Epigenetics of neurodegenerative diseases

Para-sagittal MRI of the head in a patient with benign familial macrocephaly.

Neurodegenerative diseases are a heterogenous group of complex disorders linked by the degeneration of neurons in either the peripheral nervous system or the central nervous system. Their underlying causes are extremely variable and complicated by various genetic and/or environmental factors. These diseases cause progressive deterioration of the neuron resulting in decreased signal transduction and in some cases even neuronal death. Peripheral nervous system (PNS) diseases may be further categorized by the type of nerve cell (motor, sensory, or both) affected by the disorder. Effective treatment of these diseases is often prevented by lack of understanding of the underlying molecular and genetic pathology. Epigenetic therapy is being investigated as a method of correcting the expression levels of misregulated genes in neurodegenerative diseases.

Neurodengenerative diseases of motor neurons can cause degeneration of motor neurons involved in voluntary muscle control such as muscle contraction and relaxation. This article will cover the epigenetics and treatment of amyotrophic lateral sclerosis (ALS) and spinal muscular atrophy (SMA). See the Motor Neuron Fact Sheet for details regarding other motor neuron diseases.Neurodegenerative diseases of the central nervous system can affect the brain and/or spinal cord. This article will cover the epigenetics and treatment of Alzheimer’s disease (AD), Huntington’s disease (HD), and Parkinson’s disease (PD). These diseases are characterized by chronic and progressive neuronal dysfunction, sometimes leading to behavioral abnormalities (as with PD), and, ultimately, neuronal death, resulting in dementia.

Neurodegeneration Neurodegenerative diseases of sensory neurons can cause degeneration of sensory neurons involved in transmitting sensory information such as hearing and seeing. The main group of sensory neuron diseases are hereditary sensory and autonomic neuropathies (HSAN) such as HSAN I, HSAN II, and Charcot-Marie-Tooth Type 2B (CMT2B).[1] Though some sensory neuron diseases are recognized as neurodegenerative, epigenetic factors have not yet been clarified in the molecular pathology and as such will not be covered in this article.

Epigenetics and epigenetic drugs

The nucleus of a human cell showing the location of euchromatin

The term epigenetics refers to three levels of gene regulation: (1) DNA methylation, (2) histone modifications, and (3) non-coding RNA (ncRNA) function. Briefly, histone-mediated transcriptional control occurs by the wrapping of DNA around a histone core. This DNA-histone structure is called a nucleosome; the more tightly the DNA is bound by the nucleosome, and the more tightly a string of nucleosomes are compressed among each other, the greater the repressive effect on transcription of genes in the DNA sequences near or wrapped around the histones, and vice versa (i.e. looser DNA binding and relaxed compaction leads to a comparatively derepressed state, resulting in facultative heterochromatin or, even further derepressed, euchromatin). At its most repressive state, involving many folds into itself and other scaffolding proteins, DNA-histone structures form constitutive heterochromatin. This chromatin structure is mediated by these three levels of gene regulation. The most relevant epigenetic modifications to treatment of neurodegenerative diseases are DNA methylation and histone protein modifications via methylation or acetylation.[2]

Epigenetic drugs target the proteins responsible for modifications on DNA or histone. Current epigenetic drugs include but are not limited to: HDAC inhibitors (HDACi), HAT modulators, DNA methyltransferase inhibitors, and histone demethylase inhibitors (Urdinguio et al., 2009; Peedicayil, 2013). The majority of epigenetic drugs tested for use against neurodegenerative diseases are HDAC inhibitors; however, some DNMT inhibitors have been tested as well. While the majority of epigenetic drug treatments have been conducted in mouse models, some experiments have been performed on human cells as well as in human drug trials (see table below). There are inherent risks in using epigenetic drugs as therapies for neurodegenerative disorders as some epigenetic drugs (e.g. HDACis such as sodium butyrate) are non-specific in their targets, which leaves potential for off-target epigenetic marks causing unwanted epigenetic modifications.

 Epigenetic Drugs
Function Classification Drug ALS AD HD PD SMA
DNA-methylation inhibitor chemical analogue of cytidine Azathioprine M (ny) M (ny)
HDAC inhibitor (small molecule) benzamide M344 MC 19
fatty acid Sodium butyrate M (y) 5, 6, 7 ; H (ny) D (y) 11 M (y) 14; R (y) 15;

D (y) 16, 18; H (ny)

 MC 20; M (y) 21; H (ny)
Sodium phenylbutyrate M (y) 1; H (y) 2 M (y) 8; H (ny) H (ys) 12 MC 20; H (v) 21, 22
Valproic acid M (y) 2; H (ni) 3 M (y) 9; H (ny) D (y) 11 R (y) 17; H (ny) MC 23, 24; M (y) 25;

H (v) 26, 27, 28, 29

hydroxamic acid Trichostatin A M (y) 4; H (ny) M (y) 10; H (ny) MC 13; D (y) 11 M (y) 30, 31; H (ny)
Vorinostat (suberanilohydroxamic acid-SAHA) M (y) 9; H (ny) MC 13; D (y) 11 D (y) 18 MC 32, 33; M (y) 34; H (ny)
Disease: amyotrophic lateral sclerosis (ALS), Alzheimer’s disease (AD), Huntington's disease (HD), spinal muscular atrophy (SMA), Parkinson's disease (PD)
Tested on: mouse (M), only mouse cells (MC), human (H), Drosophila (D), rat (R)
Successful treatment: yes (y), yes but with side effects (ys), not yet (ny), variable (v), no improvement (ni)
References: listed by column (disease) and by ascending row (drug) order
ALS: (1) Del Signore et al., 2009; Petri et al., 2006 (2) Cudkowicz et al., 2009 (3) Piepers et al., 2009; (4) Yoo et al., 2011
AD: (5) Fischer et al., 2007; (6) Ricobaraza et al., 2010; (7) Govindarajan et al., 2011; (8) Ricobaraza et al., 2012; (9) Kilgore et al., 2010; (10) Francis et al., 2009
HD: (11) Steffan et al., 2001 (12) Gardian et al., 2005 (13) Dompierre et al., 2007
PD: (14) Zhou et al., 2011 (15) Rane et al., 2012 (16) St. Laurent et al., 2013 (17) Monti et al., 2010 (18) Kontopolous et al., 2006
SMA: (19) Riessland et al., 2006 (20) Andreassi et al., 2004 (21) Mercuri et al., 2007 (22) Brahe et al., 2005 (23) Sumner et al., 2003 (24) Brichta et al., 2003 (25) Tsai et al., 2006 (26) Weihl et al., 2006 (27) Piepers et al., 2010 (28) Swoboda et al., 2010 (29) Darbar et al., 2011 (30) Narver et al., 2008 (31) Avila et al., 2007 (32) Hahnan et al., 2006 (33) Kernochan et al., 2005 (34) Riessland et al., 2010

Neurodegenerative diseases of motor neurons

Amyotrophic lateral sclerosis (ALS)

Amyotrophic Lateral Sclerosis (ALS), also known as Lou Gehrig’s disease, is a motor neuron disease that involves neurogeneration. All skeletal muscles in the body are controlled by motor neurons that communicate signals from the brain to the muscle through a neuromuscular junction. When the motor neurons degenerate, the muscles no longer receive signals from the brain and begin to waste away. ALS is characterized by stiff muscles, muscle twitching, and progressive muscle weakness from muscle wasting. The parts of the body affected by early symptoms of ALS depend on which motor neurons in the body are damaged first, usually the limbs. As the disease progresses most patients are unable to walk or use their arms and eventually develop difficulty speaking, swallowing and breathing. Most patients retain cognitive function and sensory neurons are generally unaffected. Patients are often diagnosed after the age of 40 and the median survival time from onset to death is around 3–4 years. In the final stages, patients can lose voluntary control of eye muscles and often die of respiratory failure or pneumonia as a result of degeneration of the motor neurons and muscles required for breathing. Currently there is no cure for ALS, only treatments that may prolong life.

Genetics and Underlying Causes

To date, multiple genes and proteins have been implicated in ALS. One of the common themes between many of these genes and their causative mutations is the presence of protein aggregates in motor neurons (Dewey et al., 2012). Other common molecular features in ALS patients are altered RNA metabolism (Polymenidou et al., 2012) and general histone hypoacetylation (Rouaux et al., 2003).

SOD1

Chromossome 21
The SOD1 gene on chromosome 21 that codes for the superoxide dismutase protein is associated with 2% of cases and is believed to be transmitted in an autosomal dominant manner (Battistini et al., 2009; Anderson et al., 1996). Many different mutations in SOD1 have been documented in ALS patients with varying degrees of progressiveness (Anderson et al., 1996). SOD1 protein is responsible for destroying naturally occurring, but harmful superoxide radicals produced by the mitochondria. Most of the SOD1 mutations associated with ALS are gain-of-function mutations in which the protein retains its enzymatic activity, but aggregate in motor neurons causing toxicity (Bruijn et al., 1998; Furukawa et al., 2006). Normal SOD protein is also implicated in other cases of ALS due to potentially cellular stress (Boillee et al., 2006). Researchers have developed an ALS mouse model through gain-of-function mutations in SOD1 (Cudkowicz et al., 1997).

c9orf72

Recently a gene called c9orf72 was found to have a hexanucleotide repeat in the non-coding region of the gene in association with ALS and ALS-FTD (DeJesus-Hernandez et al., 2011; Renton et al., 2011; Majounie et al., 2012). These hexanucleotide repeats may be present in up 40% of familial ALS cases and 10% of sporadic cases. C9orf72 likely functions as a guanine exchange factor for a small GTPase, but this is likely not related to the underlying cause of ALS (Yoshimura et al., 2010). The hexanucleotide repeats are likely causing cellular toxicity after they are spliced out of the c9orf72 mRNA transcripts and accumulate in the nuclei of affected cells (Lee et al., 2013).

UBQLN2

The UBQLN2 gene encodes the protein ubiquilin 2 which is responsible for controlling the degradation of ubiquitinated proteins in the cell. Mutations in UBQLN2 interfere with protein degradation resulting in neurodegeneration through abnormal protein aggregation (Han-Xiang et al., 2011). This form of ALS is X chromosome-linked and dominantly inherited and can also be associated with dementia.

Epigenetic Treatment with HDAC inhibitors

ALS patients and mouse models show general histone hypoacetylation that can ultimately trigger apoptosis of cells (Rouaux et al., 2004). In experiments with mice, HDAC inhibtors counteract this hypoacetylation, reactivate aberrantly down-regulated genes, and counteract apoptosis initiation (Ryu et al., 2005; Yoo et al., 2011). Furthermore, HDAC inhibitors are known to prevent SOD1 protein aggregates in vitro (Corcoran et al., 2004).

Sodium Phenylbutyrate

Sodium phenylbutyrate treatment in a SOD1 mouse model of ALS showed improved motor performance and coordination, decreased neural atrophy and neural loss, and increased weight gain (Del Signore et al., 2009; Petri et al., 2006). Release of pro-apoptotic factors was also abrogated as well as a general increase in histone acetylation (Ryu et al., 2005). A human trial using phenylbuturate in ALS patients showed some increase in histone acetylation, but the study did not report whether ALS symptoms improved with treatment (Cudkowicz et al., 2009).

Valproic Acid

Valproic acid in mice studies restored histone acetylation levels, increased levels of pro-survival factors, and mice showed improved motor performance (Crochemore et al., 2009). However, while the drug delayed the onset of ALS, it did not increase lifespan or prevent denervation (Rouaux et al., 2007). Human trials of valproic acid in ALS patients did not improve survival or slow progression (Piepers et al., 2009).

Trichostatin A

Trichostatin A trials in mouse ALS models restored histone acetylation in spinal neurons, decreased axon demyelination, and increased survival of mice (Yoo et al., 2011).

Spinal Muscular Atrophy (SMA)

Main Wiki article: Spinal Muscular Atrophy
Alpha motor neurons are derived from the basal plate (basal lamina).

Spinal muscular atrophy (SMA) is an autosomal recessive motor neuron disease caused by mutations in the SMN1 gene (Brzustowicz et al., 1990). Symptoms vary greatly with each subset of SMA and the stage of the disease. General symptoms include overall muscle weakness and poor muscle tone including extremities and respiratory muscles leading to difficulty walking, breathing, and feeding. Depending on the type of SMA, the disease can present itself from infancy through adulthood. As SMN protein generally promotes the survival of motor neurons, mutations in SMN1 results in slow degeneration motor neurons leading to progressive system-wide muscle wasting. Specifically, over time, decreased levels of SMN protein results in gradual death of the alpha motor neurons in the anterior horn of the spinal cord and brain. Muscles depend on connections to motor neurons and the central nervous system to stimulate muscle maintenance and therefore degeneration of motor neurons and subsequent denervation of muscles lead to loss of muscle control and muscle atrophy. The muscles of the lower extremities are often affected first followed by upper extremities and sometime the muscles of respiration and mastication. In general, proximal muscle are always affected more than distal muscle.

Genetic Cause

Spinal muscular atrophy is linked to genetic mutations in the SMN1 (Survival of Motor Neuron 1) gene. The SMN protein is widely expressed in neurons and serves many functions within neurons including spliceosome construction, mRNA axon transport, neurite outgrowth during development, and neuromuscular junction formation. The causal function loss in SMA is currently unknown.

SMN1 is located in a telomeric region of human chromosome 5 and also contains SMN2 in a centromeric region. SMN1 and SMN2 are nearly identical except for a single nucleotide change in SMN2 resulting in an alternative splicing site where intron 6 meets exon 8. This single base pair change leads to only 10-20% of SMN2 transcripts resulting in fully functional SMN protein and 80-90% of transcripts leading to a truncated protein that is rapidly degraded. Most SMA patients have 2 or more copies of the SMN2 gene with more copies resulting a decrease in disease severity (Prior et al., 2009). Most SMA patients have either point mutations or a deletion in exon 7 often leading to a protein product similar to the truncated and degraded version of the SMN2 protein. In SMA patients this small amount of functional SMN2 protein product allows for the some neurons to survive.

Epigenetic Treatment through SMN2 gene activation

Although SMA is not caused by an epigenetic mechanism, therapeutic drugs that target epigenetic marks may provide SMA patients with some relief, halting or even reversing the progression of the disease. As SMA patients with higher copy numbers of the SMN2 gene have less severe symptoms, researchers predicted that epigenetic drugs that increased SMN2 mRNA expression would increase the amount of functional SMN protein in neurons leading to a reduction in SMA symptoms. Histone deacetylase (HDAC) inhibitors are the main compounds that have been tested to increase SMN2 mRNA expression. Inhibiting HDACs would allow for hyperacetylation of the SMN2 gene loci theoretically resulting in an increase in SMN2 expression (Kernochan et al., 2005). Many of these HDAC inhibitors (HDACi) are first tested in mouse models of SMA created through a variety of mutations in the mouse SMN1 gene. If the mice show improvement and the drug does not cause very many side effects or toxicity, the drug may be used in human clinical trials. Human trials with all of the below HDAC inhibitors are extremely variable and often impacted by the patient's exact SMA subtype.

Quisinostat is effective at low doses resulting in some improved neuromuscular function in mouse model of SMA, but survival was not increased (Schreml et al., 2012). No human trials have been conducted.
Sodium butyrate was the first HDAC inhibitor tested in SMA mouse models. It prolonged SMA mouse life span by 35% and showed increased levels of SMN protein in spinal cord tissue (Mercuri et al., 2007; Andreassi et al., 2004). However, sodium butyrate has not been used in human trials to date.
Sodium phenybutyrate increases SMN2 full length mRNA transcripts in cell culture but drug application must be repeated in order to maintain results (Andreassi et al., 2004). Human trials show mixed results with one study showing increased SMA transcript levels in blood and improved motor function (Brahe et al. 2005), but a larger trial showing no effects on disease progression or motor function (Mercuri et al., 2007).
Valproic acid added to cells from SMA patients increased SMN2 mRNA and protein levels and that the drug directly activates SMN2 promoter (Sumner et al., 2003; Brichta et al., 2003). In a SMA mouse model, valproic acid was added to the drinking water and restored motor neuron density and increased motor neuron number over a period of 8 months (Tsai et al., 2006). Human trials are extremely variable showing increased SMN2 levels and increased muscle strength in some trials and absolutely no effects in other trials (Weihl et al., 2006; Piepers et al., 2010; Swoboda et al., 2010; Darbar et al., 2011).
  • M344
M344 is a benzamide that shows promising results in fibroblast cell culture and increases level of splicing factors known to modulate SMN2 transcripts, but the drug was determined toxic and research has not progressed to in vivo testing (Riessland et al., 2006)
Trichostatin A treatment shows promising results in mice . In one study, Trichostatin A combined with extra nourishment in early onset mouse SMA models resulted in improved motor function and survival and delays progressive denervation of muscles (Narver et al., 2008). A second study in a SMA mouse model showed increased SMN2 transcripts with daily injections (Avila et al., 2007). No human trials have been conducted.
Vorinostat is a second generation inhibitor that is fairly non-toxic and found to be effective in cell culture at low concentrations (Hahnan et al., 2006) and increases histone acetylation at the SMN2 promoter (Kernochan et al., 2005). In a SMA mouse model, SAHA treatment resulted in weight gain, increased SMN2 transcripts levels in muscles and spinal cord, and motor neuron loss and denervation were halted (Riessland et al., 2010). No human trials have been conducted.

Neurodegenerative Diseases of the Central Nervous System

Alzheimer’s Disease (AD)

Main Wiki article: Alzheimer’s Disease

Alzheimer’s disease (AD) is the most prevalent form of dementia among the elderly. The disease is characterized behaviorally by chronic and progressive decline in cognitive function, beginning with short term memory loss, and neurologically by buildup of misfolded tau protein and associated neurofibrillary tangles, and by amyloid-beta senile plaques amyloid-beta senile plaques. Several genetic factors have been identified as contributing to AD, including mutations to the amyloid precursor protein (APP) and presenilins 1 and 2 genes, and familial inheritance of apolipoprotein E allele epsilon 4. In addition to these common factors, there are a number of other genes that have shown altered expression in Alzheimer's disease, some of which are associated with epigenetic factors.

Epigenetic Factors of Alzheimer’s Disease

ncRNA
Research has shown that a ncRNA that is encoded antisense from an intron within the beta-amyloid cleaving enzyme gene, BACE1, is involved in AD (Faghihi et al., 2008). This ncRNA, BACE1-AS (for antisense), which overlaps exon 6 of BACE1, is involved in increasing the stability of the BACE1 mRNA transcript. As that gene's name suggests, BACE1 is an enzymatic protein that cleaves the Amyloid Precursor Protein into the insoluble amyloid beta form, which then aggregates into senile plaques. With increased stability of BACE1 mRNA resulting from BACE1-AS, more BACE1 mRNA is available for translation into BACE1 protein.
miRNA factors have not consistently been shown to play a role in progression of AD. miRNAs are involved in post-transcriptional gene silencing via inhibiting translation or involvement in RNAi pathways. Some studies have shown upregulation of miRNA-146a, which differentially regulates neuroimmune-related Interleukin-1R associated kinases IRAK1 and IRAK2 expression, in human AD brain, while other studies have shown upregulation or downregulation of miRNA-9 in brain (Bennett et al., 2015).
DNA methylation
In Alzheimer’s disease cases, global DNA hypomethylation and gene-specific hypermethylation has been observed, though findings have varied between studies, especially in studies of human brains. Hypothetically, global hypomethylation should be associated with global increases in transcription, since CpG islands are most prevalent in gene promoters; gene-specific hypermethylation, however, would indicate that these hypermethylated genes are repressed by the methylation marks. Generally, repressive hypermethylation of genes related to learning and memory has been observed in conjunction with derepressive hypomethylation of neuroinflammatory genes and genes related to pathological expression of Alzheimer's disease.
Brain-derived neurotrophic factor
One study has shown reduced methylation in the long-term memory-associated temporal neocortex neurons in monozygotic twins with Alzheimer’s disease compared to the healthy twin (Mastroeni et al., 2009). Global hypomethylation of CpG dinucleotides has also been observed in hippocampus (Chouliaras et al., 2013) and in entorhinal cortex layer II (Mastroeni et al., 2010) of human AD patients, both of which are susceptible to AD pathology. These results, found by probing with immunoassays, have been challenged by studies that interrogate DNA sequence by bisulfite sequencing, a CpG transformation technique which is sensitive to CpG methylation status, in which global hypomethylation has been observed (Bakulski et al., 2012; Rao et al., 2012).
At the individual gene level, Rao et al. have reported hypomethylation and thus derepression of COX-2, inhibition of which reduces inflammation and pain, and hypermethylation of BDNF, a neurotrophic factor important for long-term memory. Expression of CREB, an activity-dependent transcription factor involved in regulating BDNF among many other genes, has also been shown to be hypermethylated, and thus repressed, in AD brains, further reducing BDNF transcription (Rao et al., 2012). Furthermore, synaptophysin (SYP), the major synaptic vesicle protein-encoding gene, has been shown to be hypermethylated and thus repressed, and transcription factor NF-κB, which is involved in immune signaling, has been shown to be hypomethylated and thus derepressed (Rao et al., 2012). Taken together, these results have elucidated a role for dysregulation of genes involved in learning and memory and synaptic transmission, as well as with immune response.
Hypomethylation has been observed in promoters of presenilin 1 (Wang et al., 2008), GSK3beta, which phosphorylates tau protein (Nicolia et al., 2010), and BACE1 (Byun et al., 2012), an enzyme that cleaves APP into the amyloid-beta form, which in turn aggregates into insoluble senile plaques. Repressive hypermethylation caused by amyloid-beta has been observed at the promoter of NEP, the gene for neprilysin, which is the major amyloid-beta clearing enzyme in the brain (Chen et al., 2009). This repression of NEP could result in a feed-forward buildup of senile plaques; combined with the observed increase in AD brains of BACE1-AS and corresponding increases in BACE1 protein and amyloid beta (Faghihi et al., 2008; see above), multiple levels of epigenetic regulation may be involved in controlling amyloid-beta formation, clearance or aggregation, and senile plaque deposition.
There may be some effect of age in levels of DNA methylation at specific gene promoters, as one study found greater levels of methylation at APP promoters in AD patients up to 70 years old, but lower levels of methylation in patients greater than 70 years old (Tohgi et al., 1999). Studies on differential DNA methylation in human AD brains remain largely inconclusive possibly owing to the high degree of variability between individuals and to the numerous combinations of factors that may lead to AD.
Histone marks
Acetylation of lysine residues on histone tails is typically associated with transcriptional activation, whereas deacetylation is associated with transcriptional repression. There are few studies investigating specific histone marks in AD. These studies have elucidated a decrease in acetylation of lysines 18 and 23 on N-terminal tails of histone 3 (H3K18 and H3K23, respectively) (Zhang et al., 2012) and increases in HDAC2 in AD brains (Graff et al., 2012) - both marks related to transcriptional repression. Age-related cognitive decline has been associated with deregulation of H4K12 acetylation, a cognitive effect that was restored in mice by induction of this mark (Peleg et al., 2010).

Treatments for epigenetic factors of Alzheimer’s disease Treatment for prevention or management of Alzheimer's disease has proven troublesome since the disease is chronic and progressive, and many epigenetic drugs act globally and not in a gene-specific manner. As with other potential treatments to prevent or ameliorate symptoms of AD, these therapies do not work to cure, but only ameliorate symptoms of the disease temporarily, underscoring the chronic, progressive nature of AD, and the variability of methylation in AD brains.

DNA methylation-directed treatments

Folate and other B vitamins
B vitamins are involved in the metabolic pathway that leads to SAM production. SAM is the donor of the methyl group utilized by DNA methyltransferases (DNMTs) to methylate CpGs. Using animal models, Fuso et al. have demonstrated restoration of methylation at previously hypomethylated promoters of presenilin 1, BACE1 and APP (Fuso et al., 2005, 2008, 2012) - a hypothetically stable epigenetic modification that should repress those genes and slow the progression of AD. Dietary SAM supplementation has also been shown to reduce oxidative stress and delay buildup of neurological hallmarks of AD such as amyloid beta and phosphorylated tau protein in transgenic AD mice.
AZA
Khan and colleagues have demonstrated a potential role for neuroglobinin attenuating amyloid-related neurotoxicity (Khan et al., 2007). 5-aza-2' deoxycitidine (AZA, or decitabine), a DNMT inhibitor, has shown some evidence for regulating neuroglobin expression, though this finding has not been tested in AD models (Zhang et al., 2011).

Histone-directed treatments

Though studies of histone marks in AD brains are few in number, several studies have looked at the effects of HDACis in treatment of Alzheimer’s disease. Class I and II HDAC inhibitors such as trichostatin A, vorinostat, and sodium butyrate, and Class III HDACis, such as nicotinamide, have been effective at treating symptoms in animal models of AD. While promising as a therapeutic in animal models, studies on the long-term efficacy of HDACis and human trials have yet to be conducted.
Sodium butyrate
Sodium butyrate is a class I and II HDACi and has been shown to recover learning and memory after 4 weeks (Fischer et al., 2007), decrease phosphorylated tau protein, and restore dendritic spine density in the hippocampus of AD transgenic mice (Ricobaraza et al., 2010). Histone acetylation resulting from diffuse sodium butyrate application is especially prevalent in the hippocampus, and genes involved in learning and memory showed increased acetylation in AD mice treated with this drug (Govindarajan et al., 2011).
Trichostatin A
Trichostatin A is also a class I and II HDACi that rescues fear learning in a fear conditioning paradigm in transgenic AD mice to wild type levels via acetylation on histone 4 lysine tails (Francis et al., 2009)
Vorinostat
Vorinostat is a class I and II HDACi that has been shown to be especially effective at inhibiting HDAC2 and restoring memory functions in non-AD models of learning deficits (Guan et al., 2009). One study showed vorinostat is effective at reversing contextual memory deficits in transgenic AD mice (Kilgore et al., 2010).

Huntington's (HD)

Main Wiki article: Huntington's disease
This is a transverse section of the striatum from a structural MR image. The striatum includes the caudate nucleus and putamen. The image also includes the globus pallidus, which is sometimes included when using the term corpus striatum.
This is a transverse section of the striatum from a structural MR image. The striatum, in red, includes the caudate nucleus (top), the putamen (right), and, when including the term 'corpus' striatum, the globus pallidus (lower left).

Huntington’s disease (HD) is an inherited disorder that causes progressive degeneration of neurons within the cerebral cortex and striatum of the brain (OMIM 143100) resulting in loss of motor functions (involuntary muscle contractions), decline in cognitive ability (eventually resulting in dementia), and changes in behavior (Urdinguio et al., 2009).

Genetics and Underlying Causes

Huntington’s is caused by an autosomal dominant mutation expanding the number of glutamine codon repeats (CAG) within the Huntingtin gene (Htt)(OMIN 613004) (http://www.omim.org/entry/143100). The Htt gene encodes for the huntingtin protein which plays a role in normal development but its exact function remains unknown (Nasir et al., 1995). The length of this CAG repeat correlates with the age-of-onset of the disease. The average person without Huntington’s has less than 36 CAG repeats present within the Htt gene. When this repeat length exceeds 36, the onset of neuronal degradation and the physical symptoms of Huntington’s can range from as early as 5 years of age (CAG repeat > 70) to as late as 80 years of age (CAG repeat < 39) (Chen et al., 2002).

This CAG expansion results in mRNA downregulation of specific genes, decreased histone acetylation, and increased histone methylation (Ryu et al., 2006; Hazeki et al., 2002). The exact mechanism of how this repeat causes gene dysregulation is unknown, but epigenome modification may play a role. For early-onset Huntington's (ages 5–15), both transgenic mice and mouse striatal cell lines show brain specific histone H3 hypoacetylation and decreased histone association at specific downregulated genes within the striatum (namely Bdnf, Cnr1, Drd2 - dopamine 2 receptor, and Penk1 - preproenkephalin) (Sadri et al., 2007). For both late- and early-onset Huntington’s, the H3 and H4 core histones associated with these downregulated genes in Htt mutants have hypoacetylation (decreased acetylation) compared to wild-type Htt (Hazeki et al., 2002; Sadri et al., 2007). This hypoacetylation is sufficient to cause tighter chromatin packing and mRNA downregulation (Hazeki et al., 2002).

Along with H3 hypoacetylation, both human patients and mice with the mutant Htt have increased levels of histone H3 lysine 9 trimethylation (Ryu et al., 2006). This increase in H3-K9 trimethylation is linked to an increased expression of the methyltransferase ESET/SETDB1 (ERG-associated protein with SET domain (ESET)), which targets and trimethylates H3-K9 residues (Ryu et al., 2006). It’s proposed that this hypermethylation may account for the onset of specific gene repression in Htt mutants (Ryu et al., 2006).

Epigenetic Treatment with HDAC inhibitors

Huntington patients and both mouse and Drosophila models show histone H3 and H4 hypoacetylation. There are currently no treatments for the disease but numerous HDAC inhibitors have been tested and shown to reverse the certain symptoms caused by the Htt mutation.

  • Sodium Butyrate
Sodium butyrate treatment slowed neuronal degeneration in Drosophila models (Steffan et al., 2001). Sodium butyrate treatment also increased histone H3 acetylation and normalized mRNA levels for mutant Htt downregulated genes (Sadri et al., 2007).
  • Valproic acid
Valproic acid treatment increased mutant Htt H3 and H4 acetylation levels comparable to wild-type Htt in Drosophila models (Steffan et al., 2001).
  • Sodium Phenylbutyrate
Sodium phenylbutyrate phase II human triasl with 12 to 15 g/day showed restored mRNA levels of Htt mutant repressed genes but also had adverse side effects such as nausea, headaches, and gain instability (Hogarth et al., 2007). Phenylbutyrate has also been shown to increase histone acetylation, decrease histone methylation, increase survival rate, and decrease the rate of neuronal degradation in Htt mutant mouse models (Gardian et al., 2005).
  • Trichostatin A
Trichostatin A (TSA) treatment increased mutant Htt H3 and H4 acetylation levels comparable to wild-type Htt in Drosophila models (Steffan et al., 2001). TSA treatment has also been shown to increase alpha-tubulin lysine 40 acetylation in mouse striatal cells and increase intracellular transport of BDNF, a brain-derived neurotrophic factor that function in nerve growth and maintenance within the brain (Dompierre et al., 2007; http://ghr.nlm.nih.gov/gene/BDNF).
  • Vorinostat (SAHA)
Vorinostat treatment slowed photoreceptor degeneration and improved longevity of adult Htt mutant Drosophila (Steffan et al., 2001). Like TSA, SAHA treatment increased alpha-tubulin lysine 40 acetylation in mouse striatal cells and also increased intracellular transport of BDNF.

Parkinson's Disease (PD)

Main Wiki article: Parkinson's Disease
Lewy bodies

Parkinson’s disease (PD) is characterized by progressive degeneration of dopaminergic neurons in the substantia nigra by causes unknown. Several genes and environmental factors (e.g. pesticide exposure) may play a role in onset of PD. Hallmarks include mutations to the alpha-synuclein gene, SNCA, as well as PARK2, PINK1, UCHL1, DJ1, and LRRK2 genes, and fibrillar accumulation of Lewy bodies from misfolded alpha-synuclein. Symptoms are most noticeably manifested in disorders of movement, including shaking, rigidity, deficits in making controlled movements, and slow and difficult walking. The late stages of the disease result in dementia and depression. Levodopa and dopaminergic therapy may ameliorate symptoms, though there is no treatment to halt progression of the disease.

Epigenetic factors of Parkinson’s disease

ncRNA
Research has shown reductions of miR-133b correlated to decreased numbers of dopaminergic neurons in the midbrain of PD patients (Kim et al., 2007). miR-132, meanwhile, is negatively correlated with dopaminergic neuron differentiation in the midbrain (Jankovic et al., 2005). miR-7 and miR-153 act to reduce alpha-synuclein levels (a hallmark of PD) but are reduced in PD brain (Doxakis, 2010).
DNA methylation
Neurons of PD patients show hypomethylation of tumor necrosis factor (TNF) alpha encoding sequence, overexpression of which leads to apoptosis of neurons (Pieper et al., 2008). Cerebrospinal fluid of PD patients also shows elevated TNF alpha (Mogi et al., 1996). Research indicates there may be a link between DNA methylation and SNCA expression (Bonsch et al., 2005; Jowaed et al., 2010). Furthermore, human and mouse models have shown reduction of nuclear DNMT1 levels in PD subjects, resulting in hypomethylated states associated with transcriptional repression (Desplats et al., 2011).
Histone marks
alpha-synuclein, the protein encoded by SNCA, can associate with histones and prevent their acetylation in concert with the HDACs HDAC1 and Sirt2 (Kontopoulos et al., 2006; Outeiro et al., 2007). Furthermore, it has been demonstrated that alpha-synuclein binds histone 3 and inhibits its acetylation in Drosophila (Kontopoulos et al., 2006). Dopamine depletion in Parkinson’s disease is associated with repressive histone modifications, including reduced H3K4me3, and lower levels of H3 and H4 lysine acetylation after levodopa therapy (a common treatment of PD).

Treatments for epigenetic factors of Parkinson’s disease Epigenetic treatments tested in models of PD are few, though some promising research has been conducted. Most treatments investigated thus far are directed at histone modifications and analysis of their roles in mediating alpha-synuclein expression and activity. Pesticides and paraquat increase histone acetylation, producing neurotoxic effects similar to those seen in PD, such as apoptosis of dopaminergic cells (Song et al., 2010, 2011). Despite this, treatment with HDACis (Harrison and Dexter, 2013) seems to have a neuroprotective effect.

  • Sodium butyrate
Several studies using different animal models have demonstrated that sodium butyrate may be effective in reducing alpha-synuclein-related neurotoxicity(Zhou et al., 2011; Rane et al., 2012). In Drosophila, sodium butyrate improved locomotor impairment and reduced early mortality rates (St. Laurent et al., 2013).
  • Valproic acid
In an inducible rat model of PD, valproic acid had a neuroprotective effect by preventing translocation of alpha-synuclein into cell nuclei (Monti et al., 2010).
  • Vorinostat
In an alpha-synuclein overexpressing Drosophila model of PD, vorinostat (as well as sodium butyrate) reduced alpha-synuclein-mediated neurotoxicity (Kontopolous et al., 2006).
  • siRNA inhibition of SIRT2
Treatment with SIRT2 inhibiting siRNA leads to reduced alpha-synuclein neurotoxicity AK-1 or AGK-2 (Outeiro et al., 2007).

See also

Notes

  1. ↑ (OMIM; Sghirlanzoni et al., 2005)
  2. ↑ (Goll et al., 2005; Bradley et al., 2007)
  3. ↑ (Bradley et al., 2007)

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