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用一种类似Gnk2的蛋白质对体细胞胚进行遗传转化,该蛋白质显示出一种假定的抗卵菌作用。

Genetic Transformation of Somatic Embryos with a Gnk2-like Protein That Reveals a Putative Anti-Oomycete Action.

作者信息

Serrazina Susana, Martínez Mª Teresa, Cano Vanesa, Malhó Rui, Costa Rita Lourenço, Corredoira Elena

机构信息

Faculdade de Ciências, BioISI-Biosystems & Integrative Sciences Institute, Universidade de Lisboa, 1749-016 Lisbon, Portugal.

Misión Biológica de Galicia, Consejo Superior de Investigaciones Científicas (MBG-CSIC), Avda Vigo s/n, Campus Vida, Apartado 122, 15705 Santiago de Compostela, Spain.

出版信息

Plants (Basel). 2022 Jan 24;11(3):304. doi: 10.3390/plants11030304.

Abstract

Holm oak is a key tree species in Mediterranean ecosystems, whose populations have been increasingly threatened by oak decline syndrome, a disease caused by the combined action of and abiotic stresses. The aim of the present study was to produce holm oak plants that overexpress the Ginkbilobin-2 homologous domain gene () that it is known to possess antifungal properties. Proembryogenic masses (PEMs) isolated from four embryogenic lines (Q8, E2, Q10-16 and E00) were used as target explants. PEMs were co-cultured for 5 days with EHA105pGnk2 and then cultured on selective medium containing kanamycin (kan) and carbenicillin. After 14 weeks on selective medium, the transformation events were observed in somatic embryos of lines Q8 and E2 and a total of 4 transgenic lines were achieved. The presence of the gene on transgenic embryos was verified by PCR, and the number of transgene copies and gene expression was estimated by qPCR. Transgenic plants were obtained from all transgenic lines after cold storage of the somatic embryos for 2 months and subsequent transfer to germination medium. In an in vitro tolerance assay with the pathogen , we observed that transgenic plants were able to survive longer than wild type.

摘要

冬青栎是地中海生态系统中的关键树种,其种群受到栎树衰退综合征的威胁日益增加,该疾病是由生物和非生物胁迫共同作用引起的。本研究的目的是培育过量表达银杏双黄酮 - 2同源结构域基因(已知具有抗真菌特性)的冬青栎植株。从四个胚性系(Q8、E2、Q10 - 16和E00)分离得到的原胚性细胞团(PEMs)用作目标外植体。PEMs与EHA105pGnk2共培养5天,然后在含有卡那霉素(kan)和羧苄青霉素的选择培养基上培养。在选择培养基上培养14周后,在Q8和E2系的体细胞胚中观察到转化事件,共获得4个转基因株系。通过PCR验证转基因胚上基因的存在,并通过qPCR估计转基因拷贝数和基因表达。将体细胞胚冷藏2个月后转移至萌发培养基,从所有转基因株系中获得了转基因植株。在对病原菌的体外耐受性试验中,我们观察到转基因植株比野生型存活时间更长。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b174/8838351/c9787d921824/plants-11-00304-g001.jpg

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