Knowledge Resource Center for Ecological Environment in Arid Area
DOI | 10.1186/1471-2229-11-17 |
Development of genic-SSR markers by deep transcriptome sequencing in pigeonpea [Cajanus cajan (L.) Millspaugh] | |
Dutta, Sutapa1,2; Kumawat, Giriraj1; Singh, Bikram P.1; Gupta, Deepak K.1; Singh, Sangeeta1; Dogra, Vivek1; Gaikwad, Kishor1; Sharma, Tilak R.1; Raje, Ranjeet S.3; Bandhopadhya, Tapas K.2; Datta, Subhojit4; Singh, Mahendra N.5; Bashasab, Fakrudin6; Kulwal, Pawan7; Wanjari, K. B.7; Varshney, Rajeev K.8; Cook, Douglas R.9; Singh, Nagendra K.1 | |
通讯作者 | Singh, Nagendra K. |
来源期刊 | BMC PLANT BIOLOGY
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ISSN | 1471-2229 |
出版年 | 2011 |
卷号 | 11 |
英文摘要 | Background: Pigeonpea [Cajanus cajan (L.) Millspaugh], one of the most important food legumes of semi-arid tropical and subtropical regions, has limited genomic resources, particularly expressed sequence based (genic) markers. We report a comprehensive set of validated genic simple sequence repeat (SSR) markers using deep transcriptome sequencing, and its application in genetic diversity analysis and mapping. Results: In this study, 43,324 transcriptome shotgun assembly unigene contigs were assembled from 1.696 million 454 GS-FLX sequence reads of separate pooled cDNA libraries prepared from leaf, root, stem and immature seed of two pigeonpea varieties, Asha and UPAS 120. A total of 3,771 genic-SSR loci, excluding homopolymeric and compound repeats, were identified; of which 2,877 PCR primer pairs were designed for marker development. Dinucleotide was the most common repeat motif with a frequency of 60.41%, followed by tri-(34.52%), hexa(2.62%), tetra- (1.67%) and pentanucleotide (0.76%) repeat motifs. Primers were synthesized and tested for 772 of these loci with repeat lengths of >= 18 bp. Of these, 550 markers were validated for consistent amplification in eight diverse pigeonpea varieties; 71 were found to be polymorphic on agarose gel electrophoresis. Genetic diversity analysis was done on 22 pigeonpea varieties and eight wild species using 20 highly polymorphic genic-SSR markers. The number of alleles at these loci ranged from 4-10 and the polymorphism information content values ranged from 0.46 to 0.72. Neighbor-joining dendrogram showed distinct separation of the different groups of pigeonpea cultivars and wild species. Deep transcriptome sequencing of the two parental lines helped in silico identification of polymorphic genic-SSR loci to facilitate the rapid development of an intra-species reference genetic map, a subset of which was validated for expected allelic segregation in the reference mapping population. Conclusion: We developed 550 validated genic-SSR markers in pigeonpea using deep transcriptome sequencing. From these, 20 highly polymorphic markers were used to evaluate the genetic relationship among species of the genus Cajanus. A comprehensive set of genic-SSR markers was developed as an important genomic resource for diversity analysis and genetic mapping in pigeonpea. |
类型 | Article |
语种 | 英语 |
国家 | India ; USA |
收录类别 | SCI-E |
WOS记录号 | WOS:000287208000001 |
WOS关键词 | EST-DERIVED MICROSATELLITES ; ORYZA-SATIVA L. ; WILD RELATIVES ; GENETIC DIVERSITY ; REPEAT MARKERS ; MALE-STERILITY ; LINKAGE MAP ; RICE ; GENOME ; WHEAT |
WOS类目 | Plant Sciences |
WOS研究方向 | Plant Sciences |
来源机构 | University of California, Davis ; International Crops Research Institute for the Semi-Arid Tropics |
资源类型 | 期刊论文 |
条目标识符 | http://119.78.100.177/qdio/handle/2XILL650/167450 |
作者单位 | 1.Indian Agr Res Inst, Natl Res Ctr Plant Biotechnol, New Delhi 110012, India; 2.Univ Kalyani, Dept Mol Biol & Biotechnol, Kalyani 741235, W Bengal, India; 3.Indian Agr Res Inst, Div Genet, New Delhi 110012, India; 4.Indian Inst Pulses Res, Kanpur 208024, Uttar Pradesh, India; 5.Banaras Hindu Univ, Inst Agr Sci, Varanasi 221005, Uttar Pradesh, India; 6.Univ Agr Sci, Dharwad 580005, Karnataka, India; 7.Panjabrao Deshmukh Krishi Vidyapeeth, Akola 444104, Maharasthra, India; 8.Int Crops Res Inst Semi Arid Trop, Patancheru 502324, AP, India; 9.Univ Calif Davis, Dept Plant Pathol, Davis, CA 95616 USA |
推荐引用方式 GB/T 7714 | Dutta, Sutapa,Kumawat, Giriraj,Singh, Bikram P.,et al. Development of genic-SSR markers by deep transcriptome sequencing in pigeonpea [Cajanus cajan (L.) Millspaugh][J]. University of California, Davis, International Crops Research Institute for the Semi-Arid Tropics,2011,11. |
APA | Dutta, Sutapa.,Kumawat, Giriraj.,Singh, Bikram P..,Gupta, Deepak K..,Singh, Sangeeta.,...&Singh, Nagendra K..(2011).Development of genic-SSR markers by deep transcriptome sequencing in pigeonpea [Cajanus cajan (L.) Millspaugh].BMC PLANT BIOLOGY,11. |
MLA | Dutta, Sutapa,et al."Development of genic-SSR markers by deep transcriptome sequencing in pigeonpea [Cajanus cajan (L.) Millspaugh]".BMC PLANT BIOLOGY 11(2011). |
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