Genome biology,
Journal Year:
2023,
Volume and Issue:
24(1)
Published: March 14, 2023
Abstract
Background
Genomic
imprinting
affects
gene
expression
in
a
parent-of-origin
manner
and
has
profound
impact
on
complex
traits
including
growth
behavior.
While
the
rat
is
widely
used
to
model
human
pathophysiology,
few
imprinted
genes
have
been
identified
this
murid.
To
systematically
identify
genomic
imprints
rat,
we
use
low
input
methods
for
genome-wide
analyses
of
DNA
methylation
profile
embryonic
extraembryonic
tissues
at
allele-specific
resolution.
Results
We
14
26
these
tissues,
respectively,
with
10
both
tissues.
Comparative
mouse
reveal
that
orthologous
associated
canonical
are
conserved
embryo
proper
Muridae
family.
However,
only
3
paternally
expressed
tissue
murids,
all
which
non-canonical
H3K27me3
imprints.
The
discovery
8
novel
unique
consistent
more
rapid
evolution
imprinting.
Meta-analysis
reveals
multiple
mechanisms
by
species-specific
may
be
established,
deposition
oocyte,
appearance
ZFP57
binding
motifs,
insertion
endogenous
retroviral
promoters.
Conclusions
In
summary,
provide
an
expanded
list
loci
extent
conservation
expression,
potential
responsible
Nature Cell Biology,
Journal Year:
2025,
Volume and Issue:
unknown
Published: Jan. 2, 2025
Abstract
The
establishment
of
naive
pluripotency
is
a
continuous
process
starting
with
the
generation
inner
cell
mass
(ICM)
that
then
differentiates
into
epiblast
(EPI).
Recent
studies
have
revealed
key
transcription
factors
(TFs)
for
ICM
formation,
but
which
TFs
initiate
EPI
specification
remains
unknown.
Here,
using
targeted
rapid
protein
degradation
system,
we
show
GABPA
not
only
regulator
major
ZGA,
also
master
specifier
required
by
regulating
47%
genes
during
E3.5
to
E4.5
transition.
Chromatin
binding
dynamics
analysis
suggests
controls
formation
at
least
partly
gene
promoters
occupied
regulators
TFAP2C
and
SOX2
establish
E4.5.
Our
study
uncovers
as
regulator,
supports
notion
mammalian
requires
dynamic
stepwise
multi-TF
regulatory
network.
Trends in Genetics,
Journal Year:
2025,
Volume and Issue:
unknown
Published: March 1, 2025
Recent
developments
in
low-input
genomics
techniques
have
greatly
advanced
the
analysis
of
order
which
DNA
is
replicated
genome
-
that
is,
replication
timing
(RT)
and
its
interrelationships
with
other
processes.
RT
correlates
or
anticorrelates
genomic-specific
parameters
such
as
gene
expression,
chromatin
accessibility,
histone
modifications,
3D
structure
genome,
but
significance
how
they
influence
each
relate
to
biological
processes
remains
unclear.
In
this
review
I
discuss
results
recent
analyses
RT,
time
at
it
remodeled
consolidated
during
embryogenesis,
influences
development
differentiation,
regulatory
mechanisms
factors
involved.
Genes & Development,
Journal Year:
2021,
Volume and Issue:
35(11-12), P. 821 - 834
Published: June 1, 2021
Genomic
imprinting
is
the
monoallelic
expression
of
a
gene
based
on
parent
origin
and
consequence
differential
epigenetic
marking
between
male
female
germlines.
Canonically,
genomic
mediated
by
allelic
DNA
methylation.
However,
recently
it
has
been
shown
that
maternal
H3K27me3
can
result
in
methylation-independent
imprinting,
termed
“noncanonical
imprinting.”
In
this
review,
we
compare
contrast
what
currently
known
about
underlying
mechanisms,
role
endogenous
retroviral
elements,
conservation
canonical
noncanonical
imprinting.
Developmental Cell,
Journal Year:
2021,
Volume and Issue:
56(21), P. 2995 - 3005.e4
Published: Nov. 1, 2021
Highlights•Comprehensive
inventory
of
epigenetic
mechanisms
that
regulate
parent-specific
imprints•Extraembryonic
ectoderm
uses
broader
array
imprinting
than
the
epiblast•G9a-mediated
pathway
controls
ERV-driven
promoters
non-canonical
imprinted
genes•Polycomb
silences
secondary
X
chromosome
targets
in
extraembryonic
ectodermSummaryGenomic
and
inactivation
(XCI)
require
to
encode
allele-specific
expression,
but
how
these
specific
tasks
are
accomplished
at
single
loci
or
across
chromosomal
scales
remains
incompletely
understood.
Here,
we
systematically
disrupt
essential
pathways
within
polymorphic
embryos
order
examine
canonical
genomic
as
well
XCI.
We
find
DNA
methylation
Polycomb
group
repressors
indispensable
for
autosomal
imprinting,
albeit
distinct
gene
sets.
Moreover,
relies
on
a
spectrum
mechanisms,
including
targeting
maternal
endogenous
retrovirus
(ERV)-driven
by
H3K9
methyltransferase
G9a.
further
identify
Polycomb-dependent
-independent
clusters
chromosome,
which
appear
reflect
domains
Xist-mediated
suppression.
From
our
data,
assemble
comprehensive
maintain
eutherian
mammals,
an
expanded
view
placental
lineage.Graphical
abstract
Nature Communications,
Journal Year:
2021,
Volume and Issue:
12(1)
Published: Dec. 2, 2021
Silencing
of
a
subset
germline
genes
is
dependent
upon
DNA
methylation
(DNAme)
post-implantation.
However,
these
are
generally
hypomethylated
in
the
blastocyst,
implicating
alternative
repressive
pathways
before
implantation.
Indeed,
embryonic
stem
cells
(ESCs),
an
overlapping
set
genes,
including
"genome-defence"
(GGD)
upregulated
following
deletion
H3K9
methyltransferase
SETDB1
or
subunits
non-canonical
PRC1
complex
PRC1.6.
Here,
we
show
that
pre-implantation
embryos
and
naïve
ESCs
(nESCs),
promoters
bound
by
PRC1.6
DNA-binding
MGA/MAX/E2F6
enriched
for
RING1B-dependent
H2AK119ub1
H3K9me3.
Accordingly,
repression
nESCs
shows
greater
dependence
on
than
DNAme.
In
contrast,
GGD
hypermethylated
epiblast-like
(EpiLCs)
their
silencing
SETDB1,
PRC1.6/RING1B
DNAme,
with
H3K9me3
DNAme
establishment
MGA
binding.
Thus,
initially
repressed
PRC1.6,
subsequently
engaged
post-implantation
embryos.
Cold Spring Harbor Perspectives in Biology,
Journal Year:
2021,
Volume and Issue:
unknown, P. a040196 - a040196
Published: July 26, 2021
François
Dossin1,2
and
Edith
Heard1
1European
Molecular
Biology
Laboratory,
Director's
Unit,
69117
Heidelberg,
Germany
Correspondence:
edith.heard{at}embl.org
↵2
Present
address:
Genome
Integrity,
Immunity
Cancer
Department
of
Immunology,
Genomes
Genetics,
Institut
Pasteur,
75015
Paris,
France.
Cells,
Journal Year:
2022,
Volume and Issue:
11(15), P. 2404 - 2404
Published: Aug. 4, 2022
Epigenetic
regulation
plays
an
essential
role
in
driving
precise
transcriptional
programs
during
development
and
homeostasis.
Among
epigenetic
mechanisms,
histone
mono-ubiquitination
has
emerged
as
important
post-transcriptional
modification.
Two
major
events
are
the
of
H2A
at
lysine
119
(H2AK119ub),
placed
by
Polycomb
repressive
complex
1
(PRC1),
H2B
120
(H2BK120ub),
heteromeric
RNF20/RNF40
complex.
Both
these
play
fundamental
roles
shaping
chromatin
landscape
cellular
identity.
In
this
review
we
summarize
current
understandings
molecular
concepts
behind
mono-ubiquitination,
focusing
on
their
recently
identified
tissue
pathologies.
Genome Research,
Journal Year:
2023,
Volume and Issue:
33(12), P. 2079 - 2093
Published: Dec. 1, 2023
Mammalian
sperm
show
an
unusual
and
heavily
compacted
genomic
packaging
state.
In
addition
to
its
role
in
organizing
the
compact
hydrodynamic
head,
it
has
been
proposed
that
chromatin
architecture
helps
program
gene
expression
early
embryo.
Scores
of
genome-wide
surveys
have
reported
patterns
accessibility,
nucleosome
localization,
histone
modification,
chromosome
folding.
Here,
we
revisit
these
studies
light
recent
reports
obtained
from
mouse
epididymis
are
contaminated
with
low
levels
cell-free
chromatin.
absence
proper
lysis,
readily
recapitulate
multiple
prominent
chromatin,
suggesting
profiles
primarily
reflect
contaminating
Removal
DNA,
appropriate
lysis
conditions,
together
required
reveal
a
state
distinct
most
previous
reports.
Using
ATAC-seq
explore
relatively
accessible
loci,
identify
landscape
open
loci
associated
development
transcriptional
control.
Histone
modification
folding
also
strongly
support
hypothesis
prior
suffer
contamination,
but
technical
challenges
reliably
preserving
head
prevent
us
confidently
assaying
true
localization
for
epigenetic
marks.
Together,
our
knowledge
mammalian
remains
largely
incomplete,
motivate
future
efforts
more
accurately
characterize
genome
organization
mature
sperm.