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OsPIN1a基因在水稻根负向光性中的作用初探 被引量:6

Preliminary Study on Function of OsPIN1a Gene in Negative Phototropism of Rice Roots
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摘要 为了探讨水稻生长素输出载体蛋白OsPIN1a与根负向光性的关系,根据GenBank数据库报道的OsPIN1a核苷酸序列,利用RT-PCR技术,设计特异引物从水稻cDNA中扩增得到生长素输出蛋白基因(OsPIN1a)。测序结果表明,OsPIN1a基因序列中GC含量达65.49%。构建该基因的GFP融合表达载体pCAMBIA-1301-OsPIN1a::GFP,对洋葱表皮细胞的瞬时表达分析表明,融合蛋白主要分布在细胞膜和细胞核内。以农杆菌介导法转化水稻中花11,PCR和GUS染色检测结果表明,目的基因片段已经整合到水稻基因组内;在单侧光照射下,转基因水稻种子根的负向光弯曲角度比野生型大约14.0%,转基因植株中OsPIN1a的表达水平也显著高于野生型植株,说明OsPIN1a可能在水稻根的负向光性反应中起重要作用。 To explore the relationship between auxin efflux protein OsPfNla and negative phototropism of rice roots, the complete open reading frame (ORF) of OsPINla was amplified based on the sequence deposited in GenBank by RT-PCR with gene-specific primers. Sequencing results show that the GC content of OsP1Nla ORF is 65.49 %. The fusion expression vector pCAMBIA-1301-OsPINla : :GFP containing OsPINla and a coding green fluorescent protein (gfp) gene was constructed and transferred into onion skin cells by the Agrobacterium turnefaciens transformation. Transient expression of the OsPINla-GFP protein showed that the protein was mainly located on the nucleus and cell membrane. Genetic transformation of japonica rice variety Zhonghua 11 was mediated by Agrobacterium tumefaciens. Molecular detection of transformed rice plants by PCR and GUS staining showed that the target construct was integrated into the genome of rice. The negative phototropism curvature of the transformed rice root were higher than that of the wild type as well as the expression level of OsPINla in transformed plants, indicating that OsPINla probably played an important role in negative phototropism curvature of rice root.
出处 《中国水稻科学》 CAS CSCD 北大核心 2013年第5期466-472,共7页 Chinese Journal of Rice Science
基金 国家自然科学基金资助项目(31071353 31100197) 绍兴文理学院科研启动费(20135004)
关键词 水稻 OsPIN1a 绿色荧光蛋白 瞬时表达 负向光性 rice OsPIN1a green fluorescent protein (GFP) transient expression negative phototropism
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  • 1王忠,顾蕴洁,莫亿伟,钱善勤.Negative phototropism of rice root and its influencing factors[J].Science China(Life Sciences),2002,45(5):485-496. 被引量:26
  • 2MoYi-wei WANGZhong QIANShan-qin GuYun-jie.Effect of Indoleacetic acid (IAA) on the Negative Phototropism of Rice Root[J].Rice science,2004,11(3):125-128. 被引量:10
  • 3Bao, F., Shen, J., Brady, S.R., Muday, G.K., Asami, T., and Yang, Z. (2004). Brassinosteroids interact with auxin to promote lateral root development in Arabidopsis. Plant Physiol. 134, 1624-1631. 被引量:1
  • 4Benkova, E., Michniewicz, M., Sauer, M., Teichmann, T., Seifertova, D., Jurgens, G., and Friml, J. (2003). Local, effluxdependent auxin gradients as a common module for plant organ formation. Cell. 115, 591-602. 被引量:1
  • 5Blilou, I., Xu, J., Wildwater, M., Willemsen, V., Paponov, I., Friml, J., Heidstra, R., Aida, M., Palme, K., and Scheres, B. (2005). The PIN auxin efflux facilitator network controls growth and patterning in Arabidopsis roots. Nature. 433, 39-44. 被引量:1
  • 6Carraro, N., Forestan, C., Canova, S., Traas, J., and Varotto, S. (2006). ZmPINla and ZmPINlb encode two novel putative candidates for polar auxin transport and plant architecture determination of maize. Plant Physiol. 142, 254-264. 被引量:1
  • 7Casimiro, I., Beeckman, T., Graham, N., Bhalerao, R., Zhang, H., Casero, R, Sandberg, G., and Bennett, M.J. (2003). Dissecting Arabidopsis lateral root development. Trends Plant Sci. 8, 165-171. 被引量:1
  • 8Chen, S., Jin, W., Wang, M., Zhang, F., Zhou, J., Jia, Q., Wu, Y., Liu, F., and Wu, R (2003). Distribution and characterization of over 1000 T-DNA tags in rice genome. Plant J. 36, 105-113. 被引量:1
  • 9Friml, J., et al. (2002). AtPIN4 mediates sink-driven auxin gradients and root patterning in Arabidopsis. Cell. 108, 661-673. 被引量:1
  • 10Friml, J., Vieten, A., Sauer, M., Weijers, D., Schwarz, H., Hamann, T., Offringa, R., and Jurgens, G. (2003). Efflux-dependent auxin gradients establish the apical-basal axis of Arabidopsis. Nature. 426, 147-153. 被引量:1

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