Current
thought
envisions
dopamine
neurons
conveying
the
reinforcing
effect
of
unconditioned
stimulus
during
associative
learning
to
axons
Drosophila
mushroom
body
Kenyon
cells
for
normal
olfactory
learning.
Here,
we
show
using
functional
GFP
reconstitution
experiments
that
and
from
axoaxonic
reciprocal
synapses.
The
receive
cholinergic
input
via
nicotinic
acetylcholine
receptors
cells;
knocking
down
these
impairs
revealing
importance
at
synapse.
Blocking
synaptic
output
conditioning
reduces
presynaptic
calcium
transients
in
neurons,
a
finding
consistent
with
communication.
Moreover,
silencing
decreases
chronic
activity
neurons.
Our
results
reveal
new
critical
role
positive
feedback
onto
through
connections
Understanding
memory
formation,
storage
and
retrieval
requires
knowledge
of
the
underlying
neuronal
circuits.
In
Drosophila,
mushroom
body
(MB)
is
major
site
associative
learning.
We
reconstructed
morphologies
synaptic
connections
all
983
neurons
within
three
functional
units,
or
compartments,
that
compose
adult
MB's
α
lobe,
using
a
dataset
isotropic
8
nm
voxels
collected
by
focused
ion-beam
milling
scanning
electron
microscopy.
found
Kenyon
cells
(KCs),
whose
sparse
activity
encodes
sensory
information,
each
make
multiple
en
passant
synapses
to
MB
output
(MBONs)
in
compartment.
Some
MBONs
have
inputs
from
KCs,
while
others
differentially
sample
modalities.
Only
6%
KC>MBON
receive
direct
synapse
dopaminergic
neuron
(DAN).
identified
two
unanticipated
classes
synapses,
KC>DAN
DAN>MBON.
DAN
activation
produces
slow
depolarization
MBON
these
DAN>MBON
can
weaken
recall.
Genetics,
Journal Year:
2017,
Volume and Issue:
205(4), P. 1373 - 1397
Published: March 30, 2017
The
advantages
of
the
model
organism
Drosophila
melanogaster,
including
low
genetic
redundancy,
functional
simplicity,
and
ability
to
conduct
large-scale
screens,
have
been
essential
for
understanding
molecular
nature
circadian
(∼24
hr)
rhythms,
continue
be
valuable
in
discovering
novel
regulators
rhythms
sleep.
In
this
review,
we
discuss
current
these
interrelated
biological
processes
wider
implications
research.
Clock
genes
period
timeless
were
first
discovered
screens
developed
1970s.
Feedback
on
their
own
transcription
forms
core
clock,
accurately
timed
expression,
localization,
post-transcriptional
modification,
function
is
thought
critical
maintaining
cycle.
Regulators,
several
phosphatases
kinases,
act
different
steps
feedback
loop
ensure
strong
rhythms.
Approximately
150
neurons
fly
brain
that
contain
components
clock
together
translate
intracellular
cycling
into
rhythmic
behavior.
We
how
groups
serve
functions
allowing
clocks
entrain
environmental
cues,
driving
behavioral
outputs
at
times
day,
flexible
responses
conditions.
neuropeptide
PDF
provides
an
important
signal
synchronize
neurons,
although
details
accomplishes
are
still
being
explored.
Secreted
signals
from
also
influence
other
tissues.
SLEEP
is,
part,
regulated
by
which
ensures
appropriate
timing
sleep,
but
amount
quality
sleep
determined
mechanisms
a
homeostatic
balance
between
wake.
Flies
useful
identifying
large
set
genes,
molecules,
neuroanatomic
loci
regulating
amount.
Conserved
aspects
regulation
flies
mammals
include
wake-promoting
roles
catecholamine
neurotransmitters
involvement
hypothalamus-like
regions,
regions
implicated
less
clear
parallels.
Sleep
subject
factors
such
as
food
availability,
stress,
social
environment.
beginning
understand
identified
molecules
interact
with
each
other,
environment,
regulate
researchers
can
take
advantage
increasing
mechanistic
behaviors,
learning
memory,
courtship,
aggression,
loss
impacts
behaviors.
thus
remain
tool
both
discovery
deep
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.
Flexible
behaviors
over
long
timescales
are
thought
to
engage
recurrent
neural
networks
in
deep
brain
regions,
which
experimentally
challenging
study.
In
insects,
circuit
dynamics
a
region
called
the
central
complex
(CX)
enable
directed
locomotion,
sleep,
and
context-
experience-dependent
spatial
navigation.
We
describe
first
complete
electron
microscopy-based
connectome
of
Annual Review of Neuroscience,
Journal Year:
2020,
Volume and Issue:
43(1), P. 465 - 484
Published: April 14, 2020
The
Drosophila
brain
contains
a
relatively
simple
circuit
for
forming
Pavlovian
associations,
yet
it
achieves
many
operations
common
across
memory
systems.
Recent
advances
have
established
clear
framework
learning
and
revealed
the
following
key
operations:
a)
pattern
separation,
whereby
dense
combinatorial
representations
of
odors
are
preprocessed
to
generate
highly
specific,
nonoverlapping
odor
patterns
used
learning;
b)
convergence,
in
which
sensory
information
is
funneled
small
set
output
neurons
that
guide
behavioral
actions;
c)
plasticity,
where
changing
mapping
input
requires
strong
reinforcement
signal,
also
modulated
by
internal
state
environmental
context;
d)
modularization,
consists
multiple
parallel
traces,
distinct
stability
flexibility
exist
anatomically
well-defined
modules
within
network.
Cross-module
interactions
allow
higher-order
effects
past
experience
influences
future
learning.
Many
these
parallels
with
processes
formation
action
selection
more
complex
brains.