Sequence determinants of human microsatellite variability

<p>Abstract</p> <p>Background</p> <p>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...

Full description

Bibliographic Details
Main Authors: Jakobsson Mattias, Sandefur Conner I, Pemberton Trevor J, Rosenberg Noah A
Format: Article
Language:English
Published: BMC 2009-12-01
Series:BMC Genomics
Online Access:http://www.biomedcentral.com/1471-2164/10/612
id doaj-55f32200ae3b41bbbdf97059e52342df
record_format Article
spelling doaj-55f32200ae3b41bbbdf97059e52342df2020-11-24T22:21:51ZengBMCBMC Genomics1471-21642009-12-0110161210.1186/1471-2164-10-612Sequence determinants of human microsatellite variabilityJakobsson MattiasSandefur Conner IPemberton Trevor JRosenberg Noah A<p>Abstract</p> <p>Background</p> <p>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.</p> <p>Results</p> <p>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.</p> <p>Conclusions</p> <p>These results suggest that sequence properties of microsatellites have a significant impact in determining the features of human microsatellite variability.</p> http://www.biomedcentral.com/1471-2164/10/612
collection DOAJ
language English
format Article
sources DOAJ
author Jakobsson Mattias
Sandefur Conner I
Pemberton Trevor J
Rosenberg Noah A
spellingShingle Jakobsson Mattias
Sandefur Conner I
Pemberton Trevor J
Rosenberg Noah A
Sequence determinants of human microsatellite variability
BMC Genomics
author_facet Jakobsson Mattias
Sandefur Conner I
Pemberton Trevor J
Rosenberg Noah A
author_sort Jakobsson Mattias
title Sequence determinants of human microsatellite variability
title_short 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_sort sequence determinants of human microsatellite variability
publisher BMC
series BMC Genomics
issn 1471-2164
publishDate 2009-12-01
description <p>Abstract</p> <p>Background</p> <p>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.</p> <p>Results</p> <p>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.</p> <p>Conclusions</p> <p>These results suggest that sequence properties of microsatellites have a significant impact in determining the features of human microsatellite variability.</p>
url http://www.biomedcentral.com/1471-2164/10/612
work_keys_str_mv AT jakobssonmattias sequencedeterminantsofhumanmicrosatellitevariability
AT sandefurconneri sequencedeterminantsofhumanmicrosatellitevariability
AT pembertontrevorj sequencedeterminantsofhumanmicrosatellitevariability
AT rosenbergnoaha sequencedeterminantsofhumanmicrosatellitevariability
_version_ 1725769352255373312