Spatial
segregation
of
mRNAs
in
the
cytoplasm
cells
is
a
well-known
biological
phenomenon
that
widely
observed
diverse
species
spanning
different
kingdoms
life.
In
mammalian
cells,
localization
has
been
documented
and
studied
quite
extensively
highly
polarized
most
notably
neurons,
where
localized
function
to
direct
protein
production
at
sites
are
distant
from
soma.
Recent
studies
have
strikingly
revealed
large
proportion
cellular
transcriptome
exhibits
distributions
even
lack
an
obvious
need
for
long-range
transport,
such
as
fibroblasts
or
epithelial
cells.
This
review
focuses
on
emerging
concepts
regarding
functional
outcomes
mRNA
targeting
We
also
discuss
regulatory
mechanisms
controlling
these
events,
with
emphasis
role
cell
mechanics
organization
cytoskeleton.
article
categorized
under:
Translation
>
Regulation
RNA
Export
Localization
Localization.
bioRxiv (Cold Spring Harbor Laboratory),
Journal Year:
2025,
Volume and Issue:
unknown
Published: Jan. 13, 2025
Summary
Long-term
memory
consolidation
is
a
dynamic
process
that
requires
heterogeneous
ensemble
of
neurons,
each
with
highly
specialized
molecular
environment.
Considerable
effort
has
been
placed
into
understanding
how
the
mechanisms
in
specific
neuron
types
are
modified
memory,
but
these
studies
often
undertaken
hours
or
days
after
training,
when
already
consolidated.
Studies
have
shown
protein
synthesis
elevated
during
early
stages
consolidation,
there
limited
information
as
to
it
impacts
neuronal
function.
We
hypothesize
mRNAs
being
translated
could
provide
clues
diverse
neurons
involved
formation
restructure
their
architecture
support
formation.
Here,
we
generate
landscape
translatome
three
dorsal
hippocampus
first
hour
contextual
consolidation.
Our
results
show
share
common
backbone
readily
mRNAs.
However,
excitatory
undergo
deep
reconfiguration
proteostatic
control,
whereas
interneurons
modify
synaptic
transmission.
demonstrate
translational
control
GADD34,
which
promotes
translation
initiation.
Finally,
differential
expression
by
can
be
explained
features
hard
coded
mRNA,
suggesting
ubiquitous
controlling
activity-dependent
translation.
Altogether,
our
work
uncovers
previously
unknown
checkpoints
and
provides
large,
available
resource
for
further
investigations
health
disease.
Journal of Alzheimer s Disease,
Journal Year:
2021,
Volume and Issue:
83(3), P. 977 - 1001
Published: Aug. 17, 2021
Oxidative
stress
is
associated
with
the
progression
of
Alzheimer's
disease
(AD).
Reactive
oxygen
species
can
modify
lipids,
DNA,
RNA,
and
proteins
in
brain.
The
products
their
peroxidation
oxidation
are
readily
detectable
at
incipient
stages
disease.
Based
on
these
products,
various
biomarker-based
strategies
have
been
developed
to
identify
oxidative
levels
AD.
Known
stress-related
biomarkers
include
lipid
F2-isoprostanes,
as
well
malondialdehyde
4-hydroxynonenal
which
both
conjugate
specific
amino
acids
proteins,
DNA
or
RNA
8-hydroxy-2'-deoxyguanosine
(8-OHdG)
8-hydroxyguanosine
(8-OHG),
respectively.
inducible
enzyme
heme
oxygenase
type
1
(HO-1)
found
be
upregulated
response
events
AD
While
global
for
early-stage
AD,
they
generally
poorly
differentiate
from
other
neurodegenerative
disorders
that
also
coincide
stress.
Redox
proteomics
approaches
provided
specificity
stress-associated
pathology
by
identification
oxidatively
damaged
pathology-specific
proteins.
In
this
review,
we
discuss
potential
combined
diagnostic
value
reported
context
eight
mRNA
newly
identified
using
a
transcriptomics
approach.
We
review
genes
involvement
regulation
Further
research
warranted
establish
protein
functionalities
molecular
mechanisms
involved
determination
status
patients.
Annual Review of Biomedical Data Science,
Journal Year:
2022,
Volume and Issue:
5(1), P. 67 - 94
Published: April 26, 2022
The
formation
of
protein
complexes
is
crucial
to
most
biological
functions.
cellular
mechanisms
governing
complex
biogenesis
are
not
yet
well
understood,
but
some
principles
cotranslational
and
posttranslational
assembly
beginning
emerge.
In
bacteria,
this
process
favored
by
operons
encoding
subunits
complexes.
Eukaryotic
cells
do
have
polycistronic
mRNAs,
raising
the
question
how
they
orchestrate
encounter
unassembled
subunits.
Here
we
review
constraints
eukaryotic
co-
folding
assembly,
including
influence
elongation
rate
on
nascent
chain
targeting,
folding,
chaperone
interactions.
Recent
evidence
shows
that
mRNAs
oligomeric
assemblies
can
undergo
localized
translation
form
cytoplasmic
condensates
might
facilitate
Understanding
interplay
between
mRNA
proteostasis
will
be
critical
defining
in
vivo.
Spatial
segregation
of
mRNAs
in
the
cytoplasm
cells
is
a
well-known
biological
phenomenon
that
widely
observed
diverse
species
spanning
different
kingdoms
life.
In
mammalian
cells,
localization
has
been
documented
and
studied
quite
extensively
highly
polarized
most
notably
neurons,
where
localized
function
to
direct
protein
production
at
sites
are
distant
from
soma.
Recent
studies
have
strikingly
revealed
large
proportion
cellular
transcriptome
exhibits
distributions
even
lack
an
obvious
need
for
long-range
transport,
such
as
fibroblasts
or
epithelial
cells.
This
review
focuses
on
emerging
concepts
regarding
functional
outcomes
mRNA
targeting
We
also
discuss
regulatory
mechanisms
controlling
these
events,
with
emphasis
role
cell
mechanics
organization
cytoskeleton.
article
categorized
under:
Translation
>
Regulation
RNA
Export
Localization
Localization.