Deciphering the epigenetic role of long non‐coding RNAs in mood disorders: Focus on human brain studies
Bhaskar Roy,
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Anuj Kumar Verma,
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Yu Funahashi
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et al.
Clinical and Translational Medicine,
Journal Year:
2025,
Volume and Issue:
15(3)
Published: March 1, 2025
Language: Английский
Decoding the complex journeys of RNAs along neurons
Nucleic Acids Research,
Journal Year:
2025,
Volume and Issue:
53(7)
Published: April 10, 2025
Abstract
Neurons
are
highly
polarized,
specialized
cells
that
must
overcome
immense
challenges
to
ensure
the
health
and
survival
of
organism
in
which
they
reside.
They
can
spread
over
meters
persist
for
decades
yet
communicate
at
sub-millisecond
millimeter
scales.
Thus,
neurons
require
extreme
levels
spatial-temporal
control.
employ
molecular
motors
transport
coding
noncoding
RNAs
distal
synapses.
Intracellular
trafficking
enables
locally
regulate
protein
synthesis
synaptic
activity.
The
way
get
loaded
onto
transported
their
target
locations,
particularly
following
plasticity,
is
explored
below.
Language: Английский
Non-coding RNA and memory
Elsevier eBooks,
Journal Year:
2025,
Volume and Issue:
unknown
Published: Jan. 1, 2025
Language: Английский
lncRNA ADEPTR loss-of-function elicits sex-specific behavioral and spine deficits
bioRxiv (Cold Spring Harbor Laboratory),
Journal Year:
2024,
Volume and Issue:
unknown
Published: May 26, 2024
Abstract
Activity-dependent
changes
in
neuronal
connections
are
fundamental
to
learning
and
long-term
memory
storage.
However,
the
precise
contribution
of
long
noncoding
RNAs
(lncRNAs)
these
modifications
remains
unclear.
In
this
study,
we
assessed
role
lncRNA
ADEPTR,
a
cAMP-modulated
localized
dendrites,
which
is
crucial
for
synapse
morphology.
By
generating
two
different
mouse
models—one
with
deletion
ADEPTR
(L-ADEPTR)
one
its
protein
interaction
region
(S-ADEPTR)—we
investigated
sex-specific
impacts
loss
function
on
learning,
memory,
dendritic
arborization,
Our
behavioral
analyses
revealed
reduction
anxiety
adult
male
mice,
while
remained
unaffected
both
models.
Systematic
evaluations
morphology
across
various
developmental
stages
(∼3-day-old
postnatal
cultures
14-
42-day-old
female
mice)
uncovered
substantial
deficits
architecture
S-
L-ADEPTR
cultures.
At
day
42,
contrast
their
counterparts,
mice
exhibited
significant
deficiency
thin
spines.
Additionally,
found
that
expression
plasticity-related
gene
BDNF,
immediate
early
cFOS
were
enhanced
cortex
hippocampus
suggesting
activation
compensatory
mechanism
protecting
against
deficits.
Collectively,
observations
underscore
shaping
behavior.
Language: Английский
lncRNA ADEPTR Loss-of-Function Elicits Sex-Specific Behavioral and Spine Deficits
Published: Jan. 1, 2024
Language: Английский
Profiling hippocampal expression of long non-coding RNA GM12371 in a rat model of vascular dementia
Egyptian Journal of Medical Human Genetics,
Journal Year:
2024,
Volume and Issue:
25(1)
Published: Oct. 6, 2024
Abstract
Background
Dementia,
characterized
by
synaptic
dysfunction
and
memory
loss,
presents
a
significant
challenge
in
medical
research.
Long
non-coding
RNAs
(lncRNAs),
known
for
their
crucial
roles
regulating
gene
expression,
represent
gap
knowledge
regarding
specific
involvement
structure,
transmission,
plasticity.
This
study
aims
to
investigate
the
dynamic
changes
hippocampal
lncRNA
GM12371
expression
response
acute
chronic
hypoperfusion
rat
brain
using
2VO
model.
Methods
The
model
was
induced
permanently
occluding
common
carotid
arteries.
Quantitative
real-time
polymerase
chain
reaction
(qRT-PCR)
used
evaluate
at
both
(day
4)
28)
stages
post-2VO
surgery.
Comparative
analysis
conducted
with
sham-operated
group.
Results
A
notable
reduction
observed
hippocampus
on
day
4
following
surgery
compared
sham
group
(
P
<
0.05).
However,
there
no
difference
between
2VO-28
groups.
Conclusion
These
findings
suggest
that
downregulation
of
is
blood
flow
but
tends
normalize
during
phase
cerebral
hypoperfusion.
regulation
may
be
adaptive
vascular
dementia.
Further
clinical
studies
are
warranted
potential
peripheral
alterations
individuals
Language: Английский
Structural basis for ring-opening fluorescence by the RhoBAST RNA aptamer.
bioRxiv (Cold Spring Harbor Laboratory),
Journal Year:
2024,
Volume and Issue:
unknown
Published: Dec. 30, 2024
Abstract
Tagging
RNAs
with
fluorogenic
aptamers
has
enabled
imaging
of
transcripts
in
living
cells,
thereby
revealing
novel
aspects
RNA
metabolism
and
dynamics.
While
a
diverse
set
been
developed,
new
generation
are
beginning
to
exploit
the
ring-opening
spirocyclic
rhodamine
dyes
achieve
robust
performance
live
mammalian
cells.
These
fluorophores
have
two
chemical
states:
colorless,
cell-permeable
state
fluorescent
zwitterionic
state.
Recently,
developed
dye
SpyRho555
almost
exclusively
adopts
closed
solution
becomes
complex
RhoBAST
aptamer.
To
understand
basis
for
RhoBAST-SpyRho555
fluorogenicity,
we
determined
crystal
structures
5-carboxytetramethylrhodamine
analogue,
MaP555.
is
organized
by
perfect
four-way
junction
that
positions
loops
form
dye-binding
pocket.
The
core
ligand
resides
between
tri-adenine
floor
single
guanine
base,
largely
driven
π-stacking
interactions.
Importantly,
unpaired
interacts
3-position
group
MaP555
stabilize
open
conformation,
supported
mutagenesis
data,
may
play
an
active
role
promoting
conformation
dye.
Graphical
Language: Английский