Huntingtons Disease Fatal Syndrome Neither Remission Nor Cure Biology Essay


Huntington's disease is a fatal syndrome with neither remission nor cure named after Doctor George Huntington in 1872. At first, it was believed that the disease sufferers were haunted by spirits or victimized as witches, and were rejected by the community. In 1872, Dr. George Huntington described the disease in detail and expressed family linkage. Over 100 years later, in 1993, the US-Venezuela Huntington's Disease Collaborative Research Project found out the causal gene which is responsible for abnormally large CAG repeat (Huntington's Disease Collaborative Research Group, 1993).

Huntington's disease is a progressive neurodegenerative genetic disorder, inherited in an autosomal dominant pattern. So, one copy of the altered gene with an expanded tri-nucleotide repeats (mutant allele) is required to develop the disease (Walker, 2007). All human beings have the Huntington gene (Htt gene), which codes for the Huntingtin protein. The Huntington gene is present on the short arm of chromosome 4, at exon 1 of the interesting transcript 15 (IT15) gene on chromosome 4p 16.3 (Rubinsztein et al., 1997). The Huntington gene contains a three Deoxyribonucleic acid (DNA) bases sequence: cytosine-adenine-guanine (CAG) repeats, known as a tri-nucleotide repeat, which varies in length between each individual and between each generation (Walker, 2007). In a normal person, this tri-nucleotide repeat consists of less than 35 CAG units (Huntington's Disease Collaborative Research Group, 1993). When the length of this repeat expansion reaches a certain threshold, beyond 35 triplets (Huntington's Disease Collaborative Research Group, 1993), it produces an abnormal protein, known as a mutant Huntingtin protein (mHtt), a cytoplasmic protein, whose presence causes slow but steady damage to specific areas of the brain (Walker, 2007). The CAG trinucleotide repeats are translated into more than 35 glutamines in the mutant Huntingtin protein of the Huntington's disease patients (Warby et al., 2010).

Different types of Huntington's disease

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There are 3 different types of Huntington's disease depending on the age of onset: juvenile form, typical form and late form (Wexler et al., 2004). These three different types are also different in the numbers of CAG repeats they possess (Wexler et al., 2004).

Table 1: Relationship between different types of Huntington's disease depending on the age of onset and number of CAG repeats (Adapted from Wexler et al., 2004)

Types of Huntington's disease

Age of onset

Mean numbers of CAG repeats


From 2 years to 20 years



From 21 years to 50 years



Older than 50 years


Genetic inheritance pattern of Huntington's disease

Huntington's disease is due to the expanded CAG tri-nucleotide repeat determined in the DNA since conception. Since Huntington's disease is the autosomal dominant inherited disease, if one parent carries the mutant gene, 50 percent of the offspring will be affected (Lipe and Bird, 2009). The genetic inheritance pattern of the Huntington's disease is described in figure 1.

Figure 1: Genetic inheritance pattern of the Huntington's disease

If one parent possesses the mutant Huntington gene, half of his or her offspring will be affected regardless of the sex of the offspring.

However, the percentage of inheritance varies from study to study suggesting that genetic is not the only component in the Huntington's disease development.

One study conducted in Southern India found that the juvenile form of Huntington's patients was inherited from their fathers (Murgod et al., 2001). Among them, the fathers of two patients showed clinical features of Huntington's disease whereas the other two were asymptomatic but they had expanded CAG repeats with the mean CAG repeats of 48.4 (Murgod et al., 2001). Moreover, only 88.5 percent of the 26 Huntington's disease patients were found to have family history in the above study. Furthermore, family history was not found in 8 percent of 171 DNA confirmed Huntington's disease patients in New South Wales (McCusker et al., 2000). Lipe and Bird's study in 2009 also mentioned that among 34 cases of the Huntington's disease patients, 68 percent had no recognized family history of this disease. Since these studies were conducted on a small scale involving few numbers of patients, great caution should be exercised in interpretation and generalization of these findings. Kartsaki and co-workers, 2006, pointed out that the lack of obvious family history of Huntington's disease was due to small CAG repeat size in their family members (Kartsaki et al., 2006) because CAG repeats size of 35-39 shows reduced penetrance and may be asymptomatic for the whole life-span (Langbehn et al., 2004). So, the absent of family history in Huntington's disease patients may be due to the small sample size and/or due to the reduced penetrance.

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The total number of CAG repeats was related to the age of onset of Huntington's disease in case of maternally inherited pattern (Snell et al., 1993). Large CAG repeat expansion pattern was unlikely to be occurred in maternally inherited patients while it was found to be vice versa in paternally inherited ones (Rubinsztein et al., 1997). However, Murgod and co-workers found no obvious difference in the age of onset between those who inherited the disease from the father when compared to those who inherited it from the mother; the mean age of disease onset was found to be 36.9 years in both cases (Murgod et al., 2001).

Interestingly, sex of the patients also affects the type of familial inheritance and age of onset of the disease. In Venezuelan sibling pairs, the prevalence of Huntington's disease between the sisters is found to be 0.49% and is higher than the prevalence of this disease between sister and brother (0.40%) and between the brothers (0.18%) (Wexler et al., 2004). In the study conducted by Roos and co-workers among 822 cases showed that the age of onset in female patients (mean age of onset = 39.9 years) were higher than that of male patients (mean age of onset = 37.5 years) (Roos et al., 1991). Furthermore, the Roos study mentioned that the mean age of onset in both male and female is lowest in the grandmother-father lineage compared to the other grandmother-mother lineage, grandfather-mother lineage and grandfather-father lineage (Roos et al., 1991). These above findings suggest that females have less severe phenotype and generate less offspring with the disease.

Homozygous Huntington's disease patients inherit two expanded tri-nucleotide repeats copies, one from each parent. However, the age of onset of the Huntington's disease is not altered (Myers et al., 1989). So, the age of onset of the Huntington's disease is independent of inheritance of one copy or two copies of an expanded CAG repeats, but dependent on the length of the tri-nucleotide repeats.

In 1994, Andrew and his colleagues reported Huntington's disease cases with no CAG repeats expansion pointing that Huntington's disease has phenocopies (Andrew et al., 1994). In their study, 1.17 percent of 1, 022 Huntington's disease patients have no CAG repeats expansion. Pedigree analysis of the Huntington's disease patients with phenocopies showed that chromosome 20p12 region encoding the prion proteins were responsible for the phenocopy effects (Xiang et al., 1998). In 1999, doppel or prion protein 2 (dublet) (Prnd) genes which are prion protein like genes were discovered as the new members for Huntington's phenocopy genes (Moore et al., 1999). Huntington's disease phenocopy patients showed atypical presentation such as epileptic seizures (Andrew et al., 1994).

CAG repeats and ethnicity in Huntington's disease

There is ethnic difference in the prevalence of the Huntington's disease. The prevalence among people of Europe and North America ranges from 2.5 to 10 per 100,000 people (Walker, 2007; Murgod et al., 2001); Indian immigrants to Britain have prevalence of 1.75 per 100,000 people (Murgod et al., 2001).

The CAG repeats expansions in Htt gene correlate to a specific predisposing haplo-group in Western Europeans (Warby et al., 2009). European Huntington's disease patients possess a specific set of twenty two tagged single nucleotide polymorphisms which make up a single haplo-group (Warby et al., 2009). This haplo-group is also seen in chromosome of general population indicating that there may be the predisposing cis-elements mutation in Htt gene in the Europeans causing the CAG repeats instability (Warby et al., 2009). However, this predisposing haplo-group for CAG expansion is not seen in the Chinese and Japanese people, meaning that the difference in the predisposing background distribution among populations explain the different prevalence of Huntington's disease in different populations (Warby et al., 2009).

Next to the 3′ end of CAG repeats in Htt gene is a CCG repeats site (Pecheux et., 1995). In the Caucasian population, expanded CAG repeats are highly associated with (CCG) 7 (Squitieri et al., 1994), whereas in the Japanese population and Chinese population, expanded CAG repeats are associated with (CCG)10 (Masuda et al., 1995; (Ma et al., 2010) suggesting that the different CCG alleles that are present in the different ethnicity produce different prevalence of Huntington's disease in different populations. (CCG) 10 is found to be accountable for the low prevalence of Huntington's disease in Japanese populace and Chinese populace as compare to the Western Europeans. The specific single nucleotide polymorphism alleles are strongly associated with the CAG repeats expansions. We need to find out the single polynucleotide polymorphisms that reveal to cis-elements responsible for the instability of the CAG repeats in Htt gene (Warby et al., 2009). By knowing this, we can develop the new therapy for the Huntington's disease patients using personalized allele-specific targets medicine.

Reasons for the expansion of CAG repeat in the Htt gene

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There are different proposals for the underlying reasons of the expansion of CAG repeats in the Htt gene. Flap endonuclease 1 (FEN1), is a structure-specific endonuclease that is involved in the correction of DNA-damage. In mammals, the loss of FEN1gene expression is embryonically lethal (Yang and Freudenreich, 2007). Normally, FEN1 protein cleaves a double flap substrate possessing the 5′ flap with a one 3′ overhangs in vitro (Rossi et al., 2006). In this case, flap equilibration is achieved by correct mechanisms of FEN1 protein, followed by ligation with DNA ligase and no CAG repeat expansion (Liu et al., 2004). FEN1 gene takes part in prevention of CAG tri-nucleotide repeat sequences instability because an increase in occurrence of CAG repeats expansion is found in FEN1 gene mutants in yeast cells with defective yeast homolog of FEN1, RAD27 (Yang and Freudenreich, 2007). Moreover, the FEN1 protein concentration is directly proportional to the length of CAG repeats, i.e., if the cells have longer CAG repeats, more FEN1 proteins are required in order to maintain the stability (Yang and Freudenreich, 2007). If concentration of FEN1 protein is limited, the unprocessed flap substrate could equilibrate into different types of intermediate structures and some of the intermediate structures will be ligated by DNA ligase resulting in expansion of the sequence (Yang and Freudenreich, 2007). This finding is supported by Henricksen and co-workers, 2002. Their study showed that FEN1 and DNA ligase competed at the flap, and when the amount of ligase is increased, there will be the ligation of unprocessed flaps causing sequence expansions (Henricksen et al., 2002). Spiro and McMurray, 2003 studied the relationship between CAG repeats expansion and FEN1 gene in FEN1 +/- mice with expanded CAG-120 repeats within the human Huntington's disease gene (Spiro and McMurray, 2003). They found that there was increase in CAG repeats expansion in the progeny of the FEN1+/- male mice. Therefore, FEN1 gene plays the role in prevention of CAG repeat expansion during the flap processing. The mechanism of FEN1 in CAG repeats expansion is demonstrated in the figure 2.

Figure 2: Role of FEN1 in CAG repeats expansion

Another factor contributing to the formation of the CAG trinucleotide repeats is defect in double strand break repair system. Meiotic recombination-11 (Mre11) gene of Saccharomyces cerevisiae is involved in the double strand break repair pathway and in Mre11-deficient strains; there is an accumulation of CAG trinucleotide repeats expansions (Sundararajan et al., 2010). Moreover, CAG repeats expansion is seen in the absence of small ubiqutin-related modifier-1(SUMO1) activating enzyme subunit-2 (sae2) genes which is also involved in double strand break repair pathway and in the absence of Rad52 gene which is involved not only in double strand break repair but also in homologous recombination (Sundararajan et al., 2010). Both double strand break repair and homologous recombination are important mechanisms for preventing the trinucleotide repeats expansion.

Another possible mechanism for CAG repeat expansions is due to the mis-match repair (MMR) system. A function for MMR system in CAG expansion is poorly understood. During DNA replication, the tri-nucleotide repeats can misalign causing an extra-helical DNA loop. DNA loops are repaired by mutS homolog2/mutS homolog3 (MSH2/MSH3) by insertion leading to the tri-nucleotide expansion in vivo (Kovtun et al., 2004). In yeast and bacterial studies, deletions of tri-nucleotide repeats tracts are more likely to occur than insertions during cell proliferation by 10-1000 times in wild type cells compared to the MMR system defective cells (Schweitzer and Livingston, 1999). Furthermore, Manley and co-workers found that when there was no MSH2, the CAG repeats expansion were not developed in germ cell lines as well as in somatic cells during the development in animals (Manley et al, 1999).

MSH2/MSH3 protein is also involved in somatic age-dependent expansion in Huntington's disease (Cleary et al., 2002). However, in the proliferating fibroblasts of the Huntington's disease patients, CAG tracts are also deleted with an intact MMR system (Spiegel et al, 1996). These findings oppose a mechanism in which MMR system is responsible for CAG repeats expansion during post-replicative repair suggesting that not only the MMR system but also the other repair systems like double strand break repair system and homologous recombination are involved in the development of the CAG repeats expansions. Role of MMR system in polyglutamine repeats is described in figure 3.

Figure 3: Role of MSH2/MSH3 in CAG repeats expansion

However, it is difficult to conclude the extent of these MMR system involved in CAG repeats expansion. It is not possible to test the role of repair mechanisms in causing CAG repeats expansions because the MMR mechanism is important in preventing the development of the abnormal new DNA strand during the DNA replication. Different cell types might be affected by different mechanisms to develop the polyglutamine repeats.

A DNA glycosylase, 7, 8-dihydro-8-oxo-guanine-DNA glycosylase-1 (OGG1), is one of the contributing factors for Huntington's disease. In Huntington's disease mice, age-dependent expansion of CAG repeats takes place alongside with the oxidative DNA damage accumulation (Kovtun et al., 2007). Importantly, absence of OGG1 protein, a DNA glycosylase, suppresses expansion in Huntington's disease mice (Kovtun et al., 2007). OGG1 null animals inhibit the CAG repeats expansions in the presence of MSH2 proteins as well as MSH2 null animals inhibit CAG repeats expansion in the presence of OGG1 proteins (Kovtun and McMurray, 2001). So, these two proteins are responsible in the development of CAG repeats expansions.

Functions of Normal Huntingtin protein

Huntington protein is 348 kDa (kilodalton), soluble (Cattaneo et al., 2001) protein and has a polyglutamine of not more than 35 residues of glutamine. Huntingtin protein contains HEAT-like repeats (Huntingtin, Elongation factor 3, protein phosphatsase 2A, TOR1) from its amino-terminus to the carboxyl-terminus. Having the HEAT-repeats structure, Huntingtin protein may possess a solenoid-like structure acting as a scaffold for interactions of multiple proteins (Takano and Gusella, 2002). Huntington's protein is cytosolic and is present not only in the brain but also in other organs like lungs, heart, liver, kidneys, lymphoblasts, etc (Sharp et al., 1995). Using the poly and mono clonal antibodies, Huntingtin proteins are detected in all over the brain and neurons (Sharp et al., 1995). In the nervous system, Huntingtin protein augments the neurotrophic factors production thereby contributing to the neuro-protective function (Cattaneo et al., 2001).

From the animal study using mice, it was found that the polyglutamine segment is not indispensable because, even though it is removed from Huntingtin protein, mice are surviving with minor symptoms (Clabough and Zeitlin, 2006). However, when the whole normal Huntingtin protein is removed, it is embryonically lethal in mice and adult cell degeneration is observed in the conditional knockout of the Htt gene in mice (Duyao et al., 1995; Nasir et al., 1995). So, Huntingtin protein is essential for life but the polyglutamine segment is not essential for life.

Moreover, Huntingtin protein has an anti-apoptotic action. Position 548 of the N-terminal of the normal Huntingtin protein is responsible for anti-apoptosis (Rigamonti et al., 2000). Huntingtin protein inhibits the pro-caspase 9 (Rigamonti et al., 2000) and it also prevents the formation of the pro-apoptotic complex, Huntington Interacting Protein-1 Protein Interactor-Huntington Interacting Protein-1 (HIPPI-HIP-1) complex (Gervais et al., 2002).

Impact of mutant Huntington protein

How mutant Htt protein containing more than 35 glutamine residues, stimulates a cascade of cellular alterations, resulting in cell dysfunction and deterioration, have not yet been fully understood (van Duijn et al., 2007). And again, the exact mechanisms of mutant Htt proteins accumulation are still unknown (Casarejos et al., 2011). The cellular toxicity sites for the mutant Huntingtin protein are not only in the nucleus (Saudou et al., 1998) but also in the cytoplasm (Panov et al., 2003). Mutant Huntingtin proteins affect many proteins present in the nucleus and cytoplasm of the cells that are involved in the gene transcription (Cha, 2000), programmed cell death (Hickey and Chesselet, 2003), mitochondrial function (Panov et al., 2003), suppression of tumor (Bae et al., 2005), release of neurotransmitter and axonal transport (Freeman and Mortan, 2004; Charrin et al., 2005). Transcriptional dysfunction of polyglutamine expansions might take a role in the development of neurotoxicity in Huntington's disease because in transgenic Huntington's disease model mouse, improve survival was seen after treating with histone deacetylase inhibitor, sodium butyrate, that modulated transcription significantly (Ferrante et al., 2003). In the nucleus, there are abnormal interactions between the abnormal polyglutamine protein and p53 tumor suppressor protein, cyclic adenosine monophosphate (cAMP) response element binding (CREB) protein (co-activator), stable protein-1 transcription factor and TATA-associated factor-130 (Mc Campbell et al., 2000; Nucifora et al., 2001; Dunah et al., 2002). Both normal and mutant form of Huntingtin protein act on stable protein-1 transcription factor and TATA-associated factor-130 but mutant Huntingtin protein has the stronger interaction than normal one (Dunah et al., 2002). Mutant Huntington proteins cause toxicity to the cells as well as impairment to the function of the wild type Huntington proteins.

Neuronal intranuclear inclusions of expanded polyglutamine protein are one of the factors that contribute to the clinical manifestation of Huntington's disease. Neuronal intranuclear inclusions of expanded polyglutamine protein are the most distinct pathological characteristic of polyglutamine diseases (DiFiglia et al., 1997). Neuronal intranuclear inclusions are correlated with toxic level of protein and disease severity (Arrasate et al., 2004). Neuronal intranuclear inclusions of mutant Huntingtin protein and progressive cerebral deterioration starting from caudate nucleus and putamen are involved in Huntington's disease pathophysiology (Arrasate et al., 2004).

In Huntington's disease, there is an impairment of the ubiquitin-proteasome system (DiFiglia et al., 1997) and this impairment is due to ubiquitin and ubiquitin-proteosome system's component localization in neuronal intranuclear inclusions (Schmidt et al., 2002). Expanded polyglutamine causes abnormal protein folding (DePril et al., 2004) and the proteins themselves directly inhibit the proteasome resulting in accumulation of the poly-ubiquitinated proteins (Bence et al., 2001). Moreover, there is accumulation of mutant Htt protein due to the impairment in the autophagy-lysosomal pathway and inhibition of the autophagy resulting in the ubiquitinated proteisn accumulation (Korolchuk et al., 2009).

Moreover, ubiquitin+1 (UBB+1), an abnormal form of ubiquitin, is accumulated in Huntington's disease (DePril et al., 2004). This UBB+1 is unable to ubiquitinate substrate polyglutamine proteins (Fischer et al., 2003). In addition, at high concentration, UBB+1 also inhibits proteasomal degradation of substrate polyglutamine proteins causing neuroblastoma cells death (van Tijn et al., 2007). UBB+1 does not induce neuropathlogy itself but together with the polyglutamine proteins, UBB+1 mediated proteasomal inhibition causes exacerbated neurological signs and symptoms (DePril et al., 2004). Differences in ubiquitin-proteasomal system effectiveness or the level at which abnormal proteins like UBB+1 deposited determine the inter-patients variation in onset of disease or extent of atrophy of corpus striatum in Huntington's disease patients (Wexler et al., 2004; McNeil et al., 1997).

Interestingly, the pre-symptomatic individuals show the abnormalities in non-neuronal tissues such as fibroblast, platelets, cultured lymphoblasts, blood-nucleated cells and skeletal muscle cells due to the presence of mutant Huntingtin protein in these tissues (Borovecki et al, 2005; Panov et al, 2005). The mutant Htt gene causes the pathological changes in any cells not only in the brain cells.

Therefore the neurological features of Huntington's disease patients are due to the polyglutamine themselves, impaired ubiquitin-proteasomal degradation system, and autophagy-lysosomal system and accumulation of the abnormal protein like UBB + 1. The impact of the mutant Huntingtin protein can be seen in neuronal as well as in non-neuronal tissues. Polyglutamine repeats become the therapeutic target in the treatment of Huntington's disease as they play the key role in the development of clinical manifestations of Huntington's disease.

Juvenile form and classical form of Huntington's disease

There are some differences between the Juvenile form and classical form of Huntington's disease. Firstly, the prevalence of Juvenile Huntington's disease is about 8-10% of cases and it rises to 70-80% if it is inherited from father (Squitieri et al., 2006). Majority of the juvenile Huntington's disease patients are inherited from their fathers (Murgod et al, 2001).

Over 60 repeats of CAG expansion, there is strict linear relationship between the age of onset of the disease and expansion mutations, implying that the onset of juvenile Huntington's disease is more closely related to length of CAG repeats than adult form (Telenius et al., 1993). Studying the candidate for gene modifiers and age at disease onset, Li and colleagues in 2003 found that juvenile Huntington's disease showed an effect specifically on gene polymorphisms (Li et al., 2003). However, in the different study conducted by MacDonald and co-workers found that there was no such effect in adult onset Huntington's disease patients (MacDonald et al., 1999).

Only in juvenile Huntington's disease patients with large repeat expansion, biochemical and biophysical changes were observed in lymphoblasts such as augmented caspase 3 action (Sawa et al., 1999), diminished potential of mitochondrial membrane (Panov et al., 2002) and enhanced cytoplasmic autophagosomes activity (Nagata et al., 2004).

In juvenile Huntington's disease, atypical motor symptoms are more common without chorea. The symptoms may include dystonia, bradykinesia, cerebral features or rigidity and are usually coupled with extensive brain atrophy (Squitieri et al., 2000a). Rigidity, although common in Juvenile form, is also found in adult onset of Huntington's disease (Squitieri et al., 2000a).

However, the juvenile form and classical Huntington's disease patients share some clinical features. Psychiatric problems and behavioral disorders are key elements of the clinical manifestation of Huntington's disease (van Duijn et al., 2007). This is of practical importance since these neuropsychiatric symptoms have a considerable impact on daily activities (Hamilton et al., 2003). The most common neuropsychiatric symptom is depressed mood occurring in 33-69% of patients (van Duijn et al., 2007).

Huntington's disease patients are easily recognized by their distinctive clinical features. They have low quality of life due to motor and psychiatric problems. Moreover, the younger the age of onset, the more severe the disease manifestation because juvenile Huntington's disease patients have larger numbers of CAG repeats.

Number of CAG repeats and Huntington's disease severity

There are many evidences of correlation between the numbers of CAG repeats and the severity of the disease. Relationship between numbers of CAG repeats and phenotypes are as follows.

Table 2: Relationship between numbers of CAG repeats and phenotype of the Huntington's disease patients

Numbers of CAG repeats



Less than 26

Normal phenotype

Warby et al., 2010


Not develop into clinical features of Huntington's disease, but have high potential for expansion mutation in meiosis and thus can have Huntington's disease offspring

Semaka et al., 2010


Incomplete penetrance. May be associated with Huntington's disease phenotype or may be asymptomatic for the whole life.

Langbehn et al., 2004

40 and above

Full penetrance

Warby et al., 2010

Degeneration of the neurons in Huntington's disease is characterized by presence of DNA fragmentation and there is a correlation between number of CAG repeats and degree of DNA fragmentation (Butterworth et al., 1998). In the same study, they found that in post-mortem striatal section of the brain of the Huntington's disease patients, number of trinucleotide (CAG) repeats was positively correlated to the extent of DNA fragmentation with the Pearson correlation value less than 0.0002 (Butterworth et al., 1998). The numbers of CAG repeats also increase the progress of atrophy in the brain area of frontal lobes and basal ganglia (Ruocco et al., 2008). Ruocco and co-workers also found that more deficits in motor and cognitive function were found in the patients with larger CAG repeats (Ruocco et al., 2008).

Brandth and co-workers found that the longer CAG repeats length was seen in younger age of onset of Huntington's disease patients with the probability value less than 0.001 among 46 samples (Brandth et al., 1996). CAG repeats more than 80-100 results in Huntington's disease before 10 years of age (Squitieri et al., 2002). Similar findings are documented by Lipe and Bird study in which thirty four cases of late Huntington's disease patients were retrospectively studied (Lipe and Bird, 2009) indicating that the longer the CAG repeats, the younger the onset of disease. Progressively more severe brain damage was observed among patients who manifest the disease at an early age (Illarioshkin et al., 1994).

Reduced penetrance, the percentage of the individuals showing the physical appearance of the genotype that they possess, is associated with late onset of disease (McNeil et al., 1997) and the late onset is associated with the small numbers of CAG repeats expansion. Therefore, CAG repeat length has an effect on the progression of the neurological signs and symptoms and the earlier the age of onset of the disease, the more severe the disease.

Do CAG repeats always cause Huntington's disease?

Huntington disease patients with classic history have more than 35 repeats of CAG and patients with triplet lengths less than 35 has not yet been reported so far. In 1994, Andrew and his colleagues stated that the patients with less than 36 CAG repeats showed symptoms like Huntington's disease but these symptoms were not due to Huntington's disease but are due to Huntington's disease phenocopies, wrong diagnosis or error in biological sample (Andrew et al., 1994). The clinical signs and symptoms of Huntington's disease may be present in the person with CAG repeats less than 35 but the repeats tracts are not stable (toward increasing size) especially when it is inherited from the father (Herishanu et al, 2009). The number of CAG repeats associated with the signs and symptoms of the Huntington's disease is varied.

CAG repeats contribute to many neurological manifestations not only the Huntington's disease. Expanded tri-nucleotide repeats are responsible for at least nineteen inherited disorders (Hu et al, 2009) such as Machado-Joseph Disease (MJD), Huntington's disease, myotonic dystrophy type 1 and several spinocerebellar ataxias (SCAs) (Pearson et al, 2005), etc. MJD is due to CAG tri-nucleotide repeats within the ataxin-3 (ATXN3) gene (Hu et al, 2009). In SCAs, there are forty CAG repeat expansion in the ataxin-1 gene (Emamian et al., 2003). CAG repeats expansion is present in different genes and produces various kinds of diseases.

Treatment of Huntington's disease

The clinical manifestation of the Huntington's disease is due to the toxic effect of the mutant Huntingtin protein fragment and there is no curable for Huntington's disease so far (Sarkar et al., 2008). The current therapy is only symptomatic. Choreic movement can be treated with haloperidol and olanzapine both of which are neuroleptic agents (de Tommaso et al., 2005). Psychiatric symptoms like depression are response to the psychotropic agents (Warby et al., 2010).

As for the curable treatment, possible regime for Huntington's disease is silencing the mutant Htt gene expression by using the RNA interference (RNAi) (Harper et al., 2005) so that there will be less formation of mutant Huntingtin protein. In their study with Huntington's disease model mouse, they found that RNAi decreased the mutant Htt gene expression and mutant Huntingtin protein formation thereby decreasing the clinical manifestation of the Huntington's disease (Harper et al., 2005).

Sanchez and co-workers also found that azo-dye Congo red inhibited the formation of the polyglutamine aggregates and increased the removal of expanded polyglutamine repeats not only in vitro but also in vivo (Sanchez et al., 2003). In the same study they also found that in transgenic Huntington's disease model mouse showed improvement in survival and clinical symptoms of Huntington's disease after infusion of Congo red dye to them (Sanchez et al., 2003).

Moreover, sodium butyrate chemotherapy improved the clinical manifestations in transgenic Huntington's disease model mouse by improving oxidative phosphorylation and transcriptional regulation as sodium butyrate augmented histone and Specificity protein-1 acetylation (Ferrante et al., 2003). Furthermore, Trehalose, one of the disaccharides sugars, can bind to the expanded polyglutamines and prevent the formation of the polyglutamine aggregates in the brain and liver thereby ameliorating the motor function and survival rate in transgenic Huntington's disease model mouse (Tanaka et al., 2004). Moreover, Trehalose produces a dose and time dependent rise in the amount of autophagy in NB69 human neuroblastoma cells thereby enhancing the elimination of abnormal proteins like mutant Huntingtin protein with polyglutamine and preventing the necrosis of NB69 by enhancing the autophagy activities i.e., increase degradation of mutant Htt protein (Casarejos et al., 2011). The advantages of Trehalose are less toxic, highly soluble and easy administration by orally (Tanaka et al., 2004).

In the study conducted by Sarkar and co-workers on African green monkey kidney cells, they found that lithium and rapamycin combination up-regulates the autophagy that degrades the mutant Huntingtin proteins (Sarkar et al., 2008). Rapamycin alone does not affectively decrease the mutant Huntingtin protein aggregates level if one third of the cell has aggregates but it decreases the aggregates if only ten percent of the cell contains aggregates in fly and mouse models of Huntington disease (Ravikumar et al., 2004). Both lithium and rapamycin are lipophilic so that they can pass the blood brain barrier (Sarkar et al., 2008) and therefore it is possible to use them in long-term treatment for Huntington's disease patients.

Since polyglutamine and polyglutamine aggregates take a central role in the development of neuropathology in the Huntington's disease, the treatments are targeting to them to get complete cure. However, these treatments are under the animal trials so far and more studies are needed in this area. Outline of pathology of Huntington's disease and possible therapeutic agents are demonstrated in the figure 4.

Figure 4: Mechanisms of Huntington's disease pathology and possible sites acting by different therapeutic agents


Huntington's disease is the autosomal dominant inherited disorder due to the CAG trinucleotide repeats expansion greater than normal limit of 35. The age of onset that disease developed is correlated to the length of the polyglutamine expansion. The longer the length of CAG repeats the younger the age of the onset of the Huntington's disease patients. The age of onset is independent of homozygous or heterozygous of the mutant gene in Huntington's disease patients but rate of disease progression is more rapid in homozygous disorder. The greater the number of CAG repeats length, the more severe the disease manifestation. Although it is the autosomal inherited disease, no family history is found in some cases. However, this may be due to the small CAG repeats size (reduced penetrance) or small study sample size. More longitudinal study with larger sample size is needed.

There is the ethnicity difference in the prevalence of Huntington's disease. Japanese and Chinese populations are less common than Europe and North-American population and this ethnic variation depends on the presence of specific predisposing haplotype.

FEN-1, MMR system, double strand break repair system, homologous recombination and OGG-1 play the role in the development of the CAG repeat expansion. Mutant Huntingtin protein containing the CAG repeats more than 35 produce the neurological signs and symptoms through their cytoplasmic and nucleus cytotoxicity. Clinical manifestations are more or less similar in Juvenile and adult form of Huntington's disease but atypical motor symptoms without chorea is more common in Juvenile form.

Currently, there is no curable regime for Huntington's disease, only symptomatic treatments can be given. Since the behavioral and psychiatric disorders disrupt the normal daily routine activities, curable therapy needs to be developed. Now we have some curative trials on transgenic Huntington's disease model mouse, we still need to prove on human beings that these therapies are effective and tolerated in human. Genetic counseling and DNA testing before marriage will prevent the transmission of disease from generation to the next generation after considering the ethical issues since there is the no cure for Huntington's disease.