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Evolutionary
developmental biology
We are interested in a broad range of problems associated with the
cellular, molecular, and evolutionary basis of biological pattern
formation. My lab utilizes a variety of molecular and "classical"
techniques of microinjection, cell labeling, ablation, and transplantation,
to address fundamental problems in developmental biology in a phylogenetic
context.
My lab is currently focused in three major areas.
The first area of interest is to understand the relationship between
radially symmetrical and bilaterally symmetrical organisms. Current
theory predicts that bilaterians are derived from a radially symmetrical
stock, yet there is little evidence for how such a transition might
have occurred. For example, what is the relationship of the oral-aboral
axis of radially symmetrical forms to the anterior-posterior of
bilaterians? How did the dorsoventral axis arise? To what degree
are the molecular events underlying patterning events conserved
in this group of animals? We are investigating these and other aspects
of early development in representatives of both anthozoan cnidarian
(corals and sea anemones) and ctenophore embryos.
The second area is to understand the evolution of
the third, "middle" embryonic germ layer (called mesoderm)
and the evolution of the nervous system in phylogenetically important
groups (e.g. including cnidarians, ctenophores, acoel flatworms,
and chaetognaths) to see if networks of gene expression observed
in bilaterian animals are used in similar ways throughout the Metazoa.
The third area of interest is to understand the
role of the early cleavage program in the segregation of developmental
potential in a wide variety of animals which share a mode of embryogenesis
known as spiral cleavage (e.g. molluscs, annelids, nemerteans, sipunculids,
echiurans, and flatworms..). Of particular interest is the mechanisms
by which dorsoventral polarity is established in members of different
spiralian phyla. We are also interested in understanding the significance
of naturally evolved variations in the spiral cleavage program such
as modifications associated with the abandonment of larval development
in order to develop directly to a miniature adult form (direct development).
Representative
publications
Finnerty, J.R., Pang, K., Burton, P., Paulson, D., and Martindale,
M.Q. 2004. Deep Origins for Bilateral Symmetry: Hox and Dpp Expression
in a sea anemone. Science, 304, 1335-1337.
Maslakova, S., Martindale, M.Q., and Norenberg,
J.L. 2004. The vestigial prototroch in a basal nemertean Carinoma
tremaphoros (Nemertea; Palaeonemertea). Evol. Dev., 6, 219-226.
Martindale, M.Q., Pang, K., and Finnerty, J.R. 2004.
Investigating the origins of triploblasty: "Mesodermal"
gene expression in a diploblastic animal, the sea anemone, Nematostella
vectensis (phylum, Cnidaria; Class Anthozoa). Development, 131,
2463-2474.
Henry, J.Q., Okusu, A., and Martindale, M.Q. 2004.
The cell lineage of the polyplochphoran, Chaetopleura apiculata:
variation in the spiralian program and implications for molluscan
evolution. Dev. Bio., 272, 145-160.
Kusserow, A., Pang, K., Sturm, C., Hrouda, M., Lentfer,
J., Technau, U., Hobmayer, B., Martindale M.Q., and Holstein, T.W.
2005. Unexpected complexity of Wnt gene family in a sea anemone.
Nature, 433, 156-160. (cover image).
Extavour, C. G., Pang, K., Matus, D.Q. and Martindale,
M.Q. 2005. vasa and nanos expression Patterns in a Sea Anemone and
the Evolution of Bilaterian Germ Cell Specification Mechanisms.
Evol. Dev., 7, 201-215.
Maxmen, A., Browne, W.E., Martindale, M.Q., and
Gonzalo Giribet, G. 2005. Neuroanatomy of sea spiders: Implications
for the evolution of the arthropod head. Nature, 437, 1144-1148.
Magie, C.R., Pang, K., Martindale, M.Q. 2005. Genomic
inventory and expression of Sox and Fox genes in the cnidarian Nematostella
vectensis. Dev. Genes Evol., 215, 618-630.
Matus, D. Q., Thomsen, G.H., and Martindale, 2006.
M.Q. "Dorso-ventral" genes are asymmetrically expressed
and involved in germ layer demarcation during cnidarian gastrulation.
Current Biology, 16, 499-505.
Lee, P.N., Kumburegama, S., Marlow, H., Martindale,
M.Q. and Wikramanayake, A. H. 2007. Evolution of the primary egg
axis in the sea anemone, Nematostella vectensis. Dev. Bio. 310,
169-186.
Browne, W.E., Schmid, B.G.M., Wimmer, E.A., and
Martindale, M.Q. 2006. Expression of otd orthologs in the amphipod
crustacean, Parhyale hawaiensis. Dev. Genes Evol., 216: 581-595
Henry, J.Q., Perry, K., and Martindale, M.Q. 2006.
Cell specification and the role of the polar lobe in the gastropod
mollusc, Crepidula fornicata. Dev. Biol. 297:295-307
Matus, D. Q., Pang, K., Marlow, H., Dunn, C., Thomsen,
G.H., and Martindale, M. Q. 2006. Molecular evidence for deep evolutionary
roots of bilaterality in animal development. PNAS. 103, 11195-11200..
Hejnol, A., Martindale, M.Q., and Henry, J.J.Q.
2007. High-resolution fate map of the gastropod snail Crepidula
fornicata: the origins of ciliary bands, nervous and muscular elements.
Dev. Bio. 305, 63-76.
Lee, P.N., Kumburegama, S., Marlow, H., Martindale,
M.Q. and Wikramanayake, A. H. 2007. Evolution of the primary egg
axis in the sea anemone, Nematostella vectensis. Dev. Bio. 310,
169-186.
Putnum, N., , Srivastava, M., Hellsten, U., Dirks,
B., Chapman, J., Salamov, A., Terry, A., Shapiro, H., Lindquist,
E., Kapitonov, V.V., Jurka, J., Genikhovich, G., Grigoriev, I.,
JGI Sequencing Team, Steele, R., Finnerty, J.R., Technau, U., Martindale,
M.Q., and Rokhsar, D. 2007. Sea anemone genome reveals the gene
repertoire and genomic organization of the eumetazoan ancestor.
2007, Science, 317, 86-94.
Adamska, M., Matus, D.Q., Adamski, M., Green, K.,
Martindale, M.Q., and Degnan, B.M. 2007. Evolutionary origin of
hedgehog proteins. Current Biology, 17, R836-37.
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