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WASH is required for the differentiation commitment of hematopoietic stem cells in a c-Myc-dependent manner.
[wiskott-aldrich syndrome]
Hematopoiesis
is
fully
dependent
on
hematopoietic
stem
cells
(
HSCs
)
that
possess
the
capacity
to
self-renew
and
differentiate
into
all
blood
cell
lineages
.
WASH
,
Wiskott-
Aldrich
syndrome
protein
(
WASP
)
and
SCAR
homologue
(
WASH
)
is
involved
in
endosomal
sorting
as
an
actin-nucleating
protein
.
Here
,
we
show
that
conditional
WASH
deletion
in
the
hematopoietic
system
causes
defective
blood
production
of
the
host
,
leading
to
severe
cytopenia
and
rapid
anemia
.
WASH
deficiency
causes
the
accumulation
of
long
-term
(
LT
)
-
HSCs
in
bone
marrow
and
perturbs
their
differentiation
potential
to
mature
blood
lineages
.
Importantly
,
WASH
is
located
in
the
nucleus
of
LT-HSCs
and
associates
with
the
nucleosome
remodeling
factor
(
NURF
)
complex
.
WASH
assists
the
NURF
complex
to
the
promoter
of
c-
Myc
gene
through
its
VCA
domain-dependent
nuclear
actin
nucleation
.
WASH
deletion
suppresses
the
transcriptional
activation
of
c-
Myc
gene
and
impairs
the
differentiation
of
LT-HSCs
.
WASH
acts
as
an
upstream
regulator
to
modulate
c-
Myc
transcription
for
hematopoietic
regulation
.
Diseases
Validation
Diseases presenting
"defective blood production of the host"
symptom
wiskott-aldrich syndrome
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