Literature DB >> 15038610

Substantial linkage disequilibrium across the dihydrolipoyl succinyltransferase gene region without Alzheimer's disease association.

Abraham M Brown1, Derek Gordon, Hsinhwa Lee, Michael Caudy, Vahram Haroutunian, John P Blass.   

Abstract

Association of the candidate gene DLST with late-onset Alzheimer's disease (LOAD) risk has been suggested on the basis of case-control studies. This gene, located on chromosome 14q24.3, encodes a subunit of a mitochondrial component known to be defective in AD, the alpha-ketoglutarate dehydrogenase complex. Positive reports have correlated different DLST alleles with LOAD, whereas other groups have failed to find any significant association. We therefore reexamined the association of DLST and LOAD in a more ethnically homogeneous series using three additional single nucleotide polymorphisms (SNP) located within or closely flanking either end of the DLST gene. Pairwise analysis of these SNPs indicated there was strong linkage disequilibrium across the DLST locus. Analysis of complex genotypes or haplotypes based upon all five SNP loci failed to identify a LOAD risk allele, suggesting that further studies of DLST in relation to AD are not warranted.

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Year:  2004        PMID: 15038610     DOI: 10.1023/b:nere.0000014833.54481.1d

Source DB:  PubMed          Journal:  Neurochem Res        ISSN: 0364-3190            Impact factor:   3.996


  35 in total

1.  Biased tests of association: comparisons of allele frequencies when departing from Hardy-Weinberg proportions.

Authors:  D J Schaid; S J Jacobsen
Journal:  Am J Epidemiol       Date:  1999-04-15       Impact factor: 4.897

2.  The frequency of founder mutations in the BRCA1, BRCA2, and APC genes in Australian Ashkenazi Jews: implications for the generality of U.S. population data.

Authors:  A Y Bahar; P J Taylor; L Andrews; A Proos; L Burnett; K Tucker; M Friedlander; M F Buckley
Journal:  Cancer       Date:  2001-07-15       Impact factor: 6.860

3.  DLST gene and Alzheimer's disease.

Authors:  H Kunugi; S Nanko; A Ueki; K Isse; H Hirasawa
Journal:  Lancet       Date:  1998-05-23       Impact factor: 79.321

4.  A DLST genotype associated with reduced risk for Alzheimer's disease.

Authors:  K F Sheu; A M Brown; B S Kristal; R N Kalaria; L Lilius; L Lannfelt; J P Blass
Journal:  Neurology       Date:  1999-04-22       Impact factor: 9.910

5.  Apparent mtDNA heteroplasmy in Alzheimer's disease patients and in normals due to PCR amplification of nucleus-embedded mtDNA pseudogenes.

Authors:  M Hirano; A Shtilbans; R Mayeux; M M Davidson; S DiMauro; J A Knowles; E A Schon
Journal:  Proc Natl Acad Sci U S A       Date:  1997-12-23       Impact factor: 11.205

6.  Association between the gene encoding the E2 subunit of the alpha-ketoglutarate dehydrogenase complex and Parkinson's disease.

Authors:  T Kobayashi; H Matsumine; S Matuda; Y Mizuno
Journal:  Ann Neurol       Date:  1998-01       Impact factor: 10.422

7.  Haplotype frequency estimation in patient populations: the effect of departures from Hardy-Weinberg proportions and collapsing over a locus in the HLA region.

Authors:  Richard M Single; Diogo Meyer; Jill A Hollenbach; Mark P Nelson; Janelle A Noble; Henry A Erlich; Glenys Thomson
Journal:  Genet Epidemiol       Date:  2002-02       Impact factor: 2.135

8.  Ancient mtDNA sequences in the human nuclear genome: a potential source of errors in identifying pathogenic mutations.

Authors:  D C Wallace; C Stugard; D Murdock; T Schurr; M D Brown
Journal:  Proc Natl Acad Sci U S A       Date:  1997-12-23       Impact factor: 11.205

9.  Apolipoprotein E: high-avidity binding to beta-amyloid and increased frequency of type 4 allele in late-onset familial Alzheimer disease.

Authors:  W J Strittmatter; A M Saunders; D Schmechel; M Pericak-Vance; J Enghild; G S Salvesen; A D Roses
Journal:  Proc Natl Acad Sci U S A       Date:  1993-03-01       Impact factor: 11.205

10.  Evidence for parent of origin effect in late-onset Alzheimer disease.

Authors:  Susan Spear Bassett; Dimitrios Avramopoulos; Daniele Fallin
Journal:  Am J Med Genet       Date:  2002-08-08
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  4 in total

1.  Mice deficient in dihydrolipoyl succinyl transferase show increased vulnerability to mitochondrial toxins.

Authors:  Lichuan Yang; Qingli Shi; Daniel J Ho; Anatoly A Starkov; Elizabeth J Wille; Hui Xu; H L Chen; Steven Zhang; Cliona M Stack; Noel Y Calingasan; Gary E Gibson; M Flint Beal
Journal:  Neurobiol Dis       Date:  2009-08-04       Impact factor: 5.996

2.  Molecular Alterations in the Cerebellum of Sporadic Creutzfeldt-Jakob Disease Subtypes with DJ-1 as a Key Regulator of Oxidative Stress.

Authors:  Waqas Tahir; Saima Zafar; Franc Llorens; Amandeep Singh Arora; Katrin Thüne; Matthias Schmitz; Nadine Gotzmann; Niels Kruse; Brit Mollenhauer; Juan Maria Torres; Olivier Andréoletti; Isidre Ferrer; Inga Zerr
Journal:  Mol Neurobiol       Date:  2016-12-14       Impact factor: 5.590

Review 3.  The alpha-ketoglutarate-dehydrogenase complex: a mediator between mitochondria and oxidative stress in neurodegeneration.

Authors:  Gary E Gibson; John P Blass; M Flint Beal; Victoria Bunik
Journal:  Mol Neurobiol       Date:  2005       Impact factor: 5.590

4.  Neuroglobin and Alzheimer's dementia: genetic association and gene expression changes.

Authors:  Megan Szymanski; Ruihua Wang; M Danielle Fallin; Susan S Bassett; Dimitrios Avramopoulos
Journal:  Neurobiol Aging       Date:  2008-11-17       Impact factor: 4.673

  4 in total

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