Photo:
Elaine Simons |
Research | Teaching | Team | Publications
e-mail: Berbee@mail.ubc.ca
office phone: (604) 822-3780
lab phone: (604) 822-2019
Professor, Dept. of Botany
B.Sc. Univ. Minnesota (1979);
Ph.D. Univ.California, Davis (1987);
Postdoctoral, Univ. Tubingen, Germany (1988);
Postdoctoral, Univ. California, Davis (1989);
Postdoctoral, Univ. California, Berkeley (1990-92).
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Research Interests:
Research in the Berbee laboratory focuses on the diversity
and molecular phylogenetics of fungi. Fungi and animals
shared a common ancestor over a billion years ago. Since
that time, animals evolved into herbivores and predators
while fungi became specialized as decay agents and recyclers
in the environment; as plant and animal pathogens; and as
symbionts contributing as mycorrhizal partners to plant
growth. Through a combination of field and laboratory work,
students and postdoctoral researchers are finding and culturing
fungi and fungus-like organisms, many of them new to science,
and then applying microscopic and molecular phylogenetic
techniques to place the origin and diversification of the
fungi in a phylogenetic context.
Current research
1. Deep divergences and ancient lineages of fungi and fungus-like
organisms (Taylor et al. 2006, Mycologia; Berbee
et al. 2007, New Phytologist). With funding from
Canada’s NSERC and from the US NSF, members of the
Berbee lab are collecting new fungi and fungus-like organisms
from aquatic environments, growing them in pure culture
whenever possible, and combining microscopic and phylogenetic
approaches to make inferences about their biology and evolutionary
origins (Marshall et al. 2008, Protist; Tsui et
al. 2009, Molecular Phylogenetics and Evolution).
Including our newly discovered organisms as well as taxa
from culture collections, they are sequencing genes that
allow reconstruction of patterns of evolutionary origin
of the fungus life style among evolutionarily divergent
fungi and fungus-like organisms.
2. Ascomycete evolution, breeding systems and systematics.
With more than 30,000 known species, the ascomycetes are
diverse and ecologically important. With the support of
NSERC, students in the Berbee lab are reconstructing patterns
of evolution in the ascomycetes. They are concentrating
on the Pleosporales, a well-defined group including many
species with adaptations to specialized habitats. Like whales
and seals, some fungi in this group originated on land but
then returned to the water. Over 60 species in the order
Pleosporales produce helicoid asexual spores many adapted
for dispersal in water and colonization of aquatic habitats.
Our analyses are showing extensive convergence in most morphological
characters and molds forming complex, barrel-shaped helical
spores to trap air bubbles for floatation arose convergently
from three, primarily terrestrial lineages in the Pleosporales
(Tsui et al. 2006, Molecular Phylogenetics and Evolution).
The Pleosporales also included many
serious pathogens of plants. To track the molecular evolution
of changes in breeding systems among these plant pathogens,
the Berbee lab is applying molecular amplification of mating
type gene DNA. The two opposite mating type genes are the
master regulators of sexual reproduction in these fungi.
In an outcrossing species, haploid individuals with opposite
mating types can mate and 50% of their haploid progeny will
be of each mating type. Asexual reproduction propagates
the parental mating type. In a selfing species, each haploid
nucleus in an individual carries the two opposite mating
type genes. Working backwards, by examining the distribution
of mating type genes in a population, we can distinguish
outcrossing from selfing individuals and sexual from asexual
populations (Inderbitzin et al. 2005, PNAS; Inderbitzin
et al.; 2006, Canadian Journal of Botany). 15,000
ascomycete species lack known sexual states and for these
fungi, our molecular genetic detection of mating type genes
will provide a tool to distinguish cryptic sexuality from
true clonality (Berbee et al. 2003, Mycological Research).
3. Mycorrhizal fungal diversity. Forestry is of great
economic importance in British Columbia (BC) and one of
the goals of foresters is to develop management strategies
that maintain the diversity of forest organisms including
fungi. Mycorrhizae are mutually beneficial associations
between fungi and roots of plants and they are required
for healthy forests. Our studies have shown that BC fungi
are highly diverse (Allen et al. 2003, New Phytologist;
Wright et al. 2009, Mycorrhiza). Even though fungi
are clearly important to tree health, which fungi are important
for particular trees in particular regions of the province
remains largely unknown. With funding from the BC Forest
Science Program, from NSERC, and with the support of the
Vancouver Mycological Society and graduate and undergraduate
students conducting research projects, we are exploring
the diversity of fungi in BC and contributing to a DNA sequence
barcode database that will facilitate identification of
our mushroom species. With these data, we will be able to
correlate the occurrence of particular fungi with tree species,
with geographical regions, and with tree growth rates. This
research helps lay the groundwork for development of conservation
management strategies for fungi and for the plant community
that requires fungal partnerships.
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| Courses
Taught (2006-2007):
Biology 209: Biology of Nonvascular
Plants
Biology 323: Structure and Reproduction of Fungi
Biology 448: Directed studies
Biology 525: Phylogenetics Workshop. To be offered in June,
2009
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| Research
Team:
Satoshi Sekimoto (Postdoctoral researcher)
Jaclyn Dee (Research assistant)
Wyth Marshall (Graduate Student)
SeaRa Lim (Graduate Student)
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| Selected
Publications:
Deep divergences and ancient lineages.
Tsui, CK-M Marshall W Yokoyama R Honda
D Lippmeier C Craven KD, Peterson PD Berbee ML. 2009.
Labyrinthulomycetes phylogeny and its implications for
the evolutionary loss of chloroplasts and gain of ectoplasmic
gliding, Molecular Phylogenetics and Evolution, in press
available online 17 October 2008, DOI: 10.1016/j.ympev.2008.09.027.
Marshall W Celio G Padamsee M McLaughlin
D Berbee M. 2008. Multiple isolations of a culturable,
motile Ichthyosporean (Mesomycetozoa, Opisthokonta) Creolimax
fragrantissima n. gen., n. sp., from marine invertebrate
digestive tracts. Protist 159, 415-433.
Berbee ML, Taylor JW. 2007. Rhynie
chert: a window into a lost world of complex plant-fungus
interactions. New Phytologist174: 475-479.
Taylor JW, Berbee ML. 2006. Dating divergences
in the Fungal Tree of Life: Review with some new analyses.
Mycologia 98: 838-849.
Ascomycete evolution.
Tsui CKM, Berbee ML. 2006. Phylogenetic
relationships and convergence of helicosporous fungi inferred
from ribosomal DNA sequences. Mol Phyl Evol 39:587-597.
Inderbitzin P Shoemaker RA O'Neill
NR Turgeon BG Berbee ML. 2006. Systematics and mating
systems of two fungal pathogens of opium poppy: the heterothallic
Crivellia papaveracea with a Brachycladium penicillatum
asexual state and a homothallic species with a B.
papaveris asexual state. Can J Bot 84 1304-1326.
Inderbitzin P Harkness J Turgeon BGT
Berbee ML. 2005. Evolution of mating type gene arrangement
in the genus Stemphylium (Ascomycetes). PNAS
102:11390-11395.
Inderbitzin P, Lim SR, Volkmann-Kohlmeyer
B, Kohlmeyer J, Berbee ML. 2004. The phylogenetic position
of Spathulospora based on DNA sequences from
dried herbarium material. Mycol Res 108: 737-748.
Berbee ML, Payne BP, Zhang G, Roberts
RG, Turgeon BG. 2003. Shared ITS DNA substitutions in
isolates of opposite mating type reveal a recombining
history for three presumed asexual species in the filamentous
ascomycete genus Alternaria. Mycol Res 107:169-182.
Mycorrhizal fungal diversity.
Wright SHA Berch SM Berbee ML. 2008.
The effect of fertilization on the below-ground diversity
and community composition of ectomycorrhizal fungi associated
with western hemlock (Tsuga heterophylla). Mycorrhiza,
in press, accepted Dec 2008.
Allen TR, Millar T, Berch SM, Berbee
ML. 2003. Culturing and direct DNA extraction find different
fungi from the same ericoid mycorrhizal roots. New Phytologist
160: 255-272.
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