biology Group, COMAV, Universitat Politècnica de València, Valencia, Spain., Sancho-Oviedo D; Cell Biology Group, COMAV, Universitat Politècnica de València, Valencia, Spain., Boutilier K; Bioscience, Wageningen University and Research, Wageningen, AA, Netherlands., Seguí-Simarro JM; Cell Biology Group, COMAV, Universitat Politècnica de València, Valencia, Spain.
Jazyk: angličtina
Zdroj: Physiologia plantarum [Physiol Plant] 2024 May-Jun; Vol. 176 (3), pp. e14405.
DOI: 10.1111/ppl.14405
Abstrakt: During microspore embryogenesis, microspores are induced to develop into haploid embryos. In Brassica napus, microspore embryogenesis is induced by a heat shock (HS), which initially produces embryogenic structures with different cell wall architectures and compositions, and with different potentials to develop into embryos. The B. napus DH4079 and DH12075 genotypes have high and very low embryo yields, respectively. In DH12075, embryo yield is greatly increased by combining HS and the histone deacetylase (HDAC) inhibitor trichostatin A (TSA). However, we show that HS + TSA inhibits embryogenesis in the highly embryogenic DH4079 line. To ascertain why TSA has such different effects in these lines, we treated DH4079 and DH12075 microspore cultures with TSA and compared the cell wall structure and composition of the different embryogenic structures in both lines, specifically the in situ levels and distribution of callose, cellulose, arabinogalactan proteins and high and low methyl-esterified pectin. For both lines, HS + TSA led to the formation of cell walls unfavorable for embryogenesis progression, with reduced levels of arabinogalactan proteins, reduced cell adhesion of inner walls and altered pectin composition. Thus, TSA effects on cell walls cannot explain their different embryogenic response to TSA. We also applied TSA to DH4079 cultures at different times and concentrations before HS application, with no negative effects on embryogenic induction. These results indicate that DH4079 microspores are hypersensitive to combined TSA and HS treatments, and open up new hypotheses about the causes of such hypersensitivity.
(© 2024 The Author(s). Physiologia Plantarum published by John Wiley & Sons Ltd on behalf of Scandinavian Plant Physiology Society.)
Databáze: MEDLINE
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