Proteome analysis of male gametophyte development in rice anthers
Date
2003
Authors
Kerim, Tursun
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In this thesis, two-dimensional electrophoresis (2-DE)-based comparative
proteomics were applied to monitor the global changes in protein expression during the
male gametophyte development in anthers of the Australian rice cultivar Doongara,
with the aim of providing a protein-level insight into the molecular mechanism
underlying this important reproductive developmental process. At the same time, this
thesis also evaluates the potential application of 2-DE based proteomics to other
aspects of plant developmental biology.
In order to collect sufficient amount of homogenous anther populations which
represent a number of discrete cellular events encompassing the process of
microsporegenesis, the cytological examination of developing anthers was done to
establish the allometric relationships between a number of growth parameters and
anther developmental stages. This provided a base for the quick and nondestructive
assessment of microspore developmental stages. From this study, a strategy for the
collection of rice anthers for six developmental stages was established using a
combination of anther length, auricle distance and days before heading. The findings
of the cytological analysis opened up the possibility of establishing rice plants as a new
model system for male gametophyte research of plants.
Anther proteome maps were established for six microspore developmental stages
within the pH ranges of 4 to 7 and 6 to 11. Over 3,500 protein spots were reproducibly
resolved in the combined pH range of 4 to 11. Comparison of proteome maps of six
developmental stages resulted in the detection of 150 differentially displayed protein
spots at various stages. Putative identities were predicted for 49 out of 155 protein
spots which were subjected to peptide mass fingerprinting (PMF) analysis. Eight low
molecular weight protein spots were matched to putative translation products of rice
expressed sequence tags (EST) by N-terminal terminal sequencing followed by
homology searches. This verified the translation of these small open reading frames
(ORF) and revealed the presence of some post translational modifications of these
proteins. By integrating the information about the functions of identified proteins and
their temporal regulation patterns, three developmentally regulated metabolic pathways
Xl
were identified and the significance of these pathways in relation to male gametophyte
development was discussed.
Based on the N-terminal sequencing data, three isoforms of rice homologues of
grass group II pollen allergens (Ory s 2) were identified and further characterized using
bioinformatics and immunochemical techniques. Polyclonal antibodies were produced
against Ory s 2 isoforms using gel-separated proteins as the antigen. Immunoblot
analysis revealed that Ory s 2 proteins are pollen specific and accumulated to high
abundance at mature pollen, indicating their possible involvement in fertilization
process. Immunochemical analysis also showed that rice group II allergens do not
possess cross-reactivity with group II allergens of other grasses.
This study produced valuable molecular data to provide some insight into the
global changes of protein expression accompanying pollen development, and identified
some developmentally regulated protein markers which have potential practical
application to other research projects. From the promising results of this proteomic
study it can be expected that our understanding of complex biological processes in
plant development will be enhanced with the availability of a fully annotated rice
genome and the application of integrated systems biology research approaches.
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Thesis (PhD)
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