您好,欢迎访问山东省农业科学院文献资源数据库平台

In vitro mutagenesis and directed screening for salt-tolerant mutants in peanut

文献类型: 外文期刊

作者: Zhao, Ming-Xia 1 ; Sun, Hai-Yan 1 ; Ji, Rui-Rui 1 ; Hu, Xiao-Hui 2 ; Sui, Jiong-Ming 1 ; Qiao, Li-Xian 1 ; Chen, Jing; 1 ;

作者机构: 1.Qingdao Agr Univ, Key Lab Plant Biotechnol Univ Shandong, Coll Life Sci, Qingdao 266109, Peoples R China

2.Shandong Acad Agr Sci, Peanut Res Inst, Qingdao 266100, Peoples R China

关键词: Peanut (Arachis hypogaea L.);PYM;In vitro mutagenesis;Directed screening;Salt-tolerant mutant

期刊名称:EUPHYTICA ( 影响因子:1.895; 五年影响因子:2.181 )

ISSN:

年卷期:

页码:

收录情况: SCI

摘要: To expand the salt-tolerant gene resources of peanut, we conducted in vitro mutagenesis with pingyangmycin (PYM) as the mutagen and directed screening with medium containing NaCl. After embryonic leaflets from mature peanut seeds (variety Huayu 22) were cultured on somatic embryogenesis-induction medium containing 4 mg/L PYM for 4 weeks, the surviving somatic embryos were sequentially transferred to a germination medium containing 15 and then 20 g/L NaCl. The 30 NaCl-tolerant plantlets obtained were grafted and transplanted in the field in 2011, and the mature seeds of 26 regenerated plants were harvested. In 2012, all seeds from each plant were sown in the field. The offspring (M-2 generation) of 23 of 26 NaCl-tolerant, regenerated plants differed from their mutagenic parent in vigor, growth habit, flowering habit, pod shape, and seed coat color, and they also exhibited trait segregation from the same NaCl-tolerant, regenerated plant. In a germination test with a 0.7 % NaCl solution and the M-3-generation seeds from 18 of the NaCl-tolerant, regenerated plants, the germination rate was substantially higher for the seeds from 6 plants than for seeds from the mutagenic parent (Huayu 22). To determine whether the changes in plant traits might be associated with gene mutations, DNA polymorphisms between the mutagenic parent and 19 M-3 generation individuals from different NaCl-tolerant, regenerated plants were analyzed with 39 pairs of SSR primers, and all mutants differed from the mutagenic parent in > 2 loci. The results indicate that the use of PYM-based mutagenesis in combination with directed in vitro screening with NaCl is effective for creating and identifying salt-tolerant mutants of peanut.

  • 相关文献

[1]Transcriptome profiling of peanut gynophores revealed global reprogramming of gene expression during early pod development in darkness. Xia, Han,Zhao, Chuanzhi,Hou, Lei,Li, Aiqin,Zhao, Shuzhen,Bi, Yuping,An, Jing,Wan, Shubo,Wang, Xingjun,Bi, Yuping,Wan, Shubo,Wang, Xingjun,Bi, Yuping,An, Jing,Zhao, Yanxiu,Wang, Xingjun. 2013

[2]High efficiency in vitro plant regeneration from epicotyl explants of Chinese peanut cultivars. Shan, Lei,Tang, Guiying,Xu, Pingli,Liu, Zhanji,Bi, Yuping,Shan, Lei,Tang, Guiying,Xu, Pingli,Liu, Zhanji,Bi, Yuping,Shan, Lei,Tang, Guiying,Xu, Pingli,Liu, Zhanji,Bi, Yuping.

[3]Isolation and characterization of a stress responsive small GTP-binding protein AhRabG3b in peanut (Arachis hypogaea L.). Yu, Shan-Lin,Sui, Jiong-Ming,Li, Rui,Fan, Qian-Cheng,Zheng, Chun-Hua,Wang, Jing-Shan,Qiao, Li-Xian,Song, Lin. 2013

[4]Modified AnM technique in combination with black and transparent film mulching in peanut production. Qin, Feifei,Takano, Tetsuo,Qin, Feifei,Xu, Hui-lian,Qin, Feifei. 2012

[5]Peanut violaxanthin de-epoxidase alleviates the sensitivity of PSII photoinhibition to heat and high irradiance stress in transgenic tobacco. Yang, Sha,Meng, De-Yun,Hou, Lin-Lin,Li, Yan,Guo, Feng,Meng, Jing-Jing,Li, Xin-Guo,Wan, Shu-Bo,Meng, De-Yun,Hou, Lin-Lin.

[6]Generation of peanut mutants by fast neutron irradiation combined with in vitro culture. Wang, Jing-Shan,Sui, Jiong-Ming,Qiao, Li-Xian,Xie, Yong-Dun,Guo, Hui-Jun,Liu, Lu-Xiang,Zhao, Li-Lan,Yu, Shan-Lin. 2015

作者其他论文 更多>>