Studies on the CTA/CTG trinucleotide repeats of ATXN8OS gene in Chinese Hans / 中华医学遗传学杂志
Zhonghua Yi Xue Yi Chuan Xue Za Zhi
; (6): 511-514, 2008.
Article
de Zh
| WPRIM
| ID: wpr-308028
Bibliothèque responsable:
WPRO
ABSTRACT
<p><b>OBJECTIVE</b>To study the normal range of (CTA/CTG)n repeats of ATXN8OS gene in Chinese Hans, and the frequency of ATXN8OS (CTA/CTG)n repeat expansion in spinocerebellar ataxia(SCA) patients in Mainland China.</p><p><b>METHODS</b>The (CTA/CTG)n repeats of ATXN8OS gene were detected using fluorescence-PCR, 8% denaturing polyacrylamide gel and capillary electrophoresis technique in 132 SCA patients in whom CAG expansion at the SCA1, SCA2, SCA3, SCA6, SCA7, SCA12, SCA17 and dentatorubral-pallidoluysian atrophy(DRPLA) loci has been excluded, and 261 healthy controls.</p><p><b>RESULTS</b>There were no obvious abnormal changes of the (CTA/CTG)n repeats of ATXN8OS gene in the 132 SCA patients. Thirty-five SCA patients were homozygotes (26.5%), and the range of CTA/CTG repeat number was 17 to 47 (24.20+/-4.57), among which 18 repeats appeared most frequently. In 261 normal controls, 70 were homozygotes (26.8%), and the range of the CTA/CTG repeat number was from 12 to 43 (24.04+/-4.53), among which 18 repeats was the most frequent.</p><p><b>CONCLUSION</b>SCA8 is a rare subtype of SCA in Mainland China. The low prevalence of SCA8 seems to be correlated with the low frequency of large (CTA/CTG)n copy number alleles in Chinese population.</p>
Texte intégral:
1
Indice:
WPRIM
Sujet Principal:
Analyse de mutations d'ADN
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Séquence nucléotidique
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Ethnies
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Études cas-témoins
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Dosage génique
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Répétitions de trinucléotides
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Ataxies spinocérébelleuses
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ARN non traduit
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Asiatiques
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Allèles
Type d'étude:
Observational_studies
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Risk_factors_studies
Limites du sujet:
Adolescent
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Adult
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Aged
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Child
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Child, preschool
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Female
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Humans
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Male
langue:
Zh
Texte intégral:
Zhonghua Yi Xue Yi Chuan Xue Za Zhi
Année:
2008
Type:
Article