bioRxiv (Cold Spring Harbor Laboratory),
Journal Year:
2024,
Volume and Issue:
unknown
Published: May 30, 2024
Gene
expression
is
tightly
controlled
during
animal
development
to
allow
the
formation
of
specialized
cell
types.
Our
understanding
how
animals
evolved
this
exquisite
regulatory
control
remains
elusive,
but
evidence
suggests
that
changes
in
chromatin-based
mechanisms
may
have
contributed.
To
investigate
possibility,
here
we
examine
gene
features
closest
relatives
animals,
choanoflagellates.
Using
Salpingoeca
rosetta
as
a
model
system,
examined
chromatin
accessibility
and
histone
modifications
at
genome
scale
compared
these
expression.
We
first
observed
accessible
regions
are
primarily
associated
with
promoters
found
no
distal
elements
resembling
enhancers
deploy
regulate
developmental
Remarkably,
modification
deposited
by
polycomb
repressive
complex
2,
H3
lysine
27
trimethylation
(H3K27me3),
appeared
function
similarly
S.
its
role
because
decorated
genes
type-specific
Additionally,
H3K27me3
marked
transposons,
retaining
what
appears
be
an
ancestral
regulating
elements.
further
uncovered
putative
new
bivalent
state
consists
4
mono-methylation
(H3K4me1).
Together,
our
discoveries
support
scenario
gene-associated
states
underpin
emerged
before
evolution
multicellularity.
PLANT PHYSIOLOGY,
Journal Year:
2024,
Volume and Issue:
194(4), P. 1998 - 2016
Published: Jan. 17, 2024
Abstract
Chromatin
plays
a
crucial
role
in
genome
compaction
and
is
fundamental
for
regulating
multiple
nuclear
processes.
Nucleosomes,
the
basic
building
blocks
of
chromatin,
are
central
these
processes,
determining
chromatin
accessibility
by
limiting
access
to
DNA
various
proteins
acting
as
important
signaling
hubs.
The
association
histones
with
nucleosomes
folding
into
higher-order
structures
strongly
influenced
variety
epigenetic
marks,
including
methylation,
histone
variants,
post-translational
modifications.
Additionally,
wide
array
chaperones
ATP-dependent
remodelers
regulate
aspects
nucleosome
biology,
assembly,
deposition,
positioning.
This
review
provides
an
overview
recent
advances
our
mechanistic
understanding
how
organization
regulated
marks
plants.
Furthermore,
we
present
current
technologies
profiling
organization.
Frontiers in Plant Science,
Journal Year:
2024,
Volume and Issue:
15
Published: April 15, 2024
When
exposed
to
low
temperatures,
plants
undergo
a
drastic
reprogramming
of
their
transcriptome
in
order
adapt
new
environmental
conditions,
which
primes
them
for
potential
freezing
temperatures.
While
the
involvement
transcription
factors
this
process,
termed
cold
acclimation,
has
been
deeply
investigated,
contribution
chromatin
regulation
remains
largely
unclear.
A
large
proportion
cold-inducible
genes
carries
repressive
mark
histone
3
lysine
27
trimethylation
(H3K27me3),
hypothesized
as
maintaining
silenced
state
absence
stress,
but
would
need
be
removed
or
counteracted
upon
stress
perception.
However,
fate
H3K27me3
during
exposure
not
studied
genome-wide.
In
study,
we
offer
an
epigenome
profiling
and
its
antagonistic
active
H3K4me3
short-term
exposure.
Both
marks
rapid
redistribution
exposure,
however,
gene
sets
undergoing
differential
methylation
are
distinct,
refuting
simplistic
idea
that
activation
relies
on
switch
from
repressed
form
enriched
H3K4me3.
Coupling
ChIP-seq
experiments
with
reveals
only
weakly
correlates
changes
expression.
Interestingly,
subset
cold-regulated
lose
induction,
indicating
is
obstacle
transcriptional
activation.
methyltransferase
curly
leaf
(clf)
mutant,
many
regulated
display
reduced
levels
activity
altered
prior
suggesting
may
serve
more
intricate
role
response
than
simply
repressing
naïve
conditions.
bioRxiv (Cold Spring Harbor Laboratory),
Journal Year:
2024,
Volume and Issue:
unknown
Published: Jan. 11, 2024
ABSTRACT
Animal
germ
cells
deploy
a
specialized
small
RNA-based
silencing
system,
called
the
PIWI-interacting
RNA
(piRNA)
pathway,
to
prevent
unwanted
expression
of
transposable
elements
and
maintain
genome
integrity.
In
Drosophila
cells,
majority
piRNA
populations
originate
from
dual-strand
clusters,
genomic
regions
highly
enriched
in
transposon
fragments,
via
an
elaborate
protein
machinery
centred
on
heterochromatin
1
homolog,
Rhino.
Although
Rhino
binds
peptides
carrying
trimethylated
H3K9
vitro,
it
is
not
fully
understood
why
vivo
only
fraction
H3K9me3-decorated
occupied
by
Recent
work
uncovered
that
recruited
subset
clusters
zinc
finger
Kipferl.
Here
we
identify
Kipferl-independent
mode
targeting
dependent
histone
H3
lysine
27
methyltransferase
Enhancer
Zeste
presence
H3K9me3
H3K27me3
marks.
At
sites,
find
Rhino,
through
its
dimeric
chromodomain,
specifically
loci
marked
both
H3K27me3.
These
results
expand
our
understanding
characteristic
binding
profile
Our
reveals
role
for
dual
modifications
defining
specificity
chromatin
protein.
Science Advances,
Journal Year:
2024,
Volume and Issue:
10(28)
Published: July 12, 2024
5-Methylcytosine
(5mC)
is
a
widespread
silencing
mechanism
that
controls
genomic
parasites.
In
eukaryotes,
5mC
has
gained
complex
roles
in
gene
regulation
beyond
parasite
control,
yet
also
been
lost
many
lineages.
The
causes
for
retention
and
its
consequences
are
still
poorly
understood.
Here,
we
show
the
protist
closely
related
to
animals
Amoebidium
appalachense
features
both
transposon
body
methylation,
pattern
reminiscent
of
invertebrates
plants.
Unexpectedly,
hypermethylated
regions
derive
from
viral
insertions,
including
hundreds
endogenized
giant
viruses,
contributing
14%
proteome.
Using
combination
inhibitors
assays,
demonstrate
silences
these
virus
insertions.
Moreover,
alternative
isolates
polymorphic
highlighting
dynamic
process
infection,
endogenization,
purging.
Our
results
indicate
critical
controlled
coexistence
newly
acquired
DNA
into
eukaryotic
genomes,
making
unique
model
understand
hybrid
origins
DNA.
bioRxiv (Cold Spring Harbor Laboratory),
Journal Year:
2024,
Volume and Issue:
unknown
Published: Jan. 8, 2024
Abstract
5-methylcytosine
(5mC)
is
a
widespread
silencing
mechanism
that
controls
genomic
parasites.
However,
in
many
eukaryotes
5mC
has
gained
complex
roles
gene
regulation
beyond
parasite
control.
Animals
are
quintessential
case
for
evolution,
as
they
show
variability
across
lineages,
ranging
from
and
transposable
element
control
to
loss
of
this
base
modification.
Here
we
the
protist
closely
related
animals
Amoebidium
appalachense
features
both
transposon
body
methylation,
pattern
reminiscent
invertebrates
plants.
Unexpectedly,
large
hypermethylated
regions
genome
derive
viral
insertions,
including
hundreds
endogenized
giant
viruses
contributing
14%
encoded
genes,
an
extent
never
reported
before
any
eukaryotic
genome.
Using
combination
inhibitors
functional
assays,
demonstrate
silences
these
virus
insertions.
Moreover,
alternative
isolates
polymorphic
highlighting
dynamic
process
infection,
endogenization
purging.
Our
results
indicate
critical
controlled
co-existence
newly
acquired
DNA
into
genomes,
making
unique
model
understand
hybrid
origins
genomes.
Nucleic Acids Research,
Journal Year:
2024,
Volume and Issue:
52(11), P. 6285 - 6297
Published: April 27, 2024
Abstract
Epigenetic
regulations,
including
chromatin
accessibility,
nucleosome
positioning
and
DNA
methylation
intricately
shape
genome
function.
However,
current
profiling
techniques
relying
on
short-read
sequencing
technologies
fail
to
characterise
highly
repetitive
genomic
regions
cannot
detect
multiple
features
simultaneously.
Here,
we
performed
Simultaneous
Accessibility
Methylation
Sequencing
(SAM-seq)
of
purified
plant
nuclei.
Thanks
the
use
long-read
nanopore
sequencing,
SAM-seq
enables
high-resolution
m6A-tagged
accessibility
together
with
endogenous
cytosine
in
plants.
Analysis
naked
revealed
significant
sequence
preference
biases
m6A-MTases,
controllable
through
a
normalisation
step.
By
applying
Arabidopsis
maize
nuclei
obtained
fine-grained
landscapes
genome-wide.
We
uncovered
crosstalk
between
within
nucleosomes
genes,
TEs,
centromeric
repeats.
also
detects
footprints
over
cis-regulatory
regions.
Furthermore,
using
single-molecule
information
provided
by
identified
extensive
cellular
heterogeneity
at
domains
antagonistic
marks,
suggesting
that
bivalency
reflects
cell-specific
regulations.
is
powerful
approach
simultaneously
study
epigenetic
unique
sequences,
opening
new
opportunities
for
investigation
mechanisms.
Communications Biology,
Journal Year:
2023,
Volume and Issue:
6(1)
Published: Nov. 10, 2023
Polycomb
group
proteins,
as
part
of
the
repressive
complexes,
are
essential
in
gene
repression
through
chromatin
compaction
by
canonical
PRC1,
mono-ubiquitylation
histone
H2A
non-canonical
PRC1
and
tri-methylation
H3K27
PRC2.
Despite
prevalent
models
emphasizing
tight
functional
coupling
between
PRC2,
it
remains
unclear
whether
this
paradigm
indeed
reflects
evolution
functioning
these
complexes.
Here,
we
conduct
a
comprehensive
analysis
presence
or
absence
cPRC1,
nPRC1
PRC2
across
entire
eukaryotic
tree
life,
find
that
both
complexes
were
present
Last
Eukaryotic
Common
Ancestor
(LECA).
Strikingly,
~42%
organisms
contain
only
showing
their
since
LECA
is
largely
uncoupled.
The
identification
ncPRC1-defining
subunits
unicellular
relatives
animals
fungi
suggests
ncPRC1
originated
before
propose
scenario
for
cPRC1
from
ncPRC1.
Together,
our
results
suggest
crosstalk
secondary
development
evolution.
International Journal of Molecular Sciences,
Journal Year:
2025,
Volume and Issue:
26(2), P. 848 - 848
Published: Jan. 20, 2025
Tanshinones,
biologically
active
diterpene
compounds
derived
from
Salvia
miltiorrhiza,
interact
with
specific
proteins
and
DNA
sequences,
influencing
signaling
pathways
in
animals
humans.
This
study
highlights
tanshinone–protein
interactions
observed
at
concentrations
achievable
vivo,
ensuring
greater
physiological
relevance
compared
to
vitro
studies
that
often
employ
supraphysiological
ligand
levels.
Experimental
data
suggest
while
tanshinones
multiple
proteomic
targets,
only
a
few
enzymes
are
significantly
affected
relevant
concentrations.
apparent
paradox
may
be
resolved
by
tanshinones’
ability
bind
influence
involved
gene
expression
or
mRNA
stability,
such
as
RNA
polymerase
II
human
antigen
R
protein.
These
trigger
secondary,
widespread
changes
expression,
leading
complex
alterations.
Although
the
current
understanding
of
remains
incomplete,
this
provides
foundation
for
deciphering
molecular
mechanisms
underlying
therapeutic
effects
S.
miltiorrhiza
diterpenes.
Additionally,
numerous
tanshinone
derivatives
have
been
developed
enhance
pharmacokinetic
properties
biological
activity.
However,
their
safety
profiles
remain
poorly
characterized,
limiting
comprehensive
insights
into
medicinal
potential.
Further
investigation
is
essential
fully
elucidate
toxicological
both
native
modified
tanshinones.