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一种新型的无固体培养基的大豆(大豆属(L)梅里尔)植株内转化方法。

A Novel Solid Media-Free In-Planta Soybean (. (L) Merr.) Transformation Approach.

作者信息

Khan Muhammad Waqar, Shaheen Aaqib, Zhang Xuebin, Dewir Yaser Hassan, Mendler-Drienyovszki Nóra

机构信息

State Key Laboratory of Crop Stress Adaptation and Improvement, Henan Joint International Laboratory for Crop Multi-Omics Research, School of Life Sciences, Henan University, Jinming Road, Kaifeng 475004, China.

State Key Laboratory of Crop Stress Adaptation and Improvement, College of Agriculture, Henan University, Kaifeng 475004, China.

出版信息

Life (Basel). 2024 Nov 1;14(11):1412. doi: 10.3390/life14111412.

Abstract

Soybean's lengthy protocols for transgenic plant production are a bottleneck in the transgenic breeding of this crop. Explants cultured on a medium for an extended duration exhibit unanticipated modifications. Stress-induced somaclonal variations and in vitro contaminations also cause substantial losses of transgenic plants. This effect could potentially be mitigated by direct shoot regeneration without solid media or in-planta transformation. The current study focused primarily on developing a rapid and effective media-free in-planta transformation technique for three soybean genotypes (Wm82) and our newly developed two hybrids, designated as ZX-16 and ZX-3. The whole procedure for a transgenic plant takes the same time as a stable grown seedling. Multiple axillary shoots were regenerated on stable-grown soybean seedlings without the ectopic expression of developmental regulatory genes. An approximate amount of 200 µL medium with a growth regulator was employed for shoot organogenesis and growth. The maximal shoot regeneration percentages in the Wm82 and ZX-3 genotypes were 87.1% and 84.5%, respectively. The stable transformation ranged from 3% to 8.0%, with an average of 5.5%. This approach seems to be the opposite of the hairy root transformation method, which allowed transgenic shoots to be regenerated on normal roots. Further improvement regarding an increase in the transformation efficiency and of this technique for a broad range of soybean genotypes and other dicot species would be extremely beneficial in achieving increased stable transformation.

摘要

大豆转基因植株生产的冗长流程是该作物转基因育种的一个瓶颈。在培养基上培养较长时间的外植体会出现意外的变异。胁迫诱导的体细胞克隆变异和体外污染也会导致转基因植株大量损失。通过无固体培养基的直接芽再生或体内转化,有可能减轻这种影响。当前的研究主要集中于为三种大豆基因型(Wm82)以及我们新培育的两个杂交品种ZX - 16和ZX - 3开发一种快速有效的无培养基体内转化技术。转基因植株的整个过程所需时间与稳定生长的幼苗相同。在稳定生长的大豆幼苗上再生出多个腋芽,且发育调控基因无异位表达。使用约200微升含有生长调节剂的培养基进行芽器官发生和生长。Wm82和ZX - 3基因型的最大芽再生率分别为87.1%和84.5%。稳定转化率在3%至8.0%之间,平均为5.5%。这种方法似乎与毛状根转化方法相反,毛状根转化方法是使转基因芽在正常根上再生。进一步提高转化效率以及将该技术应用于更广泛的大豆基因型和其他双子叶植物物种,对于实现更高的稳定转化率将极为有益。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4a49/11595655/808860ed7382/life-14-01412-g001.jpg

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