A genotyping platform assembled with high-throughput DNA extraction, codominant functional markers, and automated CE system to accelerate marker-assisted improvement of rice

被引:0
作者
Likai Chen
Weiwei Gao
Tao Guo
Cuihong Huang
Ming Huang
Jiafeng Wang
Wuming Xiao
Guili Yang
Yongzhu Liu
Hui Wang
Zhiqiang Chen
机构
[1] South China Agricultural University,National Engineering Research Center of Plant Space Breeding
来源
Molecular Breeding | 2016年 / 36卷
关键词
Rice; DNA extraction; Marker-assisted selection; Grain quality; Genotyping;
D O I
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中图分类号
学科分类号
摘要
The introgression of multiple genes into traditional cultivars using marker-assisted selection (MAS) in order to obtain favorable traits is an effective strategy to achieve improved rice lines. Genotyping of markers is a central component of the evaluation of germplasm and the selection of progeny lines. However, efficient DNA extraction and genotyping of large breeding populations still remain limiting factors in rice molecular breeding programs. This study has developed and validated a cost-effective, rapid (<1 h for 96 samples), and high-throughput (96-well format) total DNA-extraction method based on magnetic particle technology. To improve the grain-quality traits of two rice varieties, we have designed and employed an efficient codominant functional marker system (including Wx, ALK, Chalk5, and fgr genes), in combination with genotyping based on automated capillary electrophoresis. Rice lines with simultaneous improvement at multiple loci were obtained and found to have superior grain quality and to be fragrant. The genotyping pipeline established in this study represents an efficient, reliable, and precise platform for MAS.
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共 228 条
[1]  
Ahmed I(2009)High-quality plant DNA extraction for PCR: an easy approach J Appl Genet 50 105-107
[2]  
Islam M(2003)Functional markers in plants Trends Plant Sci 8 554-560
[3]  
Arshad W(1997)Microsatellites and a single-nucleotide polymorphism differentiate apparent amylose classes in an extended pedigree of US rice germplasm Theor Appl Genet 94 773-781
[4]  
Mannan A(2006)Nucleotide diversity in starch synthase IIa and validation of single nucleotide polymorphisms in relation to starch gelatinization temperature and other physicochemical properties in rice ( Theor Appl Genet 113 1171-1183
[5]  
Ahmad W(1998) L.) Plant J 14 459-465
[6]  
Mirza B(2014)Aberrant splicing of intron 1 leads to the heterogeneous 5′ UTR and decreased expression of waxy gene in rice cultivars of intermediate amylose content PLoS One 9 e85106-545
[7]  
Andersen JR(2008)Diversity of global rice markets and the science required for consumer-targeted rice breeding J Cereal Sci 47 536-58
[8]  
Lubberstedt T(2012) gene haplotypes: associations with apparent amylose content and the effect by the environment in an international rice germplasm collection Open Bioinform J 6 55-820
[9]  
Ayres NM(1991)Primer1: primer design web service for tetra-primer ARMS-PCR Nucleic Acids Res 19 1349-594
[10]  
McClung AM(2014)A simple and rapid method for the preparation of plant genomic DNA for PCR analysis Afr J Biotechnol 13 814-290