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[Combination of multiple displacement amplification with short tandem repeat polymorphismin preimplantation genetic diagnosis].
[achondroplasia]
To
explore
the
application
of
multiple
displacement
amplification
(
MDA
)
combined
with
short
tandem
repeats
(
STRs
)
in
preimplantation
genetic
diagnosis
(
PGD
)
.
MDA
was
applied
to
amplify
the
whole
genome
of
a
single
cell
and
to
retrieve
and
assemble
the
highly
heterogeneous
STR
loci
among
human
population
.
Haplotype
analytic
system
was
established
with
aiming
at
diagnosis
of
the
single
gene
diseases
by
selecting
the
STR
loci
located
within
the
pathogenic
genes
or
on
both
bounding
sides
of
the
pathogenic
genes
.
At
the
same
time
,
allele
specific
amplification
,
PCR-reverse
dot-blotting
hybridization
methods
and
gene
sequencing
methods
were
employed
for
direct
detection
of
the
pathogenic
genes
.
The
STR
loci
located
at
related
chromosomes
were
selected
to
carry
out
allele
number
analysis
on
the
basis
of
chromosome
number
and
structural
abnormality
.
In
the
study
,
12
PGD
systems
were
set
up
including
6
different
monogenic
diseases
(
spinal
muscular
atrophy
,
Duchenne
muscular
dystrophy
,
X-
linked
chronic
granulomatous
disease
,
osteopetrosis
,
achondroplasia
,
X-
linked
severe
combined
immunodeficiency
)
,
Robertsonian
translocations
,
α-thalassemia
combined
with
Robertsonian
translocation
,
α-
and
β-
double
thalassemia
,
β-thalassemia
with
HLA
typing
and
DMD
with
HLA
typing
.
Then
44
PGD
cycles
were
performed
for
35
couples
with
different
kinds
of
inherited
diseases
,
which
resulted
in
20
healthy
liveborns
(
12
singletons
and
4
twins
)
and
5
ongoing
pregnancies
.
The
clinical
pregnancy
rate
was
47
.
7
%
(
21
/
44
)
per
PGD
cycle
.
The
overall
diagnostic
rate
was
94
.
6
%
(
367
/
388
)
.
The
MDA
failed
in
3
.
6
%
(
14
/
388
)
single
blastomeres
.
The
amplification
rate
of
the
subsequent
PCR
was
97
.
1
%
and
the
average
allele
drop
out
(
ADO
)
rate
was
12
.
6
%
(
range
:
0
-
47
.
5
%
)
.
The
application
of
MDA
combined
with
STRs
provided
a
generic
PGD
approach
for
different
genetic
disorders
,
especially
for
simultaneous
diagnosis
of
two
or
more
hereditary
statuses
.
The
method
could
greatly
shorten
the
time
of
developing
PGD
system
of
new
diseases
,
which
broadens
the
indications
of
PGD
.
Diseases
Validation
Diseases presenting
"to retrieve and assemble the highly heterogeneous str loci among human population"
symptom
achondroplasia
alpha-thalassemia
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