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L. 对由Cry10Aa蛋白表达介导的咖啡果小蠹具有抗性。

L. Resistant to Coffee Berry Borer () Mediated by Expression of the Cry10Aa Protein.

作者信息

Valencia-Lozano Eliana, Cabrera-Ponce Jose Luis, Noa-Carrazana Juan C, Ibarra Jorge E

机构信息

Laboratorio de Bioinsecticidas, Departamento de Biotecnología y Bioquímica, Unidad Irapuato, Centro de Investigación y Estudios Avanzados del Instituto Politécnico Nacional (CINVESTAV), Irapuato, Mexico.

Laboratorio de Transformacion Genetica de Plantas, Departamento de Ingeniería Genética, Unidad Irapuato, Centro de Investigación y Estudios Avanzados del Instituto Politécnico Nacional (CINVESTAV), Irapuato, Mexico.

出版信息

Front Plant Sci. 2021 Oct 22;12:765292. doi: 10.3389/fpls.2021.765292. eCollection 2021.

Abstract

spp. are tropical plants used for brewing beverages from roasted and grounded seeds, the favorite drink in the world. It is the most important commercial crop plant and the second most valuable international commodity after oil. Global coffee trade relies on two species: L. (arabica coffee) comprising 60% and (robusta) comprising the remaining 40%. Arabica coffee has lower productivity and better market price than robusta. Arabica coffee is threatened by disease (i.e., coffee leaf rust), pests [i.e., or coffee berry borer (CBB) and nematodes], and susceptibility to climate change (i.e., drought and aluminum toxicity). Plant biotechnology by means of tissue culture inducing somatic embryogenesis (SE) process, genetic transformation, and genome editing are tools that can help to solve, at least partially, these problems. This work is the continuation of a protocol developed for stable genetic transformation and successful plant regeneration of arabica coffee trees expressing the (Bt) toxin Cry10Aa to induce CBB resistance. A highly SE line with a high rate of cell division and conversion to plants with 8-month plant regeneration period was produced. To validate this capability, gene expression analysis of master regulators of SE, such as BABY BOOM (BBM), FUS3, and LEC1, embryo development, such as EMB2757, and cell cycle progression, such as ETG1 and MCM4, were analyzed during induction and propagation of non-competent and highly competent embryogenic lines. The particle bombardment technique was used to generate stable transgenic lines after 3 months under selection using hygromycin as selectable marker, and 1 month in plant regeneration. Transgenic trees developed fruits after 2 years and demonstrated expression of the Bt toxin ranging from 3.25 to 13.88 μg/g fresh tissue. Bioassays with transgenic fruits on CBB first instar larvae and adults induced mortalities between 85 and 100% after 10 days. In addition, transgenic fruits showed a seed damage lower than 9% compared to 100% of control fruits and adult mortality. This is the first report on stable transformation and expression of the Cry10Aa protein in coffee plants with the potential to control CBB.

摘要

咖啡属植物是热带植物,其烘焙和研磨后的种子用于酿造饮品,是全球最受欢迎的饮品。它是最重要的商业作物,也是仅次于石油的第二大最具价值的国际商品。全球咖啡贸易依赖两种咖啡豆:阿拉比卡咖啡豆(占60%)和罗布斯塔咖啡豆(占40%)。阿拉比卡咖啡豆的产量低于罗布斯塔咖啡豆,但市场价格更高。阿拉比卡咖啡豆受到疾病(如咖啡叶锈病)、害虫(如咖啡果小蠹或咖啡果蛀虫以及线虫)的威胁,并且易受气候变化(如干旱和铝毒性)的影响。通过组织培养诱导体细胞胚胎发生(SE)过程、遗传转化和基因组编辑的植物生物技术是可以至少部分帮助解决这些问题的工具。这项工作是为阿拉比卡咖啡树稳定遗传转化和成功植株再生所开发方案的延续,该方案用于表达苏云金芽孢杆菌(Bt)毒素Cry10Aa以诱导对咖啡果蛀虫的抗性。培育出了一个具有高细胞分裂率且8个月植株再生期就能转化为植株的高体细胞胚胎发生系。为了验证这种能力,在无能力和高能力胚性系的诱导和增殖过程中,分析了体细胞胚胎发生的主要调节因子(如婴儿潮蛋白(BBM)、FUS3和LEC1)、胚胎发育(如EMB2757)以及细胞周期进程(如ETG1和MCM4)的基因表达。使用颗粒轰击技术,以潮霉素作为选择标记,在选择3个月后以及植株再生1个月后,生成了稳定的转基因系。转基因树在2年后结出果实,Bt毒素的表达量在每克鲜组织3.25至13.88微克之间。用转基因果实对咖啡果蛀虫一龄幼虫和成虫进行的生物测定显示,10天后死亡率在85%至100%之间。此外与100%的对照果实相比,转基因果实的种子损伤率低于9%,且成虫死亡率也较低。这是关于咖啡植株中Cry10Aa蛋白稳定转化和表达以及具有控制咖啡果蛀虫潜力的首次报道。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b873/8569674/bd88ed8061ee/fpls-12-765292-g0001.jpg

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