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利用成熟种子的胚轴,通过根癌农杆菌介导的基因转移实现蓖麻(Ricinus communis L.)的稳定遗传转化。

Stable genetic transformation of castor (Ricinus communis L.) via Agrobacterium tumefaciens-mediated gene transfer using embryo axes from mature seeds.

作者信息

Sujatha M, Sailaja M

机构信息

Crop Improvement Section, Directorate of Oilseeds Research, Rajendranagar, Hyderabad, 500030, India.

出版信息

Plant Cell Rep. 2005 Mar;23(12):803-10. doi: 10.1007/s00299-004-0898-4. Epub 2004 Dec 3.

Abstract

A protocol for the transformation of castor embryo axes using the pCAMBIA vector 1304 in disarmed Agrobacterium tumefaciens strain EHA105 is presented. Co-cultivated explants were initially subjected to expansion and proliferation on MS medium with 0.5 mg l(-1) TDZ followed by three cycles of selection on medium with 0.5 mg l(-1) BA and increasing concentrations of hygromycin (20-40-60 mg l(-1)). Selected shoot clusters were transferred to medium with 0.5 mg l(-1) BA for proliferation and 0.2 mg l(-1) BA for shoot elongation. Elongated shoots were rooted on half-strength MS medium with 2.0 mg l(-1) NAA. The presence and stable integration of the hpt gene was confirmed through PCR, RT-PCR, PCR-Southern blot, sequence analysis, Southern blot analysis and PCR analysis of progeny. Southern blot analysis of the primary transformants showed single copy integration and progeny analysis revealed monogenic inheritance of the introduced gene. This paper reports the first successful attempt at producing transgenic castor.

摘要

本文介绍了一种利用携带pCAMBIA载体1304的无致病力根癌农杆菌EHA105菌株转化蓖麻胚轴的方法。共培养的外植体最初在含有0.5 mg l(-1)噻二唑素(TDZ)的MS培养基上进行扩增和增殖,随后在含有0.5 mg l(-1)苄氨基嘌呤(BA)和逐渐增加浓度潮霉素(20 - 40 - 60 mg l(-1))的培养基上进行三轮筛选。筛选出的芽簇转移到含有0.5 mg l(-1) BA的培养基上进行增殖,在含有0.2 mg l(-1) BA的培养基上进行芽伸长。伸长的芽在含有2.0 mg l(-1)萘乙酸(NAA)的1/2强度MS培养基上生根。通过PCR、RT-PCR、PCR- Southern杂交、序列分析、Southern杂交分析以及后代的PCR分析,证实了潮霉素磷酸转移酶(hpt)基因的存在及其稳定整合。对初级转化体的Southern杂交分析显示单拷贝整合,后代分析揭示了导入基因的单基因遗传。本文报道了首次成功培育转基因蓖麻的尝试。

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