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Farnesyl-diphosphate synthase is localized in peroxisomes.
[neonatal adrenoleukodystrophy]
In
this
study
,
we
have
investigated
the
subcellular
localization
of
farnesyl-diphosphate
synthase
(
FPP
synthase
)
.
FPP
synthase
produces
FPP
,
which
is
utilized
in
the
synthesis
of
squalene
,
cholesterol
,
farnesylated
and
geranylgeranylated
proteins
,
dolichols
,
coenzyme
Q
,
and
the
isoprenoid
moiety
of
heme
a
.
This
enzyme
is
found
in
the
100
,
000
x
g
supernatant
fraction
of
cells
or
tissues
and
has
been
considered
to
be
a
cytoplasmic
protein
.
In
this
study
,
analysis
of
FPP
synthase
activity
and
protein
in
fractionated
rat
liver
together
with
immunofluorescent
and
immunoelectron
microscopy
studies
demonstrated
unequivocally
that
FPP
synthase
is
largely
localized
in
peroxisomes
.
These
data
,
in
combination
with
the
previous
observation
that
mevalonate
kinase
is
predominantly
localized
in
peroxisomes
,
suggest
that
peroxisomes
are
the
major
site
of
synthesis
of
FPP
from
mevalonate
.
We
also
demonstrate
that
in
liver
tissue
obtained
from
patients
with
peroxisomal
deficiency
diseases
(
Zellweger
syndrome
and
neonatal
adrenoleukodystrophy
)
,
the
activities
of
five
enzymes
involved
in
isoprenoid
synthesis
,
namely
mevalonate
kinase
,
phosphomevalonate
kinase
,
mevalonate-diphosphate
decarboxylase
,
isopentenyl-diphosphate
isomerase
,
and
FPP
synthase
,
are
significantly
reduced
,
consistent
with
a
peroxisomal
localization
of
these
enzymes
.
Diseases
Validation
Diseases presenting
"phosphomevalonate kinase"
symptom
neonatal adrenoleukodystrophy
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