Duchenne`s muscular dystrophy

advertisement
Muscular
dystrophy
Dr. Derakhshandeh
1
Muscular dystrophy
(MD)




a group of rare inherited muscle diseases
muscle fibers are unusually susceptible to damage
Muscles, primarily voluntary muscles, become
progressively weaker
In some types of muscular dystrophy, heart
muscles, other involuntary muscles and other
organs are affected
2
voluntary & in voluntary muscles
3
Duchenne's muscular dystrophy (Xp21.2)


The types of muscular dystrophy:
 a genetic deficiency of the protein
dystrophin :
 dystrophinopathies
Duchenne's muscular dystrophy :


the most severe form of dystrophinopathy.
It occurs mostly:

in young boys
4
Dystrophin






a large (427 kD) cytoskeletal protein
structure with an actin-binding domain at the
amino terminus (N)
The carboxy-terminal domains associate with a
large transmembrane complex of glycoproteins
directly bind with elements of the extracellular
Dystrophin: likely plays a critical role in
establishing connections between the internal,
actin-based cytoskeleton and the external
basement membrane
Its absence may lead to increased membrane
fragility
5
Dystrophin
6
Duchenne's muscular
dystrophy
Difficulty getting up from a lying or
sitting position
 Weakness in lower leg muscles,
resulting in difficulty running and
jumping
 Waddling gait
 Mild mental retardation, in some
cases

7
Waddling gait
8
In the late stages of muscular
dystrophy, fat and connective tissue
often replace muscle fibers.
9
10
DMD
11
Orthopaedic management of patients
with Duchenne's muscular dystrophy
12
Duchenne's muscular
dystrophy
X-linked inheritance
Prevalence 0.003-0.05/1,000 total
 Signs and symptoms of Duchenne's
usually appear between the ages of 2
and 5
 It first affects the muscles of the
pelvis, upper arms and upper legs.
 By late childhood, most children with
this form of muscular dystrophy are
unable to walk.

13
Most die by their late teens or early
20s, often from pneumonia,
respiratory muscle weakness or
cardiac complications.
 Some people with Duchenne's MD may
exhibit curvature of their spine
(scoliosis).

14
Becker's muscular dystrophy




This type of muscular dystrophy is a
milder form of dystrophinopathy.
It generally affects older boys and
young men, and progresses more
slowly, usually over several decades.
Signs and symptoms of Becker's MD
are similar to those of Duchenne's.
The onset of the signs and symptoms
is generally later, from age 2 to 16.
15
Multiplex PCR images
Iranian J Publ Health, Vol. 32, No. 3, pp.47-53, 2003
S Kheradmand kia , DD Farhud , S Zeinali , AR Mowjoodi, H Najmabadi ,
F Pourfarzad, P Derakhshandeh-Peykar
,
16
-/- +/+
-/+ +/y -/+ +/y
-/- +/+
-/+ -/y +/+ +/y
Iranian J Publ Health, Vol. 32, No. 3, pp.47-53, 2003
17
Iranian J Publ Health, Vol. 32, No. 3, pp.47-53, 2003
18
19
MLPA
Multiplex Ligation-dependent Probe
Amplification
20
MLPA
21
MLPA analysis of the human DMDgene in a normal male
22
Agarose-gel analysis of DMD
deletion patient
23
The MLPA reaction & five major
steps
1) DNA denaturation and hybridisation of MLPA
probes
2) ligation reaction
3) PCR reaction
4) separation of amplification products by
electrophoresis
5) data analysis
24
The MLPA reaction I





first step: the DNA is denatured and incubated
overnight with a mixture of MLPA probes
MLPA probes consist of two separate
oligonucleotides, each containing one of the
PCR primer sequences
The two probe oligonucleotides hybridize to
immediately adjacent target sequences
Only when the two probe oligonucleotides are
both hybridised to their adjacent targets can
they be ligated during the ligation reaction
only ligated probes will be exponentially
amplified during the subsequent PCR reaction
25
The MLPA reaction II




the number of probe ligation products is a
measure for the number of target sequences in
the sample
The amplification products are separated using
capillary electrophoresis
Probe oligonucleotides that are not ligated only
contain one primer sequence. As a
consequence, they cannot be amplified
exponentially and will not generate a signal.
The removal of unbound probes is therefore
unnecessary in MLPA and makes the MLPA
method easy to perform.
26
Advantages of MLPA





methods which were primarily developed for detecting point
mutations, such as sequencing and DHPLC (denaturing
high-performance liquid chromatography), generally fail to detect
copy numbers changes
Southern blot analysis, will not always detect small deletions
and is not ideal as a routine technique
comparing MLPA to FISH, MLPA not only has the advantage
of being a multiplex technique, but also one in which very
small (50-70 nt) sequences are targeted
Moreover, MLPA can be used on purified DNA
The over 300 probe sets now available are dedicated to
applications ranging from the relatively common (Duchenne,
DiGeorge syndrome, SMA)
27
MAPH
Multiplex Amplifiable Probe
Hybridisation
28
MAPH
 Detection
of
deletions/duplication mutations
in Duchenne Muscular
Dystrophy using: MAPH
29
MAPH

Although ~95% of deletions can be detected in
males using multiplex PCR

other methods must be used to determine
duplications, as well as the carrier status of
females
The most commonly applied methods are
quantitative multiplex PCR and quantitative
Southern blotting

30
MAPH




Using high-quality Southern blots it is possible
to perform a quantitative analysis and detect
duplications
this technique is time consuming
it is difficult to exactly determine the duplication
it can be difficult to detect duplications in
females and triplications will be missed
Armour et al (Nucl.Acids Res. 2000)
31

system for analyzing all 79 exons of the
DMD gene for deletions and duplications

MAPH is based on a quantitative PCR of
short DNA probes recovered after
hybridization to immobilized genomic DNA
32
33






1 ug of denatured genomic DNA is spotted
on a small nylon filter
hybridized overnight in a solution
containing one of the probe mixes
Following stringent washing the next day
the filter is placed in a PCR tube
and a short PCR reaction is performed
This releases the specifically-bound probes
into the solution
An aliquot of this is transferred to a second,
quantitative PCR reaction
34

alterations can be examined by using a set
of short probes (140-600 bp)

After washing and PCR the differently sized
products resolved and quantified measured

The amount of probe amplified depends on
the number of hybridising targets and
therefore on the copy number of the
corresponding locus in the test DNA
35
36
MAPH dystrophin probe sets A/B: The
two probes sets encompassing
all exons in normal individuals
37
A relative comparison is made between the
band intensities or peak heights
38
39
Outline of the MAPH technique
40
A: a female deleted for exons 49 and 51
B: a control female
C: a female duplicated for the exons 49 and 51
D: a male deleted for exons 49 and 51
41
Analysis of exon products on a micro-array
PCR-fragments containing DMD exons are spotted in triplicate on each array
top left exons 1-24
bottom left exons 49-72
top right exons 25-48
bottom right exons 73-79
42
Applications

areas such as cancer risk (BRCA1 and
HNPCC)

learning disability (US: "mental retardation")

muscular dystrophy (DMD/BMD)
neuromuscular disorders (SMA)
43
Download