Oilseed crops are diverse in the plant kingdom and belong to several families. In India, oilseed crops occupy an important position in the export earning potential by ranking in billions of dollars every year. However, the slow growth in the domestic production of oilseeds has not been able to keep pace with the increasing demand in the country, leading to more import, and resulting in high inflation rates. Low and unstable yields of most oilseed crops, and uncertainty in returns to investment results from the continued cultivation of oilseeds as rainfed, cover and high stressed environment crops leading to the situation of high demand supply gap. The production of high yielding oilseed cultivars by reconstituting the genetic architecture is of utmost importance to regain the economy returns. Oilseed crops are good sources of oil, protein, sugars, minerals and even vitamins. The oilseeds like groundnut, sesame, soybean and niger are important sources of nutrients and thus are consumed either directly or as ingredients of other food items.

The diverse agro-ecological conditions of India are well suited for several indigenous and naturalised annual oilseed crops. Among the nine oilseed crops grown in the country, seven are of edible oils (soybean, groundnut, rapeseed-mustard, sunflower, sesame, safflower and niger) and two are of non-edible oils (castor and linseed). India is the fourth largest oilseed producing country after USA, China and Brazil. Among the large number of oilseeds grown here, sesame lies at the sixth position of production after soybean, cotton seed, groundnut, sunflower and mustard (National Productive Council, New Delhi). It is predominantly grown in Uttar Pradesh, Rajasthan, Orissa, Gujarat, Andhra Pradesh, Tamil Nadu, Karnataka, West Bengal, Bihar and Assam. The largest producer and exporter of sesame seed in 2011 was Myanmar, secondly India followed by China, Ethiopia, Nigeria and Uganda [1] . China is the world’s largest consumer and 70% of world’s sesame crop is grown in Asia followed by Africa having a gross share of 26% in the world.

Wild relatives of crop plants constitute an increasingly important resource for improving agricultural production and for maintaining agricultural agro-ecosystems. They have contributed many useful genes to crop plants and modern varieties of crops that contain genes from their wild relatives. The conservation and use of crop wild relatives are essential elements for increasing food security, eliminating poverty and maintaining the environment. Wild species have proved useful to crop improvement as source of pest and disease resistance, stress tolerance, in providing valuable information on species relationship revealing crop evolution patterns. Wild sesame species are reported to possess several desirable traits such as high harvest index and other yield components (multilocular capsules per leaf axil, full seed set, large or medium sized seeds etc.), determinate growth habit with uniform ripening, early maturity, photo and thermal insensitivity, high seed retention, high nutritional quality (high oil and protein, high sesamin and sesamolin contents, reduced anti-nutritional factors and oxalic acid in seeds). Wild sesame species are likely to exhibit tolerance to different pests and diseases i.e. resistance to biotic (Phytophthora blight, Cercospora spot, Alternaria leaf spot, phyllody, leaf curl virus etc. and abiotic (waterlogging, drought and salinity) stresses [26] -[28] .

Sesame seed is rich in oil , contains high amounts of (83% - 90%) unsaturated fatty acids, mainly linoleic acid (37% - 47%), oleic acid (35% - 43%), palmitic (9% - 11%) and stearic acid (5% - 10%) with trace amount of linolenic acid [35] . The seeds are a rich source of antioxidants and bioactive compounds including phenolics, phytosterols, phytates, polyunsaturated fatty acids and short chain peptides. Sesame cake is a rich source of protein, carbohydrate and mineral nutrients. Sesame seeds have special significance for human nutrition on account of its high content of sulphur amino acids and phytosterols. The potential distribution of bioactive components in sesame seed have been presented in Figure 1. Sesame seed possess many health promoting effects some of which have been attributed to a group of compounds called lignans (sesamin, sesamolin, sesaminol and sesamolinol). Sesame seed also contains lignan aglycones in oil and lignan glucosides [36] . The antioxidative agents (sesamin, sesamolin, sesamol and sesaminol glucosides along with tocopherol make the oil highly stable and therefore have a long shelf life [37] [38] . Among the vitamins in the sesame seed, the presence of vitamin E is very interesting in relation to the effectiveness of sesame seed as a health food. Sesame seeds are a rich source of phytates and in defatted sesame meal it is 5.18%, compared with 1% in soybean meal and 1.5% in isolated soybean protein [39] . However, the high content of phytic acid and oxalic acid in sesame seed hinders the use of sesame protein as food [40] .

In agriculture, the main objective of plant breeder is to improve the existing cultivars, which are deficient in one or more traits by crossing such cultivars with lines that possess the desired trait. A conventional breeding programme thus involves crossing whole genomes followed by selection of the superior recombinants from among the several segregation products. Indeed, such a procedure is laborious and time consuming, involving several crosses, generations and careful phenotypic selection along with the linkage drag (tight linkage of the undesired loci with the desired loci) may make it further difficult to achieve the desired objective. It is essential to raise the

quality of sesame oil by breeding. Marker-assisted selection breeding can provide a dramatic improvement in the efficiency with which breeders can select traits of desirable combination of genes. This can be used to monitor DNA sequence variation in and among the species and create new sources of genetic variation by introducing new and economically important traits from wild relatives, landraces etc.

Genetic diversity of crops holds an important role in sustainable development and food security [41] . The presence of wild relatives, landraces, introgressed lines and elite cultivars enable selection of superior lines for trait enhancement. It is also important for selection of parents that can be used in plant breeding programs. Improvement of a crop species requires good knowledge on genetic diversity. Diversity studies can be carried out by using various methods such as morphological, biochemical and molecular markers. Morphology study has been a primary tool to estimate genetic differences among sesame genotypes. Several studies based on morphological markers have revealed presence of high genetic diversity in sesame populations [31] [42] [43] . Genetic divergence in sesame (Sesamum indicum L.) landraces based on qualitative and quantitative traits has also been studied [44] . The study revealed a considerable level of variation in 105 sesame accessions collected from diverse ecologies of Pakistan for a number of morphologic and agronomic traits, while limited diversity was observed among the accessions for characters like stem hairiness, flower color (white with purple shading), seed color and to some extent phyllody disease.

However, morphological markers have limitations in their ability to estimate genetic diversity because of strong influence from environmental factors, which make them highly dependent on the cultivation conditions. Biochemical studies involve study of allelic variants of enzymes known as isozymes. This technique utilizes enzymatic functions and is a powerful method of measuring allele frequencies for specific genes. Isozyme studies have been performed in sesame varieties for genetic diversity studies [45] . However, the major disadvantages shown by biochemical markers include their limited number and influence by environmental factors or the developmental stage of the plant, thus sharing similarity to morphological markers [46] .

DNA markers are the most widely used type of marker predominantly due to their abundance and thus these have overcome the limitations shown by morphological and biochemical markers. Molecular markers techniques such as amplified fragment length polymorphism (AFLP), random amplified polymorphic DNA (RAPD), inter simple sequence repeats (ISSR) and simple sequence repeats (SSR) have been widely used in genetic diversity studies in sesame. RAPD study carried out on sesame reported a high genetic diversity of 0.35 among 58 sesame accessions from the Indian subcontinent and other countries [2] . RAPD markers reported a genetic diversity among 38 Turkish sesame accessions ranging from 0.14 to 0.40 [47] . Similarly, high genetic diversity of sesame was reported in Vietnam and Cambodia using RAPD estimated by percent polymorphism (83%) and genetic distance coefficient (0.03 - 0.31) [48] . An ISSR based study on sesame germplasm from Korea and other countries have revealed a low level of polymorphism and genetic distance coefficient between populations (0 to 0.25) [49] . Recently, genetic diversity studies based on ISSR have been carried out in cultivated sesame and related wild species in east Africa [50] . Six reliable ISSR primers generated 51 amplification fragments of which 70.6% were polymorphic.

Low genetic diversity (0.14 - 0.21) among groups was reported in 32 sesame germplasm collections using amplified fragment length polymorphism studies [51] . Additionally, genetic diversity studies based on AFLP have been performed in 96 sesame germplasm collections collected from all over the world [52] . The studies have reported similarity of geographical origin and morphological characteristics of sesame accessions with AFLP pattern and thus demonstrated that for genetic relatedness studies, AFLP is a reliable tool in sesame.

Most recent molecular markers utilized in tagging genes of economic importance include SSR and SNPs. Microsatellites are one of the most commonly used molecular markers to determine the genetic diversity in crop species. However, only a few studies used microsatellites to evaluate genetic diversity in sesame [53] . Study based on ten SSR markers to analyse pattern of genetic variation within and among 50 sesame populations representing the existing Ethiopian collections have been carried out [54] . The workers reported small genetic divergence for between populations than within populations.

Genetic diversity has been evaluated based on phylogenetic relationships and population structure of sesame using microsatellite markers developed from an SSR-enriched genomic DNA library of sesame [55] . A high level of polymorphism was revealed among the accessions. The population structure analysis indicated frequent hybridization and introgression events. Studies based on comparative potential of phenotypic, ISSR and SSR markers for characterization of sesame (Sesamum indicum L.) varieties from India have been performed [56] . The morphological clustering suggested that there was no geographical structure discernable and the varieties were clustered independently of their geographical regions. In contrast, the ISSR- and SSR-based dendrogram analyses showed that all of the genotypes clearly clustered into their respective geographical groups. Studies based on application of microsatellite polymorphisms to evaluate the diversity in seed oil content and fatty acid composition have been performed in Nigerian sesame accessions [57] . The variability in the accessions based on microsatellite markers was closely related to the variation in oil yield and fatty acid composition, which could be potentially beneficial in efforts towards marker assisted selection for these traits.

A variety of molecular markers have been successfully used for detection of their associations with major traits of economic value in several crop plants, amongst which SNP plays an important role [58] .

Single nucleotide variations in genome sequence of individuals of a population are known as SNPs. They are the most abundant molecular markers in the genome and are widely dispersed throughout genomes with a variable distribution among species. Several instances of mutations are generally observed in diverse crop species. Sequence variation examined within two lignin biosynthetic genes (cinnamoyl CoA reductase (CCR) and cinnamyl alcohol dehydrogenase 2 (CAD2) in Eucalyptus globulus [59] . Twenty-one single nucleotide polymorphisms (SNPs) were identified in the exons of CCR, of which nine were neutral mutations and 12 were missense mutations. DNA sequence variations in coding regions of two lignin genes, Cinnamate 4-hydroxylase (C4H) and Cinnamyl alcohol dehydrogenase (CAD) from Acacia mangium and Acacia auriculiformis have been demonstrated [60] . Twenty eight and thirty two SNPs were identified in the coding region of C4H and CAD region. Thus, variations in the two genes may lead to changes in phenotypic characteristics of the trees.

Recently, genome of sesame crop has been sequenced by a group from China [61] . The valuable information on genome brings in a new era of functional and comparative genomic studies in sesame. The comparative studies on domesticates, i.e. S. indicum and wild relatives would increase our understanding of limitations posed by domesticated germplasm and potential of utilization of wild relatives in crop improvement programs. In addition, sesame breeding objectives to create new varieties with high oil quality and yield potential, resistance to pathogens, water logging and drought stress would be efficiently fulfilled [62] . With the advent of high-throughput sequencing technology, abundant information on DNA sequences for the genomes of many plant species has been generated. Expressed Sequence Tags (ESTs) of many crop species has been generated and thousands of sequences have been annotated as putative functional genes using powerful bioinformatics tools. The basic objective of effective breeding programs could be achieved by improving the quality of crop plants, a direct function of their metabolite content. In addition, the quality of plant tissues determines their commercial value in relation to its flavour, fragrance, shelf life, physical attributes, etc. [63] [64] .

Comparative analyses of ESTs have been studied in Sesamum indicum and Arabidopsis thaliana developing seeds [65] . They were able to identify genes involved in accumulation of seed storage products and in the biosynthesis of antioxidant lignans. Thus, analysis of ESTs from Sesamum indicum and Arabidopsis thaliana resulted in similar and different gene expression profiles in the two during seed development and identification of large number of sesame seed specific genes. In addition, full length enriched cDNA library has been generated for developing sesame seeds resulting in 41,248 ESTs [66] . Studies based on identification of homologous genes involved in oil biosynthesis with some conservative transcription factors such as LEC1 (LEAFY COTYLE- DON1), PKL (PICKLE), WRI1 (WRINKLED1) regulating oil biosynthesis have been performed. 117 ESTs were possibly found to be involved in sesame lignan biosynthesis.

Molecular markers have been developed to identify morphological traits of sesame such as growth habit and closed capsule trait [67] . Recently, a high-density genetic map was constructed for sesame based on large scale marker development by specific length amplified fragment (SLAF) sequencing [68] . Specific length amplified fragment sequencing (SLAF-seq) is a recently developed high-resolution strategy for large-scale de novo SNP discovery and genotyping. The map was constructed using an F2 population and the SLAF-seq approach, which allowed the efficient development of a large number of polymorphic markers in a short time. The results obtained from the study not only provides a platform for gene/QTL fine mapping, map-based gene isolation, and molecular breeding for sesame, but also serve as a reference for positioning sequence scaffolds on a physical map, to assist in the process of assembling the sesame genome sequence.

Moreover, biotechnology techniques such as in vitro regeneration and genetic transformation have also been developed for sesame [69] .

Even though the sesame crop has high nutritional, medicinal and agricultural value it is losing out as an oilseed. In spite of being a good source of “healthy oil” in terms of presence of high amounts of PUFA and high antioxidant content, it is not grown on a large extent due to very poor yields [70] [71] . The decreasing crop yield can be attributed to its cultivation in un-irrigated areas, lack of varietal replacement through development of hybrids. Low productivity has been attributed to cultivation of low yielding dehiscent varieties with low harvest index values, significant yield loss during threshing, indeterminate growth, uneven ripening of capsules and lack of improved varieties tolerant to biotic and abiotic stresses like diseases, pests and drought [72] -[74] . For meeting the required yield, advantages of the crop need to be explored such as oil quality, antioxidants, drought tolerance, low cost of production and improvement in soil water percolation Table 1. The low seed yield of sesame is a consequence of a lack in breeding attention [72] . Sesame production is also limited by pests, diseases, lack of uniform maturity of capsules, and seed shattering [75] . Inspite of huge repertoire of sesame germplasm collections available in India, limited research efforts on the use of conventional and biotechnological methodologies have resulted in minimal success in developing biotic and abiotic stress-tolerant cultivars. The absence of efficient in vitro regeneration protocols further provides challenges for development of desired novel sesame genotypes.

Molecular markers are useful for a variety of purposes relevant to crop improvement. The most important of these uses is the indirect marker assisted selection (MAS) exercised during plant breeding. For this purpose, molecular markers need to be amenable to automation and high throughput approaches. The use of molecular markers is based on naturally occurring DNA polymorphism, which forms the basis for designing strategies to exploit for applied purposes. It is essential to raise the quality of sesame oil by breeding. Marker-assisted selection breeding can provide a dramatic improvement in the efficiency with which breeders can select with desirable combination of genes. They can be used to monitor DNA sequence variation in and among the species and create new sources of genetic variation by introducing new and economically important traits from wild relatives, landraces etc.

The breeding efforts in sesame should be targeted on production of white seeded varieties with high returns, short duration of the crop, drought resistance, phyllody resistance, semi-rabi condition, high-temperature tolerance, higher yields, improved plant architecture and indehiscent capsules. The research on sesame breeding has enabled the selection of superior genotypes with high nutritional value. Thorough investigation of genotypes led to detection of lines with increased seed tocopherol, lignan content and high amounts of unsaturated fatty acids [25] [29] . These results have contributed to the identification of the genetic basis underlying the trait, which is a good starting point for future breeding advances in this field. The future research efforts on sesame breeding should be targeted on detection of correlation between oil content and domestication events in sesame as this would be of immense value to the breeders. The great variability for nutritional attributes suggests that these selected accessions may be as useful as parents in hybridization programs to produce sesame with value added traits. In addition, the importance of sesame for value addition of sesame oil has been ignored and thus attention should be given to develop varieties with high amount of unsaturated and polyunsaturated fatty acids. The development of varieties with low or zero anti-nutritional factors like oxalic and phytic acids needs attention for its value addition. In addition, the efforts should also be made to develop low free fatty acid (<2%) sesame varieties.

Therefore, studies on this valuable oilseed sesame with high antioxidant and nutraceutical value should not be undermined as it possess potential market niches and it is of utmost importance to unlock the untapped genetic variation hidden in the sesame germplasm. The exploitation of wild sesame germplasm for breeding purposes would enable substantial expansion of gene pool of domesticates and incorporation of novel traits, particularly pest and disease resistance (phyllody disease), high yield and enhanced oil quality.