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Rapid and reliable detection of α-globin copy number variations by quantitative real-time PCR.
[alpha-thalassemia]
Alpha-thalassemia
is
the
most
common
human
genetic
disease
worldwide
.
Copy
number
variations
in
the
form
of
deletions
of
α-globin
genes
lead
to
α-thalassemia
while
duplications
of
α-globin
genes
can
cause
a
severe
phenotype
in
β-thalassemia
carriers
due
to
accentuation
of
globin
chain
imbalance
.
It
is
important
to
have
simple
and
reliable
methods
to
identify
unknown
or
rare
deletions
and
duplications
in
cases
in
which
thalassemia
is
suspected
but
can
not
be
confirmed
by
multiplex
gap-
PCR
.
Here
we
describe
a
copy
number
variation
assay
to
detect
deletions
and
duplications
in
the
α-globin
gene
cluster
(
HBA-CNV
)
.
Quantitative
real-time
PCR
was
performed
using
four
TaqMan
®
assays
which
specifically
amplify
target
sequences
representing
both
the
α-globin
genes
,
the
-
α
3
.
7
deletion
and
the
HS
-
40
region
.
The
copy
number
for
each
target
was
determined
by
the
2
-
ΔΔCq
method
.
To
validate
our
method
,
we
compared
the
HBA-CNV
method
with
traditional
gap-
PCR
in
108
samples
from
patients
referred
to
our
laboratory
for
hemoglobinopathy
evaluation
.
To
determine
the
robustness
of
the
four
assays
,
we
analyzed
samples
with
and
without
deletions
diluted
to
obtain
different
DNA
concentrations
.
The
HBA-CNV
method
identified
the
correct
copy
numbers
in
all
108
samples
.
All
four
assays
showed
the
correct
copy
number
within
a
wide
range
of
DNA
concentrations
(
3
.
2
-
100
Â
ng
/
μL
)
,
showing
that
it
is
a
robust
and
reliable
method
.
By
using
the
method
in
routine
diagnostics
of
hemoglobinopathies
we
have
also
identified
several
deletions
and
duplications
that
are
not
detected
with
conventional
gap-
PCR
.
HBA-CNV
is
able
to
detect
all
known
large
deletions
and
duplications
affecting
the
α-globin
genes
,
providing
a
flexible
and
simple
workflow
with
rapid
and
reliable
results
.
Diseases
Validation
Diseases presenting
"simple workflow"
symptom
alpha-thalassemia
familial hypocalciuric hypercalcemia
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