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Sequence determinants of human microsatellite variability

BACKGROUND: Microsatellite loci are frequently used in genomic studies of DNA sequence repeats and in population studies of genetic variability. To investigate the effect of sequence properties of microsatellites on their level of variability we have analyzed genotypes at 627 microsatellite loci in...

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Autores principales: Pemberton, Trevor J, Sandefur, Conner I, Jakobsson, Mattias, Rosenberg, Noah A
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2806349/
https://www.ncbi.nlm.nih.gov/pubmed/20015383
http://dx.doi.org/10.1186/1471-2164-10-612
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author Pemberton, Trevor J
Sandefur, Conner I
Jakobsson, Mattias
Rosenberg, Noah A
author_facet Pemberton, Trevor J
Sandefur, Conner I
Jakobsson, Mattias
Rosenberg, Noah A
author_sort Pemberton, Trevor J
collection PubMed
description BACKGROUND: Microsatellite loci are frequently used in genomic studies of DNA sequence repeats and in population studies of genetic variability. To investigate the effect of sequence properties of microsatellites on their level of variability we have analyzed genotypes at 627 microsatellite loci in 1,048 worldwide individuals from the HGDP-CEPH cell line panel together with the DNA sequences of these microsatellites in the human RefSeq database. RESULTS: Calibrating PCR fragment lengths in individual genotypes by using the RefSeq sequence enabled us to infer repeat number in the HGDP-CEPH dataset and to calculate the mean number of repeats (as opposed to the mean PCR fragment length), under the assumption that differences in PCR fragment length reflect differences in the numbers of repeats in the embedded repeat sequences. We find the mean and maximum numbers of repeats across individuals to be positively correlated with heterozygosity. The size and composition of the repeat unit of a microsatellite are also important factors in predicting heterozygosity, with tetra-nucleotide repeat units high in G/C content leading to higher heterozygosity. Finally, we find that microsatellites containing more separate sets of repeated motifs generally have higher heterozygosity. CONCLUSIONS: These results suggest that sequence properties of microsatellites have a significant impact in determining the features of human microsatellite variability.
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spelling pubmed-28063492010-01-14 Sequence determinants of human microsatellite variability Pemberton, Trevor J Sandefur, Conner I Jakobsson, Mattias Rosenberg, Noah A BMC Genomics Research article BACKGROUND: Microsatellite loci are frequently used in genomic studies of DNA sequence repeats and in population studies of genetic variability. To investigate the effect of sequence properties of microsatellites on their level of variability we have analyzed genotypes at 627 microsatellite loci in 1,048 worldwide individuals from the HGDP-CEPH cell line panel together with the DNA sequences of these microsatellites in the human RefSeq database. RESULTS: Calibrating PCR fragment lengths in individual genotypes by using the RefSeq sequence enabled us to infer repeat number in the HGDP-CEPH dataset and to calculate the mean number of repeats (as opposed to the mean PCR fragment length), under the assumption that differences in PCR fragment length reflect differences in the numbers of repeats in the embedded repeat sequences. We find the mean and maximum numbers of repeats across individuals to be positively correlated with heterozygosity. The size and composition of the repeat unit of a microsatellite are also important factors in predicting heterozygosity, with tetra-nucleotide repeat units high in G/C content leading to higher heterozygosity. Finally, we find that microsatellites containing more separate sets of repeated motifs generally have higher heterozygosity. CONCLUSIONS: These results suggest that sequence properties of microsatellites have a significant impact in determining the features of human microsatellite variability. BioMed Central 2009-12-16 /pmc/articles/PMC2806349/ /pubmed/20015383 http://dx.doi.org/10.1186/1471-2164-10-612 Text en Copyright ©2009 Pemberton et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research article
Pemberton, Trevor J
Sandefur, Conner I
Jakobsson, Mattias
Rosenberg, Noah A
Sequence determinants of human microsatellite variability
title Sequence determinants of human microsatellite variability
title_full Sequence determinants of human microsatellite variability
title_fullStr Sequence determinants of human microsatellite variability
title_full_unstemmed Sequence determinants of human microsatellite variability
title_short Sequence determinants of human microsatellite variability
title_sort sequence determinants of human microsatellite variability
topic Research article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2806349/
https://www.ncbi.nlm.nih.gov/pubmed/20015383
http://dx.doi.org/10.1186/1471-2164-10-612
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