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The open chromatin landscape of Kaposi's sarcoma-associated herpesvirus.
[primary effusion lymphoma]
Kaposi
's
sarcoma
-associated
herpesvirus
(
KSHV
)
is
an
oncogenic
gammaherpesvirus
which
establishes
latent
infection
in
endothelial
and
B
cells
,
as
well
as
in
primary
effusion
lymphoma
(
PEL
)
.
During
latency
,
the
viral
genome
exists
as
a
circular
DNA
minichromosome
(
episome
)
and
is
packaged
into
chromatin
analogous
to
human
chromosomes
.
Only
a
small
subset
of
promoters
,
those
which
drive
latent
RNAs
,
are
active
in
latent
episomes
.
In
general
,
nucleosome
depletion
(
"
open
chromatin
"
)
is
a
hallmark
of
eukaryotic
regulatory
elements
such
as
promoters
and
transcriptional
enhancers
or
insulators
.
We
applied
formaldehyde-assisted
isolation
of
regulatory
elements
(
FAIRE
)
followed
by
next
-generation
sequencing
to
identify
regulatory
elements
in
the
KSHV
genome
and
integrated
these
data
with
previously
identified
locations
of
histone
modifications
,
RNA
polymerase
II
occupancy
,
and
CTCF
binding
sites
.
We
found
that
(
i
)
regions
of
open
chromatin
were
not
restricted
to
the
transcriptionally
defined
latent
loci
;
(
ii
)
open
chromatin
was
adjacent
to
regions
harboring
activating
histone
modifications
,
even
at
transcriptionally
inactive
loci
;
and
(
iii
)
CTCF
binding
sites
fell
within
regions
of
open
chromatin
with
few
exceptions
,
including
the
constitutive
LANA
promoter
and
the
vIL
6
promoter
.
FAIRE-identified
nucleosome
depletion
was
similar
among
B
and
endothelial
cell
lineages
,
suggesting
a
common
viral
genome
architecture
in
all
forms
of
latency
.
Diseases
Validation
Diseases presenting
"open chromatin"
symptom
primary effusion lymphoma
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