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利用愈伤组织作为外植体的杂交杨 84K(×)高效 -介导转化方法。

An Efficient -Mediated Transformation Method for Hybrid Poplar 84K ( × ) Using Calli as Explants.

机构信息

State Key Laboratory of Tree Genetics and Breeding, Key Laboratory of Tree Breeding and Cultivation of the State Forestry Administration, Research Institute of Forestry, Chinese Academy of Forestry, Beijing 100091, China.

College of Forestry, Inner Mongolia Agricultural University, Hohhot 010019, China.

出版信息

Int J Mol Sci. 2022 Feb 17;23(4):2216. doi: 10.3390/ijms23042216.

Abstract

A highly efficient -mediated transformation method is needed for the molecular study of model tree species such as hybrid poplar 84K ( × cv. '84K'). In this study, we report a callus-based transformation method that exhibits high efficiency and reproducibility. The optimized callus induction medium (CIM1) induced the development of calli from leaves with high efficiency, and multiple shoots were induced from calli growing on the optimized shoot induction medium (SIM1). Factors affecting the transformation frequency of calli were optimized as follows: concentration sets at an OD of 0.6, infective suspension with an acetosyringone (AS) concentration of 100 µM, infection time of 15 min, cocultivation duration of 2 days and precultivation duration of 6 days. Using this method, transgenic plants are obtained within approximately 2 months with a transformation frequency greater than 50%. Polymerase chain reaction (PCR), reverse transcription-PCR (RT-PCR) and β-galactosidase (GUS) histochemical staining analyses confirmed the successful generation of stable transformants. Additionally, the calli from leaves were subcultured and used to obtain new explants; the high transformation efficiency was still maintained in subcultured calli after 6 cycles. This method provides a reference for developing effective transformation protocols for other poplar species.

摘要

需要一种高效的介导转化方法来进行模式树种(如杂种杨 84K(× cv. '84K'))的分子研究。在这项研究中,我们报告了一种基于愈伤组织的转化方法,该方法具有高效性和可重复性。优化的愈伤组织诱导培养基(CIM1)能高效诱导叶片产生愈伤组织,且在优化的芽诱导培养基(SIM1)上生长的愈伤组织可诱导出多个芽。优化了影响愈伤组织转化频率的因素,结果如下:OD 值为 0.6 的 浓度设置、100 μM 乙酰丁香酮(AS)的浸染悬浮液、15 分钟的浸染时间、2 天的共培养时间和 6 天的预培养时间。使用该方法,可在大约 2 个月内获得转化频率大于 50%的转基因植物。聚合酶链反应(PCR)、反转录-PCR(RT-PCR)和β-半乳糖苷酶(GUS)组织化学染色分析证实了稳定转化体的成功生成。此外,叶片来源的愈伤组织可以进行继代培养并获得新的外植体;继代培养的愈伤组织在 6 个循环后仍保持较高的转化效率。该方法为其他杨树物种开发有效的转化方案提供了参考。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/576b/8879841/a4320129756e/ijms-23-02216-g001.jpg

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