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Recessive mutations in PCBD1 cause a new type of early-onset diabetes.
[phenylketonuria]
Mutations
in
several
genes
cause
nonautoimmune
diabetes
,
but
numerous
patients
still
have
unclear
genetic
defects
,
hampering
our
understanding
of
the
development
of
the
disease
and
preventing
pathogenesis-oriented
treatment
.
We
used
whole-genome
sequencing
with
linkage
analysis
to
study
a
consanguineous
family
with
early
-onset
antibody-negative
diabetes
and
identified
a
novel
deletion
in
PCBD
1
(
pterin-
4
α-carbinolamine
dehydratase
/
dimerization
cofactor
of
hepatocyte
nuclear
factor
1
α
)
,
a
gene
that
was
recently
proposed
as
a
likely
cause
of
diabetes
.
A
subsequent
reevaluation
of
patients
with
mild
neonatal
hyperphenylalaninemia
due
to
mutations
in
PCBD
1
from
the
BIODEF
database
identified
three
additional
patients
who
had
developed
HNF
1
A
-
like
diabetes
in
puberty
,
indicating
early
β-cell
failure
.
We
found
that
Pcbd
1
is
expressed
in
the
developing
pancreas
of
both
mouse
and
Xenopus
embryos
from
early
specification
onward
showing
colocalization
with
insulin
.
Importantly
,
a
morpholino-mediated
knockdown
in
Xenopus
revealed
that
pcbd
1
activity
is
required
for
the
proper
establishment
of
early
pancreatic
fate
within
the
endoderm
.
We
provide
the
first
genetic
evidence
that
PCBD
1
mutations
can
cause
early
-onset
nonautoimmune
diabetes
with
features
similar
to
dominantly
inherited
HNF
1
A
-
diabetes
.
This
condition
responds
to
and
can
be
treated
with
oral
drugs
instead
of
insulin
,
which
is
important
clinical
information
for
these
patients
.
Finally
,
patients
at
risk
can
be
detected
through
a
newborn
screening
for
phenylketonuria
.
Diseases
Validation
Diseases presenting
"early specification onward"
symptom
phenylketonuria
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