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MicroTom——一种用于功能基因组学的高通量模型转换系统。

MicroTom--a high-throughput model transformation system for functional genomics.

作者信息

Dan Yinghui, Yan Hua, Munyikwa Tichafa, Dong Jimmy, Zhang Yanling, Armstrong Charles L

机构信息

Monsanto Company, 700 Chesterfield Parkway, Chesterfield, MO 63017, USA.

出版信息

Plant Cell Rep. 2006 May;25(5):432-41. doi: 10.1007/s00299-005-0084-3. Epub 2005 Dec 9.

Abstract

We have developed a high-throughput Agrobacterium-mediated transformation model system using both nptII and the 5-enolpyruvylshikimate-3-phosphate synthase gene from Agrobacterium tumefaciens strain CP4 (cp4) based selections in MicroTom, a miniature rapid-cycling cherry tomato variety. With the NPTII selection system, transformation frequency calculated as independent transgenic events per inoculated explant ranged from 24 to 80% with an average of 56%, in industrial production scale transformation experiments. For CP4, with glyphosate selection, the average transformation frequency was 57%. Stable transformation frequency was positively correlated with transient expression (R=0.85), and variable with the genes of interest. DNA integration and germline transformation were confirmed by biological assay, Southern Blot analysis, and R(1) phenotype segregation. Transgene expression was observed in leaf, root, stem, flower, and fruit tissues of the transgenic plants. Ninety-five percent of transgenic events coexpressed two introduced genes based on beta-glucuronidase (GUS) and neonmycin phosphotransferase II (NPTII) expression. Seventy-five percent of transgenic events contained one to two copies of the introduced uidA (GUS) gene based on Southern analysis. Transgenic plants from the cotyledon explants to the transgenic plants transferred to soil were produced within about 2-3 months depending on the genes of interest. The utility of this MicroTom model transformation system for functional genomic studies, such as identification of genes related to important agricultural traits and gene function, is discussed.

摘要

我们利用来自根癌农杆菌CP4菌株的nptII基因和5-烯醇丙酮酸莽草酸-3-磷酸合酶基因(cp4),基于微型快速循环樱桃番茄品种MicroTom中的筛选,开发了一种高通量农杆菌介导的转化模型系统。在工业生产规模的转化实验中,使用NPTII筛选系统时,以每个接种外植体的独立转基因事件计算的转化频率为24%至80%,平均为56%。对于cp4,使用草甘膦筛选时,平均转化频率为57%。稳定转化频率与瞬时表达呈正相关(R = 0.85),并且因目的基因而异。通过生物学测定、Southern杂交分析和R(1)表型分离证实了DNA整合和种系转化。在转基因植物的叶、根、茎、花和果实组织中观察到了转基因表达。基于β-葡萄糖醛酸酶(GUS)和新霉素磷酸转移酶II(NPTII)的表达,95%的转基因事件共表达了两个导入基因。根据Southern分析,75%的转基因事件含有一至两个拷贝的导入uidA(GUS)基因。从子叶外植体到转移到土壤中的转基因植物,根据目的基因的不同,大约在2至3个月内产生。讨论了这种MicroTom模型转化系统在功能基因组学研究中的实用性,例如鉴定与重要农业性状和基因功能相关的基因。

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