Movement
is
a
key
feature
of
animal
systems,
yet
its
embryonic
origins
are
not
fully
understood.
Here,
we
investigate
the
genetic
basis
underlying
onset
movement
in
Drosophila
focusing
on
role
played
by
small
non-coding
RNAs
(microRNAs,
miRNAs).
To
this
end,
first
develop
quantitative
behavioural
pipeline
capable
tracking
large
populations
fly
embryos,
and
using
system,
discover
that
miRNA
miR-2b-1
plays
emergence
movement.
Through
combination
spectral
analysis
motor
patterns,
cell
sorting
RNA
situs,
reconstitution
tests,
neural
optical
imaging
define
influences
exerting
actions
developing
nervous
system.
Furthermore,
through
bioinformatics
coupled
to
manipulation
expression
phenocopy
tests
identify
previously
uncharacterised
(but
evolutionarily
conserved)
chloride
channel
encoding
gene
–
which
term
Mo
vement
Modula
tor
(
Motor
)
as
target
mechanistically
links
Cell-specific
null
mutant
background,
followed
assays
analyses,
suggest
affects
effects
sensory
elements
circuitry,
rather
than
domain.
Our
work
thus
reports
system
regulating
movement,
suggesting
other
miRNAs
likely
play
developmental
process
well
species.
bioRxiv (Cold Spring Harbor Laboratory),
Год журнала:
2024,
Номер
unknown
Опубликована: Март 13, 2024
The
gut
undergoes
peristaltic
movements
regulated
by
intricate
cellular
interactions.
How
there
interactions
emerge
in
the
developing
remains
poorly
explored
due
to
a
lack
of
model
system.We
here
developed
novel
contractile
organoid
that
is
derived
from
muscle
layer
chicken
embryonic
hindgut.
contained
smooth
cells
(SMCs)
and
interstitial
Cajal
(ICCs;
pacemaker)
with
few
enteric
neurons,
underwent
periodic
contractions.
formed
self-organization
morphological
arrangements
ICCs
(internal)
SMCs
(peripheral),
allowing
identification
these
live.
GCaMP-Ca2+
imaging
analyses
revealed
Ca2+
transients
between
ICC-ICC,
SMC-SMC
or
SMC-ICC
were
markedly
coordinated.
Pharmacological
studies
further
suggested
role
gap
junctions
ICC-to-SMC
signaling,
also
possible
mechanical
feedback
SMC's
contraction
ICC's
pace-making
activities.
In
addition,
two
organoids
different
rhythm
became
synchronized
when
mediated
SMCs,
unveiling
contribution
pace-making.
this
study
offers
useful
understand
how
coordination
between/among
maintained
during
development.
Movement
is
a
key
feature
of
animal
systems,
yet
its
embryonic
origins
are
not
fully
understood.
Here
we
investigate
the
genetic
basis
underlying
onset
movement
in
Drosophila
focusing
on
role
played
by
small
non-coding
RNAs
(microRNAs,
miRNAs).
To
this
end,
first
develop
quantitative
behavioural
pipeline
capable
tracking
large
populations
fly
embryos,
and
using
system,
discover
that
miRNA
miR-2b-1
plays
emergence
movement.
Through
combination
spectral
analysis
motor
patterns,
cell
sorting
RNA
situs
,
reconstitution
tests,
neural
optical
imaging
define
influences
exerting
actions
developing
nervous
system.
Furthermore,
through
bioinformatics
coupled
to
manipulation
expression
phenocopy
tests
identify
previously
uncharacterised
(but
evolutionarily
conserved)
chloride
channel
encoding
gene
–
which
term
Janus
as
target
mechanistically
links
Cell-specific
null
mutant
background,
followed
assays
analyses,
suggest
affects
effects
sensory
elements
circuitry,
rather
than
domain.
Our
work
thus
reports
system
regulating
movement,
suggesting
other
miRNAs
likely
play
developmental
process
well
species.
bioRxiv (Cold Spring Harbor Laboratory),
Год журнала:
2024,
Номер
unknown
Опубликована: Май 26, 2024
Direct
measurement
of
neural
activity
in
freely
moving
animals
is
essential
for
understanding
how
the
brain
controls
and
represents
behaviors.
Genetically
encoded
calcium
indicators
report
as
changes
fluorescence
intensity,
but
motion
confounds
quantitative
fluorescence.
Translation,
rotation,
deformation
movements
intervening
scattering
or
auto-fluorescent
tissue
all
alter
amount
fluorescent
light
captured
by
a
microscope.
Compared
to
single-photon
approaches,
two
photon
microscopy
less
sensitive
off-target
fluorescence,
more
motion,
imaging
has
always
required
anchoring
microscope
brain.
We
developed
closed-loop
resonant
axial-scanning
high-speed
(CRASH2p)
real-time
3D
correction
unrestrained
animals,
without
implantation
reference
markers.
complemented
CRASH2p
with
novel
scanning
strategy
multi-stage
registration
pipeline.
performed
volumetric
ratiometrically
corrected
functional
CNS
Drosophila
larvae
discovered
previously
unknown
correlates
behavior.
Movement
is
a
key
feature
of
animal
systems,
yet
its
embryonic
origins
are
not
fully
understood.
Here
we
investigate
the
genetic
basis
underlying
onset
movement
in
Drosophila
focusing
on
role
played
by
small
non-coding
RNAs
(microRNAs,
miRNAs).
To
this
end,
first
develop
quantitative
behavioural
pipeline
capable
tracking
large
populations
fly
embryos,
and
using
system,
discover
that
miRNA
miR-2b-1
plays
emergence
movement.
Through
combination
spectral
analysis
motor
patterns,
cell
sorting
RNA
situs
,
reconstitution
tests,
neural
optical
imaging
define
influences
exerting
actions
developing
nervous
system.
Furthermore,
through
bioinformatics
coupled
to
manipulation
expression
phenocopy
tests
identify
previously
uncharacterised
(but
evolutionarily
conserved)
chloride
channel
encoding
gene
–
which
term
Mo
vement
Modula
tor
(
Motor)
as
target
mechanistically
links
Cell-specific
null
mutant
background,
followed
assays
analyses,
suggest
affects
effects
sensory
elements
circuitry,
rather
than
domain.
Our
work
thus
reports
system
regulating
movement,
suggesting
other
miRNAs
likely
play
developmental
process
well
species.
Movement
is
a
key
feature
of
animal
systems,
yet
its
embryonic
origins
are
not
fully
understood.
Here,
we
investigate
the
genetic
basis
underlying
onset
movement
in
Drosophila
focusing
on
role
played
by
small
non-coding
RNAs
(microRNAs,
miRNAs).
To
this
end,
first
develop
quantitative
behavioural
pipeline
capable
tracking
large
populations
fly
embryos,
and
using
system,
discover
that
miRNA
miR-2b-1
plays
emergence
movement.
Through
combination
spectral
analysis
motor
patterns,
cell
sorting
RNA
situs,
reconstitution
tests,
neural
optical
imaging
define
influences
exerting
actions
developing
nervous
system.
Furthermore,
through
bioinformatics
coupled
to
manipulation
expression
phenocopy
tests
identify
previously
uncharacterised
(but
evolutionarily
conserved)
chloride
channel
encoding
gene
–
which
term
Mo
vement
Modula
tor
(
Motor
)
as
target
mechanistically
links
Cell-specific
null
mutant
background,
followed
assays
analyses,
suggest
affects
effects
sensory
elements
circuitry,
rather
than
domain.
Our
work
thus
reports
system
regulating
movement,
suggesting
other
miRNAs
likely
play
developmental
process
well
species.