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Title

Mining, characterization and validation of EST derived microsatellites from the transcriptome database of Allium sativum L

 

Authors

Subodh Kumar Chand, Satyabrata Nanda, Ellojita Rout & Raj Kumar Joshi*

 

Affiliation

Functional Genomics laboratory, Centre of Biotechnology, Siksha O Anusandhan University, Bhubaneswar-751003, India

 

Email

rajkumar.joshi@yahoo.co.in; *Corresponding author

 

Article Type

Hypothesis

 

Date

Received February 07, 2015; Accepted February 28, 2015; Published March 31, 2015

 

Abstract

Expressed Sequence Tags (ESTs) with comprehensive transcript information are valuable resources for development of molecular markers as they are derived from conserved genic regions. The present study highlights the mining of EST database to deduce the class I hyper variable SSRs in A. sativum. From 21694 garlic EST sequences, 642 non-redundant SSRs were identified with an average frequency of 1 per 14.9 kb of garlic transcriptome. The most abundant SSR motifs were the mononucleotides (32.86%) followed by trinucleotides (28.50%) and dinucleotides (13.39%). Among the individual SSRs, (A/T)n accounted for the highest number (137; 21.33%) followed by (G/C)n (74; 11.52%) and (AAG)n (63;9.81%). Primers designed from a robust set of 7 AsEST-SSRs resulted in the amplification of 63 polymorphic alleles in 14 accessions of garlic. The resolving power of the markers varied from 4.286 (AsSSR7) to 18.143 (AsSSR13) while the average marker index (MI) was 5.087. These EST-SSRs markers for garlic could be useful for the improvement of garlic linkage map and could be used for evaluating genetic variation and comparative genomics studies in Allium species.

 

Keywords

Allium sativum, expressed sequences tags, EST-SSRs, SSR motifs

 

Citation

Chand et al. Bioinformation 11(3): 145-150 (2015)
 

Edited by

P Kangueane

 

ISSN

0973-2063

 

Publisher

Biomedical Informatics

 

License

This is an Open Access article which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. This is distributed under the terms of the Creative Commons Attribution License.