FEBS Journal,
Journal Year:
2024,
Volume and Issue:
unknown
Published: June 29, 2024
Within
the
three-dimensional
(3D)
nuclear
space,
genome
organizes
into
a
series
of
orderly
structures
that
impose
important
influences
on
gene
regulation.
T
lymphocytes,
crucial
players
in
adaptive
immune
responses,
undergo
intricate
transcriptional
remodeling
upon
activation,
leading
to
differentiation
specific
effector
and
memory
cell
subsets.
Recent
evidence
suggests
activation
is
accompanied
by
dynamic
changes
architecture
at
multiple
levels,
providing
unique
biological
context
explore
functional
relevance
molecular
mechanisms
3D
organization.
Here,
we
summarize
recent
advances
link
reorganization
programs
conversion
fates
during
differentiation.
We
further
discuss
how
various
chromatin
regulators,
including
CCCTC-binding
factor
several
transcription
factors,
collectively
modulate
this
process.
PLoS Biology,
Journal Year:
2025,
Volume and Issue:
23(1), P. e3003009 - e3003009
Published: Jan. 24, 2025
The
organization
of
the
human
genome
in
space
and
time
is
critical
for
transcriptional
regulation
cell
fate
determination.
However,
robust
methods
tracking
or
genomic
interactions
over
living
cells
are
lacking.
Here,
we
developed
a
multicolor
DNA
labeling
system,
ParSite,
to
simultaneously
track
triple
loci
U2OS
cells.
tricolor
ParSite
system
derived
from
T
.
thermophilus
ParB/ParSc
(
Tt
ParB/ParSc)
by
rational
design.
We
mutated
interface
between
ParB
ParSc
generated
new
pair
ParBm
ParSm
labeling.
insertions
16
base-pair
palindromic
into
allow
dual-color
imaging
A
labeled
could
be
colocalized
with
p53-binding
protein
1
(53BP1)
response
CRISPR/Cas9-mediated
double-strand
breaks
(DSBs).
permits
promoter
terminator
dynamics
APP
gene,
which
spans
290
kilobases
length.
Intriguingly,
hybrid
ParS
(ParSh)
half-ParSc
half-ParSm
enables
visualization
third
locus
independent
ParSm.
3
distance
36,
89,
352
downstream
C3
repeat
locus,
respectively.
In
sum,
multiple
Current Opinion in Genetics & Development,
Journal Year:
2022,
Volume and Issue:
73, P. 101898 - 101898
Published: Jan. 10, 2022
In
the
mammalian
cell
nucleus,
chromosomes
are
folded
differently
in
interphase
and
mitosis.
Interphase
relatively
decondensed
display
at
least
two
unique
layers
of
higher-order
organization:
topologically
associating
domains
(TADs)
cell-type-specific
A/B
compartments,
which
correlate
well
with
early/late
DNA
replication
timing
(RT).
mitosis,
these
structures
rapidly
disappear
but
gradually
reconstructed
during
G1
phase,
coincident
establishment
RT
program.
However,
also
change
dynamically
differentiation
reprogramming,
yet
we
surprisingly
ignorant
about
relationship
between
their
cycle
dynamics
developmental
dynamics.
this
review,
summarize
recent
findings
on
topic,
discuss
how
processes
might
be
coordinated
each
other
its
potential
significance.
Advanced Science,
Journal Year:
2024,
Volume and Issue:
11(32)
Published: June 26, 2024
Abstract
CRISPR‐based
genomic‐imaging
systems
have
been
utilized
for
spatiotemporal
imaging
of
the
repetitive
genomic
loci
in
living
cells,
but
they
are
still
challenged
by
limited
signal‐to‐noise
ratio
(SNR)
at
a
non‐repetitive
locus.
Here,
an
efficient
system
is
proposed,
termed
CRISPR/Pepper‐tDeg,
engineering
CRISPR
sgRNA
scaffolds
with
degron‐binding
Pepper
aptamers
binding
fluorogenic
proteins
fused
Tat
peptide
derived
degron
domain
(tDeg).
The
target‐dependent
stability
switches
both
and
protein
allow
this
to
image
telomeres
sensitively
5‐fold
higher
SNR
than
conventional
CRISPR/MS2‐MCP
using
“always‐on”
fluorescent
tag.
Subsequently,
CRISPR/Pepper‐tDeg
applied
simultaneously
label
track
two
different
loci,
centromeres,
cells
combining
systems.
Given
further
improved
split
design,
extended
sequence
only
one
aptamer
insertions.
Neither
complex
design
nor
difficult
plasmid
construction
required,
greatly
reducing
technical
barriers
define
organization
dynamics
thus
demonstrating
large
application
potential
biological
research,
clinical
diagnosis
therapy.
FEBS Journal,
Journal Year:
2024,
Volume and Issue:
unknown
Published: June 29, 2024
Within
the
three-dimensional
(3D)
nuclear
space,
genome
organizes
into
a
series
of
orderly
structures
that
impose
important
influences
on
gene
regulation.
T
lymphocytes,
crucial
players
in
adaptive
immune
responses,
undergo
intricate
transcriptional
remodeling
upon
activation,
leading
to
differentiation
specific
effector
and
memory
cell
subsets.
Recent
evidence
suggests
activation
is
accompanied
by
dynamic
changes
architecture
at
multiple
levels,
providing
unique
biological
context
explore
functional
relevance
molecular
mechanisms
3D
organization.
Here,
we
summarize
recent
advances
link
reorganization
programs
conversion
fates
during
differentiation.
We
further
discuss
how
various
chromatin
regulators,
including
CCCTC-binding
factor
several
transcription
factors,
collectively
modulate
this
process.