Abstract

BackgroundAlpha satellite is the major repeated DNA element of primate centromeres. Evolution of these tandemly repeated sequences has led to the existence of numerous families of monomers exhibiting specific organizational patterns. The limited amount of information available in non-human primates is a restriction to the understanding of the evolutionary dynamics of alpha satellite DNA.ResultsWe carried out the targeted high-throughput sequencing of alpha satellite monomers and dimers from the Cercopithecus solatus genome, an Old World monkey from the Cercopithecini tribe. Computational approaches were used to infer the existence of sequence families and to study how these families are organized with respect to each other. While previous studies had suggested that alpha satellites in Old World monkeys were poorly diversified, our analysis provides evidence for the existence of at least four distinct families of sequences within the studied species and of higher order organizational patterns. Fluorescence in situ hybridization using oligonucleotide probes that are able to target each family in a specific way showed that the different families had distinct distributions on chromosomes and were not homogeneously distributed between chromosomes.ConclusionsOur new approach provides an unprecedented and comprehensive view of the diversity and organization of alpha satellites in a species outside the hominoid group. We consider these data with respect to previously known alpha satellite families and to potential mechanisms for satellite DNA evolution. Applying this approach to other species will open new perspectives regarding the integration of satellite DNA into comparative genomic and cytogenetic studies.Electronic supplementary materialThe online version of this article (doi:10.1186/s12864-016-3246-5) contains supplementary material, which is available to authorized users.

Highlights

  • Alpha satellite is the major repeated DNA element of primate centromeres

  • We decided to extract DNA from two bands corresponding to monomers and dimers of alpha satellites from an agarose gel and implemented high throughput sequencing on an Ion Torrent sequencing platform providing reads up to 400 nucleotide in length

  • As a further control of the consistency between the results from fluorescence in situ hybridization (FISH) experiments and sequence analysis, we showed that a 13-mer locked nucleic acid (LNA) probe that was designed to target the four C1 to C4 groups of sequences provided signals that overlapped with the combined signals of probes targeting each group, i.e. was able to label all chromosomes within the centromeric and pericentromeric regions (Additional file 1: Figure S6)

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Summary

Introduction

Alpha satellite is the major repeated DNA element of primate centromeres. Evolution of these tandemly repeated sequences has led to the existence of numerous families of monomers exhibiting specific organizational patterns. Alpha satellite DNA is made of tandemly repeated AT-rich monomers that are about 170 bp in length and organized in head-to-tail orientation [11, 12]. Over the last 30 years, the systematic cloning and sequencing of many alpha satellite DNAs, combined with fluorescence in situ hybridization (FISH) experiments, has provided a thorough knowledge of alpha satellite DNA diversity and organization patterns in the human genome [11, 15, 16] and, to a much lesser extent, in other primates [17,18,19,20]

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