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Characterization of the Poly-T Variant in the TOMM40 Gene in Diverse Populations
We previously discovered that a polymorphic, deoxythymidine-homopolymer (poly-T, rs10524523) in intron 6 of the TOMM40 gene is associated with age-of-onset of Alzheimer's disease and with cognitive performance in elderly. Three allele groups were defined for rs10524523, hereafter ‘523’, based o...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3281049/ https://www.ncbi.nlm.nih.gov/pubmed/22359560 http://dx.doi.org/10.1371/journal.pone.0030994 |
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author | Linnertz, Colton Saunders, Ann M. Lutz, Michael W. Crenshaw, Donna M. Grossman, Iris Burns, Daniel K. Whitfield, Keith E. Hauser, Michael A. McCarthy, Jeanette J. Ulmer, Megan Allingham, Rand Welsh-Bohmer, Kathleen A. Roses, Allen D. Chiba-Falek, Ornit |
author_facet | Linnertz, Colton Saunders, Ann M. Lutz, Michael W. Crenshaw, Donna M. Grossman, Iris Burns, Daniel K. Whitfield, Keith E. Hauser, Michael A. McCarthy, Jeanette J. Ulmer, Megan Allingham, Rand Welsh-Bohmer, Kathleen A. Roses, Allen D. Chiba-Falek, Ornit |
author_sort | Linnertz, Colton |
collection | PubMed |
description | We previously discovered that a polymorphic, deoxythymidine-homopolymer (poly-T, rs10524523) in intron 6 of the TOMM40 gene is associated with age-of-onset of Alzheimer's disease and with cognitive performance in elderly. Three allele groups were defined for rs10524523, hereafter ‘523’, based on the number of ‘T’-residues: ‘Short’ (S, T≤19), ‘Long’ (L, 20≤T≤29) and ‘Very Long’ (VL, T≥30). Homopolymers, particularly long homopolymers like ‘523’, are difficult to genotype because ‘slippage’ occurs during PCR-amplification. We initially genotyped this locus by PCR-amplification followed by Sanger-sequencing. However, we recognized the need to develop a higher-throughput genotyping method that is also accurate and reliable. Here we describe a new ‘523’ genotyping assay that is simple and inexpensive to perform in a standard molecular genetics laboratory. The assay is based on the detection of differences in PCR-fragment length using capillary electrophoresis. We discuss technical problems, solutions, and the steps taken for validation. We employed the novel assay to investigate the ‘523’ allele frequencies in different ethnicities. Whites and Hispanics have similar frequencies of S/L/VL alleles (0.45/0.11/0.44 and 0.43/0.09/0.48, respectively). In African-Americans, the frequency of the L-allele (0.10) is similar to Whites and Hispanics; however, the S-allele is more prevalent (0.65) and the VL-allele is concomitantly less frequent (0.25). The allele frequencies determined using the new methodology are compared to previous reports for Ghanaian, Japanese, Korean and Han Chinese cohorts. Finally, we studied the linkage pattern between TOMM40-‘523’ and APOE alleles. In Whites and Hispanics, consistent with previous reports, the L is primarily linked to ε4, while the majority of the VL and S are linked to ε3. Interestingly, in African-Americans, Ghanaians and Japanese, there is an increased frequency of the ‘523’S-APOEε4 haplotype. These data may be used as references for ‘523’ allele and ‘523’-APOE haplotype frequencies in diverse populations for the design of research studies and clinical trials. |
format | Online Article Text |
id | pubmed-3281049 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-32810492012-02-22 Characterization of the Poly-T Variant in the TOMM40 Gene in Diverse Populations Linnertz, Colton Saunders, Ann M. Lutz, Michael W. Crenshaw, Donna M. Grossman, Iris Burns, Daniel K. Whitfield, Keith E. Hauser, Michael A. McCarthy, Jeanette J. Ulmer, Megan Allingham, Rand Welsh-Bohmer, Kathleen A. Roses, Allen D. Chiba-Falek, Ornit PLoS One Research Article We previously discovered that a polymorphic, deoxythymidine-homopolymer (poly-T, rs10524523) in intron 6 of the TOMM40 gene is associated with age-of-onset of Alzheimer's disease and with cognitive performance in elderly. Three allele groups were defined for rs10524523, hereafter ‘523’, based on the number of ‘T’-residues: ‘Short’ (S, T≤19), ‘Long’ (L, 20≤T≤29) and ‘Very Long’ (VL, T≥30). Homopolymers, particularly long homopolymers like ‘523’, are difficult to genotype because ‘slippage’ occurs during PCR-amplification. We initially genotyped this locus by PCR-amplification followed by Sanger-sequencing. However, we recognized the need to develop a higher-throughput genotyping method that is also accurate and reliable. Here we describe a new ‘523’ genotyping assay that is simple and inexpensive to perform in a standard molecular genetics laboratory. The assay is based on the detection of differences in PCR-fragment length using capillary electrophoresis. We discuss technical problems, solutions, and the steps taken for validation. We employed the novel assay to investigate the ‘523’ allele frequencies in different ethnicities. Whites and Hispanics have similar frequencies of S/L/VL alleles (0.45/0.11/0.44 and 0.43/0.09/0.48, respectively). In African-Americans, the frequency of the L-allele (0.10) is similar to Whites and Hispanics; however, the S-allele is more prevalent (0.65) and the VL-allele is concomitantly less frequent (0.25). The allele frequencies determined using the new methodology are compared to previous reports for Ghanaian, Japanese, Korean and Han Chinese cohorts. Finally, we studied the linkage pattern between TOMM40-‘523’ and APOE alleles. In Whites and Hispanics, consistent with previous reports, the L is primarily linked to ε4, while the majority of the VL and S are linked to ε3. Interestingly, in African-Americans, Ghanaians and Japanese, there is an increased frequency of the ‘523’S-APOEε4 haplotype. These data may be used as references for ‘523’ allele and ‘523’-APOE haplotype frequencies in diverse populations for the design of research studies and clinical trials. Public Library of Science 2012-02-16 /pmc/articles/PMC3281049/ /pubmed/22359560 http://dx.doi.org/10.1371/journal.pone.0030994 Text en Linnertz et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Linnertz, Colton Saunders, Ann M. Lutz, Michael W. Crenshaw, Donna M. Grossman, Iris Burns, Daniel K. Whitfield, Keith E. Hauser, Michael A. McCarthy, Jeanette J. Ulmer, Megan Allingham, Rand Welsh-Bohmer, Kathleen A. Roses, Allen D. Chiba-Falek, Ornit Characterization of the Poly-T Variant in the TOMM40 Gene in Diverse Populations |
title | Characterization of the Poly-T Variant in the TOMM40 Gene in Diverse Populations |
title_full | Characterization of the Poly-T Variant in the TOMM40 Gene in Diverse Populations |
title_fullStr | Characterization of the Poly-T Variant in the TOMM40 Gene in Diverse Populations |
title_full_unstemmed | Characterization of the Poly-T Variant in the TOMM40 Gene in Diverse Populations |
title_short | Characterization of the Poly-T Variant in the TOMM40 Gene in Diverse Populations |
title_sort | characterization of the poly-t variant in the tomm40 gene in diverse populations |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3281049/ https://www.ncbi.nlm.nih.gov/pubmed/22359560 http://dx.doi.org/10.1371/journal.pone.0030994 |
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