Abstract
BackgroundPectins are one of the main components of plant cell walls. They are secreted to the wall as highly methylesterified forms that can be de-esterified by pectin methylesterases (PMEs). The degree of methylesterification of pectins changes during development, PMEs are involved in the cell wall remodeling that occurs during diverse plant developmental processes. Nevertheless, the functional meaning of pectin-related wall remodeling in different cell types and processes remains unclear. In vivo, the microspore follows the gametophytic pathway and differentiates to form the pollen grain. In vitro, the microspore can be reprogrammed by stress treatments becoming a totipotent cell that starts to proliferate and follows the embryogenic pathway, a process known as microspore embryogenesis.ResultsTo investigate if the change of developmental programme of the microspore towards embryogenesis involves changes in pectin esterification levels, which would cause the cell wall remodeling during the process, in the present study, dynamics of PME expression and degrees of pectin esterification have been analysed during microspore embryogenesis and compared with the gametophytic development, in Brassica napus. A multidisciplinary approach has been adopted including BnPME gene expression analysis by quantitative RT-PCR, fluorescence in situ hybridization, immuno-dot-blot and immunofluorescence with JIM5 and JIM7 antibodies to reveal low and highly-methylesterified pectins. The results showed that cell differentiation at advanced developmental stages involved induction of BnPME expression and pectin de-esterification, processes that were also detected in zygotic embryos, providing additional evidence that microspore embryogenesis mimics zygotic embryogenesis. By contrast, early microspore embryogenesis, totipotency and proliferation were associated with low expression of BnPME and high levels of esterified pectins.ConclusionsThe results show that the change of developmental programme of the microspore involves changes in pectin esterification associated with proliferation and differentiation events, which may cause the cell wall remodeling during the process. The findings indicate pectin-related modifications in the cell wall during microspore embryogenesis, providing new insights into the role of pectin esterification and cell wall configuration in microspore totipotency, embryogenesis induction and progression.
Highlights
Pectins are one of the main components of plant cell walls
Microspore embryogenesis progression involves induction of Brassica napus pectin methylesterase (BnPME) expression and increasing pectin de-esterification levels in cell walls In this study, we have investigated if the change of developmental programme of the microspore towards embryogenesis involved changes in pectin esterification levels, accomplished by Pectin methylesterase (PME) activity, which would suggest cell wall remodeling during the process
Our results allowed the in situ identification of defined cell wall distribution patterns of pectin esterification associated with cell totipotency, proliferation and differentiation
Summary
Pectins are one of the main components of plant cell walls They are secreted to the wall as highly methylesterified forms that can be de-esterified by pectin methylesterases (PMEs). The degree of methylesterification of pectins changes during development, PMEs are involved in the cell wall remodeling that occurs during diverse plant developmental processes. Microspore embryogenesis is a widely used method to generate genetic variability by obtaining microsporederived embryos and double-haploid plants with many applications for plant breeding [15] This process involves the reprogramming of the immature pollen— the microspore— towards a different developmental pathway and the onset of proliferation and differentiation events, which lead to embryo formation and haploid and doublehaploid plant regeneration [16, 17]. Some plant cell wall polymers are regulated during plant development, the functional meaning of wall changes in different cell types and processes remains unclear
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