Molecular Basis of Some Neurological Disorders
Said IsmailDept. of Biochemistry
Molecular Basis of Neurological Disorders
Neurological Disorders
disorders which involve: - The central nervous system (brain, brainstem and cerebellum) - The peripheral nervous system (including cranial and peripheral nerves)
Major examples:Neurodegenerative diseases:
- affecting movement - Parkinson's disease (PD) - Huntington's disease (HD)
- memory loss and Dementia - Alzheimer StrokeEpilepsy and SeizuresNeoplasmsHeadaches
Molecular Basis of Neurological Disorders
Common causes:
- Inherited genetic abnormalities
- Problems in the immune system
- Injury to the brain or nervous system
- other diseases such as Diabetes
Molecular Basis of Neurological Disorders
WHO numbers: March 2007
Hundreds of million worldwide are affected by neurological disorders:
Examples:
50 million: epilepsy;62 million: cerebrovascular disease; 326 million: migraine; 24 million: Alzheimer disease & other dementias
- 6.8 million people die every year as a result of neurological disorders
Molecular Basis of Neurological Disorders
Huntington’s Disease (HD):
- Major example of inherited neurological disorders (ND)
- Unlike other common NDs:single genetic cause in all patients (ie single disease mechanism)
- Symptoms: - abnormal body movements called chorea and a lack of coordination
- Also involves behavioral and intellectual problems
- Age of onset:all ages but majority in middle age
- Death typically occurs 15 years after motor symptoms onset
Molecular Basis of Neurological Disorders
HD Inheritance and Genetics:
- All cases: due to expansion of the CAG tri-nucleotide repeat in the HD gene
- HD gene is found on short arm of chromosome 4
- There are normally: 6 – 34 CAG units (>34 repeats result in HD)
- In rare HD Heterozygotes, the longer repeat determines the age of onset (the second repeat has no effect):
HD is autosomal dominance (at least in regard to age of onset)
Molecular Basis of Neurological Disorders
Molecular Basis of Neurological Disorders
Inheritance of Huntington disease
The extended CAG repeat:
- CAG repeat: located in coding sequence near 5’ end of HD geneWhen CAG is > 34: Inheritance is meiotically not stable (specially from father)
(Child usually has longer CAG region compared to father (earlier onset)
Age of Onset: depend largely on length of CAG repeat (The Longer the CAG repeat the Younger the onset of disease)
NO correlation between CAG length and Duration of disease (onset to death)
Only Little effect of CAG length on progression of symptoms
So, Mechanism of disease onset night be different from mechanism of disease progression
Molecular Basis of Neurological Disorders
Correlation of HD CAG-repeat length with age at onset
Molecular Basis of Neurological Disorders
Cont.
- CAG repeats: Encodes a poly-Glutamine tract beginning 18 aa of the N-terminus
- HD protein: “Huntingtin” large (> 3,100 aa)
- expressed in both neuronal and non-neuronal tissues
- expression not limited to neurons affected in HD !!
- Expanded CAG repeats and extended polyglutamine tract have been found in other proteins involved in other inherited neurodegenerative dis.s
Molecular Basis of Neurological Disorders
Toxic effect of HD polyglutamine tract:
- Still not very clear
- Only the N-terminus of Huntingtin is necessary for HD symptoms
- General hypothesis:- HD is a conformational disease in which the pathogenic pathway is triggered In some manner by protein mis-folding and its consequences including Formation of aggregate structures
Molecular Basis of Neurological Disorders
Alzheimer’s disease:
- Most common cause of Dementia (50-60 %)
- First described 100 years ago by Alois Alzheimer, Germany.
- Dementia: - < 1% in people aged 60-64 years
- 24 – 33% in people over 85 years
- World wide: - 24 million in 2004- 81 million in 2040 (due to increased life expectancy)
- Familial and sporadic forms
Molecular Basis of Neurological Disorders
Molecular Basis of Neurological Disorders
Genetics of Alzheimer’s:
- “Familial” type:
- Autosomal dominant disorder with onset before 65 years
- Rare: prevalence below 0.1%
- Genes involved:
- Presenilin 1 (PSEN1) & Presenilin 2 (PSEN2): most familial cases- Amyloid precursor protein (APP): only few cases
Molecular Basis of Neurological Disorders
“Sporadic” type: - Almost 80% is linked to genetic factors - Apolipoprotein E (APOE) ε4 allele: most important predisposing risk factor - APOE: is a cholesterol transporter in Brain
(APOE4: low efficiency variant in reuse of membrane lipids and repair)
- Hetero APOE ε4: 3 fold increase in risk - Homo APOE ε4: 15 fold increase in risk
- APOE ε4 allele affects mainly the age of onset:- each allele copy lower age of onset by 10 years
- NO other gene has been shown to have similar significance (probably because sporadic form are the result of accumulated smalleffects of several genes plus the environmental factors)
Molecular Basis of Neurological Disorders
Molecular Basis of Neurological Disorders
PROTEIN CHROMOSOME GENE
S182 14 Presenilin-1 STM2 1 Presenilin-2 APP 21 Amyloid Precursor Protein APOE 19 ApoLipoprotein e
Genetic Causes of Alzheimer's Disease
Familial
Sporadic
Parkinson’s Disease (PD):
- The second most common adult onset neurological condition
- Affects over 1% of people over 65 years
- Main symptoms: bradykinisia, tremor, and rigidity
- Sporadic PD:
- only little gene association has been uncovered so far (5-10%)
- caused by a combination of environmental toxins acting via inhibition of the mitochondrial respiratory chain to produce dopaminergic cell loss and inclusion bodies leading to increase in oxidative stress.
Molecular Basis of Neurological Disorders
celebrity patients: Michael J. Fox and Muhammad Ali
Molecular Basis of Neurological Disorders
Familial PD:
- rare
- Some variants are autosomal recessive and some are autosomal dominant
- Ex1: DJ-1 gene:- causes an autosomal recessive type of PD- Normal DJ-1 appears to provide neuro-protection against
oxidative stress caused by mitochondrial toxins (Mutated DJ-1 does not)
- Ex 2: PINK1 gene:- also causes an autosomal recessive type of PD
- also have neuroprotective properties against a variety of cellular stresses
(mutated forms (eg G309D) lose such properties)
- Ex 3: parkin and α-synuclein: involved in juvenile and early-onset PD - parkin gene: autosomal dominant - α-synuclein: autosomal recessive
Molecular Basis of Neurological Disorders
Table 1. Summary of the genes accounting for the Mendelian forms of PD and the major published mutations identified in these genes
AD, autosomal dominant; AR, autosomal recessive, Homozygous mutations are only shown for genes causing autosomal recessive PD. Although several heterozygous mutations have been identified in all genes causing autosomal recessive PD, the pathological significance remains unclear. aThe G2019S mutation in the LRRK2 gene has been reported a number of times and appears to account for 3–7% familial PD and 1–1.6% of so-called ‘sporadic PD’ (57,58,59).
Mutations identified Inheritance pattern
Gene Chromosomal location
Locus
Missense mutations: A53T, A30P, E46K duplication, triplication AD
Alpha-synuclein 4q21–q23
Park 1 and 4
Exon deletions and duplications; frameshift mutations 13, nonsense mutations 6, missense mutations 27 AR Parkin 6q25.2–q27 Park 2
AD Unknown 2p13 Park 3
Missense mutation I93M AD UCHL-1 4p14 Park 5
Missense mutations: G309D, A168P, H271Q, E417G, L347P; nonsense mutations: W437X, R246X; frameshift mutation: 1573_1574insTTAG AR PINK1 1p35–36 Park 6
Exonic deletion: exons 1–5; missense mutations: L166P, M26I, E64D AR DJ-1 1p36 Park 7
Missense mutations: L1114L, I1122V, I1371V, I2020T, R1441C, Y1699C, R1441G, G2019Sa AD LRRK2
12p11.2–q13.1 Park 8
AR Unknown 1p36 Park 9
Autosomal recessive inheritance where both parents carry the faulty parkin gene.
Autosomal dominant inheritance when one parent either has PD or has the faulty α-synuclein gene copy.
Epilepsy:
- 40% of cases are associated with genetic factors
- Genetic Epilepsies:
1. Mendelian disorders: single major locus account for segregation of disease
2. Non-Mendelian (complex) diseases:several gene loci implicated in addition to environmental factors
or by maternal inheritance pattern of mitochondrial DNA
3. Chromosomal disorder:Gross cytogenetic abnormality is present
Molecular Basis of Neurological Disorders
Mendelian:
- Over 200 Mendelian diseases include epilepsy in their phenotype- BUT, all are rare (1% of all patients)- Channelopathies: arise from mutation in both voltage-gated and ligand-gated ion ion channels
complex:
- Most common familial type of epilepsy
Chromosomal:
- Trisomy 21 (Down Syndrome) - Trisomy 12p
Molecular Basis of Neurological Disorders
Neuroscience and Stem cell research:
- Promising animal model and human experiments
- Political and ethical debate !!- USA: September 2001 restrictions by Bush
- Example Target Disorders:
- Neurodegenerative disorders: Parkinson’s & Huntington’s: localized degeneration: easier cell therapy Alzheimer: affected neurons are less defined
- Spinal cord injuries
Molecular Basis of Neurological Disorders
MAKING THE HEADLINESFROM STEM CELLS TO NEURONS LOST IN ALZHEIMER’Spublished 4/3/2011 in the journal Stem Cells (Kessler and Bissonnette)Northwestern Medicine researchers for the first time have transformed a human embryonic stem cell into a critical type of neuron that dies early in Alzheimer’s disease and is a major cause of memory loss.This new ability to reprogram stem cells and grow a limitless supply of the human neurons will enable a rapid wave of drug testing for Alzheimer’s disease, allow researchers to study why the neurons die and could potentially lead to transplanting the new neurons into people with Alzheimer’s.These critical neurons, called basal forebrain cholinergic neurons, help the hippocampus retrieve memories in the brain.
Human Skin Cells Transformed into Stem Cells and then NeuronsIn new, unpublished research: Northwestern Medicine scientists also have discovered a second novel way to make the neurons. They made human embryonic stem cells (called induced pluripotent stem cells) from human skin cells and then transformed these into the neurons.Scientists made these stem cells and neurons from skin cells of three groups of people: Alzheimer’s patients, healthy patients with no family history of Alzheimer’s, and healthy patients with an increased likelihood of developing the disease due to a family history of Alzheimer’s because of genetic mutations or unknown reasons.
Video
Molecular Basis of Neurological Disorders