Ramasamy Manikandan, Mora Victoria, Damaj Mona B, Padilla Carmen S, Ramos Ninfa, Rossi Denise, Solís-Gracia Nora, Vargas-Bautista Carol, Irigoyen Sonia, DaSilva Jorge A, Mirkov T Erik, Mandadi Kranthi K
a Texas A&M AgriLife Research & Extension Center , Weslaco , TX , USA.
b Department of Soil & Crop Sciences , Texas A&M University , TX , USA.
GM Crops Food. 2018;9(4):211-227. doi: 10.1080/21645698.2018.1553836. Epub 2018 Dec 17.
Sugarcane and energycane ( spp. hybrids) are prominent sources of sugar, ethanol, as well as high-value bioproducts globally. Genetic analysis for trait improvement of sugarcane is greatly hindered by its complex genome, limited germplasm resources, long breeding cycle, as well as recalcitrance to genetic transformation. Here, we present a biolistic-based transformation and bioreactor-based micro-propagation system that has been utilized successfully to transform twelve elite cane genotypes, yielding transformation efficiencies of up to 39%. The system relies on the generation of embryogenic callus from sugarcane and energycane apical shoot tissue, followed by DNA bombardment of embryogenic leaf roll discs (approximately one week) or calli (approximately 4 weeks). We present optimal criteria and practices for selection and regeneration of independent transgenic lines, molecular characterization, as well as a bioreactor-based micro-propagation technique, which can aid in rapid multiplication and analysis of transgenic lines. The cane transformation and micro-propagation system described here, although built on our previous protocols, has significantly accelerated the process of producing and multiplying transgenic material, and it is applicable to other varieties. The system is highly reproducible and has been successfully used to engineer multiple commercial sugarcane and energycane varieties. It will benefit worldwide researchers interested in genomics and genetics of sugarcane photosynthesis, cell wall, and bioenergy related traits.
甘蔗和能源甘蔗(品种杂交种)是全球糖、乙醇以及高价值生物产品的主要来源。甘蔗复杂的基因组、有限的种质资源、漫长的育种周期以及对遗传转化的难处理性,极大地阻碍了其性状改良的遗传分析。在此,我们展示了一种基于生物弹道法的转化和基于生物反应器的微繁殖系统,该系统已成功用于转化12个优良甘蔗基因型,转化效率高达39%。该系统依赖于从甘蔗和能源甘蔗顶芽组织产生胚性愈伤组织,随后对胚性叶卷圆盘(约一周)或愈伤组织(约4周)进行DNA轰击。我们提出了独立转基因系选择和再生、分子鉴定的最佳标准和做法,以及一种基于生物反应器的微繁殖技术,该技术有助于转基因系的快速繁殖和分析。这里描述的甘蔗转化和微繁殖系统,虽然基于我们之前的方案构建,但显著加速了转基因材料的生产和繁殖过程,并且适用于其他品种。该系统具有高度可重复性,已成功用于培育多个商业甘蔗和能源甘蔗品种。它将惠及全球对甘蔗光合作用、细胞壁以及生物能源相关性状的基因组学和遗传学感兴趣的研究人员。