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Effort and Contribution of T-DNA Insertion Mutant Library for Rice Functional Genomics Research in China:Review and Perspective 被引量:4

Effort and Contribution of T-DNA Insertion Mutant Library for Rice Functional Genomics Research in China:Review and Perspective
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摘要 With the completion of the rice (Oryza sativa L.) genome-sequencing project, the rice research community proposed to characterize the func- tion of every predicted gene in rice by 2020. One of the most effective and high-throughput strategies for studying gene function is to employ genetic mutations induced by insertion elements such as T-DNA or transposons. Since 1999, with support from the Ministry of Science and Technology of China for Rice Functional Genomics Programs, large-scale T-DNA insertion mutant populations have been generated in Huazhong Agricultural University, the Chinese Academy of Sciences and the Chinese Academy of Agricultural Sciences. Currently, a total of 372,346 mutant lines have been generated, and 58,226 T-DNA or Tos17 flanking sequence tags have been isolated. Using these mutant resources, more than 40 genes with potential applications in rice breeding have already been identified. These include genes involved in biotic or abiotic stress responses, nutrient metabolism, pollen development, and plant architecture. The functional analysis of these genes will not only deepen our understanding of the fundamental biological questions in rice, but will also offer valuable gene resources for developing Green Super Rice that is high-yielding with few inputs even under the poor growth conditions of many regions of Africa and Asia. With the completion of the rice (Oryza sativa L.) genome-sequencing project, the rice research community proposed to characterize the func- tion of every predicted gene in rice by 2020. One of the most effective and high-throughput strategies for studying gene function is to employ genetic mutations induced by insertion elements such as T-DNA or transposons. Since 1999, with support from the Ministry of Science and Technology of China for Rice Functional Genomics Programs, large-scale T-DNA insertion mutant populations have been generated in Huazhong Agricultural University, the Chinese Academy of Sciences and the Chinese Academy of Agricultural Sciences. Currently, a total of 372,346 mutant lines have been generated, and 58,226 T-DNA or Tos17 flanking sequence tags have been isolated. Using these mutant resources, more than 40 genes with potential applications in rice breeding have already been identified. These include genes involved in biotic or abiotic stress responses, nutrient metabolism, pollen development, and plant architecture. The functional analysis of these genes will not only deepen our understanding of the fundamental biological questions in rice, but will also offer valuable gene resources for developing Green Super Rice that is high-yielding with few inputs even under the poor growth conditions of many regions of Africa and Asia.
出处 《Journal of Integrative Plant Biology》 SCIE CAS CSCD 2012年第12期953-966,共14页 植物学报(英文版)
基金 supported by the National Natural Science Foundation of China(30970172) the 863 Project Grant2012AA10A304 the Program for New Century Excellent Talents in University
关键词 Flanking sequence tags functional genomics insertion site RICE T-DNA insertion mutant library. Flanking sequence tags functional genomics insertion site rice T-DNA insertion mutant library.
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  • 1朱英,蔡秀玲,王宗阳.用无启动子的GUS报告基因捕获水稻基因启动子[J].植物生理与分子生物学学报,2003,29(4):289-294. 被引量:8
  • 2王爱民,陈石燕,沈革志,王新其,鞠丹花,王钟林,王宗阳,蔡秀玲.Ac/Ds(GUS)结构介导的水稻启动子捕获系统的建立[J].植物生理与分子生物学学报,2005,31(6):575-580. 被引量:11
  • 3吴关庭,郎春秀,胡张华,陈笑芸,王伏林,金卫,陈锦清.应用反义PEP基因表达技术提高稻米脂肪含量[J].植物生理与分子生物学学报,2006,32(3):339-344. 被引量:20
  • 4Ayliffe, M.A., Agostino, A., Clarke, B.C., Furbank, R., von Caemmerer, S., Pryor, A.J., 2009. Suppression of the barley uroporphyrinogen Ⅲ synthase gene by a Ds activation tagging element generates developmental photo- sensitivity. Plant Cell 21,814-831.
  • 5Boese, Q.E, Spano, A.J., Li, J.M., Timko, M.E, 1991. Aminolevulinic acid dehydratase in pea (Pisum-Sativum L.). J. Biol. Chem. 266, 17060-17066.
  • 6Chou, K.C., Shen, H.B., 2008. Cell-PLoc: a package of web servers for pre- dicting subcellular localization of proteins in various organisms. Nat. Protoco. 3, 153-162.
  • 7Danon, A., Miersch, O., Felix, G., Camp, R.G., Apel, K., 2005. Concurrent activation of cell death-regulating signaling pathways by singlet oxygen in Arabidopsis thaliana. Plant J. 41, 68-80.
  • 8Edwards, K., Johnstone, C., Thompson, C., 1991. A simple and rapid method for the preparation of plant genomic DNA for PCR analysis. Nucleic Acids Res. 19, 1349.
  • 9Gray, J., Janick-Buckner, D., Buckner, B., Close, RS., Johal, G.S., 2002. Light- dependent death of maize llsl cells is mediated by mature chloroplasts. Plant Physiol. 130, 1894-1907.
  • 10Grimm, B., 1998. Novel insights in the control of tetrapyrrole metabolism of higher plants. Curr. Opin. Plant Biol. 1,245-250.

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