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Systematic isolation and characterization of cDNAs encoding AAA proteins from human brain.
[adrenomyeloneuropathy]
The
AAA
(
ATPases
Associated
with
various
cellular
Activities
)
domain
characterizes
a
diverse
superfamily
of
proteins
.
Mutations
in
genes
encoding
AAA-domains
cause
a
variety
of
human
diseases
including
cystic
fibrosis
,
Zellweger
syndrome
,
adrenomyeloneuropathy
,
and
dystonia
.
Recently
,
mutations
in
two
AAA-containing
proteins
paraplegin
and
spastin
have
been
shown
to
cause
two
types
of
hereditary
spastic
paraplegia
(
HSP
)
.
The
HSPs
are
genetically
heterogeneous
degenerative
spinal
cord
disorders
characterized
by
lower
extremity
weakness
and
spasticity
.
Clinical
similarity
between
various
genetic
types
of
HSP
led
us
to
propose
that
different
genetic
types
of
HSP
were
due
to
common
biochemical
abnormalities
including
disturbances
in
related
proteins
.
For
this
reason
,
we
sought
to
identify
novel
AAA-containing
proteins
as
potential
candidates
for
HSP
and
related
neurodegnerative
disorders
.
We
used
degenerative
PCR
,
based
on
the
conserved
AAA
peptide
sequence
to
systematically
clone
and
characterize
AAA
genes
expressed
in
human
brain
.
We
analyzed
646
clones
and
identified
19
known
AAA-containing
proteins
including
spastin
and
paraplegin
,
AAA-containing
genes
that
cause
HSP
.
In
addition
,
we
identified
14
unique
DNA
inserts
representing
novel
putative
AAA-containing
proteins
.
Four
of
these
novel
genes
are
hypothetical
AAA
proteins
and
the
rest
of
novel
clones
matched
sequences
of
yet
uncharacterized
expressed
sequence
tags
(
ESTs
)
.
Fourteen
novel
AAA-containing
proteins
are
potential
candidates
for
human
diseases
including
degenerative
neurologic
disorders
,
and
their
further
analysis
is
ongoing
(
Tab
.
1
,
Fig
.
1
,
Ref
.
22
)
.
Diseases
Validation
Diseases presenting
"and their further analysis is ongoing"
symptom
adrenomyeloneuropathy
zellweger syndrome
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