Abstract

Background2b-RAD (type IIB endonucleases restriction-site associated DNA) approach was invented by Wang in 2012 and proven as a simple and flexible method for genome-wide genotyping. However, there is still plenty of room for improvement for the existent 2b-RAD approach. Firstly, it doesn’t include the samples pooling in library preparation as other reduced representation libraries. Secondly, the information of 2b-RAD tags, such as tags numbers and distributions, in most of species are unknown. The purposes of the research are to improve a new 2b-RAD approach which possesses samples pooling, moreover to figure out the characteristic and application potentiality of 2b-RAD tags by bioinformatics analysis.ResultsTwelve adapter1 and an adapter2 were designed. A library approach comprising digestion, ligation, pooling, PCR and size selection were established. For saving costs, we used non-phosphorylated adapters and indexed PCR primers. A F2 population of rice (Oryza sativa .L) was genotyped to validate the new approach. On average, 2000332 high quality reads of each sample were obtained with high evenness. Totally 3598 markers containing 3804 SNPs were discovered and the missing rate was 18.9%. A genetic linkage map of 1385 markers was constructed and 92% of the markers’ orders in the genetic map were in accordance with the orders in chromosomes. Meanwhile, the bioinformatics simulation in 20 species showed that the BsaXI had the most widespread recognition sites, indicating that 2b-RAD tags had a powerful application potentiality for high density genetic map. Using modified adapters with a fix base in 3′end, 2b-RAD was also fit for QTL studies with low costs.ConclusionsAn improved 2b-RAD genotyping approach was established in this research and named as I2b-RAD. The method was a simple, fast, cost-effective and multiplex sequencing library approach. It could be adjusted by selecting different enzymes and adapters to fit for alternative uses including chromosomes assembly, QTL fine mapping and even natural population analysis.Electronic supplementary materialThe online version of this article (doi:10.1186/1471-2164-15-956) contains supplementary material, which is available to authorized users.

Highlights

  • IntroductionGenotyping with the molecular markers - detecting the heritable polymorphisms among the individuals of one or more populations - are employed in many regions in modern biological research including phylogeny, evolution, plant breeding and disease research, etc

  • Genotyping with the molecular markers - detecting the heritable polymorphisms among the individuals of one or more populations - are employed in many regions in modern biological research including phylogeny, evolution, plant breeding and disease research, etc. [1,2,3].The classical molecular markers, such as restriction fragment length polymorphisms (RFLPs), randomly amplified polymorphic DNA (RAPD), amplified fragment length polymorphisms (AFLPs) and simple sequence repeats (SSRs) were proven to be powerful in genotyping

  • By the detection of restriction enzymes (REs) sites, we found BsaXI sites were more than EcoRI, especially in Oryza sativa

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Summary

Introduction

Genotyping with the molecular markers - detecting the heritable polymorphisms among the individuals of one or more populations - are employed in many regions in modern biological research including phylogeny, evolution, plant breeding and disease research, etc. The classical molecular markers, such as restriction fragment length polymorphisms (RFLPs), randomly amplified polymorphic DNA (RAPD), amplified fragment length polymorphisms (AFLPs) and simple sequence repeats (SSRs) were proven to be powerful in genotyping. Based on gel electrophoresis, these methods usually take long time and high labor costs with large samples size. The DNA polymorphisms with artificial bands counting are prone to error. These methods generally produce limited markers, making it difficult to construct high density genetic map that is essential for chromosomes assembly.

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