Albers, D. S. and S. J. Augood (2001). "New insights into
progressive supranuclear palsy." Trends Neurosci24(6): 347-53.
Increased oxidative damage and mitochondrial dysfunction have been suggested to
play crucial roles in the pathogenesis of several neurodegenerative diseases,
including Parkinson's disease and Alzheimer's disease. In this review, we will
focus on progressive supranuclear palsy (PSP), a rare parkinsonian disorder with
tau pathology. Particular emphasis is placed on the genetic and biochemical data
that has emerged, offering new perspectives into the pathogenesis of this
devastating disease, especially the contributory roles of oxidative damage and
mitochondrial dysfunction.
Arvanitakis, Z. and Z. K. Wszolek (2001). "Recent advances in the understanding
of tau protein and movement disorders." Curr Opin Neurol14(4):
491-7.
Tau plays an important role in movement disorders. The accumulation of
pathological tau is a major substrate of frontotemporal dementia and
parkinsonism linked to chromosome 17, progressive supranuclear palsy, and
corticobasal degeneration. Over the past year, several new mutations on the tau
gene have been found. These mutations have been classified into three groups: (i)
mutations in constitutively spliced exons; (ii) mutations in the alternatively
spliced exon 10; and (iii) mutations of the exon 10 5' splice site. Some
patients presenting with frontotemporal dementia and parkinsonism linked to
chromosome 17 transiently respond to levodopa therapy. The significance of Pick
bodies was recognized by a recent study on kindred with the Glu342Val tau
mutation. In sporadic cases of progressive supranuclear palsy, the presence of
the H1 haplotype was found to be a risk factor. Corticobasal degeneration shares
a common genetic background with progressive supranuclear palsy. This opens the
question of whether corticobasal degeneration represents a separate disorder or
a spectrum of disease with progressive supranuclear palsy. However,
distinguishing features are observed, and include oculomotor abnormalities,
which may help to differentiate these two disorders on clinical grounds. Despite
recent advances in the understanding of the tauopathies, there are still no
curative therapies available. It is hoped that studies in transgenic tau animal
models will lead to the development of successful treatments.
Delacourte, A. (2001). "The molecular parameters of tau pathology. Tau as a
killer and a witness." Adv Exp Med Biol487: 5-19.
Farrer, M., D. M. Maraganore, et al. (2001). "alpha-Synuclein gene haplotypes
are associated with Parkinson's disease." Hum Mol Genet10(17):
1847-51.
We report haplotype analysis of the alpha-synuclein gene in Parkinson's disease
(PD), extending earlier reports of an association with a polymorphism within the
gene promoter. This analysis showed significant differences in haplotypes
between PD cases and controls. Our analyses demonstrate that genetic variability
in the alpha-synuclein gene is a risk factor for the development of PD. These
genetic findings are analogous to the tau haplotype over-represented in
progressive supranuclear palsy and further extend the similarity in the
etiologies and pathogeneses of the synucleinopathies and tauopathies.
Goedert, M. (2001). "The significance of tau and alpha-synuclein inclusions in
neurodegenerative diseases." Curr Opin Genet Dev11(3): 343-51.
Intracellular filamentous inclusions made of either the microtubule-associated
protein tau or the protein alpha-synuclein define the majority of cases of
neurodegenerative disease. Mutations in the tau gene in familial forms of
frontotemporal dementia and in the alpha-synuclein gene in familial cases of
Parkinson's disease have provided causal links between the dysfunction of these
proteins and neurodegeneration. Over the past year, several novel tau gene
mutations have been identified and more has been learned about possible
mechanisms by which tau gene mutations lead to frontotemporal dementia.
Experimental animal models have provided a link between tau filament formation
and nerve cell degeneration. Along similar lines, animal models have been
produced that result in the formation of alpha-synuclein filaments and the
degeneration of dopaminergic nerve cells. Building on previous work, synthetic
alpha-synuclein filaments have been shown to exhibit the characteristics of
amyloid.
Goedert, M., M. G. Spillantini, et al. (2001). "From genetics to pathology: tau
and alpha-synuclein assemblies in neurodegenerative diseases." Philos Trans R
Soc Lond B Biol Sci356(1406): 213-27.
The most common degenerative diseases of the human brain are characterized by
the presence of abnormal filamentous inclusions in affected nerve cells and
glial cells. These diseases can be grouped into two classes, based on the
identity of the major proteinaceous components of the filamentous assemblies.
The filaments are made of either the microtubule-associated protein tau or the
protein alpha-synuclein. Importantly, the discovery of mutations in the tau gene
in familial forms of frontotemporal dementia and of mutations in the alpha-synuclein
gene in familial forms of Parkinson's disease has established that dysfunction
of tau protein and alpha-synuclein can cause neurodegeneration.
Golbe, L. I., A. M. Lazzarini, et al. (2001). "The tau A0 allele in Parkinson's
disease." Mov Disord16(3): 442-7.
Parkinson's disease (PD) is primarily an alpha-synucleinopathy, rather than a
tauopathy, but there is evidence for an indirect association of tau with the
pathogenetic process in PD. We therefore assessed the frequency in PD of the tau
A0 allele, a dinucleotide repeat marker that has been associated with a sporadic
tauopathy, progressive supranuclear palsy (PSP). We found the A0 allele to
comprise 79.2% of 758 alleles from PD patients and 71.2% of 264 control alleles
(P = 0.008). We also performed a meta-analysis of three previous reports, two of
which failed to produce statistically significant results. Taken together, they
also support a PD/A0 allelic association, even after correction for misdiagnosis
of PSP as PD (P< 0.001). The A0/A0 genotype frequency in our patients (62.3%)
did not differ significantly from that in controls (53.0%, P = 0.062), but the
meta-analysis, even after correction for misdiagnosis, showed a significant
result, with P = 0.002. The frequency of A0 allele and the A0/A0 genotype were
compatible with Hardy-Weinberg equilibrium. The frequency of the A0 allele and
the A0/A0 genotype in our patients with familial PD was not significantly
greater than in those with sporadic PD. We conclude that the tau protein may
play a small role in the pathogenesis of PD and that biochemical
characterization of this role may suggest opportunities for PD prophylaxis.
Copyright 2001 Movement Disorder Society.
Henderson, J. M., W. P. Gai, et al. (2001). "Parkinson's disease with late
Pick's dementia." Mov Disord16(2): 311-9.
We report a case in which typical clinical features of idiopathic Parkinson's
disease existed for seven years prior to the development of significant
behavioral and cognitive changes and severe dementia. The patient presented with
right-sided resting tremor, bradykinesia, and rigidity, which were highly
responsive to levodopa. Serial neuropsychological evaluation revealed no
evidence of dementia until late in the disease. The patient deteriorated rapidly
eight years into the disease, requiring full care. She died 16 years after
symptom onset and post-mortem neuropathological analysis revealed Lewy body
Parkinson's disease and Pick's disease. To our knowledge, this is the first
non-familial case with this combination of clinical history and pathologically
confirmed disease to be reported in the literature. The absence of a family
history of any neurological disease sets this case apart from the recently
described genetic cases of frontotemporal dementia with Parkinsonism linked to
chromosome 17. In addition, the relatively late onset of dementia in
frontotemporal dementia is atypical. While there is considerable debate
regarding the cause of dementia in idiopathic Parkinson's disease, our case
illustrates that Pick's disease is one such cause. Copyright 2001 Movement
Disorder Society.
Ingelson, M., S. F. Fabre, et al. (2001). "Increased risk for frontotemporal
dementia through interaction between tau polymorphisms and apolipoprotein E
epsilon4." Neuroreport12(5): 905-9.
The tau gene has an important role in frontotemporal dementia (FTD) as
pathogenic mutations have been found in hereditary forms of the disease.
Furthermore, a certain extended tau haplotype has been shown to increase the
risk for progressive supranuclear palsy, corticobasal degeneration, Parkinson's
disease and, in interaction with the apolipoprotein E (apoE) epsilon4 allele,
Alzheimer's disease. By microsatellite analysis we investigated an intronic tau
polymorphism, in linkage disequilibrium with the extended tau haplotype, in FTD
patients (n = 36) and healthy controls (n = 39). No association between any of
the tau alleles/genotypes and FTD was seen, but certain tau alleles and apoE
epsilon4 interactively increased the risk of FTD (p = 0.006). We thus propose
that this extended tau haplotype in combination with apoE epsilon4 is a genetic
risk factor for FTD.
Lev, N. and E. Melamed (2001). "Heredity in Parkinson's disease: new findings."
Isr Med Assoc J3(6): 435-8.
Multiple factors have been hypothesized over the last century to be causative or
contributory for Parkinson's disease. Hereditary factors have recently emerged
as a major focus of Parkinson's disease research. Until recently most of the
research on the etiology of Parkinson's disease concentrated on environmental
factors, and the possibility that genetic factors contribute significantly to
the pathogenesis of Parkinson's disease has been neglected. However, it has
become increasingly apparent that even in sporadic cases, the disease most
likely reflects a combination of genetic susceptibility and an unknown
environmental insult. Moreover, the identification of genes and proteins that
may cause hereditary parkinsonism substantially contributes to our ability to
understand the pathogenesis of Parkinson's disease and may help in the early
identification of the disease and its treatment. The discovery of
alpha-synuclein mutations in families with autosomal dominant Parkinson's
disease sheds light on its role in sporadic Parkinson's disease. It seems that
this protein tends to aggregate when the cellular milieu is altered [14-16]. The
question as to the exact changes that cause its deposition remains open. One of
the major possibilities is oxidative stress [16]. The role of these aggregates
in neuronal cell death is also still unclear. Transgenic mice expressing
wild-type human alpha-synuclein developed progressive accumulation of
alpha-synuclein and ubiquitin-immunoreactive inclusions in neurons in the
neocortex, hippocampus and the substantia nigra. These alterations were
associated with loss of dopaminergic terminals and motor impairments [24]. This
finding suggests that accumulation of alpha-synuclein may play a causal role in
sporadic Parkinson's disease as well. The parkin protein seems to be a crucial
survival factor for nigral neurons [15]. The parkin protein is related to the
ubiquitin pathway, which is important in the elimination of damaged proteins.
Ubiquitin-mediated degradation of proteins plays a central role in the control
of numerous processes, including signal transduction, receptor and
transcriptional regulations, programmed cell death, and breakdown of abnormal
proteins that may interfere with normal cell functions. Further studies on the
function of Parkin protein and its relation to the ubiquitin pathway could
elucidate at least one of the molecular mechanisms of nigral neuronal death. A
mutation in the ubiquitin carboxy-teminal hydrolase L1 gene also implies the
importance of the ubiquitin pathway in Parkinson's disease. Abnormal tau protein
was found to be the cause of familial frontotemporal dementia and parkinsonism.
It tends to form filamentous structures, which may lead to neuronal death.
Elucidation of the molecular mechanism of neuronal death in this disease may
contribute to our understanding of sporadic diseases with tau accumulation, such
as corticobasal degeneration, progressive supranuclear palsy, Pick's disease,
Alzheimer's disease and possibly also the pathogenesis of Parkinson's disease.
Other genetic loci have been identified by linkage analysis of patients with
familial parkinsonism. These loci conceal other genes and proteins that may be
pivotal factors in the pathogenesis of Parkinson's disease. The discovery of
genetic mutations in patients with parkinsonism may offer us new insights into
the understanding of the pathways leading to neuronal death and development of
Parkinson's disease. It may also help in the early identification of susceptible
people to this disease and possibly in developing new treatment strategies.
Martin, E. R., W. K. Scott, et al. (2001). "Association of single-nucleotide
polymorphisms of the tau gene with late-onset Parkinson disease." Jama
286(18): 2245-50.
CONTEXT: The human tau gene, which promotes assembly of neuronal microtubules,
has been associated with several rare neurologic diseases that clinically
include parkinsonian features. We recently observed linkage in idiopathic
Parkinson disease (PD) to a region on chromosome 17q21 that contains the tau
gene. These factors make tau a good candidate for investigation as a
susceptibility gene for idiopathic PD, the most common form of the disease.
OBJECTIVE: To investigate whether the tau gene is involved in idiopathic PD.
DESIGN, SETTING, AND PARTICIPANTS: Among a sample of 1056 individuals from 235
families selected from 13 clinical centers in the United States and Australia
and from a family ascertainment core center, we tested 5 single-nucleotide
polymorphisms (SNPs) within the tau gene for association with PD, using
family-based tests of association. Both affected (n = 426) and unaffected (n =
579) family members were included; 51 individuals had unclear PD status.
Analyses were conducted to test individual SNPs and SNP haplotypes within the
tau gene. MAIN OUTCOME MEASURE: Family-based tests of association, calculated
using asymptotic distributions. RESULTS: Analysis of association between the
SNPs and PD yielded significant evidence of association for 3 of the 5 SNPs
tested: SNP 3, P =.03; SNP 9i, P =.04; and SNP 11, P =.04. The 2 other SNPs did
not show evidence of significant association (SNP 9ii, P =.11, and SNP 9iii, P
=.87). Strong evidence of association was found with haplotype analysis, with a
positive association with one haplotype (P =.009) and a negative association
with another haplotype (P =.007). Substantial linkage disequilibrium (P<.001)
was detected between 4 of the 5 SNPs (SNPs 3, 9i, 9ii, and 11). CONCLUSIONS:
This integrated approach of genetic linkage and positional association analyses
implicates tau as a susceptibility gene for idiopathic PD.
Miyamoto, K., A. Ikemoto, et al. (2001). "A case of frontotemporal dementia and
parkinsonism of early onset with progressive supranuclear palsy-like features."
Clin Neuropathol20(1): 8-12.
We report a patient with frontotemporal degeneration and parkinsonism with
mental retardation. The patient was a 54-year-old man who had parkinsonism that
resembled progressive supranuclear palsy, frontotemporal degeneration and
myoclonus. His family included many affected members. Neuropathologically, there
was degeneration of the frontal and temporal cortices, the basal ganglia, the
brainstem and the cerebellum. Microscopically, neuronal loss was severe in the
frontal and temporal cortex, the globus pallidus, substantia nigra, red nucleus
and dentate nucleus. Fibrillary changes were found in neurons and glia that were
immunostained for tau. Although we could not define the genetic abnormalities,
we thought that this case might have involved frontotemporal dementia and
parkinsonism linked to chromosome 17.
Pastor, P., E. Pastor, et al. (2001). "Familial atypical progressive
supranuclear palsy associated with homozigosity for the delN296 mutation in the
tau gene." Ann Neurol49(2): 263-7.
Heterozygous missense and splice-site mutations in the tau gene have been
previously identified in familial frontotemporal dementia with autosomal
dominant inheritance. Here we report a Spanish kindred in which two brothers
born from a third-degree consanguineous marriage were both affected with
atypical progressive supranuclear palsy. A homozygous deletion at codon 296
(delN296) was identified in one of the affected siblings. Among the heterozygous
carriers, two members with probable Parkinson's disease were identified, but
none of heterozygotes developed atypical parkinsonism. The delN296 mutation lies
in the sequence corresponding to the second tubulin-binding repeat of tau
protein and affects one asparagine residue absolutely conserved in other
species. This finding indicates that homozygous mutations in the tau gene may
also cause hereditary tauopathies.
Simon, H. H., H. Saueressig, et al. (2001). "Fate of midbrain dopaminergic
neurons controlled by the engrailed genes." J Neurosci21(9):
3126-34.
Deficiencies in neurotransmitter-specific cell groups in the midbrain result in
prominent neural disorders, including Parkinson's disease, which is caused by
the loss of dopaminergic neurons of the substantia nigra. We have investigated
in mice the role of the engrailed homeodomain transcription factors, En-1 and
En-2, in controlling the developmental fate of midbrain dopaminergic neurons.
En-1 is highly expressed by essentially all dopaminergic neurons in the
substantia nigra and ventral tegmentum, whereas En-2 is highly expressed by a
subset of them. These neurons are generated and differentiate their dopaminergic
phenotype in En-1/En-2 double null mutants, but disappear soon thereafter. Use
of an En-1/tau-LacZ knock-in mouse as an autonomous marker for these neurons
indicates that they are lost, rather than that they change their
neurotransmitter phenotype. A single allele of En-1 on an En-2 null background
is sufficient to produce a wild type-like substantia nigra and ventral
tegmentum, whereas in contrast a single allele of En-2 on an En-1 null
background results in the survival of only a small proportion of these
dopaminergic neurons, a finding that relates to the differential expression of
En-1 and En-2. Additional findings indicate that En-1 and En-2 regulate
expression of alpha-synuclein, a gene that is genetically linked to Parkinson's
disease. These findings show that the engrailed genes are expressed by midbrain
dopaminergic neurons from their generation to adulthood but are not required for
their specification. However, the engrailed genes control the survival of
midbrain dopaminergic neurons in a gene dose-dependent manner. Our findings also
suggest a link between engrailed and Parkinson's disease.