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Functional characterization of pendrin mutations found in the Israeli and Palestinian populations.
[pendred syndrome]
Pendrin
is
a
transport
protein
exchanging
chloride
for
other
anions
,
such
as
iodide
in
the
thyroid
gland
or
bicarbonate
in
the
inner
ear
.
Mutations
in
the
SLC
26
A
4
gene
encoding
for
pendrin
are
responsible
for
both
syndromic
(
Pendred
syndrome
)
and
non-syndromic
(
non-syndromic
enlarged
vestibular
aqueduct
,
EVA
)
hearing
loss
.
Besides
clinical
and
radiological
assessments
,
molecular
and
functional
studies
are
essential
for
the
correct
diagnosis
of
Pendred
syndrome
and
non-syndromic
EVA
.
While
a
broad
spectrum
of
mutations
found
in
the
Caucasian
population
has
been
functionally
characterized
,
little
is
known
about
mutations
specifically
occurring
in
the
populations
of
the
Middle
East
.
Here
we
show
the
characterization
of
the
ion
transport
activity
of
three
pendrin
mutations
previously
found
in
deaf
patients
with
EVA
in
the
Israeli
Jewish
and
Palestinian
Arab
populations
,
i
.
e
.
V
239
D
,
G
334
V
X
335
and
I
487
Y
FSX
39
.
Wild
type
and
mutated
pendrin
allelic
variants
were
functionally
characterized
in
a
heterologous
over-expression
system
.
The
Cl
(
-
)
/
I
(
-
)
and
Cl
(
-
)
/
OH
(
-
)
exchange
activities
were
assessed
by
fluorometric
methods
suitable
for
measuring
iodide
fluxes
and
the
intracellular
pH
.
Both
the
Cl
(
-
)
/
I
(
-
)
and
the
Cl
(
-
)
/
OH
(
-
)
exchange
activities
of
pendrin
V
239
D
,
G
334
V
X
335
and
I
487
Y
FSX
39
were
significantly
reduced
with
respect
to
the
wild
type
,
with
V
239
D
displaying
a
residual
iodide
transport
.
Functional
assays
confirmed
the
diagnosis
of
non-syndromic
EVA
due
to
SLC
26
A
4
mutations
performed
by
radiological
and
molecular
tests
in
deaf
patients
belonging
to
the
Israeli
Jewish
and
Palestinian
Arab
populations
.
The
new
finding
that
the
V
239
D
mutation
displays
residual
function
suggests
that
the
symptoms
caused
by
this
mutation
could
be
ameliorated
by
a
pendrin
'
activator
'
,
if
available
.
Diseases
Validation
Diseases presenting
"eva"
symptom
pendred syndrome
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