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一种新型启动子优先赋予甘蔗茎杆维管束和贮藏薄壁组织中的基因表达。

A novel promoter confers gene expression preferentially in the vascular bundle and storage parenchyma of the sugarcane culm.

作者信息

Gao San-Ji, Damaj Mona B, Park Jong-Won, Wu Xiao-Bin, Sun Sheng-Ren, Chen Ru-Kai, Mirkov T Erik

机构信息

National Engineering Research Center for Sugarcane, Fujian Agriculture and Forestry University, Fuzhou, 350002 Fujian China.

Texas A&M AgriLife Research, Weslaco, TX 78596 USA.

出版信息

Biotechnol Biofuels. 2017 Jul 4;10:172. doi: 10.1186/s13068-017-0850-9. eCollection 2017.

Abstract

BACKGROUND

species such as sugarcane and energy cane are key players in the expanding bioeconomy for sugars, bioenergy, and production of high-value proteins. Genomic tools such as culm-regulated promoters would be of great value in terms of improving biomass characteristics through enhanced carbon metabolism for sugar accumulation and/or fiber content for biofuel feedstock. Unlike the situation in dicots, monocot promoters currently used are limited and mostly derived from highly expressed constitutive plant genes and viruses. In this study, a novel promoter region of (SCBV; genus , family ), was cloned and mapped by deletion analysis and functionally characterized transiently in monocot and dicot species and stably in sugarcane.

RESULTS

In silico analysis of [1816 base pair (bp)] identified two putative promoter regions (PPR1 and PPR2) with transcription start sites (TSS1 and TSS2) and two TATA-boxes (TATAAAT and ATATAA), and several vascular-specific and regulatory elements. Deletion analysis revealed that the 710 bp region spanning PPR2 (with TSS2 and ATATAA) at the 3' end of retained the full promoter activity in both dicots and monocots, as shown by transient expression of the () gene. In sugarcane young leaf segments, directed a 1.8- and 2.4-fold higher transient expression than the common maize () and 35S promoters, respectively. In transgenic sugarcane, conferred a preferential expression of the () gene in leaves and culms and specifically in the culm storage parenchyma surrounding the vascular bundle and in vascular phloem cells. Among the transgenic events and tissues characterized in this study, the promoter frequently produced higher GUS activity than the or 35S promoters in a manner that was not obviously correlated with the transgene copy number.

CONCLUSIONS

The newly developed plant viral promoter is distinct from the few existing promoters in its sequence and expression pattern. The potential of as a tissue-regulated promoter with a strong activity in the culm vascular bundle and its storage parenchyma makes it useful in sugarcane engineering for improved carbon metabolism, increased bioenergy production, and enhanced stress tolerance.

摘要

背景

甘蔗和能源甘蔗等物种在不断发展的生物经济中,对于糖类、生物能源以及高价值蛋白质的生产起着关键作用。诸如茎调控启动子之类的基因组工具,对于通过增强碳代谢以积累糖分和/或提高生物燃料原料的纤维含量来改善生物量特性具有重要价值。与双子叶植物的情况不同,目前使用的单子叶植物启动子有限,且大多源自高表达的组成型植物基因和病毒。在本研究中,克隆了一种新型的(甘蔗杆状病毒;杆状病毒属,杆状病毒科)启动子区域,并通过缺失分析进行定位,在单子叶植物和双子叶植物物种中进行了瞬时功能表征,在甘蔗中进行了稳定功能表征。

结果

对[1816个碱基对(bp)]的电子分析确定了两个推定的启动子区域(PPR1和PPR2),带有转录起始位点(TSS1和TSS2)以及两个TATA框(TATAAAT和ATATAA),还有几个维管束特异性元件和调控元件。缺失分析表明,位于3'端跨越PPR2(带有TSS2和ATATAA)的710 bp区域在双子叶植物和单子叶植物中均保留了完整的启动子活性,如()基因的瞬时表达所示。在甘蔗幼叶片段中,相较于常见的玉米()和35S启动子,分别使瞬时表达提高了1.8倍和2.4倍。在转基因甘蔗中,使()基因在叶片和茎中优先表达,特别是在维管束周围的茎贮藏薄壁组织和维管束韧皮部细胞中表达。在本研究中表征的转基因事件和组织中,启动子通常比或35S启动子产生更高的GUS活性,且这种方式与转基因拷贝数没有明显相关性。

结论

新开发的植物病毒启动子在序列和表达模式上与现有的少数启动子不同。作为一种在茎维管束及其贮藏薄壁组织中具有强活性的组织调控启动子,其潜力使其在甘蔗工程中可用于改善碳代谢、增加生物能源产量以及增强胁迫耐受性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7123/5496340/93613fe1c20f/13068_2017_850_Fig1_HTML.jpg

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