Dr.
Beatrice Holton
Associate Professor
and Co Chair
Department
of Biology/Microbiology
800 Algoma Ave.
UW Oshkosh
Oshkosh, W 54901
(920)
424-7087 or 424-1102
holton@uwosh.edu
Education
and Training:
B.A.
University of California, San Diego,
1974 (degree in Biology)
PhD.
University of Oregon, Eugene, 1980
(degree in Developmental Biology)
Postdoctoral
Research Fellow:
Pasteur Institute, Paris, France,
1980-83
University of California, Berkeley, 1983-1987
Courses
that I teach:
Biology 105 Concepts in Biology: Unity (usually Fall semester)
Biology 323 Introductory Molecular and Cell Biology (usually Fall semester)
Biology 372 Advanced Molecular and Cell Biology
Biology 316 Developmental Biology
Biology 317 Cell/Developmental Biology Laboratory
Biology 373 Biology Spring Field Trip
Research Interests:
What is a developmental biologist?
I am
a cell and developmental biologist. Developmental
biologists are interested in how single cells (e.g. fertilized eggs) give rise
to entire organisms that consist of multiple tissue types.
What chemical signals direct some cells to become neurons, for example,
whereas others become pigment cells? What
physical forces shape the developing embryo?
What factors control cellular and tissue movement so that embryonic
features develop? These are only a
few of the hundreds of questions that drive the research of developmental
biologists.
My
particular research interests:
FORMATION
OF THE AMNIOTIC MEMBRANE DURING CHICK DEVELOPMENT
Very
early in chick development the embryo is simply a population of cells in the
midst of a circular sheet of cells (the blastodisc).
As development proceeds, this sheet buckles at the anterior (head) end
and forms a fold. This fold rises
above the head of the embryo, collapses over the head and then moves down the
embryo until it, and a similar fold from the posterior, completely enclose the
embryo in the amniotic sac. My
laboratory is interested in two broad aspects of this phenomenon:
1)
The fold, as it moves down the embryo, appears to be under tension.
Preliminary work from this lab suggests that the tension is important for
proper embryonic trunk alignment. If
tension is vital to proper formation of the embryo and the membrane, how is that
tension controlled? Cell
proliferation or cell death could regulate this tension.
Two students in my laboratory are examining the contribution of each to
formation of the amniotic membrane.
2)
As the fold progresses down the embryo it seems that it must either
unroll or tractor down the embryo, or it must zip together as a body bag would
enclose a body. A student is
currently examining the physical process by which the membrane expands and
envelopes the embryo. She is also
mapping the position of cells that seem to be under tension and those that are
not. Her aim is to understand
better the source of the tension that seems so important for development.
Another student is examining changes to the cytoskeleton in individual
amniotic cells as the membrane forms.
Students
currently in my laboratory:
Evrard, Yvette – Master’s degree student who graduated from UWO with a double major in Biology and Art. She was supported Summer 2002 with a Faculty/Graduate Student Collaborative Grant.
Pulver,
Rebecca – Master’s degree student who graduated from UWO with a major in
Biology. She began research in my
lab as an undergraduate and was supported by a Faculty/Undergraduate Student
Collaborative Grant.
Tilkens,
Pennie – Master’s degree student who currently teaches at Green Bay
Technical College.
Govani,
Shaheda – Undergraduate, first year student….just getting started!
Most
Recent
Presentations (*denotes student co-authors):
Pulver,
R.*, Evrard, Y.*, Tilkens, P.* and Holton, B. Control
of tension across the chorioamniotic membrane. Society for Developmental Biology 61st Annual
Meeting, Madison, Wisconsin, July 21-25, 2002.
Macdonald,
T.E.* and Holton, B. PI3 kinase activity
affects formation and expansion of the amniotic membrane in avian embryos.
Society for Developmental Biology 59th Annual Meeting,
Boulder, Colorado, June 7-11, 2000.
Publications
(*denotes student co-authors):
Evrard, Y.A.*, Mohammad-Zadeh, L.* and Holton, B. (2004)
"Alterations in CA2+-dependent and
cAMP-dependent signaling pathways affect
neurogenesis and melanogenesis of quail neutral crest."
Development Genes and Evolution
214(4):193-199.
McDermott,
C.M., Nho, C.W.*, Howard, W.* and Holton, B.
(1998) "The cyanobacterial toxin, microcystin-LR, can induce
apoptosis in a variety of cell types."
Toxicon 3(12):1981-1996.
Holton,
B., Wu, X., Tsapin, A.I., Kramer, D.M., Malkin,R.
and Kallas,T. (1996)
"Reconstitution of the 2Fe-2S Center and g=1.89
Electron Paramagnetic Resonance Signal into Overproduced Nostoc sp. PCC 7906
Rieske Protein." Biochemistry
35:15485-15493.
Holton,
B., C.J. Wedeen, C.J., S.H. Astrow* and D.A. Weisblat (1994) "Localization
of Polyadenylated RNA's During Teloplasm Formation and Cleavage of Leech
Embryos." (1994) Roux Archives
Developmental Biology 204:46-53.
Holton, B.,
Middleton, K.*, Zarka, D.*, Alsaadi, R.* and T. Kallas. (1992).
"Overproduction of the Rieske Fe-S protein and preparations for mutagenesis
of the cytochrome b6f complex in cyanobacteria.
In: Progress
in Photosynthesis Research, Proc. IXth Intl. Congr. Photosynthesis (N.
Murata, ed.) Vol. II, Kluwer Academic Publishers, Dordrecht
pg. 567-570.
Astrow,
S.*, B. Holton and D.A. Weisblat. (1989) "Teloplasm Formation in a Leech Helobdella
triseriallis Is a Microtubule-dependent Process." Developmental Biology 135, 306-319.
Holton,
B., S. Astrow * and D.A. Weisblat. (1989) "Animal and Vegetal Teloplasm(s)
Mix in the Early Embryo of the Leech Helobdella
triserialis." Developmental
Biology 131, 182-188.
Weisblat,
D.A., S. Astrow, S.* Bissen, R. Ho, B. Holton and S. Settle. (1987) "Early
Events Associated with Cell Fate in Leech Embryos." in Genetic
Regulation of Development, W.S. Loomis, ed., Alan R. Liss, N.Y. 265-285.
Astrow,
S.*, B. Holton and D.A. Weisblat. (1987) "Centrifugation Redistributes
Factors Determining Cleavage Patterns in Leech Embryos." Developmental
Biology 120, 270-283.
Changeux,
J.-P., F. Bon, J. Cartaud, A. Devillers-Thiery, J. Giraudat*, T. Heidman*, B.
Holton, H.O. Nghiem, J.-L. Popot, R. Van Rapenbusch, S. Tzartos. (1983) "Allosteric
Properties of the Acetylcholine Receptor Protein from Torpedo
marmorata." Cold Spring Harbor
Symposia on Quantitative Biology 48, 35-52.
Holton,
B.* and J.A. Weston. (1982) "Analysis of Glial Cell Differentiation in
Peripheral Nervous Tissue. II. Neurons Promote S100 Synthesis by Purified Glial
Precursor Cell Populations." Developmental
Biology 89,72-81.
Holton,
B.* and J.A. Weston. (1982) "Analysis of Glial Cell Differentiation in
Peripheral Nervous Tissue. I.S100 Accumulation in Quail Embryo Spinal Ganglion
Cultures." Developmental Biology
89, 64-71.