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Expression of Cyclin D1 in zebrafish embryo
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Expression of Cyclin D1 in zebrafish embryo
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Description
Identifier
Thesis
2115
Author
Ji, Min, 1969-
Title
Expression
of
Cyclin
D1
in
zebrafish
embryo
Publisher
Central Connecticut State University
Date
2010
Resource Type
Master's Thesis
Notes
Cyclin
D1
is
the
major
regulator
of
cell
cycle
---
the
division
of
cells
to
copy
themselves
.
Cyclin
D1
is
the
product
of
ccnd1
gene
and
plays
an
important
role
in
regulation
of
cell
cycle
transition
from
G1
phase
to
S
phase
. The
cell
cycles
of
zebrafish
embryonic
cells
in the
developmental
early
stage
are
very
short
and
synchronous
.
DNA
replication
(S
phase)
and
mitosis
(M
phase)
can
be
observed
, but there
is
not
detectable
G1
or
G2
phase
of the
cell
cycle
in
zebrafish
early
developmental
stage
.
Subsequently
,
cell
cycles
gradually
lengthen
and
cells
gradually
lose
synchrony
during
the
embryonic
development
.
It
will be
very
important
to
know
when
and
where
the
ccnd1
starts
to
express
in
zebrafish
embryo
during
the
embryogenesis
.
We
have
implemented
in
situ
hybridization
to
localize
the
ccnd1
gene’s
transcript
during
zebrafish
embryogenesis
.
We
have
found
that
ccnd1
gene
is
expressed
in the
surface
of
germ
ring
during
gastrulation
period
of
zebrafish
embryo
,
which
is
as
early
as the
stage
at
5.7
hpf
(hours
post
fertilization)
.
MyoD
is
an
important
gene
regulating
muscle
formation
during
embryogenesis
.
MyoD
and
cyclin
D1
had been
reported
to
antagonize
each
other
. To
better
understand
how
cyclin
D1
and
MyoD
regulate
each
other
,
we
have also
localized
MyoD
gene
transcript
in
zebrafish
embryo
by in
situ
hybridization
.
We
have
found
that
MyoD
expressed
in the
tail
of
embryo
dorsal
side
at the
shield
stage
(6
hpf)
following
the
stage
of
ccnd1
expression
.
MyoD
transcript-localized
cells
formed
a
unique
pattern
. The
patches
of
cells
with
MyoD
transcript
elongated
and
formed
a
pair
of
narrow
longitudinal
rows
,
which
lay
on
either
side
of the
prospective
notochord
. The
expressing
patterns
and
locations
of
two
genes
are
different
.
Some
locations
of
two
genes’
transcripts
seem
to
overlap
.
Further
experiments
using
fluorescent
in
situ
hybridization
(FISH)
need
to be
done
to
detect
both
ccnd1
and
MyoD
genes’
transcripts
in the
same
cells
in the
embryo
to
check
if
both
genes
can
be
co-localized
in the
same
cells
in
different
stage
of
embryogenesis
.
Subject
Cyclins
Zebra danio
Cells -- Growth -- Regulation
Department
Department of Biomolecular Sciences
Advisor
Martin-Troy, Kathy
Type
Text
Digital Format
application/pdf
Language
eng
OCLC number
703420784
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