RNA Biology,
Год журнала:
2024,
Номер
21(1), С. 1 - 13
Опубликована: Окт. 10, 2024
(RNA-binding
motif
protein
3)
is
a
stress
responsive
gene,
which
maintains
cellular
homeostasis
and
promotes
survival
upon
various
harmful
stimuli.
Rbm3
shows
conserved
structural
molecular
similarities
to
heterogeneous
nuclear
ribonucleoproteins
(hnRNPs),
regulate
all
steps
of
the
mRNA
metabolism.
Growing
evidence
pointing
towards
broader
role
in
gene
expression.
Here,
we
demonstrate
that
deficiency
linked
transcriptome-wide
pre-mRNA
splicing
alterations,
can
be
reversed
through
co-expression
from
cDNA.
Using
an
MS2
tethering
assay,
show
regulates
splice
site
selection
similar
other
hnRNP
proteins
when
recruited
between
two
competing
5
Abstract
Enhanced
expression
of
the
cold‐shock
protein
RNA
binding
motif
3
(RBM3)
is
highly
neuroprotective
both
in
vitro
and
vivo
.
Whilst
upstream
signalling
pathways
leading
to
RBM3
have
been
described,
precise
molecular
mechanism
cold
induction
remains
elusive.
To
identify
temperature‐dependent
modulators
RBM3,
we
performed
a
genome‐wide
CRISPR‐Cas9
knockout
screen
using
RBM3‐reporter
human
iPSC‐derived
neurons.
We
found
that
mRNA
levels
are
robustly
regulated
by
several
splicing
factors,
with
heterogeneous
nuclear
ribonucleoprotein
H1
(HNRNPH1)
being
strongest
positive
regulator.
Splicing
analysis
revealed
moderate
hypothermia
significantly
represses
inclusion
poison
exon,
which,
when
retained,
targets
for
nonsense‐mediated
decay.
Importantly,
show
HNRNPH1
mediates
this
cold‐dependent
exon
skipping
via
its
thermosensitive
interaction
G‐rich
within
exon.
Our
study
provides
novel
mechanistic
insights
into
regulation
further
therapeutic
strategies.
The EMBO Journal,
Год журнала:
2025,
Номер
44(3), С. 877 - 902
Опубликована: Янв. 2, 2025
The
cellular
concentrations
of
splicing
factors
(SFs)
are
critical
for
controlling
alternative
splicing.
Most
serine
and
arginine-enriched
(SR)
protein
SFs
regulate
their
own
concentration
via
a
homeostatic
feedback
mechanism
that
involves
regulation
inclusion
non-coding
'poison
exons'
(PEs)
target
transcripts
nonsense-mediated
decay.
importance
SR
PE
during
animal
development
is
largely
unknown
despite
ultra-conservation
across
genomes.
To
address
this,
we
used
mouse
genetics
to
disrupt
an
ultra-conserved
in
the
Tra2b
gene
encoding
Tra2β.
Focussing
on
germ
cell
development,
found
deletion
causes
azoospermia
due
catastrophic
death
meiotic
prophase.
Failure
proceed
through
meiosis
was
associated
with
increased
expression
sufficient
drive
aberrant
Tra2β
hyper-responsive
splice
patterns.
Although
prophase,
spared
earlier
mitotically
active
cells,
even
though
these
still
required
function.
Our
data
indicate
control
prevents
accumulation
toxic
levels
incompatible
This
unexpected
connection
male
fertility
helps
explain
indicates
evaluating
function
models.
Macroautophagy/autophagy
is
the
principal
mechanism
that
mediates
delivery
of
various
cellular
cargoes
to
lysosomes
for
degradation
and
recycling,
has
been
reported
play
a
crucial
role
in
colorectal
cancer
(CRC)
pathogenesis
progression.
Targeting
autophagy
may
be
promising
therapeutic
strategy
CRC.
However,
specific
functions
potential
mechanisms
CRC
remain
unclear.
In
present
study,
we
discovered
PTK6
(protein
tyrosine
kinase
6)
could
activate
inhibit
apoptosis.
physically
interacted
with
HNRNPH1
mediated
phosphorylation
at
Y210
HNRNPH1,
which
promoted
latter's
liquid-liquid
phase
separation
(LLPS).
Furthermore,
LLPS
formed
biomolecular
condensates
triggered
splicing-switching
NBR1
exon
10
inclusion
transcript,
thereby
activating
suppressing
apoptosis
Additionally,
PDO
CDX
models
indicated
tilfrinib,
an
inhibitor
targeting
PTK6,
growth.
Overall,
our
findings
reveal
novel
PTK6-HNRNPH1-NBR1
regulatory
axis
provide
therapy
target
Communications Biology,
Год журнала:
2024,
Номер
7(1)
Опубликована: Апрель 30, 2024
Adaptation
to
hypothermia
is
important
for
skeletal
muscle
cells
under
physiological
stress
and
used
therapeutic
(mild
at
32
°C).
We
show
that
hypothermic
preconditioning
°C
72
hours
improves
the
differentiation
of
myoblasts
using
both
C2C12
primary
isolated
from
3
month
18-month-old
mice.
analyzed
cold-shock
proteome
exposed
(32
6
48
h)
identified
significant
changes
in
pathways
related
RNA
processing
central
carbon,
fatty
acid,
redox
metabolism.
The
analysis
revealed
levels
protein
RBM3,
an
RNA-binding
protein,
increases
with
acute
chronic
exposure
stress,
necessary
enhanced
maintenance
mitochondrial
also
overexpression
RBM3
37
sufficient
promote
metabolism,
cellular
proliferation,
myoblasts.
Proteomic
overexpressing
enrichment
involved
acid
metabolism
electron
transport
chain.
Overall,
we
a
critical
factor
can
be
controlling
metabolic
network
FEBS Letters,
Год журнала:
2023,
Номер
597(18), С. 2250 - 2287
Опубликована: Июль 31, 2023
Human
pluripotent
stem
cells
(hPSCs)
are
uniquely
suited
to
study
human
development
and
disease
promise
revolutionize
regenerative
medicine.
These
applications
rely
on
robust
methods
manipulate
gene
function
in
hPSC
models.
This
comprehensive
review
aims
both
empower
scientists
approaching
the
field
update
experienced
cell
biologists.
We
begin
by
highlighting
challenges
with
manipulating
expression
hPSCs
their
differentiated
derivatives,
relevant
solutions
(transfection,
transduction,
transposition,
genomic
safe
harbor
editing).
then
outline
how
perform
constitutive
or
inducible
loss-,
gain-,
change-of-function
experiments
models,
using
historical
(RNA
interference,
transgenesis,
homologous
recombination)
modern
programmable
nucleases
(particularly
CRISPR/Cas9
its
i.e.,
CRISPR
activation,
base
editing,
prime
further
describe
extension
of
these
approaches
for
arrayed
pooled
functional
studies,
including
emerging
single-cell
methods,
related
design
analytical
bioinformatic
tools.
Finally,
we
suggest
some
directions
future
advancements
all
areas.
Mastering
combination
transformative
technologies
will
unprecedented
advances
biology
iScience,
Год журнала:
2024,
Номер
27(4), С. 109435 - 109435
Опубликована: Март 6, 2024
Both
therapeutic
hypothermia
and
neural
stem
cells
(NSCs)
transplantation
have
shown
promise
in
neuroprotection
repair
after
brain
injury.
However,
the
effects
of
on
neuronal
differentiation
NSCs
are
not
elucidated.
In
this
study,
we
aimed
to
investigate
whether
mild
promoted
cultured
transplanted
human
(hNSCs).
A
significant
increase
rate
hNSCs
was
found
when
exposed
35°C,
from
33%
45%
CNS Neuroscience & Therapeutics,
Год журнала:
2024,
Номер
30(6)
Опубликована: Июнь 1, 2024
Abstract
Aim
Recent
studies
have
extensively
investigated
hypothermia
as
a
therapeutic
approach
for
mitigating
neural
damage.
Despite
this,
bibliometric
analyses
specifically
focusing
on
this
area
remain
scarce.
Consequently,
study
aims
to
comprehensively
outline
the
historical
framework
of
research
and
pinpoint
future
directions
trends.
Methods
Articles
spanning
from
2003
2023,
relevant
both
“neuroprotection”
“hypothermia”,
were
sourced
Web
Science
Core
Collection.
The
CiteSpace
software
facilitated
comprehensive
evaluation
analysis
these
publications.
This
included
examining
annual
productivity,
collaboration
among
nations,
institutions,
authors,
well
network
co‐cited
references,
authors
journals,
co‐occurrence
keywords,
their
respective
clusters
trends,
all
which
visualized.
Results
2103
articles
neuroprotection
effects
hypothermia,
noting
consistent
increase
in
publications
since
1992.
United
States,
University
California
System,
Ji
Xunming
emerged
most
productive
nation,
institution,
author,
respectively.
Analysis
top
10
revealed
that
seven
focused
infants
with
hypoxic–ischemic
encephalopathy,
while
three
addressed
cardiac
arrest.
Shankaran
S
journal
Stroke
frequently
author
journal,
Keyword
cluster
identified
ischemic
stroke
primary
focus
therapy
historically,
arrest
neonatal
encephalopathy
emerging
current
foci.
Conclusions
neuroprotective
suggest
may
mitigate
damage
associated
conditions.
However,
application
treatment
remains
confined
animal
models
vitro
studies,
notable
absence
evidence
multicenter
randomized
controlled
trials
(RCTs).
Further
is
required
address
gap.