Nucleic Acids Research,
Journal Year:
2022,
Volume and Issue:
51(3), P. e16 - e16
Published: Dec. 20, 2022
Abstract
Proper
RNA
localisation
is
essential
for
physiological
gene
expression.
Various
kinds
of
genome-wide
approaches
permit
to
comprehensively
profile
subcellular
transcriptomes.
Among
them,
cell
fractionation
methods,
that
couple
RNase
treatment
isolated
organelles
the
sequencing
protected
transcripts,
remain
most
widely
used,
mainly
because
they
do
not
require
genetic
modification
studied
system
and
can
be
easily
implemented
in
any
cells
or
tissues,
including
non-model
species.
However,
suffer
from
numerous
false-positives
since
incompletely
digested
contaminant
RNAs
still
captured
erroneously
identified
as
resident
transcripts.
Here
we
introduce
Controlled
Level
Contamination
coupled
deep
(CoLoC-seq)
a
new
transcriptomics
approach
efficiently
bypasses
this
caveat.
CoLoC-seq
leverages
classical
enzymatic
kinetics
tracks
depletion
dynamics
transcripts
gradient
an
exogenously
added
RNase,
with
without
organellar
membranes.
By
means
straightforward
mathematical
modelling,
infers
topology
robustly
distinguishes
between
genuinely
resident,
luminal
merely
abundant
surface-attached
contaminants.
Our
generic
performed
well
on
human
mitochondria
principle
applicable
other
membrane-bounded
organelles,
plastids,
compartments
vacuolar
system,
extracellular
vesicles,
viral
particles.
Frontiers in Cell and Developmental Biology,
Journal Year:
2022,
Volume and Issue:
10
Published: June 9, 2022
Background:
The
different
pharmacological
effects
of
drugs
in
people
can
be
explained
by
the
polymorphisms
drug
metabolism-related
genes.
Emerging
studies
have
realized
importance
genes
treatment
and
prognosis
cancers,
including
ovarian
cancer
(OV).
In
this
study,
using
comprehensive
bioinformatics
western
blot,
we
identified
that
gene,
ADH1B,
was
significantly
down-regulated
OV
cells
tissues.
patients
with
a
high
level
ADH1B
presented
good
prognosis.
We
also
found
negative
correlation
between
expression
activity
chemotherapeutic
agents,
such
as
cyclophosphamide.
addition,
positive
correlations
were
observed
multiple
immune
checkpoints,
LAG3
HAVCR2.
infiltration
analysis
further
indicated
aberrantly
expressed
might
important
roles
regulating
macrophages
neutrophils
Then,
co-expression
conducted
top
three
enriched
KEGG
pathways
spliceosome,
RNA
transport,
DNA
replication.
conclusion,
gene
its
interactive
network
play
an
essential
role
regulation
therapeutic
response
maybe
promising
targets
for
patients.
Life,
Journal Year:
2023,
Volume and Issue:
13(4), P. 945 - 945
Published: April 4, 2023
In
elaborating
and
maintaining
myelin
sheaths
on
multiple
axons/segments,
oligodendrocytes
distribute
translation
of
some
proteins,
including
basic
protein
(MBP),
to
sites
sheath
assembly,
or
MSAS.
As
mRNAs
located
at
these
are
selectively
trapped
in
vesicles
during
tissue
homogenization,
we
performed
a
screen
identify
mRNAs.
To
confirm
locations,
used
real-time
quantitative
polymerase
chain
reaction
(RT-qPCR),
measure
mRNA
levels
(M)
'non-myelin'
pellet
(P)
fractions,
found
that
five
(
bioRxiv (Cold Spring Harbor Laboratory),
Journal Year:
2024,
Volume and Issue:
unknown
Published: June 27, 2024
Summary
mRNA
localization
to
subcellular
compartments
is
a
widely
used
mechanism
that
functionally
contributes
numerous
processes.
targeting
can
be
achieved
upon
recognition
of
RNA
cargo
by
molecular
motors.
However,
our
understanding
how
this
accomplished
limited,
especially
in
higher
organisms.
We
focus
on
pathway
targets
mRNAs
peripheral
protrusions
mammalian
cells
and
important
for
cell
migration.
Trafficking
occurs
through
active
transport
microtubules,
mediated
the
KIF1C
kinesin.
Here,
we
identify
RNA-binding
protein
CNBP,
as
factor
required
protrusions.
CNBP
binds
directly
GA-rich
sequences
3’UTR
protrusion
targeted
mRNAs.
also
interacts
with
recruitment
their
trafficking
microtubules
periphery.
This
work
provides
reveals
motor-adaptor
complex
The
mechanics
of
how
proteins
are
generated
from
mRNA
is
increasingly
well
understood.
However,
much
less
known
about
protein
production
coordinated
and
orchestrated
within
the
crowded
intracellular
environment,
especially
in
eukaryotic
cells.
Recent
studies
suggest
that
localized
sites
exist
for
specific
proteins.
These
have
been
termed
"translation
factories"
roles
complex
formation,
localization,
inheritance,
translation
regulation
postulated.
In
this
article,
we
review
evidence
supporting
at
these
sites,
details
their
mechanism
likely
functional
significance.
Finally,
consider
key
uncertainties
regarding
elusive
structures
This
article
categorized
under:
Translation
>
Mechanisms
RNA
Export
Localization
Regulation.
bioRxiv (Cold Spring Harbor Laboratory),
Journal Year:
2024,
Volume and Issue:
unknown
Published: Aug. 9, 2024
Abstract
Centrosomes
rely
upon
proteins
within
the
pericentriolar
material
to
nucleate
and
organize
microtubules.
Several
mRNAs
also
reside
at
centrosomes,
although
less
is
known
about
how
why
they
accumulate
there.
We
previously
showed
that
local
Centrocortin
(
Cen
)
mRNA
supports
centrosome
separation,
microtubule
organization,
viability
in
Drosophila
embryos.
Here,
using
as
a
model,
we
examine
mechanisms
of
centrosomal
localization.
find
while
N’-terminus
sufficient
for
protein
enrichment
multiple
domains
cooperate
concentrate
this
location.
further
identify
an
N’-terminal
motif
conserved
among
dynein
cargo
adaptor
test
its
contribution
RNA
Our
results
support
model
whereby
enables
accumulation
own
centrosomes
through
mechanism
requiring
active
translation,
microtubules,
motor
complex.
Taken
together,
our
data
uncover
basis
translation-dependent
localization
required
mitotic
integrity.
Summary
Enrichment
fidelity.
This
study
describes
underlying
co-translational
targeting
involving
motor,
highly
binding
coding
sequence.
BioEssays,
Journal Year:
2023,
Volume and Issue:
45(4)
Published: Feb. 24, 2023
Localized
mRNA
translation
is
a
biological
process
that
allows
to
be
translated
on-site,
which
proposed
provide
fine
control
in
protein
regulation,
both
spatially
and
temporally
within
cell.
We
recently
reported
Vasa,
an
RNA-helicase,
promising
factor
appears
regulate
this
on
the
spindle
during
embryonic
development
of
sea
urchin,
yet
detailed
roles
functional
mechanisms
Vasa
are
still
largely
unknown.
In
review
article,
elucidate
these
remaining
questions,
we
first
summarize
prior
knowledge
our
recent
findings
area
research
further
discuss
how
may
function
localized
translation,
contributing
efficient
regulation
rapid
embryogenesis
cancer
cell
regulation.
RNA,
Journal Year:
2023,
Volume and Issue:
29(11), P. 1623 - 1643
Published: Aug. 15, 2023
It
is
known
that
mRNAs
and
the
machinery
translates
them
are
not
uniformly
distributed
throughout
cytoplasm.
As
a
result,
expression
of
some
genes
localized
to
particular
parts
cell
this
makes
it
possible
carry
out
important
activities,
such
as
growth
signaling,
in
three-dimensional
space.
However,
functions
gene
fully
understood,
underlying
mechanisms
enable
have
been
determined
many
cases.
One
consideration
could
help
addressing
these
challenges
role
quality
control
(QC)
monitor
translating
ribosomes.
On
global
level,
QC
pathways
critical
for
detecting
aberrant
translation
events,
ribosome
stalls
while
translating,
responding
by
activating
stress
resolving
problematic
ribosomes
at
molecular
level.
unclear
how
pathways,
even
when
active
cell,
affect
local
translation.
Importantly,
themselves
reported
be
enriched
proximity
organelles,
but
extent
activity
remains
largely
unknown.
Here,
we
describe
major
review
studies
begun
explore
their
roles
Given
limited
data
area,
also
pose
broad
questions
about
possibilities
limitations
facilitate
with
goal
offering
ideas
future
experimentation.
bioRxiv (Cold Spring Harbor Laboratory),
Journal Year:
2023,
Volume and Issue:
unknown
Published: April 26, 2023
Numerous
proteins
are
targeted
to
two
or
multiple
subcellular
destinations
where
they
exert
distinct
functional
consequences.
The
balance
between
such
differential
targeting
is
thought
be
determined
post-translationally,
relying
on
protein
sorting
mechanisms.
Here,
we
show
that
can
additionally
by
mRNA
location
and
translation
rate,
through
modulating
binding
specific
interacting
partners.
Peripheral
localization
of
the