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ARMS Molecular Marker for Identifying Long Mesocotyl Genotype gy1Kasa in Rice (Oryza sativa) |
LI Hao-Shu1,*, CHANG Yuan2,*, LIU Chun-Mei3, ZHANG Yu-Han1, YANG Yi-Rong1, QIN Guan-Nan3,4,** |
1 Biotechnology Research Institute, Chinese Academy of Agricultural Sciences, Beijing 100081, China;
2 College of Life Sciences, Capital Normal University, Beijing 100048, China;
3 Key Laboratory of Agro-Ecological Processes in Subtropical Region / Institute of Subtropical Agriculture, Chinese Academy of Sciences, Changsha 410125, China;
4 University of Chinese Academy of Sciences, Beijing 100049, China |
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Abstract Rice (Oryza sativa), one of the most important food crops, feeds more than 50% of the world's population. Mesocotyl is the first internode of rice seedlings when grown in dark. Rice varieties with longer mesocotyl will come up out of soil easier under direct seeding conditions. In previous studies, 5 quantitative trait loci (QTLs) regulating the length of mesocotyl have been identified from 'Kasalath' (O. sativa ssp. indica cv. Kasalath) with long mesocotyl, one of which has been fine mapped into gaoyao1 gene (GY1) (LOC_Os01g67430). Compared with dominant GY1Nip from 'Nipponbare' (O. sativa ssp. japonica cv. Nipponbare), a G→T mutation occurred at 376 bp of the coding region of recessive gy1Kasa in 'Kasalath', which resulted in the elongation of the mesocotyl. gy1Kasa exists in a variety of natural germplasm resources, all of whom exhibits long mesocotyl phenotype. In order to promote the application of gy1Kasa in breeding of rice suitable for direct seeding, a molecular marker was developed by Amplification Refractory Mutation System (ARMS) to identify the functional nucleotide polymorphism (FNP) of GY1. The molecular marker, denominated as gy1fnp, contained 4 primers located in the conserved flanking region of SNP376. A 470 bp fragment could be amplified by gy1fnpaf and gy1fnpar in both genotypes; a 194 bp fragment could only be amplified in homozygous gy1Kasa (FNP site was T) by gy1fnpbf and gy1fnpar; a 315 bp fragment could only be amplified in GY1Nip (FNP site was G) by gy1fnpaf and gy1fnpbr. All 3 fragments could be amplified in heterozygous genotype. The results of agarose gel electrophoresis showed that different genotypes of GY1 could be distinguished accurately and clearly. Sanger sequencing showed that the difference of banding patterns was caused by SNP376. Investigation of F2 population of 'Kasalath' / 'Nipponbare' showed that homozygous gy1Kasa identified by gy1fnp linked with long mesocotyl phenotype. Taken together, it was concluded that gy1fnp developed in this study could accurately distinguish 2 alleles and heterozygous genotypes of GY1 recognized by SNP276 using only one PCR reaction followed by agarose gel electrophoresis with convenience, rapidness and low cost. Marker gy1fnp could promote the application of gy1Kasa in direct seeding rice breeding by molecular Marker Assisted Selection (MAS). Marker gy1fnp could also identify the genotype of GY1 in rice germplasm resources quickly, which was of great significance for genetic analysis and breeding practice. In addition, the successful development of gy1fnp was helpful to reduce genetic noise caused by GY1 and facilitated map based on cloning of other mesocotyl genes.
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Received: 15 November 2019
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Corresponding Authors:
**qinguannan13@mails.ucas.ac.cn *The authors who contribute equally
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[1] 陈涛, 骆名瑞, 张亚东, 等. 2013. 利用四引物扩增受阻突变体系PCR技术检测水稻低直链淀粉含量基因Wx-mq[J]. 中国水稻科学, 27(5): 529-534.
(Chen T, Luo M R, Zhang Y D, et al.2013. Detection of Wx-mq gene for low amylose content by tetra primer amplification refractory mutation system PCR in rice[J]. China Journal of Rice Science, 27(5): 529-534.)
[2] 田孟祥, 余本勋, 张时龙, 等. 2016. 一种水稻高氮利用率NRT1.1B基因功能标记的开发与应用[J]. 分子植物育种, 14(2): 410-416.
(Tian M X, Yu B X, Zhang S L, et al.2016. Development and application of a functional marker for high nitrogen-use efficiency NRT1.1B gene in rice[J]. Molecular Plant Breeding, 14(2): 410-416.)
[3] 肖国樱, 陈芬, 孟秋成, 等, 2015. 论湖南水稻育种的主攻方向和技术策略[J]. 杂交水稻, 30(04): 1-5, 8.(Xiao G Y, Chen F, Meng Q C, et al., 2015. Key targets and technical strategy for rice breeding in Hunan province[J]. Hybrid Rice, 30(04): 1-5, 8.)
[4] 肖国樱, 邓力华, 翁绿水, 等. 2018. 水稻耐逆境种质创新研究十年回顾[J]. 农业现代化研究, 39(6): 945-952.
(Xiao G Y, Deng L H, Weng L S, et al.2018. Germplasm innovation of stress tolerance in rice: Progress we have made in past decade[J]. Research of Agricultural Modernization, 39(6): 945-952.)
[5] 张羽, 王胜宝, 冯志峰, 等. 2011. 陕西省水稻种质资源的香味基因检测[J]. 西北农林科技大学学报(自然科学版), 39(4): 55-59, 68.(Zhang Y, Wang S B, Feng Z F, et al. 2011. Detection of fgr gene in rice germplasm resources in Shaanxi Province[J]. Journal of Northwest A&F University (Nat. Sci. Ed.), 39(4): 55-59, 68.)
[6] 张羽, 张晓娟, 杨凤娇, 等. 2013. 水稻稻瘟病抗性基因Pi-ta的SNP检测方法[J]. 中国水稻科学 , 27(3): 325-328.
(Zhang Y, Zhang X J, Yang F J, et al.SNP-based detecting method of rice blast resistance gene Pi-ta[J]. China Journal of Rice Science, 27(3): 325-328.)
[7] Cai H, Morishima H.2002. QTL clusters reflect character associations in wild and cultivated rice[J]. Theoretical and Applied Genetics, 104(8): 1217-1228.
[8] Goff S A, Ricke D, Lan T H, et al.2002. A draft sequence of the rice genome (Oryza sativa. L. ssp. japonica)[J]. Science, 296(5565): 92-100.
[9] Lee H S, Sasaki K, Higashitani A, et al.2012. Mapping and characterization of quantitative trait loci for mesocotyl elongation in rice (Oryza sativa L.)[J]. Rice, 5(1): 13.
[10] Lee H S, Sasaki K, Kang J W, et al.2017. Mesocotyl elongation is essential for seedling emergence under deep-seeding condition in rice[J]. Rice, 10(1): 32.
[11] Lu Q, Zhang M, Niu X, et al.2016. Uncovering novel loci for mesocotyl elongation and shoot length in indica rice through genome-wide association mapping[J]. Planta, 243(3): 645-657.
[12] Pandey S, Mortimer M, Wade L, et al.2002. Direct seeding: Research strategies and opportunities[M]. Los Baños (Philippines): International Rice Research Institute; Metro Manila, Philippines, pp. 214-257.
[13] Sun S Y, Wang T, Wang L L, et al.2018. Natural selection of a GSK3 determines rice mesocotyl domestication by coordinating strigolactone and brassinosteroid signaling[J]. Nature Communications, 9(1): 2523.
[14] Wang M, Li W, Fang C, et al.2018. Parallel selection on a dormancy gene during domestication of crops from multiple families[J]. Nature Genetics, 50(10): 1435-1441.
[15] Wu J, Feng F, Lian X, et al.2015. Genome-wide Association Study (GWAS) of mesocotyl elongation based on re-sequencing approach in rice[J]. BMC Plant Biology, 15(1): 218.
[16] Xiong Q, Ma B, Lu X, et al.2017. Ethylene-inhibited jasmonic acid biosynthesis promotes mesocotyl/coleoptile elongation of etiolated rice seedlings[J]. Plant Cell, 29(10): 1053-1072.
[17] Yu J, Hu S N, Wang J, et al.2002. A draft sequence of the rice genome (Oryza sativa L. ssp. indica)[J]. Science, 296(5565): 79-92.
[18] Zhao H, Yao W, Ouyang Y, et al.2014. RiceVarMap: A comprehensive database of rice genomic variations[J]. Nucleic Acids Research, 43(D1): D1018-D1022.
[19] Zhao Y, Zhao W, Jiang C, et al.2018. Genetic architecture and candidate genes for deep-sowing tolerance in rice revealed by Non-syn GWAS[J]. Frontiers in Plant Science, 9(1): 332. |
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