Studies on multi-layer aleurone mutants in cereals and their nutritional significance
Abstract
Aleurone cells in the cereal bran fraction store the greatest
amount of nutritional components encompassing dietary fibre,
phenolic compounds, antioxidants, minerals, phytate, B vitamins
and lipid. I observed a substantial enhancement in these
nutrients in a novel rice mutant thick aleurone 2 (ta2)
possessing a multi-layer aleurone - from about two cells to 12
cells thick. Histological assay of ta2 showed that the aleurone
cell structure and tissue organization remained similar to
wild-type characteristics.
Nutritional analyses of wholegrain flour of field-grown ta2 rice
showed concurrent increases in dietary fibre (up 66%), phenolic
compounds (up 43%), antioxidants (up 84%), minerals (up 14-23%)
and phytate (up 18%), vitamin B3 (up 21%), B6 (up 33%), B9 (up
32%), lipid (up 50%) and simple sugars (up 170%). The field-grown
ta2 rice has normal grain morphology, seed size, and weight,
suggesting a high potential for being developed as commercially
viable bio-fortified rice for consumption.
The rice ta2 mutation was mapped to LOC_Os01g11900, corresponding
to OsROS1a gene, where a guanine nucleotide was substituted by
adenosine at Chr1:6451738. This nucleotide substitution created
an alternative RNA splicing site, which resulted in an in-frame
insertion of seven amino acids in the OsROS1A protein. Our
collaborator in IB-CAS subsequently isolated seven additional
multi-layer aleurone rice mutations in OsROS1a by TILLING. All
eight mutations were amino acid substitutions; knockout mutations
may be lethal. Together these results implied that the thick
aleurone trait was achieved through the reduction but not the
elimination of OsROS1a activity. However, I still cannot reject
the hypothesis that the thick aleurone trait is caused by a gain
of function. In the gain of function hypothesis, ta2 mutation can
result in in new function in OsROS1a which facilitates the
differentiation of endosperm progenitor cells or the
trans-differentiation of starchy endosperm cells to aleurone
cells during caryopsis development.
I attempted to mimic the desired multi-layer aleurone trait to
increase the nutritional value in wheat. I identified three wheat
homologs of rice OsROS1a, namely TraeROS1a-5A, -5B and -5D.
Quantitative PCR and TraeROS1a-5B gene promoter::GUS fusion
analyses supported TraeROS1a being expressed in immature
endosperm tissues. A suite of wheat transgenics was developed to
modulate TraeROS1a gene function in wheat. I used RNAi and
artificial microRNA for down-regulation of TraeROS1a. Also, I
conducted CRISPR/Cas9 gene editing of the endogenous TraeROS1a
gene. Both methods were aimed at knocking down one or two of the
three wheat TraeROS1a gene homeologs so as to reduce the total
enzyme activity of ROS1A protein. In addition, other genes, CR4
and DEK1, which have previously been shown to affect aleurone
development in maize, were modified in wheat. Barley HvCR4 and
HvDEK1 genes were ectopically expressed in wheat under starchy
endosperm-specific Bx17 or aleurone-specific LTP2 promoters, in
further attempts to increase signal perception and induction of
multi-layer aleurones. Detailed genotypic and phenotypic analyses
have begun on these transgenics, however, completion of this work
is beyond the scope of this thesis.
Plant transgenics were mainly focused on single nutrient
enhancement. This research provides a novel example of multiple
nutritional enhancements by the modification of a single gene in
cereal crops.
Description
Keywords
Citation
Collections
Source
Type
Book Title
Entity type
Access Statement
License Rights
Restricted until
Downloads
File
Description