The
non-B
DNA
structures
can
act
as
dynamic
functional
genomic
elements
regulating
gene
expression.
Among
them,
G4s
and
R-loops
are
two
of
the
best
studied.
interplay
between
emerging
in
repair,
replication
transcription.
A
comprehensive
picture
native
co-localized
living
cells
is
currently
lacking.
Here,
we
describe
development
HepG4-seq
an
optimized
HBD-seq
methods,
which
robustly
capture
R-loops,
respectively,
cells.
We
successfully
employed
these
methods
to
establish
maps
human
HEK293
mouse
embryonic
stem
(mESCs).
discovered
that
dynamically
altered
a
cell
type-dependent
manner
largely
localized
at
active
promoters
enhancers
transcriptional
genes.
further
demonstrated
helicase
Dhx9
direct
major
regulator
modulates
formation
resolution
R-loops.
Depletion
impaired
self-renewal
differentiation
capacities
mESCs
by
altering
transcription
-
associated
Taken
together,
our
work
established
endogenous
prevalently
persisted
regulatory
regions
genes
involved
regulation
their
linked
genes,
opening
door
for
exploring
broader
roles
disease.
Immunological Reviews,
Год журнала:
2024,
Номер
unknown
Опубликована: Дек. 2, 2024
ABSTRACT
The
sensing
of
nucleic
acids
by
DEAD/H‐box
helicases,
specifically
retinoic
acid‐inducible
gene
I
(RIG‐I)
and
melanoma
differentiation‐associated
protein
5
(MDA5),
plays
a
critical
role
in
inducing
antiviral
immunity
following
infection.
However,
this
helicase
family
includes
many
additional
proteins
whose
immune
functions
have
not
been
investigated.
While
numerous
helicases
contribute
to
immunity,
they
employ
diverse
mechanisms
beyond
the
direct
acids.
Some
members
also
identified
play
proviral
(promoting
virus
replication/propagation)
roles
during
infections,
regulate
other
non‐viral
regulation
autoimmunity
cancer.
This
review
synthesizes
known
emerging
broader
highlights
ongoing
efforts
target
these
therapeutically.
bioRxiv (Cold Spring Harbor Laboratory),
Год журнала:
2024,
Номер
unknown
Опубликована: Май 9, 2024
Recombinant
adeno-associated
viral
vectors
(rAAV)
hold
an
intrinsic
ability
to
stimulate
homologous
recombination
(AAV-HR)
and
are
the
most
used
in
clinical
settings
for
bioRxiv (Cold Spring Harbor Laboratory),
Год журнала:
2024,
Номер
unknown
Опубликована: Июнь 4, 2024
Abstract
The
non-B
DNA
structures
can
act
as
dynamic
functional
genomic
elements
regulating
gene
expression.
Among
them,
G4s
and
R-loops
are
two
of
the
best
studied.
interplay
between
emerging
in
repair,
replication
transcription.
A
comprehensive
picture
native
co-localized
living
cells
is
currently
lacking.
Here,
we
describe
development
HepG4-seq
an
optimized
HBD-seq
methods,
which
robustly
capture
R-loops,
respectively,
cells.
We
successfully
employed
these
methods
to
establish
maps
human
HEK293
mouse
embryonic
stem
(mESCs).
discovered
that
dynamically
altered
a
cell
type-dependent
manner
largely
localized
at
active
promoters
enhancers
transcriptional
genes.
further
demonstrated
helicase
Dhx9
direct
major
regulator
modulates
formation
resolution
R-loops.
Depletion
impaired
self-renewal
differentiation
capacities
mESCs
by
altering
transcription
-
associated
Taken
together,
our
work
established
endogenous
prevalently
persisted
regulatory
regions
genes
involved
regulation
their
linked
genes,
opening
door
for
exploring
broader
roles
disease.
The
non-B
DNA
structures
can
act
as
dynamic
functional
genomic
elements
regulating
gene
expression.
Among
them,
G4s
and
R-loops
are
two
of
the
best
studied.
interplay
between
emerging
in
repair,
replication
transcription.
A
comprehensive
picture
native
co-localized
living
cells
is
currently
lacking.
Here,
we
describe
development
HepG4-seq
an
optimized
HBD-seq
methods,
which
robustly
capture
R-loops,
respectively,
cells.
We
successfully
employed
these
methods
to
establish
maps
human
HEK293
mouse
embryonic
stem
(mESCs).
discovered
that
dynamically
altered
a
cell
type-dependent
manner
largely
localized
at
active
promoters
enhancers
transcriptional
genes.
further
demonstrated
helicase
Dhx9
direct
major
regulator
modulates
formation
resolution
R-loops.
Depletion
impaired
self-renewal
differentiation
capacities
mESCs
by
altering
transcription
-
associated
Taken
together,
our
work
established
endogenous
prevalently
persisted
regulatory
regions
genes
involved
regulation
their
linked
genes,
opening
door
for
exploring
broader
roles
disease.