Development, Characterization, and Cross Species/Genera Transferability of Novel EST-SSR Markers in Lentil, with Their Molecular Applications

• Published in: Plant molecular biology reporter Vol. 38; no. 1; pp. 114 - 129
• Main Authors: Singh, Dharmendra, Singh, Chandan Kumar, Tribuvan, Kishor U, Tyagi, Punit, Taunk, Jyoti, Tomar, Ram Sewak Singh, Kumari, Shanti, Tripathi, Kuldeep, Kumar, Ashok, Gaikwad, Kishor, Yadav, Rajendra Kumar, Pal, Madan
• Format: Journal Article
• Language: English
• Published: New York Springer US 01-03-2020; Springer Nature B.V
• Subjects: Annotations; Bioinformatics; Biomarkers; Biomedical and Life Sciences; Carbohydrates; Cluster analysis; Expressed sequence tags; Fibers; Gene mapping; Gene sequencing; Genera; Genetic resources; Genotypes; Germplasm; Legumes; Leguminous plants; Life Sciences; Mapping; Metabolomics; Minerals; Original Paper; Phylogeny; Plant Breeding/Biotechnology; Plant Sciences; Population structure; Proteomics; Ribonucleic acid; RNA; Species; Vitamins; Lentil; Cross-genera transferability; Genetic diversity; Unigene sequences; RNA-Seq; EST-SSR
• ISSN: 0735-9640; 1572-9818
• DOI: 10.1007/s11105-019-01184-z

Lentil is nutritionally important crop for human diet and enriched with quality protein, complex carbohydrates, fibers, essential minerals, and vitamins. However, genetic improvement of lentil is hampered largely due to unattributed and unexploited genetic and genomic resources. To administer genomic resources in lentil, we have identified 9949 EST-SSR loci from lentil RNA Seq data and validated 50 of them using 234 genotypes representing various
Lens
species and 34 accessions of 12 different legumes. Out of 50 EST-SSRs, 46 were polymorphic with polymorphic information content (PIC) ranging from 0.16–0.74. The transferability of these markers exhibited varied levels from 45.1 to 71.3% across the cultivated/wild species of lentil and from 10.8 to 54.3% across the twelve legume genera. On the basis of total identified EST-SSRs, mononucleotide (51%) repeat proportion was high followed by trinucleotide (30%) and dinucleotide (14%) repeat. Population structure and cluster analysis classified all the studied genotypes into 4 groups. However, principal coordinate analysis (PCA) was able to group genotypes based on their area of collection. Annotation of all the 46 polymorphic marker sequences revealed that most of the markers linked to genes involved in metabolism of plants. Further, polymorphic markers were also used for linkage mapping in F
3
population where 4 markers were found to be linked with a map distance of 72.5 cM. The newly developed markers represent an impressive tool for characterization of germplasm, genetic linkage mapping, phylogenetic studies, as well as to determine disparity in taxonomic status of subspecies of the genus
Lens
.