Transgene-free genome editing in potato, a clonally propagated crop - strategies and future prospects.

IF 3.6 3区 生物学 Q1 PLANT SCIENCES
Neha Sharma, Kanika Thakur, Rasna Zinta, Ishani Shaunak, Sudha Batta, Ankush Saini, Rutika Sehgal, Suhani Bhagta, Brajesh Singh, Ajay Kumar Thakur
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引用次数: 0

Abstract

Clustered regularly interspaced short palindromic repeats (CRISPR)-associated protein (Cas)-based genome editing technology has come out as very precise and effective tool for targeted modification in the gene of interest and offers unprecedented potentials in crop improvement. However, in the present regulatory framework for commercialization of genome edited crops, in many countries including India, the edited lines must be transgene-free. In India, only site directed nuclease (SDN) I and SDN II category of genome edited events which are transgene-free are permitted for commercialization. Potato is a vegetatively propagated crop, having autotetraploid genome and is highly heterozygous in nature. Removal of the transgene from potato genome of edited lines through genetic segregation, either by crossing or selfing, is not the appropriate method as the elite background of the genome gets disturbed due to heterozygous nature of the crop. Every individual seed of potato, i.e. true potato seed (TPS) behaves like a different individual than the parental line and is unable to maintain the genetic identity. In this review article, we have discussed several strategies that can be enacted for generation of transgene-free genome edited lines in potato. This article will provide deeper insight and enhance understandings about the optimum use of CRISPR as non-GMO technology in the genetic enhancement of potato and to adopt the best strategies in editing this important tuberous, clonally propagated crop.

无性系繁殖作物马铃薯的无转基因基因组编辑策略及未来展望。
基于聚类规则间隔短回文重复序列(CRISPR)相关蛋白(Cas)的基因组编辑技术已经成为对目标基因进行靶向修饰的非常精确和有效的工具,并在作物改良方面提供了前所未有的潜力。然而,在目前基因组编辑作物商业化的监管框架中,在包括印度在内的许多国家,编辑的品系必须是无转基因的。在印度,只有位点定向核酸酶(SDN) I和SDN II类基因组编辑事件不含转基因,才允许商业化。马铃薯是一种无性繁殖作物,具有同源四倍体基因组,本质上是高度杂合的。通过遗传分离,无论是通过杂交还是自交,从马铃薯编辑系基因组中去除转基因都不是合适的方法,因为由于作物的杂合性,基因组的精英背景受到干扰。马铃薯的每一粒种子,即真正的马铃薯种子(TPS)表现得与亲本系不同,无法保持遗传同一性。在这篇综述文章中,我们讨论了几种可以制定的策略,以产生无转基因的马铃薯基因组编辑系。本文将对CRISPR作为非转基因技术在马铃薯遗传增强中的最佳应用提供更深入的见解和理解,并在编辑这种重要的块茎无性繁殖作物时采用最佳策略。
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来源期刊
CiteScore
7.10
自引率
0.00%
发文量
126
期刊介绍: Founded in 1995, Physiology and Molecular Biology of Plants (PMBP) is a peer reviewed monthly journal co-published by Springer Nature. It contains research and review articles, short communications, commentaries, book reviews etc., in all areas of functional plant biology including, but not limited to plant physiology, biochemistry, molecular genetics, molecular pathology, biophysics, cell and molecular biology, genetics, genomics and bioinformatics. Its integrated and interdisciplinary approach reflects the global growth trajectories in functional plant biology, attracting authors/editors/reviewers from over 98 countries.
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