May David B, Pfotenhauer Alexander C, Concha Bryn L, Li Li, Jones Samantha M, Harbison Stacee A, Martin Lana H, Clark Lindsey A, Occhialini Alessandro, Stewart C Neal, Lenaghan Scott C
Center for Agricultural Synthetic Biology, University of Tennessee Institute of Agriculture, Knoxville, TN, 37996, USA.
Department of Plant Sciences, University of Tennessee Knoxville, 2431 Joe Johnson Dr, Knoxville, TN, 37996, USA.
Plant Cell Rep. 2025 Aug 8;44(9):196. doi: 10.1007/s00299-025-03583-x.
Synthetic biology, monocots, transgene expression, genetic regulatory elements, protoplasts, fluorometry. Given the preeminent status of monocotyledonous species in global agriculture, efforts toward enhancing their yield, resilience, and quality with synthetic biology (SynBio) approaches are warranted. We therefore sought to assemble and characterize a toolkit of genetic regulatory elements to address the relative paucity of components appropriate for genetic engineering in cereals and grasses. Here, we present an 80-member combinatorial parts library consisting of 17 promoter, 17 5' untranslated region (UTR), 18 promoter-5'UTR fusion, and 28 3'UTR sequences derived from viral, microbial, and plant sources. Evaluation of the effects of 77 combinations of these elements on GFP reporter expression in Zea mays protoplasts revealed a 74.5-fold dynamic range of expression levels. Novel combinations of the CaMV 35S promoter and viral 5'UTR sequences generated reporter expression levels that approximated the strong CsVMV viral promoter-5'UTR fusion. Newly identified 3'UTR sequences from plant small heat shock protein (HSP) species regulated impressive enhancements of reporter expression that exceeded the widely used 35S, ocs, and nos terminators. To assess cross-clade compatibility of the regulatory element combinations, reporter cassettes were also transiently assayed in Nicotiana benthamiana leaves using agroinfiltration. A total of 34 regulatory element combinations exhibited interspecific activity, 14 of which displayed similar impacts on reporter gene expression across the two species. This toolkit will enable tunable transgene expression in monocots suitable for myriad SynBio applications including genome editing, manipulation of metabolic pathways, and genetic circuit construction.
合成生物学、单子叶植物、转基因表达、遗传调控元件、原生质体、荧光测定法。鉴于单子叶植物物种在全球农业中的卓越地位,有必要采用合成生物学(SynBio)方法来提高其产量、抗逆性和品质。因此,我们试图组装并表征一套遗传调控元件工具包,以解决适合谷物和禾本科植物基因工程的元件相对较少的问题。在此,我们展示了一个由80个成员组成的组合元件库,该库由17个启动子、17个5'非翻译区(UTR)、18个启动子-5'UTR融合序列和28个3'UTR序列组成,这些序列来源于病毒、微生物和植物。对这些元件的77种组合对玉米原生质体中绿色荧光蛋白(GFP)报告基因表达的影响进行评估,结果显示表达水平的动态范围为74.5倍。CaMV 35S启动子和病毒5'UTR序列的新组合产生的报告基因表达水平接近强大的CsVMV病毒启动子-5'UTR融合序列。新鉴定的来自植物小热激蛋白(HSP)物种的3'UTR序列显著增强了报告基因的表达,超过了广泛使用的35S、ocs和nos终止子。为了评估调控元件组合的跨进化枝兼容性,还使用农杆菌浸润法在本氏烟草叶片中对报告盒进行了瞬时检测。共有34种调控元件组合表现出种间活性,其中14种对两个物种的报告基因表达产生了相似的影响。这个工具包将使单子叶植物中的转基因表达能够被调控,适用于包括基因组编辑、代谢途径操纵和遗传回路构建在内的众多合成生物学应用。