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The non-synonymous polymorphism at position 114 of the WRN protein affects cholesterol efflux in vitro and correlates with cholesterol levels in vivo.
[werner syndrome]
Werner
syndrome
(
WS
)
is
a
recessive
disorder
characterized
by
the
premature
onset
of
a
number
of
age-related
diseases
.
The
objective
of
the
present
study
was
to
examine
the
degree
of
associations
between
non-synonymous
coding
Single
Nucleotide
Polymorphisms
(
SNPs
)
in
the
WRN
gene
and
markers
of
obesity
,
diabetes
,
and
hypertension
using
meta
-analyses
publically
available
and
to
test
their
effect
in
WS
fibroblasts
.
The
P-
value
,
after
genomic
control
correction
,
for
each
non-synonymous
coding
SNP
present
in
the
WRN
gene
was
retrieved
from
the
International
Consortium
for
Blood
Pressure
Genome-
Wide
Association
Study
,
the
Genome
Wide
Associations
Scans
for
Total
Cholesterol
,
HDL-cholesterol
,
LDL-cholesterol
and
triglycerides
,
and
the
Meta
-
Analyses
of
Glucose
and
Insulin
-related
traits
Consortium
.
For
SNPs
significantly
associated
with
cholesterol
traits
,
we
generated
expression
vectors
containing
the
amino
acid
changes
and
measured
cholesterol
uptake
and
efflux
in
transfected
WS
fibroblasts
.
One
SNP
(
rs
2230009
)
changing
a
valine
for
an
isoleucine
at
position
114
of
the
WRN
protein
was
nominally
associated
with
cholesterol
and
LDL-cholesterol
measurements
(
P-
values
<
0
.
05
)
.
Interestingly
,
a
WRN
cDNA
expression
vector
bearing
a
valine
at
position
114
instead
of
isoleucine
significantly
affected
cholesterol
efflux
in
WS
fibroblasts
.
These
results
implicate
a
functional
effect
of
this
WRN
polymorphism
on
cholesterol
metabolism
.
Diseases
Validation
Diseases presenting
"blood pressure"
symptom
acute rheumatic fever
adrenal incidentaloma
alpha-thalassemia
cadasil
congenital adrenal hyperplasia
congenital diaphragmatic hernia
cushing syndrome
fabry disease
familial mediterranean fever
lymphangioleiomyomatosis
pendred syndrome
proteus syndrome
scrub typhus
systemic capillary leak syndrome
thoracic outlet syndrome
typhoid
von hippel-lindau disease
werner syndrome
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