Research Interests
My
primary interest is in studying the evolution of morphological
diversity from a phylogenetic and developmental perspective. My
goal is to integrate phylogenetic hypotheses with underlying mechanisms
of gene action to explain how morphological diversity arises. I
am particularly interested in the evolution of developmental pathways,
primarily from a developmental morphology point of view, but stretching
into shifts in timing and location of patterns of gene expression.
I have also had success in identifying candidate genes for developmental
and morphological evolution through QTL analyses of species crosses
where the two parents differ significantly in important morphological
characters. I see a developmental focus as key in integrating morphological
and genetic studies. Understanding the evolution of development
in the framework of molecular phylogenies allows us to link the
developmental trajectories of a population of individuals with
those changes in trajectory that lead to morphologically distinguishable
species. This approach attempts to bridge the gap between micro-evolutionary
processes and macro-evolutionary patterns.
Inflorescence
diversity in the millet grasses (Paniceae, Poaceae)
I am presently
working on a number of inter-related projects linking evolution
and development in grasses. The first project concerns inflorescence
diversity in the 'bristle clade' millet grasses. This group includes
the three large genera Setaria, Pennisetum and Cenchrus,
and contains foxtail millet (S. italica) and pearl millet
(P. glaucum). All members of the group have bristles (sterile
branchlets) as well as spikelets in the inflorescence, but inflorescences
range from condensed heads with many orders of branching to elongate
racemose panicles with few orders of branching. The inflorescence
diversity in these three genera has been studied in a phylogenetic
context, using the chloroplast markers ndhF and trnL, and has confirmed
the close relationship between Pennisetum and Cenchrus,
but has surprisingly suggested that both Pennisetum and Setaria are
paraphyletic. The developmental analyses have shown that only a
few developmental changes are need to create the diversity of inflorescences
seen at maturity. Work is also underway in the lab by undergraduates
Anya Penley and Shelby Kleweis, who are sequencing the nuclear
markers phytochrome B and a variable intron of knotted1 respectively.
These will be used to further elucidate the relationships of the
subclades within the 'bristle clade', as well as to test for suspected
patterns of hybridization within the group. Two papers from this
work have recently been published.
A related project
in the lab is a survey of inflorescence development and morphology
in the panicoid grasses, a large group of some 3000 species that
contains maize, sorghum and sugarcane. The survey, undertaken together
with recent master's graduate Ken Hiser, master's candidate Emilie
Bess and Professor Elizabeth Kellogg, is
a continuation of work started by Professor Kellogg and Lucia LeRoux.
A comparison of groups based on inflorescence types with groups
obtained from analysis of molecular marker sequences shows that
similar inflorescence forms have evolved repeatedly in different
groups. This may imply that only a few genes control the developmental
inflorescence morphology.
Quantitative
Trait Loci (QTL) studies in foxtail millet
To examine the
hypothesis that changes in inflorescence morphology are due to
the action of only a few genes of largeeffect, we are doing a QTL
analysis of a cross between foxtail millet (S. italica)
and green millet (S. viridis), the wild species from which S.
italica was domesticated. The seed for this cross was donated
by our collaborators Drs. Katrien Devos and Mike Gale, of the John
Innes Center, Norwich, U.K. The two parents have very different
inflorescences, and the 120 segregating F2 populations show different
combinations of inflorescence morphology traits. By relating the
distribution of morphological traits across the F2 populations
to a genomic map prepared from RFLP markers by our collaborators
at the John Innes Center, we can establish areas on the chromosomes
that control the expression of these traits. This work has shown
that only a few major gene clusters control most of the variation
in inflorescence form. Comparative mapping of QTL from the foxtail
millet genome to the maize and rice genomes has allowed likely
candidate genes to be identified. In several cases, map hybridization
of probes of those candidate genes has shown that they are in the
genome regions predicted through comparative mapping. Some QTL
regions, however, do not have any likely candidate genes (as identified
through similar mutant phenotypes), and these are the focus of
our present investigations.
Floral development
and variation in Winteraceae
My interests
arising from my PhD research on floral development and floral variation
in the basal angiosperm family Winteraceae are both evolutionary
and structural. In particular, the method by which different floral
morphologies in the family arise through modifications of the developmental
process remains an important focus, especially in the Australian
genus Tasmannia, where two sharply different developmental
programs can be found. The study of floral variation in Drimys
winteri has revealed that apical meristem size and shape have
a major influence on eventual floral form. Variation in these physical
parameters is dependent on the position of the flower in the inflorescence,
resulting in flowers on a single tree that vary greatly in organ
number and arrangement. Two papers from this work have recently
been published.
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