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The testis anion transporter TAT1 (SLC26A8) physically and functionally interacts with the cystic fibrosis transmembrane conductance regulator channel: a potential role during sperm capacitation.
[pendred syndrome]
The
Slc
26
gene
family
encodes
several
conserved
anion
transporters
implicated
in
human
genetic
disorders
,
including
Pendred
syndrome
,
diastrophic
dysplasia
and
congenital
chloride
diarrhea
.
We
previously
characterized
the
TAT
1
(
testis
anion
transporter
1
;
SLC
26
A
8
)
protein
specifically
expressed
in
male
germ
cells
and
mature
sperm
and
showed
that
in
the
mouse
,
deletion
of
Tat
1
caused
male
sterility
due
to
a
lack
of
sperm
motility
,
impaired
sperm
capacitation
and
structural
defects
of
the
flagella
.
Ca
(
2
+
)
,
Cl
(
-
)
and
HCO
(
3
)
(
-
)
influxes
trigger
sperm
capacitation
events
required
for
oocyte
fertilization
;
these
events
include
the
intracellular
rise
of
cyclic
adenosine
monophosphate
(
cAMP
)
and
protein
kinase
A
(
PKA
)
-
dependent
protein
phosphorylation
.
The
cystic
fibrosis
transmembrane
conductance
regulator
(
CFTR
)
is
expressed
in
mature
sperm
and
has
been
shown
to
contribute
to
Cl
(
-
)
and
HCO
(
3
)
(
-
)
movements
during
capacitation
.
Furthermore
,
several
members
of
the
SLC
26
family
have
been
described
to
form
complexes
with
CFTR
,
resulting
in
the
reciprocal
regulation
of
their
activities
.
We
show
here
that
TAT
1
and
CFTR
physically
interact
and
that
in
Xenopus
laevis
oocytes
and
in
CHO
-K
1
cells
,
TAT
1
expression
strongly
stimulates
CFTR
activity
.
Consistent
with
this
,
we
show
that
Tat
1
inactivation
in
mouse
sperm
results
in
deregulation
of
the
intracellular
cAMP
content
,
preventing
the
activation
of
PKA-dependent
downstream
phosphorylation
cascades
essential
for
sperm
activation
.
These
various
results
suggest
that
TAT
1
and
CFTR
may
form
a
molecular
complex
involved
in
the
regulation
of
Cl
(
-
)
and
HCO
(
3
)
(
-
)
fluxes
during
sperm
capacitation
.
In
humans
,
mutations
in
CFTR
and
/
or
TAT
1
may
therefore
be
causes
of
asthenozoospermia
and
low
fertilizing
capacity
of
sperm
.
Diseases
Validation
Diseases presenting
"sperm results in deregulation of the intracellular camp content"
symptom
pendred syndrome
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