Epigenetic marks or not? The discovery of novel DNA modifications in eukaryotes
Wei-Ying Meng,
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Zixin Wang,
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Yunfang Zhang
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et al.
Journal of Biological Chemistry,
Journal Year:
2024,
Volume and Issue:
300(4), P. 106791 - 106791
Published: Feb. 23, 2024
Language: Английский
The Mammalian Oocyte: A Central Hub for Cellular Reprogramming and Stemness
Islam M. Saadeldin,
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Seif Ehab,
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Mashan Essa F Alshammari
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et al.
Stem Cells and Cloning Advances and Applications,
Journal Year:
2025,
Volume and Issue:
Volume 18, P. 15 - 34
Published: Feb. 1, 2025
The
mammalian
oocyte
is
pivotal
in
reproductive
biology,
acting
as
a
central
hub
for
cellular
reprogramming
and
stemness.
It
uniquely
contributes
half
of
the
zygotic
nuclear
genome
entirety
mitochondrial
genome,
ensuring
individual
development
health.
Oocyte-mediated
reprogramming,
exemplified
by
transfer,
resets
somatic
cell
identity
to
achieve
pluripotency
has
transformative
potential
regenerative
medicine.
This
process
critical
understanding
differentiation,
improving
assisted
technologies,
advancing
cloning
stem
research.
During
fertilization,
maternal-zygotic
transition
shifts
developmental
control
from
maternal
factors
activation,
establishing
totipotency.
Oocytes
also
harbor
that
guide
remodeling,
epigenetic
modifications,
metabolic
enabling
early
embryogenesis.
Structures
like
mitochondria,
lipid
droplets,
cytoplasmic
lattices
contribute
energy
production,
molecular
regulation,
organization.
Recent
insights
into
components,
such
ooplasmic
nanovesicles
endolysosomal
vesicular
assemblies
(ELVAS),
highlight
their
roles
maintaining
homeostasis,
protein
synthesis,
efficiency.
By
unraveling
mechanisms
inherent
oocytes,
we
advance
our
cloning,
therapy,
highlighting
valuable
significance
biology
Language: Английский
Distinct dynamics of parental 5-hydroxymethylcytosine during human preimplantation development regulate early lineage gene expression
Dan Liang,
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Rui Yan,
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Xin Long
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et al.
Nature Cell Biology,
Journal Year:
2024,
Volume and Issue:
26(9), P. 1458 - 1469
Published: July 30, 2024
The
conversion
of
DNA
5-methylcytosine
(5mC)
to
5-hydroxymethylcytosine
(5hmC)
by
TET
enzymes
represents
a
significant
epigenetic
modification,
yet
its
role
in
early
human
embryos
remains
largely
unknown.
Here
we
showed
that
the
embryo
inherited
amount
5hmCs
from
an
oocyte,
which
unexpectedly
underwent
de
novo
hydroxymethylation
during
growth.
Furthermore,
generation
5hmC
paternal
genome
after
fertilization
roughly
followed
maternal
pattern,
was
linked
methylation
dynamics
and
regions
sustained
methylation.
persisted
until
eight-cell
stage
exhibited
high
enrichment
at
OTX2
binding
sites,
whereas
knockdown
compromised
expression
lineage
genes.
Specifically,
depletion
affected
activation
embryonic
genes,
further
evaluated
ectopically
expressing
mouse
Tet3
embryos.
These
findings
revealed
distinct
unravelled
multifaceted
functions
development.
Language: Английский
Role of epigenetic regulation in diminished ovarian reserve
Journal of Assisted Reproduction and Genetics,
Journal Year:
2024,
Volume and Issue:
unknown
Published: Dec. 7, 2024
Diminished
ovarian
reserve
(DOR)
is
characterized
by
a
decrease
in
the
number
and
quality
of
oocytes,
with
its
incidence
increasing
annually.
Its
pathogenesis
remains
unclear,
making
it
one
most
challenging
problems
field
assisted
reproduction.
Epigenetic
modification,
molecular
mechanism
affecting
genomic
activity
expression
without
altering
DNA
sequence,
has
been
widely
studied
reproductive
medicine
attracted
considerable
attention
regarding
DOR.
This
review
comprehensively
examines
various
epigenetic
regulatory
changes
granulosa
cells
(OGCs)
oocytes
during
methylation
plays
crucial
role
regulating
cell
function,
hormone
production,
oocyte
development,
maturation,
senescence.
Histone
modifications
are
involved
follicular
activation,
while
non-coding
RNAs,
such
as
long
noncoding
RNAs
(lncRNAs)
microRNAs
(miRNAs),
regulate
function
development.
N6-methyladenosine
(m6A)
associated
age-related
clocks
based
on
show
potential
predicting
Furthermore,
discusses
for
utilizing
mechanisms
to
better
diagnose
manage
Language: Английский
Low-complexity regions in fungi display functional groups and are depleted in positively charged amino acids
Kamil Steczkiewicz,
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Aleksander Kossakowski,
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Stanisław Janik
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et al.
NAR Genomics and Bioinformatics,
Journal Year:
2025,
Volume and Issue:
7(1)
Published: Jan. 7, 2025
Reports
on
the
diversity
and
occurrence
of
low-complexity
regions
(LCR)
in
Eukaryota
are
limited.
Some
studies
have
provided
a
more
extensive
characterization
LCR
proteins
prokaryotes.
There
is
growing
body
knowledge
about
plethora
biological
functions
attributable
to
LCRs.
However,
it
hard
determine
what
extent
observed
phenomena
apply
fungi
since
most
fungal
LCRs
were
limited
model
yeasts.
To
fill
this
gap,
we
performed
survey
across
all
tree
life
branches.
We
show
that
abundance
with
positively
correlated
proteome
size.
present
protein
domains
but
do
not
overlap
domain
regions.
associated
many
duplicated
domains.
The
quantity
particular
amino
acids
deviates
from
background
frequency
clear
over-representation
functional
groups
negative
charge.
Moreover,
discovered
each
lineage
favors
distinct
expansions.
Early
diverging
lineages
differ
composition
pointing
at
different
evolutionary
trajectory
group.
Language: Английский
The global phosphorylation landscape of mouse oocytes during meiotic maturation
The EMBO Journal,
Journal Year:
2024,
Volume and Issue:
unknown
Published: Sept. 10, 2024
Abstract
Phosphorylation
is
a
key
post-translational
modification
regulating
protein
function
and
biological
outcomes.
However,
the
phosphorylation
dynamics
orchestrating
mammalian
oocyte
development
remains
poorly
understood.
In
present
study,
we
apply
high-resolution
mass
spectrometry-based
phosphoproteomics
to
obtain
first
global
in
vivo
quantification
of
mouse
phosphorylation.
Of
more
than
8000
phosphosites,
75%
significantly
oscillate
64%
exhibit
marked
upregulation
during
meiotic
maturation,
indicative
dominant
regulatory
role.
Moreover,
identify
numerous
novel
phosphosites
on
proteins
few
highly
conserved
oocytes
from
different
species.
Through
functional
perturbations,
demonstrate
that
status
specific
sites
participates
modulating
critical
events
including
metabolism,
translation,
RNA
processing
meiosis.
Finally,
combine
inhibitor
screening
enzyme-substrate
network
prediction
discover
previously
unexplored
kinases
phosphatases
are
essential
for
maturation.
sum,
our
data
define
landscape
phosphoproteome,
enabling
in-depth
mechanistic
insights
into
developmental
control
germ
cells.
Language: Английский