Circadian
neurons
within
animal
brains
orchestrate
myriad
physiological
processes
and
behaviors,
but
the
contribution
of
these
to
regulation
sleep
is
not
well
understood.
To
address
this
deficiency,
we
leveraged
single-cell
RNA
sequencing
generate
a
comprehensive
census
transcriptomic
cell
types
Drosophila
clock
neurons.
We
focused
principally
on
enigmatic
DN3s,
which
constitute
most
fly
brain
were
previously
almost
completely
uncharacterized.
These
DN3s
are
organized
into
12
clusters
with
unusual
gene
expression
features
compared
more
well-studied
further
show
that
uncharacterized
DN3
subtypes
promote
through
G
protein–coupled
receptor,
TrissinR
.
Our
findings
indicate
an
intricate
behavior
by
highlight
their
remarkable
diversity
in
functional
properties.
Making
inferences
about
the
computations
performed
by
neuronal
circuits
from
synapse-level
connectivity
maps
is
an
emerging
opportunity
in
neuroscience.
The
mushroom
body
(MB)
well
positioned
for
developing
and
testing
such
approach
due
to
its
conserved
architecture,
recently
completed
dense
connectome,
extensive
prior
experimental
studies
of
roles
learning,
memory,
activity
regulation.
Here,
we
identify
new
components
MB
circuit
Drosophila,
including
visual
input
output
neurons
(MBONs)
with
direct
connections
descending
neurons.
We
find
unexpected
structure
sensory
inputs,
transfer
information
different
modalities
MBONs,
modulation
that
dopaminergic
(DANs).
provide
insights
into
circuitry
used
integrate
outputs,
between
central
complex
inputs
DANs,
feedback
MBONs.
Our
results
a
foundation
further
theoretical
work.
Many
different
functions
are
regulated
by
circadian
rhythms,
including
those
orchestrated
discrete
clock
neurons
within
animal
brains.
To
comprehensively
characterize
and
assign
cell
identity
to
the
75
pairs
of
Drosophila
neurons,
we
optimized
a
single-cell
RNA
sequencing
method
assayed
neuron
gene
expression
at
times
day.
The
data
identify
least
17
categories
with
striking
spatial
regulation
expression.
Transcription
factor
is
prominent
likely
contributes
robust
oscillation
many
transcripts,
that
encode
cell-surface
proteins
previously
shown
be
important
for
recognition
synapse
formation
during
development.
other
clock-regulated
genes
also
constitute
an
resource
future
mechanistic
functional
studies
between
and/or
temporal
signaling
circuits
elsewhere
in
fly
brain.
Journal of Neuroscience,
Год журнала:
2009,
Номер
29(8), С. 2597 - 2610
Опубликована: Фев. 25, 2009
The
neuropeptide
pigment-dispersing
factor
(PDF)
is
a
key
transmitter
in
the
circadian
clock
of
Drosophila
melanogaster.
PDF
necessary
for
robust
activity
rhythms
and
thought
to
couple
oscillations
neurons.
However,
little
known
about
action
on
individual
Here,
we
combined
period
–luciferase
reporter
system
with
immunolabeling
proteins
wild-type
Pdf
01
mutants
dissect
effects
specific
subgroups
Additionally,
levels
were
elevated
higher
than
normal
using
neural
mutants,
correlation
analysis
locomotor
protein
staining
served
determine
periods
cells.
We
found
that
has
multiple
neurons:
In
some
groups
neurons,
was
required
maintaining
cells,
others,
synchronous
cycling
members.
Other
neurons
cycled
high
amplitude
absence
PDF,
but
affected
their
intrinsic
speed.
Sometimes
shortened
sometimes
lengthened
period.
Our
observations
indicate
crucial
adjusting
amplitude,
period,
phase
different
players
clock.
Under
natural
conditions
may
be
adapting
Drosophila'
s
varying
photoperiods.
Indeed,
show
here
are
not
able
adapt
long
photoperiods
manner.
PLoS Biology,
Год журнала:
2008,
Номер
6(3), С. e69 - e69
Опубликована: Март 18, 2008
Clock
output
pathways
are
central
to
convey
timing
information
from
the
circadian
clock
a
diversity
of
physiological
systems,
ranging
cell-autonomous
processes
behavior.
While
molecular
mechanisms
that
generate
and
sustain
rhythmicity
at
cellular
level
well
understood,
it
is
unclear
how
this
further
structured
control
specific
behavioral
outputs.
Rhythmic
release
pigment
dispersing
factor
(PDF)
has
been
proposed
propagate
time
day
core
pacemaker
cells
downstream
targets
underlying
rhythmic
locomotor
activity.
Indeed,
such
changes
in
PDF
intensity
represent
only
known
mechanism
through
which
circuit
could
communicate
with
its
output.
Here
we
describe
novel
phenomenon
involving
extensive
remodeling
axonal
terminals
circuit,
display
higher
complexity
during
significantly
lower
nighttime,
both
under
daily
cycles
constant
conditions.
In
support
nature,
cycling
lost
bona
fide
clockless
mutants.
We
propose
clock-controlled
structural
plasticity
as
candidate
contributing
transmission
cells.
The Journal of Comparative Neurology,
Год журнала:
2006,
Номер
500(1), С. 47 - 70
Опубликована: Ноя. 10, 2006
The
clock-gene-expressing
lateral
neurons
are
essential
for
the
locomotor
activity
rhythm
of
Drosophila
melanogaster.
Traditionally,
these
divided
into
three
groups:
dorsal
(LN(d)),
large
ventral
(l-LN(v)),
and
small
(s-LN(v)),
whereby
latter
group
consists
four
that
express
neuropeptide
pigment-dispersing
factor
(PDF)
a
fifth
PDF-negative
neuron.
So
far,
only
l-LN(v)
PDF-positive
s-LN(v)
have
been
shown
to
project
accessory
medulla,
neuropil
contains
circadian
pacemaker
center
in
several
insects.
We
show
here
other
also
arborize
predominantly
forming
postsynaptic
sites.
Both
LN(d)
anatomically
well
suited
connect
medullae.
Whereas
may
receive
ipsilateral
photic
input
from
Hofbauer-Buchner
eyelet,
invade
mainly
contralateral
medulla
thus
side.
differentiate
during
midmetamorphosis.
They
do
so
close
proximity
one
another
s-LN(v),
suggesting
cell
groups
derive
common
precursors.
Journal of Neuroscience,
Год журнала:
2006,
Номер
26(9), С. 2531 - 2543
Опубликована: Март 1, 2006
The
molecular
mechanisms
of
circadian
rhythms
are
well
known,
but
how
multiple
clocks
within
one
organism
generate
a
structured
rhythmic
output
remains
mystery.
Many
animals
show
bimodal
activity
with
morning
(M)
and
evening
(E)
bouts.
One
long-standing
model
assumes
that
two
mutually
coupled
oscillators
underlie
these
bouts
different
sensitivities
to
light.
Three
groups
lateral
neurons
(LN)
three
dorsal
govern
behavioral
rhythmicity
Drosophila
.
Recent
data
suggest
the
LN
(the
ventral
subset
small
cells
cells)
plausible
candidates
for
M
E
oscillator,
respectively.
We
provide
evidence
neuronal
respond
differently
light
can
be
completely
desynchronized
from
another
by
constant
light,
leading
components
free-run
periods.
As
expected,
long-period
component
started
bout.
However,
short-period
originated
not
exclusively
peak
more
prominently
peak.
This
reveals
an
interesting
deviation
original
Pittendrigh
Daan
(1976)
suggests
subgroup
acts
as
“main”
oscillator
controlling
in