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1
Morphogenic Regulators and Improve Monocot Transformation.形态发生调控因子与改善单子叶植物转化
Plant Cell. 2016 Sep;28(9):1998-2015. doi: 10.1105/tpc.16.00124. Epub 2016 Sep 6.
2
Generation of transgenic energy cane plants with integration of minimal transgene expression cassette.整合最小转基因表达盒的转基因能源甘蔗植株的生成
Curr Pharm Biotechnol. 2015;16(5):407-13.
3
Effects of tissue type and promoter strength on transient GUS expression in sugarcane following particle bombardment.组织类型和启动子强度对粒子轰击后甘蔗瞬时 GUS 表达的影响。
Plant Cell Rep. 1993 Oct;12(12):666-70. doi: 10.1007/BF00233416.
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Enhanced transgene expression in sugarcane by co-expression of virus-encoded RNA silencing suppressors.通过共表达病毒编码的 RNA 沉默抑制子提高甘蔗中的转基因表达。
PLoS One. 2013 Jun 14;8(6):e66046. doi: 10.1371/journal.pone.0066046. Print 2013.
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Recovery of bovine lysozyme from transgenic sugarcane stalks: extraction, membrane filtration, and purification.从转基因甘蔗茎中回收牛溶菌酶:提取、膜过滤和纯化。
Bioprocess Biosyst Eng. 2013 Oct;36(10):1407-16. doi: 10.1007/s00449-012-0878-y. Epub 2013 Jan 18.
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High-throughput assessment of transgene copy number in sugarcane using real-time quantitative PCR.利用实时定量 PCR 对甘蔗中转基因拷贝数进行高通量评估。
Plant Cell Rep. 2012 Jan;31(1):167-77. doi: 10.1007/s00299-011-1150-7. Epub 2011 Sep 28.
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Unprecedented enhancement of transient gene expression from minimal cassettes using a double terminator.使用双终止子实现最小启动子盒中转录瞬时基因表达的空前增强。
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Sugarcane DIRIGENT and O-methyltransferase promoters confer stem-regulated gene expression in diverse monocots.甘蔗 DIR 蛋白和 O-甲基转移酶启动子在多种单子叶植物中赋予茎调控的基因表达。
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The P0 gene of Sugarcane yellow leaf virus encodes an RNA silencing suppressor with unique activities.甘蔗黄叶病毒的P0基因编码一种具有独特活性的RNA沉默抑制因子。
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一种基于生物弹道技术的遗传转化系统,适用于多种甘蔗和能源甘蔗品种。

A biolistic-based genetic transformation system applicable to a broad-range of sugarcane and energycane varieties.

作者信息

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

机构信息

a Texas A&M AgriLife Research & Extension Center , Weslaco , TX , USA.

b Department of Soil & Crop Sciences , Texas A&M University , TX , USA.

出版信息

GM Crops Food. 2018;9(4):211-227. doi: 10.1080/21645698.2018.1553836. Epub 2018 Dec 17.

DOI:10.1080/21645698.2018.1553836
PMID:30558472
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6343536/
Abstract

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.

摘要

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。