Go to:
Logótipo
Comuta visibilidade da coluna esquerda
Você está em: Start > Publications > View > High germinal instability of the (CTG)(n) at the SCA8 locus of both expanded and normal alleles
Publication

Publications

High germinal instability of the (CTG)(n) at the SCA8 locus of both expanded and normal alleles

Title
High germinal instability of the (CTG)(n) at the SCA8 locus of both expanded and normal alleles
Type
Article in International Scientific Journal
Year
2000
Authors
Silveira, I
(Author)
Other
The person does not belong to the institution. The person does not belong to the institution. The person does not belong to the institution. View Authenticus page Without ORCID
Alonso, I
(Author)
Other
The person does not belong to the institution. The person does not belong to the institution. The person does not belong to the institution. View Authenticus page Without ORCID
Guimaraes, L
(Author)
Other
The person does not belong to the institution. The person does not belong to the institution. The person does not belong to the institution. View Authenticus page Without ORCID
Mendonca, P
(Author)
Other
The person does not belong to the institution. The person does not belong to the institution. The person does not belong to the institution. Without AUTHENTICUS Without ORCID
Santos, C
(Author)
Other
The person does not belong to the institution. The person does not belong to the institution. The person does not belong to the institution. Without AUTHENTICUS Without ORCID
Maciel, P
(Author)
Other
The person does not belong to the institution. The person does not belong to the institution. The person does not belong to the institution. View Authenticus page Without ORCID
de Matos, JMF
(Author)
Other
The person does not belong to the institution. The person does not belong to the institution. The person does not belong to the institution. Without AUTHENTICUS Without ORCID
Costa, M
(Author)
Other
The person does not belong to the institution. The person does not belong to the institution. The person does not belong to the institution. Without AUTHENTICUS Without ORCID
Barbot, C
(Author)
Other
The person does not belong to the institution. The person does not belong to the institution. The person does not belong to the institution. View Authenticus page Without ORCID
Tuna, A
(Author)
Other
The person does not belong to the institution. The person does not belong to the institution. The person does not belong to the institution. Without AUTHENTICUS Without ORCID
Jose Barros
(Author)
Other
View Personal Page You do not have permissions to view the institutional email. Search for Participant Publications View Authenticus page Without ORCID
Jardim, L
(Author)
Other
The person does not belong to the institution. The person does not belong to the institution. The person does not belong to the institution. Without AUTHENTICUS Without ORCID
Coutinho, P
(Author)
Other
The person does not belong to the institution. The person does not belong to the institution. The person does not belong to the institution. View Authenticus page Without ORCID
Sequeiros, J
(Author)
ICBAS
View Personal Page You do not have permissions to view the institutional email. Search for Participant Publications View Authenticus page View ORCID page
Journal
Vol. 66
Pages: 830-840
ISSN: 0002-9297
Publisher: Elsevier
Other information
Authenticus ID: P-001-0M9
Abstract (EN): The autosomal dominant spinocerebellar ataxias (SCAs) are a group of late-onset, neurodegenerative disorders for which 10 loci have been mapped (SCA1, SCA2, SCA4-SCA8, SCA10, MJD, and DRPLA). The mutant proteins have shown an expanded polyglutamine tract in SCA1, SCA2, MJD/SCA3, SCA6, SCA7, and DRPLA; a glycine-to-arginine substitution was found in SCA6 as well. Recently, an untranslated (CTG), expansion on chromosome 13q was described as being the cause of SCA8. We have now (1) assessed the repeat size in a group of patients with ataxia and a large number of controls, (2) examined the intergenerational transmission of the repeat, and (3) estimated the instability of repeat size in the sperm of one patient and two healthy controls. Normal SCA8 chromosomes showed an apparently trimodal distribution, with classes of small (15-21 CTGs), intermediate (22-37 CTGs), and large (40-91 CTGs) alleles; large alleles accounted for only0.7% of all normal-size alleles. No expanded alleles (greater than or equal to 100 CTGs) were found in controls. Expansion of the CTC; tract was found in five families with ataxia; expanded alleles (all paternally transmitted) were characterized mostly by repeat-size contraction. There was a high germinal instability of both expanded and normal alleles: in one patient, the expanded allele (152 CTGs) had mostly contraction in size (often into the normal range); in the sperm of two normal controls, contractions were also more frequent, but occasional expansions into the upper limit of the normal size range were also seen. In conclusion, our results show (1) no overlapping between control (15-91) and pathogenic (100-152) alleles and (2) a high instability in spermatogenesis (both for expanded and normal alleles), suggesting a high mutational rate at the SCA8 locus.
Language: English
Type (Professor's evaluation): Scientific
No. of pages: 11
Documents
We could not find any documents associated to the publication.
Related Publications

Of the same journal

A COMMENT ON THE DEMONSTRATION OF ERYTHROCYTIC AMINOTRANSFERASES ON STARCH GELS (1983)
Another Publication in an International Scientific Journal
AMORIM, A
Pseudodominant transmission of hereditary hemochromatosis in a family from a small geographic area: genealogical and genetic analysis. (2000)
Summary of Presentation in an International Conference
mola-vieira, l; macedo, p; paiva, c; serpa, l; brandao, h; almeida-mello, j; rodrigues, p; porto, g
Y-chromosomal diversity in Europe is clinal and influenced primarily by geography, rather than by language (2000)
Article in International Scientific Journal
Rosser, ZH; Zerjal, T; Hurles, ME; Adojaan, M; Alavantic, D; Amorim, A; Amos, W; Armenteros, M; Arroyo, E; Barbujani, G; Beckman, G; Beckman, L; Bertranpetit, J; Bosch, E; Bradley, DG; Brede, G; Cooper, G; Corte Real, HBSM; de Knijff, P; Decorte, R...(mais 43 authors)
The tumor-necrosis-factor receptor-associated periodic syndrome: New mutations in TNFRSF1A, ancestral origins, genotype-phenotype studies, and evidence for further genetic heterogeneity of periodic fevers (2001)
Article in International Scientific Journal
Aksentijevich, I; Galon, J; Soares, M; Mansfield, E; Hull, K; Oh, HH; Goldbach Mansky, R; Dean, J; Athreya, B; Reginato, AJ; Henrickson, M; Pons Estel, B; O¿Shea, JJ; Kastner, DL
The phylogeography of Brazilian Y-chromosome lineages (2001)
Article in International Scientific Journal
Carvalho Silva, DR; Santos, FR; Rocha, J; Pena, SDJ

See all (17)

Recommend this page Top
Copyright 1996-2025 © Faculdade de Direito da Universidade do Porto  I Terms and Conditions  I Acessibility  I Index A-Z
Page created on: 2025-08-20 at 06:58:27 | Privacy Policy | Personal Data Protection Policy | Whistleblowing