SCA8 repeat expansion

Large CTA/CTG repeat alleles in neurological disorders and functional implications

Yih Ru Wu, I. Cheng Chen, Bing Wen Soong, Shih Huan Kao, Ghin Chueh Lee, Shu Yi Huang, Hon Chung Fung, Guey Jen Lee-Chen, Chiung Mei Chen

Research output: Contribution to journalArticle

9 Citations (Scopus)

Abstract

Spinocerebellar ataxia type 8 (SCA8) involves bidirectional expression of CUG (ATXN8OS) and CAG (ATXN8) expansion transcripts. The pathogenesis of SCA8 is complex and the spectrum of clinical presentations is broad. In the present study, we assessed the SCA8 repeat size ranges in Taiwanese Parkinson's disease, Alzheimer's disease and atypical parkinsonism and investigated the genetic variation modulating ATXN8 expression. Thirteen large SCA8 alleles and a novel ATXN8 -62 G/A promoter SNP were found. There is a significant difference in the proportion of the individuals carrying SCA8 larger alleles in atypical parkinsonism (P = 0.044) as compared to that in the control subjects. In lymphoblastoid cells carrying SCA8 large alleles, treatment of MG-132 or staurosporine significantly increases the cell death or caspase 3 activity. Although expressed at low steady-state, ATXN8 expression level is significantly higher (P = 0.012) in cells with SCA8 large alleles than that of the control cells. The ATXN8 transcriptional activity was significantly higher in the luciferase reporter construct containing the -62G allele than that containing the -62A allele in both neuroblastoma and embryonic kidney cells. Therefore, our preliminary results suggest that ATXN8 gene -62 G/A polymorphism may be functional in modulating ATXN8 expression.

Original languageEnglish
Pages (from-to)437-444
Number of pages8
JournalHuman Genetics
Volume125
Issue number4
DOIs
Publication statusPublished - 2009

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Nervous System Diseases
Alleles
Parkinsonian Disorders
Staurosporine
Spinocerebellar ataxia 8
Luciferases
Neuroblastoma
Caspase 3
Single Nucleotide Polymorphism
Parkinson Disease
Alzheimer Disease
Cell Death
Kidney
Genes

ASJC Scopus subject areas

  • Genetics
  • Genetics(clinical)

Cite this

Wu, Y. R., Chen, I. C., Soong, B. W., Kao, S. H., Lee, G. C., Huang, S. Y., ... Chen, C. M. (2009). SCA8 repeat expansion: Large CTA/CTG repeat alleles in neurological disorders and functional implications. Human Genetics, 125(4), 437-444. https://doi.org/10.1007/s00439-009-0641-x

SCA8 repeat expansion : Large CTA/CTG repeat alleles in neurological disorders and functional implications. / Wu, Yih Ru; Chen, I. Cheng; Soong, Bing Wen; Kao, Shih Huan; Lee, Ghin Chueh; Huang, Shu Yi; Fung, Hon Chung; Lee-Chen, Guey Jen; Chen, Chiung Mei.

In: Human Genetics, Vol. 125, No. 4, 2009, p. 437-444.

Research output: Contribution to journalArticle

Wu, YR, Chen, IC, Soong, BW, Kao, SH, Lee, GC, Huang, SY, Fung, HC, Lee-Chen, GJ & Chen, CM 2009, 'SCA8 repeat expansion: Large CTA/CTG repeat alleles in neurological disorders and functional implications', Human Genetics, vol. 125, no. 4, pp. 437-444. https://doi.org/10.1007/s00439-009-0641-x
Wu, Yih Ru ; Chen, I. Cheng ; Soong, Bing Wen ; Kao, Shih Huan ; Lee, Ghin Chueh ; Huang, Shu Yi ; Fung, Hon Chung ; Lee-Chen, Guey Jen ; Chen, Chiung Mei. / SCA8 repeat expansion : Large CTA/CTG repeat alleles in neurological disorders and functional implications. In: Human Genetics. 2009 ; Vol. 125, No. 4. pp. 437-444.
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