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Engineered minichromosomes in plants

机译:植物工程微染色体

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Engineered minichromosomes have been produced in several plant species via telomere-mediated chromosomal truncation. This approach bypasses the complications of the epigenetic nature of centromere function in plants, which has to date precluded the production of minichromosomes by the re-introduction of centromere sequences to a plant cell. Genes to be added to a cleaved chromosome are joined together with telomere repeats on one side. When these constructs are introduced into plant cells, the genes are ligated to the broken chromosomes but the telomere repeats will catalyze the formation of a telomere on the other end cutting the chromosome at that point. Telomere-mediated chromosomal truncation is sufficiently efficient that very small chromosomes can be generated consisting of basically the endogenous centromere and the added transgenes. The added transgenes provide a platform onto which it should be possible to assemble a synthetic chromosome to specification. Combining engineered minichromosomes with doubled haploid breeding should greatly expedite the transfer of transgenes to new lines and to test the interaction of transgenes in new background genotypes. Potential basic and applied applications of synthetic chromosomes are discussed.
机译:通过端粒介导的染色体截短,已在几种植物中产生了工程化的微染色体。这种方法绕过了植物着丝粒功能的表观遗传特性的复杂性,迄今为止,该方法已无法通过将着丝粒序列重新引入植物细胞中来产生微型染色体。将要添加到裂解染色体的基因在一侧与端粒重复序列连接在一起。当将这些构建体引入植物细胞后,基因被连接到断裂的染色体上,但是端粒的重复将催化端粒在另一端切割染色体时形成。端粒介导的染色体截短足够有效,可以产生非常小的染色体,基本上由内源着丝粒和添加的转基因组成。添加的转基因提供了一个平台,可以在该平台上组装符合规格的合成染色体。将工程化的微型染色体与单倍体繁殖加倍结合,可以极大地加快转基因向新品系的转移,并测试新背景基因型中转基因的相互作用。讨论了合成染色体的潜在基础和应用前景。

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