Analysis of genetic differentiation and genomic variation to reveal potential regions of importance during maize improvement

文献类型: 外文期刊

第一作者: Wu, Xun

作者: Wu, Xun;Li, Yongxiang;Li, Xin;Li, Chunhui;Shi, Yunsu;Song, Yanchun;Li, Yu;Wang, Tianyu;Wu, Xun;Zheng, Zuping

作者机构:

关键词: Genomic variation;Subpopulation differentiation;Zea mays L

期刊名称:BMC PLANT BIOLOGY ( 影响因子:4.215; 五年影响因子:4.96 )

ISSN: 1471-2229

年卷期: 2015 年 15 卷

页码:

收录情况: SCI

摘要: Background: Exploring genetic differentiation and genomic variation is important for both the utilization of heterosis and the dissection of the genetic bases of complex traits. Methods: We integrated 1857 diverse maize accessions from America, Africa, Europe and Asia to investigatetheir genetic differentiation, genomic variation using 43,252 high-quality single-nucleotide polymorphisms(SNPs), combing GWAS and linkage analysis strategy to exploring the function of relevant genetic segments. Results: We uncovered many more subpopulations that recently or historically formed during the breeding process. These patterns are represented by the following lines: Mo17, GB, E28, Ye8112, HZS, Shen137, PHG39, B73, 207, A634, Oh43, Reid Yellow Dent, and the Tropical/subtropical (TS) germplasm. A total of 85 highly differentiated regions with a D-ESI of more than 0.2 were identified between the TS and temperate subpopulations. These regions comprised 79 % of the genetic variation, and most were significantly associated with adaptive traits. For example, the region containing the SNP tag PZE. 108075114 was highly differentiated, and this region was significantly associated with flowering time (FT)-related traits, as supported by a genome-wide association study (GWAS) within the interval of FT-related quantitative trait loci (QTL). This region was also closely linked to zcn8 and vgt1, which were shown to be involved in maize adaptation. Most importantly, 197 highly differentiated regions between different subpopulation pairs were located within an FT-or plant architecture-related QTL. Conclusions: Here we reported that 700 1000 SNPs were necessary needed to robustly estimate the genetic differentiation of a naturally diverse panel. In addition, 13 subpopulations were observed in maize germplasm, 85 genetic regions with higher differentiation between TS and temperate maize germplasm, 197 highly differentiated regions between different subpopulation pairs, which contained some FT-related QTNs/QTLs/genes supported by GWAS and linkage analysis, and these regions were expected to play important roles in maize adaptation.

分类号:

  • 相关文献

[1]Identification of Sesame Genomic Variations from Genome Comparison of Landrace and Variety. Wei, Xin,Zhu, Xiaodong,Yu, Jingyin,Wang, Linhai,Zhang, Yanxin,Li, Donghua,Zhou, Rong,Zhang, Xiurong. 2016

[2]Genomic variation of the rice Rim2/Hipa superfamily and dendrogram and fingerprinting analysis of rice germplasm based on Rim2/Hipa paralog display. Tian, PF,Wang, JJ,Wu, G,Li, Q,Lu, BR,He, ZH. 2006

[3]Improved Detection and Characterization of Copy Number Variations Among Diverse Pig Breeds by Array CGH. Wang, Jiying,Jiang, Jicai,Wang, Haifei,Kang, Huimin,Zhang, Qin,Liu, Jian-Feng,Wang, Jiying. 2015

[4]High Variation in Single Nucleotide Polymorphisms (SNPs) and Insertions/Deletions (Indels) in the Highly Invasive Bemisia tabaci (Gennadius) (Hemiptera: Aleyrodidae) Middle East-Asia Minor 1 (MEAM1). Sun, H. B.,Wan, F. H.,Guo, J. Y.,Zhang, G. F.,Wan, F. H.,Guo, J. Y.. 2013

[5]Rapid diversification of five Oryza AA genomes associated with rice adaptation. Zhang, Qun-Jie,Zhu, Ting,Xia, En-Hua,Shi, Chao,Liu, Yun-Long,Zhang, Yun,Liu, Yuan,Jiang, Wen-Kai,Zhao, You-Jie,Mao, Shu-Yan,Zhang, Li-Ping,Huang, Hui,Jiao, Jun-Ying,Xu, Ping-Zhen,Yao, Qiu-Yang,Yang, Li-Li,Gao, Ju,Gao, Li-Zhi,Zhang, Qun-Jie,Zhu, Ting,Xia, En-Hua,Shi, Chao,Liu, Yuan,Yao, Qiu-Yang,Zeng, Fan-Chun,Gao, Ju,Tao, Da-Yun,Wang, Yue-Ju,Bennetzen, Jeffrey L..

[6]Quantitative Trait Loci for Asian Corn Borer Resistance in Maize Population Mc37 x Zi330. Li Xia,He Kang-lai,Wang Zhen-ying,Bai Shu-xiong,Li Xia. 2010

[7]Increasing maize seed weight by enhancing the cytoplasmic ADP-glucose pyrophosphorylase activity in transgenic maize plants. Wang, Zhangying,Chen, Xiaoping,Wang, Jianhua,Liu, Tingsong,Liu, Yan,Zhao, Li,Wang, Guoying. 2007

[8]Spatial distribution of rhizodeposit carbon of maize (Zea mays L.) in soil aggregates assessed by multiple pulse C-13 labeling in the field. Qiao, Yunfa,Miao, Shujie,Li, Na,Han, Xiaozeng,Zhang, Bin,Zhang, Bin.

[9]Potential of tropical maize populations for improving an elite maize hybrid. Yong, Hongjun,Wang, Jianjun,Liu, Zhipeng,Li, Mingshun,Zhang, Degui,Li, Xinhai,Zhang, Shihuang. 2011

[10]Stimulated fine root growth benefits maize nutrient uptake under optimized nitrogen management. Zeng, X.,Peng, Y.,Peng, Y.. 2017

[11]Recessive allelic variations of three microsatellite sites within the O2 gene in maize. Yang, W,Zheng, YL,Ni, S,Wu, J.

[12]Cloning and characterization of maize ZmSPK1, a homologue to nonfermenting1-related protein kinase2. Zou, HW,Zhang, XH,Zhao, JR,Yang, Q,Wu, ZY,Wang, FG,Huang, CL. 2006

作者其他论文 更多>>