Literature DB >> 8836199

Cloning (CAG/GTC)n STSs by an Alu-(CAG/GTC)n PCR method: an approach to human chromosome 12 and spinocerebellar ataxia 2 (SCA2).

M A Pujana1, V Volpini, X Estivill.   

Abstract

We report here an Alu-(CAG/GTC)n PCR method for the cloning of STSs with (CAG/GTC)n sequences. We have applied this method to genomic DNA of a somatic cell hybrid containing human chromosome 12 where linkage has been found for a known familiar dominant ataxia (SCA2), which is thought to be due to a (CAG/GTC)n expansion. We have isolated several clones containing (CAG/GTC)n sequences, which include previously identified sequences that map to chromosome 12. This method could be a new PCR approach for the cloning of repeats based on their proximity to Alu sequences.

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Mesh:

Year:  1996        PMID: 8836199      PMCID: PMC146120          DOI: 10.1093/nar/24.18.3651

Source DB:  PubMed          Journal:  Nucleic Acids Res        ISSN: 0305-1048            Impact factor:   16.971


  17 in total

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2.  Androgen receptor gene mutations in X-linked spinal and bulbar muscular atrophy.

Authors:  A R La Spada; E M Wilson; D B Lubahn; A E Harding; K H Fischbeck
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3.  Mapping of DNA instability at the fragile X to a trinucleotide repeat sequence p(CCG)n.

Authors:  E J Kremer; M Pritchard; M Lynch; S Yu; K Holman; E Baker; S T Warren; D Schlessinger; G R Sutherland; R I Richards
Journal:  Science       Date:  1991-06-21       Impact factor: 47.728

4.  An optimized Alu-PCR primer pair for human-specific amplification of YACs and somatic cell hybrids.

Authors:  D A Tagle; F S Collins
Journal:  Hum Mol Genet       Date:  1992-05       Impact factor: 6.150

5.  A one-tube plasmid DNA mini-preparation suitable for sequencing.

Authors:  G Del Sal; G Manfioletti; C Schneider
Journal:  Nucleic Acids Res       Date:  1988-10-25       Impact factor: 16.971

6.  An unstable triplet repeat in a gene related to myotonic muscular dystrophy.

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7.  Novel triplet repeat containing genes in human brain: cloning, expression, and length polymorphisms.

Authors:  S H Li; M G McInnis; R L Margolis; S E Antonarakis; C A Ross
Journal:  Genomics       Date:  1993-06       Impact factor: 5.736

8.  Chromosomal assignment of the second locus for autosomal dominant cerebellar ataxia (SCA2) to chromosome 12q23-24.1.

Authors:  S Gispert; R Twells; G Orozco; A Brice; J Weber; L Heredero; K Scheufler; B Riley; R Allotey; C Nothers
Journal:  Nat Genet       Date:  1993-07       Impact factor: 38.330

9.  Unstable expansion of CAG repeat in hereditary dentatorubral-pallidoluysian atrophy (DRPLA).

Authors:  R Koide; T Ikeuchi; O Onodera; H Tanaka; S Igarashi; K Endo; H Takahashi; R Kondo; A Ishikawa; T Hayashi
Journal:  Nat Genet       Date:  1994-01       Impact factor: 38.330

10.  Dentatorubral and pallidoluysian atrophy expansion of an unstable CAG trinucleotide on chromosome 12p.

Authors:  S Nagafuchi; H Yanagisawa; K Sato; T Shirayama; E Ohsaki; M Bundo; T Takeda; K Tadokoro; I Kondo; N Murayama
Journal:  Nat Genet       Date:  1994-01       Impact factor: 38.330

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