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Acta Agron Sin ›› 2011, Vol. 37 ›› Issue (10): 1897-1903.doi: 10.3724/SP.J.1006.2011.01897

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Utilization of Tissue Specific Expressing Promoter RSS1P in TiERF1 Transgenic Wheat

1中国农业科学院作物科学研究所 / 农作物基因资源与基因改良国家重大科学工程 / 农业部作物遗传育种重点实验室,北京 100081; 2山东农业大学农学院,山东泰安 2701082; 3江苏省农业科学院,江苏南京 210014   

  1. 1 National Key Facility for Crop Gene Resources and Genetic Improvement / Key Laboratory of Crop Genetic and Breeding, Ministry of Agriculture / Institute of Crop Sciences, Chinese Academy of Agricultural Sciences, Beijing 100081, China; 2 College of Agronomy, Shandong Agricultural University, Tai’an 271018, China; 3 Jiangsu Academy of Agricultural Sciences, Nanjing 210014, China
  • Received:2010-11-05 Revised:2011-06-25 Online:2011-10-12 Published:2011-07-28
  • Contact: 张增艳, E-mail: zhangzy@mail.caas.net.cn, Tel: 010-82108781; 李斯深, E-mail: ssli@sdau.edu.cn E-mail:lizhao0504@163.com

Abstract: A sucrose synthase-1 promoter (RSS1P) was cloned from rice leaf, and subcloned in-fused with 5′-terminate of the gene of ethylene responsive factor of Thinopyrum intermedium (TiERF1) to form the RSS1P::TiERF1 expressing cassette. The expressing cassette replaced the Ubi::bar gene expression cassette of pAHC20 to produce the phloem-specific expressing vector pA20-RSS1P::TiERF1. The selective mark bar was deleted in the pA20-RSS1P::TiERF1 vector, which is safe for the ecosystem. Using the method of bombardment, the vector DNAs of pA20-RSS1P::TiERF1 andpAHC20 with bar gene were co-transformed to young embryo callus of wheat cultivar Yangmai 12. The RSS1P::TiERF1 transgenic plants in T0 and T1 generations were subjected to PCR, PCR-Southern, RT-PCR, and Q-RT-PCR analyses, and Rhizoctonia cerealis resistance tests. The molecular detection results showed that the transgene RSS1P::TiERF1 was introduced into Yangmai 12 and was inheritable. In the RSS1P::TiERF1 transgenic wheat plants, expression of TiERF1 was detected in root, stem, and leaf except seed. The highest expression level was observed in root. Compared to the untransformated Yangmai 12, resistance to R. cerealis in the RSS1P::TiERF1 transgenic wheat plants was obviously improved, which was similar to that in the Ubi::TiERF1 transgenic wheat plants. The agronomic traits of RSS1P::TiERF1 transgenic plants had no obvious changes compared to untransformated Yangmai 12. These results suggest that RSS1P promoter is feasible to be used for developing new transgenic wheat germplasm.

Key words: Rice sucrose synthase-1 promoter, Phloem-specific expression, Transgenic wheat, Ethylene responsive factor of Thinopyrum intermedium

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