期刊文献+

T-DNA插入水稻群体中卷叶突变体R1-A2的遗传分析 被引量:15

GENETIC ANALYSIS OF A ROLLED-LEAF MUTANT IN RICE POPULATION OF T-DNA INSERTION
下载PDF
导出
摘要 在根癌农杆菌介导的T-DNA(携带有除草剂Basta抗性基因bar和Ds因子)转化中花11水稻群体中,获得了一个叶片发生明显内卷的突变体R1-A。经过连续三代的分离鉴定,获得突变体的纯合株(R1-A2),并与中花11号进行杂交,在调查的36个F_1植株中,全部表现为卷叶,并对Basta除草剂都表现为抗性。在852个F_2单株中,卷叶为645株,正常叶207株,卷叶和正常叶的比例为3:1,其中,卷叶株均对Basta表现抗性,正常叶株均对Basta表现敏感,表明卷叶性状和Basta抗性存在着共分离关系。用扩增Ds因子的引物,对F_2中45个卷叶抗性株进行PCR鉴定,都获得预期长度的Ds因子片段,进一步表明在这些卷叶的植株中都有T-DNA的插入;而30个正常叶敏感株都不能检测到Ds的特征片段。在以卷叶突变(R1-A2)为回交亲本的F_1B_1植株中,全部植株表现卷叶;在以中花11号为回交亲本的F_1B_1植株中,卷叶和正常叶植株的分离比为1:1。上述结果表明该卷叶突变是个显性突变,受一个基因所控制,且该基因的突变与T-DNA的插入有关。 A rolled-leaf mutant was obtained in a T-DNA( containing bar gene and Ds element) insertion population, which consist of transgenic japonica rice Zhonghua 11 mediated by Agrobacterium tumefaciens. Through self-hybridization of three generations, one of trait-purified mutants(R1-A2) was obtained and used as parent to cross with variety Zhonghua 11. The leaves of 36 FI plants investigated were rolled and resistent to herbicide Basta. Among 852 p2 plants, the segregation ratio of rolled leaves to normal leaves(645:207) was consistent with 3:1. All rolled-leaf plants were resistent to herbicide Basta, and all normal leaf plants were sensitive to herbicide Basta. These results showed that the trait of rolled-leaf is co-segregated with Basta resistance. The total DNA of 45 rolled-leaf plants and 30 normal leaf plants in F2 population were amplified to test the presence of T-DNA by Ds primers. The results showed that the positive band were amplified in all rolled-leaf plants, but not in every normal leaf plant. In F1B1 progenies, all plants which derived from backcross parent R1-A2 were rolled leaves; while variety Zhonghua 11 was used as backcross parent, the segregation ratio of rolled-leaf to normal leaf was consistent with 1:1. Taking these data together, it indicated that the rolled-leaf mutant was co-segregation with T-DNA and controlled by single dominant gene.
出处 《实验生物学报》 CSCD 北大核心 2003年第6期459-464,共6页 Acta Biologiae Experimentalis Sinica
基金 国家科技部863(2001AA222221) 国家重点基础研究发展规划项目(G1999011601)的资助
关键词 T-DNA插入 水稻 群体 卷叶突变体 R1-A2 遗传 Rice( Oryza stativa L.). T-DNA insetion. Rolled-leaf mutant
  • 相关文献

参考文献19

  • 1Walbot, V., 1992, Strategies for mutagenesis and gene cloning using trartsposon tagging and T-DNA insertional mutagenesis. Plant Mol. Biol., 43:49 - 82.
  • 2张景六.转座因子标签法[J].植物生理学通讯,1993,29(6):467-470. 被引量:9
  • 3Aarts, M. G., P. Corzaan, W. J. Stiekema and A.Pereira, 1993, Transposon tagging of a male sterility gene in Arabidopsis. Nature, 363: 715-717.
  • 4Bancroft, I., J. D. G Jones and C. Dean, 1993, Heterologous transposon tagging of the DRL1 locus in Arabidopsis . Plant Cell, 5: 631-638.
  • 5Long, D., M. Martin, E. Sundberg, J. Swinburne, P.Puangsomlee and G. Coupland, 1993, The maize transposable element system Ac/Ds as a mutagen in Arabidopsis : identification of an albino mutation induced by Ds insertion. Proc. Natl. Acad. Sci. USA, 90:10370 -10374.
  • 6James, D.W., E. Lim, J. Keller, I. Plooy, E. Ralston and H. K. Dooner, 1995, Directed tagging of the Arabidopsis fattyasid elongation 1 (FAE1) gene with themaize transposon Activator. Plant Cell, 7:309 - 319.
  • 7Sagasser, M., G.H. Lu, K. Hahlbrock and B. Weisshaar, 2002, A. thaliana TRANSPARENT TESTA 1 is involved in seed coat development and defines the WIP subfamily of plant zinc finger proteins. Genes Dev., 16:138- 149.
  • 8Chuck, G., T. Robbins, C. Nijjar, E. Ralston, N.Courtney-Gutterson and H. K. Dooner, 1993, Tagging and cloning of a petunia flower colour gene with the maize transposable element Activator. Plant Cell, 5:371 -378.
  • 9Whitham, S., S. P. Dinesh-Kumar, D. Choi, R.Hehl, C. Corr and B. Baker, 1994, The product of the tobacco mosaic virus resistance gene N: similarity to Tolland the Interleukin-1 receptor. Cell, 78:1101 - 1115.
  • 10Jones, D. A., C. M. Thomas, K. E. Hammond-Kosack, P. J. Balint-Kurti and D.G. Jones, 1994, Isolation of the tomato Cf-9 gene for resistance to Cladosporium fuluvm by transposon tagging. Science, 266 : 789 -793.

二级参考文献44

共引文献141

同被引文献195

引证文献15

二级引证文献92

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部