The Role of Polyglutamine Expansions in Huntington’s Disease Essay

Huntingtons disease (HD) is an autosomal dominant imperfect neurodegenerative disorder characterized by personality changes, motor impairment and subcortical dementia. It is associated with a selective neuronal cell death occurring primarily in the cerebral mantle and striatum. (Scherzinger et al, 1997). HD causes emotional problems, uncontrolled movements and the loss of thinking ability. It can lead to disablement and death from the illness. There are two forms of this disease adult- blast and early-onset (juvenile). Adult onset is by the far close to common for HD symptoms develop at middle 30s/40s, an individual will live an aver succession of 20 years later symptoms and signs begin. Premature signs and symptoms are depression, involuntary movements, trouble learning new information, sad coordination and balance this can all progress very severely. When HD develops into twitching or jerking this is referred as Chorea. HD can be referred to Huntington Chorea. HD usually h as a mid-life onset, notwithstanding a juvenile form, defined by onset of symptoms before the age of 21 years, is present in about 7% of HD cases. (Nance, 2001) It has similar symptoms hitherto the disease progresses more quickly than adult onset form. Gente (1985) results showed findings by others, that the most juvenile-onset patients inherit the gene from their fathers and that the late-onset form is more frequently inherited from bear upon mothers. The disorder is caused by CAG/polyglutamine (poly Q) repeat expansions in the first exon of a gene encoding a large 350 kDa protein of unknown function. (Scherzinger et al, 1997) Zhang et al put in that due to the expansion of polyQ repeats within the proteincauses neurodegenerative disease. Expansion of CAG repeats coding f... ..., C. and Bates, G, P. (2004). Huntingtin and the molecular pathogenesis of Huntingtons disease. EMBO reports 5. 958-963Nance, M, A. and Myers, R, H. (2001)Panov, A, V., Gutekunst, C., Leavitt, B, R., Hayden, M, R., Burke, J, R., Strittmatter, W, J. And Greenamyre, J, T. (2002) Early mitochondrial calcium defects in Huntingtons Disease are a direct effect of Polyglutamines. Nature neuroscience. Volume 5 no 8Ross, C, A. (2002). Polyglutamine Pathogenesis Emergence of Unifying Mechanism for Huntingtons Disease and Related Disorders. Neuron, Vol. 35,819-822.Scherzinger, E., Lurz, R., Turmaine, M., Mangiarini, L., Hollenbach, Birgit., Hasenbank, R., Bates, G, P., Davies, S, W., Lehrach, H and Wanker, E, E. (1997). Huntington-Encoded Polyglutamine Expansions Form Amyloid-like Protein Aggregates In Vitro and In Vivo. Cell, Vol.90, 549-558.Zhang,