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Development,cross-species/genera transferability of novel EST-SSR markers and their utility in revealing population structure and genetic diversity in sugarcane
Authors:Ram K Singh  Satya N Jena  Suhail Khan  Sonia Yadav  Nandita Banarjee  Saurabh Raghuvanshi  Vasudha Bhardwaj  Sanjay K Dattamajumder  Raman Kapur  Sushil Solomon  M Swapna  Sangeeta Srivastava  Akhilesh K Tyagi
Institution:1. Indian Institute of Sugarcane Research (ICAR), Rai Bareli Road, Lucknow-226002, U.P., India;2. Plant Molecular Biology Laboratory, National Botanical Research Institute, Lucknow-226001, India;3. Centre for Desert Agriculture, King Abdullah University of Science and Technology (KAUST), Thuwal 23955-6900, Saudi Arabia;4. Department of Plant Molecular Biology, University of Delhi South Campus, Benito Juarez Road, New Delhi-110021, India;5. National Institute of Plant Genome Research, Aruna Asaf Ali Marg, P.O. Box No. 10531, New Delhi-110 067, India
Abstract:Sugarcane (Saccharum spp. hybrid) with complex polyploid genome requires a large number of informative DNA markers for various applications in genetics and breeding. Despite the great advances in genomic technology, it is observed in several crop species, especially in sugarcane, the availability of molecular tools such as microsatellite markers are limited. Now-a-days EST-SSR markers are preferred to genomic SSR (gSSR) as they represent only the functional part of the genome, which can be easily associated with desired trait. The present study was taken up with a new set of 351 EST-SSRs developed from the 4085 non redundant EST sequences of two Indian sugarcane cultivars. Among these EST-SSRs, TNR containing motifs were predominant with a frequency of 51.6%. Thirty percent EST-SSRs showed homology with annotated protein. A high frequency of SSRs was found in the 5′UTR and in the ORF (about 27%) and a low frequency was observed in the 3′UTR (about 8%). Two hundred twenty-seven EST-SSRs were evaluated, in sugarcane, allied genera of sugarcane and cereals, and 134 of these have revealed polymorphism with a range of PIC value 0.12 to 0.99. The cross transferability rate ranged from 87.0% to 93.4% in Saccharum complex, 80.0% to 87.0% in allied genera, and 76.0% to 80.0% in cereals. Cloning and sequencing of EST-SSR size variant amplicons revealed that the variation in the number of repeat-units was the main source of EST-SSR fragment polymorphism. When 124 sugarcane accessions were analyzed for population structure using model-based approach, seven genetically distinct groups or admixtures thereof were observed in sugarcane. Results of principal coordinate analysis or UPGMA to evaluate genetic relationships delineated also the 124 accessions into seven groups. Thus, a high level of polymorphism adequate genetic diversity and population structure assayed with the EST-SSR markers not only suggested their utility in various applications in genetics and genomics in sugarcane but also enriched the microsatellite marker resources in sugarcane.
Keywords:EST-SSRs  expressed sequence tag-simple sequence repeats  UTR  untranslated region  gSSR  genomic simple sequence repeat  UPGMA  unweighted pair group method with arithmetic mean  PIC  polymorphism information content  SUCEST  sugarcane expressed sequence tag  DNR  dinucleotide repeat  TNR  trinucleotide repeat  TtNR  tetranucleotide repeat  PNR  pentanucleotide repeat  HNR  hexanucleotide repeat  IISR  Indian Institute of Sugarcane Research  Pop  population  ISMC  International Sugarcane Microsatellite Consortium  UGMS  unigene microsatellite markers
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