METTL14 regulates proliferation and differentiation of duck myoblasts through targeting MiR-133b
Qicheng Jiang,
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Tieshan Xu,
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Hailong Zhou
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et al.
PLoS ONE,
Journal Year:
2025,
Volume and Issue:
20(3), P. e0320659 - e0320659
Published: March 28, 2025
The
development
of
duck
pectoral
muscle
has
a
significant
impact
on
meat
quality,
and
miRNA
m6A
modification
play
key
roles
in
this
process.
In
the
early
stage,
by
using
MeRIP-seq
miRNA-seq
to
analyze
tissue
embryos
at
day
13
(E13),
19
(E19),
27
(E27)
incubation,
we
found
that
METTL14,
as
core
component
methylation
transferase
complex,
showed
differences
expression
different
developmental
stages
may
have
an
important
development.
study,
qRT-PCR
detection
revealed
proliferation
differentiation
marker
genes
CDK2,
CyclinD1,
MYOG
MYHC
varied
stages,
with
highest
level
E13
lowest
METTL14
same
stage.
After
constructing
overexpression
interference
vectors
for
promoted
embryo
myoblasts
inhibited
differentiation,
while
accelerated
differentiation.
particular,
increased
miR-133b,
whose
precursor
sequence
contains
sites,
suggesting
participate
regulation
affecting
miR-133b.
This
study
provides
new
insights
into
molecular
mechanisms
offers
potential
targets
genetic
improvement
muscle.
Language: Английский
m6A RNA methylation dynamics during in vitro maturation of cumulus-oocyte complexes derived from adult or prepubertal sheep
Chiara Cosseddu,
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Sara Succu,
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Adele Frau
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et al.
Journal of Assisted Reproduction and Genetics,
Journal Year:
2025,
Volume and Issue:
unknown
Published: March 18, 2025
Language: Английский
METTL3-m6A methylase regulates the osteo-/odontogenic potential of stem cells from apical papilla via NFIC in apical periodontitis.
Youyu Zhu,
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Xiang Ge,
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Zhi Chen
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et al.
Experimental Cell Research,
Journal Year:
2025,
Volume and Issue:
448(2), P. 114576 - 114576
Published: April 23, 2025
Stem
cells
from
the
apical
papilla
(SCAPs)
show
strong
odontogenic
ability
and
can
form
root
dentin.
However,
underlying
mechanisms
that
control
differentiation
of
SCAPs
in
an
inflammatory
environment
need
further
exploration.
In
present
study,
we
explored
regulatory
role
METTL3
originating
tooth
with
periodontitis.
derived
healthy
teeth
periodontitis
(AP-SCAPs)
were
successfully
isolated
cultured.
The
expressions
tumor
necrosis
factor-a
(TNF-a)
interleukin-6
(IL-6)
higher
AP-SCAPs.
A
decrease
expression
accompanied
decreased
osteo-/odontogenic
Exploring
on
AP-SCAPs
revealed
overexpression
upregulated
silencing
exerted
opposite
effect.
Overexpression
suppressed
TNF-α
IL-6
AP-SCAPs,
whereas
knockdown
these
enhanced
expression.
regulates
modulates
their
response.
Furthermore,
methylation
level,
mRNA,
protein
nuclear
factor-IC
(NFIC)
during
mineralization
induction.
NFIC
attenuated
METTL3-overexpressed
conclusion,
METTL3-mediated-m6A
via
NFIC.
This
paper
elucidates
a
novel
mechanism
regulating
may
be
new
target
for
regenerative
endodontic
treatment.
Language: Английский
METTL14 Promotes Vascular Smooth Muscle Cell Proliferation and Neointima Formation via m6A Methylation TEAD1 mRNA
LIANG WANG,
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G.L Xia,
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Yan Tang
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et al.
Journal of Biochemical and Molecular Toxicology,
Journal Year:
2025,
Volume and Issue:
39(5)
Published: May 1, 2025
ABSTRACT
Vascular
smooth
muscle
cell
(VSMC)
proliferation
and
neointimal
hyperplasia
critically
contribute
to
atherosclerosis
post‐angioplasty
restenosis.
Building
on
our
prior
discovery
that
TEA
domain
transcription
factor
1
(TEAD1)
regulates
VSMCs
differentiation,
we
now
investigate
methyltransferase‐like
14
(METTL14)
in
vascular
remodeling.
METTL14
expression
was
significantly
upregulated
human
carotid
atherosclerotic
plaques
versus
control
arteries,
correlating
with
dedifferentiation.
This
pattern
recapitulated
murine
wire‐induced
injury
models
during
neointima
formation.
Functionally,
overexpression
suppressed
contractile
markers
while
accelerating
migration
coronary
artery
cells
(HCASMCs).
Conversely,
knockdown
attenuated
injury‐induced
In
Vivo.
Mechanistically,
stabilizes
TEAD1
mRNA
through
m6A
modification
at
nucleotide
513,
enhancing
YAP1/TEAD1
signaling.
Both
513nt
mutation
inhibitor
VT103
abolished
METTL14‐driven
phenotypic
changes,
restoring
differentiation
suppressing
proliferation.
Collectively,
findings
establish
METTL14‐mediated
of
as
a
novel
mechanism
promoting
pathology,
highlighting
its
therapeutic
potential
for
cardiovascular
diseases.
Language: Английский
METTL3 shapes m6A epitranscriptomic landscape for successful human placentation
Ram Kumar,
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Rajnish Kumar,
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Avishek Ganguly
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et al.
bioRxiv (Cold Spring Harbor Laboratory),
Journal Year:
2024,
Volume and Issue:
unknown
Published: July 13, 2024
Methyltransferase-like
3
(METTL3),
the
catalytic
enzyme
of
methyltransferase
complex
for
m6A
methylation
RNA,
is
essential
mammalian
development.
However,
importance
METTL3
in
human
placentation
remains
largely
unexplored.
Here,
we
show
that
a
fine
balance
function
trophoblast
cells
successful
placentation.
Both
loss-of
and
gain-in
functions
are
associated
with
adverse
pregnancies.
A
subset
recurrent
pregnancy
losses
preterm
pregnancies
often
loss
expression
progenitors.
In
contrast,
induced
fetal
growth
restriction
(FGR).
Our
analyses
showed
maintenance
TSC
self-renewal
their
differentiation
to
extravillous
(EVTs).
TSCs
promotes
syncytiotrophoblast
(STB)
Global
RNA
modification
METTL3-RNA
interaction
regulates
modifications
on
mRNA
molecules
critical
regulators,
including
Language: Английский
METTL14 depletion induces trophoblast cell dysfunction by inhibiting miR–21-5p processing in an m6A-dependent manner
Xiaoli Qin,
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Xiaona Huo,
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Junpeng Dong
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et al.
International Immunopharmacology,
Journal Year:
2024,
Volume and Issue:
142, P. 113200 - 113200
Published: Sept. 27, 2024
Language: Английский
Evidence for the potential role of m6A modification in regulating autophagy in models of amyotrophic lateral sclerosis
CytoJournal,
Journal Year:
2024,
Volume and Issue:
21, P. 33 - 33
Published: Sept. 30, 2024
Amyotrophic
lateral
sclerosis
(ALS)
is
a
devastating
neurodegenerative
disease.
Research
indicates
that
N6-methyladenosine
(m6A)
modification
plays
crucial
role
in
cellular
autophagy
during
ALS
development.
This
study
investigates
the
of
ALS,
with
focus
on
effect
messenger
ribonucleic
acid
m6A
methylation
disease
progression.
Language: Английский
Exploring Potential Diagnostic Biomarkers for Mechanical Asphyxia in the Heart Based on Proteomics Technology
Yuebing Huang,
No information about this author
Hai Qiu,
No information about this author
Qianling Chen
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et al.
International Journal of Molecular Sciences,
Journal Year:
2024,
Volume and Issue:
25(23), P. 12710 - 12710
Published: Nov. 26, 2024
Mechanical
asphyxia
presents
a
challenging
diagnostic
issue
in
forensic
medicine
due
to
its
often
covert
nature,
and
the
signs
visible
during
an
autopsy
are
usually
not
specific.
Despite
some
progress
understanding
hypoxia's
effects,
traditional
methods'
inherent
limitations
might
overlook
new
biomarkers
mechanical
asphyxia.
This
study
employed
4D-DIA
proteomics
explore
protein
expression
profiles
of
cardiac
samples
under
conditions
Proteomic
analysis
identified
271
371
differentially
expressed
proteins
strangulation
suffocation
groups,
respectively,
compared
control
group.
Seventy-eight
were
across
different
groups
GO
KEGG
showed
enrichment
pathways,
including
complement
coagulation
cascades,
cAMP
cGMP-PKG
signaling
inflammatory
mediator
regulation
TRP
channels,
phagosomes.
Through
stringent
selection
based
on
interactions,
ALKBH5,
NAA10,
CLPB
as
potential
biomarkers.
ALKBH5
increased
models,
while
NAA10
downregulated;
these
biomarker
changes
validated
both
animal
models
human
samples.
highlights
discovering
reliable
biomarkers,
which
can
enhance
specificity
diagnosis
practice,
provide
insights
into
pathophysiological
mechanisms
asphyxia,
offer
perspectives
for
diagnosing
Language: Английский