Abstract

BackgroundSimple Sequence Repeat (SSR) or microsatellite markers are valuable for genetic research. Experimental methods to develop SSR markers are laborious, time consuming and expensive. In silico approaches have become a practicable and relatively inexpensive alternative during the last decade, although testing putative SSR markers still is time consuming and expensive. In many species only a relatively small percentage of SSR markers turn out to be polymorphic. This is particularly true for markers derived from expressed sequence tags (ESTs). In EST databases a large redundancy of sequences is present, which may contain information on length-polymorphisms in the SSR they contain, and whether they have been derived from heterozygotes or from different genotypes. Up to now, although a number of programs have been developed to identify SSRs in EST sequences, no software can detect putatively polymorphic SSRs.ResultsWe have developed PolySSR, a new pipeline to identify polymorphic SSRs rather than just SSRs. Sequence information is obtained from public EST databases derived from heterozygous individuals and/or at least two different genotypes. The pipeline includes PCR-primer design for the putatively polymorphic SSR markers, taking into account Single Nucleotide Polymorphisms (SNPs) in the flanking regions, thereby improving the success rate of the potential markers. A large number of polymorphic SSRs were identified using publicly available EST sequences of potato, tomato, rice, Arabidopsis, Brassica and chicken.The SSRs obtained were divided into long and short based on the number of times the motif was repeated. Surprisingly, the frequency of polymorphic SSRs was much higher in the short SSRs.ConclusionPolySSR is a very effective tool to identify polymorphic SSRs. Using PolySSR, several hundred putative markers were developed and stored in a searchable database. Validation experiments showed that almost all markers that were indicated as putatively polymorphic by polySSR were indeed polymorphic. This greatly improves the efficiency of marker development, especially in species where there are low levels of polymorphism, like tomato. When combined with the new sequencing technologies PolySSR will have a big impact on the development of polymorphic SSRs in any species.PolySSR and the polymorphic SSR marker database are available from .

Highlights

  • Simple Sequence Repeat (SSR) or microsatellite markers are valuable for genetic research

  • When combined with the new sequencing technologies PolySSR will have a big impact on the development of polymorphic SSRs in any species

  • Large numbers of polymorphic SSRs were identified by PolySSR from publicly available expressed sequence tags (ESTs) sequences of potato, tomato, rice, Arabidopsis, Brassica and chicken

Read more

Summary

Introduction

Simple Sequence Repeat (SSR) or microsatellite markers are valuable for genetic research. A number of programs have been developed to identify SSRs in EST sequences, no software can detect putatively polymorphic SSRs. Microsatellites, or simple sequence repeats (SSRs), are tandem repeats of 1–6 nucleotides and are present in all eukaryotic genomes. Microsatellites, or simple sequence repeats (SSRs), are tandem repeats of 1–6 nucleotides and are present in all eukaryotic genomes Based on their locus-specificity, high level of polymorphism (due to their multi-allelic nature), co-dominant inheritance, relative abundance and reproducibility, SSRs have become valuable tools for genetic mapping, association mapping, comparative mapping, diversity analysis, and QTL analysis [1,2,3]. The large number of expressed sequence tags (ESTs) deposited in public databases is a valuable resource to develop SSR markers. The versatility of the tool was shown in a number of species (potato, tomato, Brassica, rice, Arabidopsis and chicken)

Methods
Results
Discussion
Conclusion
Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.