|
|
Effects on Mapping the Gene of Green-revertible Chlorina 2 (grc2) Using SLAF-seq BSA in Rice (Oryza sativa) |
TAN Yan-Ning1, YU Dong1, 2, SHENG Xia-Bing1, 2, KANG Wei-Wei2, LI Zhe-Li1, 3, DUAN Mei-Juan3, YUAN Ding-Yang1, 3, * |
1 State Key Laboratory of Hybrid Rice, Hunan Hybrid Rice Research Center, Changsha 410125, China; 2 College of Biosciences and Biotechnology, Hunan Agricultural University, Changsha 410128, China; 3 College of Agronomy, Hunan Agricultural University, Changsha 410128, China |
|
|
Abstract SLAF-seq BSA, integrated traditional bulk segregant analysis (BSA) with specific-locus amplified fragment sequencing (SLAF-seq), makes it possible to quickly locate qualitative trait genes. However, little is known about the reliability of its mapping results. In this study, the green-revertible chlorina gene (grc2) in rice (Oryza sativa) was selected as a target for comparing the mapping results provided with map-based mapping and SLAF-seq BSA. Firstly, 5302 SLAF markers were identified which showed single nucleotide polymorphism between 'grc2' and 'Y58S' (a cultivar presenting normally green leaves) by SLAF-seq. Later, the wild-type bulk and the mutant bulk were established, each consisting of 100 plants from a F2 population of 'Y58S'/'grc2'. By automatically calculating the genotype frequency in two pools, 13 SLAF markers were found associated with grc2 which accorded with an expected separation ratio of 33∶66 for paternal / maternal in wild-type bulk and 99∶1 in mutant bulk at 0.01 level. Interestingly, all of the associated markers were distributed on two neighbour regions of 0.98~1.21 Mb and 1.57~1.99 Mb on Chromosome 6 referenced as '93-11' (an indica cultivar). Furthermore, two markers named AM1 and AM6 on the first region were confirmed linkaged with grc2, just exhibiting a genetic distance of 0.625 cM and 0 cM respectively. While referenced as 'Nipponbare' (a japonica cultivar), it was observed that the first region just covered the mapping area with traditional method, indicating the result of SLAF-seq BSA is for consulting. Therefore, the results presented herein supported SLAF-seq BSA would be a useful tool for rapidly obtaining the region associated with qualitative trait gene.
|
Received: 23 July 2019
|
|
Corresponding Authors:
*yuandingyang@hhrrc.ac.cn
|
|
|
|
1 陈竹锋, 严维, 王娜,等. 2014. 利用改进的MutMap方法克隆水稻雄性不育基因[J]. 遗传, 36(1): 85-93. (Chen Z F, Yan W, Wang N, et al.2014. Cloning of a rice male sterility gene by a modified MutMap method[J]. Hereditas, 36(1): 85-93.) 2 谭炎宁, 孙学武, 袁定阳, 等. 2015. 水稻单叶独立转绿型黄化突变体grc2的鉴定与基因精细定位[J]. 作物学报, 41(6): 831-837. (Tan Y N, Sun X W, Yuan D Y, et al.2015. Identification and Fine Mapping of Green-Revertible Chlorina Gene grc2 in Rice (Oryza sativa L.)[J]. Acta Agronomica Sinica, 41(6): 831-837.) 3 Abe A, Kosugi S, Yoshida K, et al.2012. Genome sequencing reveals agronomically important loci in rice using MutMap[J]. Nature Biotechnology, 30(2): 174-178. 4 Chen S, Wang W, Su J, et al.2016. Rapid identification of rice blast resistance gene by specific length amplified fragment sequencing[J]. Biotechnology & Biotechnological Equipment, 30(3): 1-7. 5 Chen W, Yao J, Chu L, et al.2015. Genetic mapping of the nulliplex-branch gene (gb_nb1) in cotton using next-generation sequencing[J]. Theoretical & Applied Genetics, 128(3): 539-547. 6 Li Y, Zeng X, Zhao Y, et al.2017. Identification of a new rice low-tiller mutant and association analyses based on the SLAF-seq method[J]. Plant Molecular Biology Reporter, 35(1): 72-82. 7 Livaja M, Wang Y, Wieckhorst S, et al.2013. BSTA: A targeted approach combines bulked segregant analysis with next- generation sequencing and de novo transcriptome assembly for SNP discovery in sunflower[J]. BMC Genomics, 14: 628. 8 McCouch S, Teytelman L, Xu Y, et al.2002. Development and mapping of 2240 new SSR Markers for rice (Oryza sativa L.)[J]. DNA Research, 9(6): 199-207. 9 Michelmore R, Paran I, Kesseli R.1991. Identification of markers linked to disease-resistance genes by bulked segregant analysis: A rapid method to detect markers in specific genomic regions by using segregating populations[J]. Proceedings of the National Academy of Sciences of USA, 88(21): 9828-9832. 10 Miller M, Dunham J, Amores A, et al.2007. Rapid and cost-effective polymorphism identification and genotyping using restriction site associated DNA (RAD) markers[J]. Genome Research, 17(2): 240-248. 11 Nasu S, Suzuki J, Ohta R, et al.2002. Search for and analysis of single nucleotide polymorphisms (SNPs) in Rice (Oryza sativa, Oryza rufipogon) and establishment of SNP markers[J]. DNA Research, 9(5): 163-171. 12 Satoshi W, Chikaharu T, Tatsuki O, et al.2017. Identification of quantitative trait loci for flowering time by a combination of restriction site-associated DNA sequencing and bulked segregant analysis in soybean[J]. Breeding Science, 67(3): 277-285. 13 Shen Y, Jiang H, Jin J, et al.2004. Development of genome-wide DNA polymorphism database for map-Based cloning of Rice Genes[J]. Plant Physiology, 135(3): 1198-1205. 14 Song J, Li J, Sun J, et al.2018. Genome-wide association mapping for cold tolerance in a core collection of rice (Oryza sativa L.) landraces by using high-density single nucleotide polymorphism markers from specific-locus amplified fragment sequencing[J]. Frontiers in Plant Science, 9: 875. 15 Sun X, Liu D, Zhang X, et al.2013. SLAF-seq: An efficient method of large-scale De Novo SNP discovery and genotyping using high-throughput sequencing[J]. Plos One, 8(3): e58700. 16 Tanksley S, Ganal M, Martin G.1995. Chromosome landing: A paradigm for map-based gene cloning in plants with large genomes[J]. Trends in Genetics, 11(2): 63-68. 17 Takagi H, Abe A, Yoshida K, et al.2013. QTL-seq: Rapid mapping of quantitative trait loci in rice by whole genome resequencing of DNA from two bulked populations[J]. The Plant Journal, 74(1): 174-183. 18 Trick M, Adamski N, Mugford S, et al.2012. Combining SNP discovery from next-generation sequencing data with bulked segregant analysis (BSA) to fine-map genes in polyploid wheat[J]. BMC Plant Biology, 12(1): 14. 19 Xia C, Chen L L, Rong T Z, et al.2015. Identification of a new maize inflorescence meristem mutant and association analysis using SLAF-seq method[J]. Euphytica, 202(1): 35-44. 20 Xu F, Sun X, Chen Y, et al.2015a. Rapid identification of major QTLs associated with rice grain weight and their utilization[J]. Plos One, 10(3): e0122206. 21 Xu X, Lu L, Zhu B, et al.2015b. QTL mapping of cucumber fruit flesh thickness by SLAF-seq[J]. Scientific Reports, 5: 15829. 22 Yang X, Nong B, Xia X, et al.2017. Rapid identification of a new gene influencing low amylose content in rice landraces (Oryza sativa, L.) using genome-wide association study with specific-locus amplified fragment sequencing[J]. Genome, 60(6): 465-472. 23 Yang X, Xia X, Zeng Y, et al.2018. Identification of candidate genes for gelatinization temperature, gel consistency and pericarp color by GWAS in rice based on SLAF-sequencing[J]. Plos One, 13(5): e0196690. 24 Zhang X, Wang G, Chen B, et al.2018. Candidate genes for first flower node identified in pepper using combined SLAF-seq and BSA[J]. Plos One, 13(3): e0194071. |
[1] |
CAO Ying-Jiang, YOU Shu-Mei, JIANG Kai-Feng, ZHANG Tao, YANG Li, YANG Qian-Hua, WAN Xian-Qi, LI Zhao-Xiang, GAO-Lei, Zheng Jia-Kui. QTL Mapping for Yield-related Traits of Rice Restorer Line Luhui8258 (Oryza sativa)[J]. 农业生物技术学报, 2020, 28(4): 594-604. |
|
|
|
|