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植物中转基因 Norovirus Narita 104 衣壳蛋白 mRNA 的假多聚腺苷酸化。

Spurious polyadenylation of Norovirus Narita 104 capsid protein mRNA in transgenic plants.

机构信息

Center for Infectious Diseases and Vaccinology (CIDV), The Biodesign Institute at Arizona State University, 1001 South McAllister Avenue, Tempe, AZ 85287-5401, USA.

出版信息

Plant Mol Biol. 2011 Feb;75(3):263-75. doi: 10.1007/s11103-010-9725-1. Epub 2011 Jan 4.

Abstract

Noroviruses are members of the family Caliciviridae, and cause a highly communicable gastroenteritis in humans. We explored the potential to develop a plant-based vaccine against Narita 104 virus, a Genogroup II Norovirus. In stably transgenic potato, we obtained very poor expression of Narita 104 virus capsid protein (NaVCP) despite the use of a strong constitutive promoter (dual enhancer 35S) driving the native coding sequence. We identified potentially detrimental sequence motifs that could mediate aberrant mRNA processing via spurious polyadenylation signals. Northern blots and RT-PCR analysis of total RNA revealed truncated transcripts that suggested premature polyadenylation. Site-directed mutagenesis to remove one potential polyadenylation near-upstream element resulted in an increased expression of NaVCP when transiently expressed in leaves of Nicotiana benthamiana. Further, cloning of the truncated cDNAs from transgenic NaVCP potato plants and transiently transfected N. benthamiana allowed us to identify at least ten different truncated transcripts resulting from premature polyadenylation of full length NaVCP transcripts. Comparative studies using real time PCR analysis from cDNA samples revealed lower accumulation of full length transcripts of NaVCP as compared to those from a gene encoding Norwalk Virus capsid protein (a related Genogroup I Norovirus) in transiently transfected plants. These findings provide evidence for impaired expression of NaVCP in transgenic plants mediated by spurious polyadenylation signals, and demonstrate the need to scrupulously search for potential polyadenylation signals in order to improve transgene expression in plants.

摘要

诺如病毒属于杯状病毒科,会导致人类高度传染性的肠胃炎。我们探索了针对 Narita 104 病毒(一种属 II 型诺如病毒)开发植物源性疫苗的潜力。在稳定的转基因马铃薯中,尽管使用了强组成型启动子(双增强子 35S)驱动天然编码序列,但我们获得的 Narita 104 病毒衣壳蛋白(NaVCP)表达水平非常低。我们确定了潜在的有害序列基序,这些序列基序可能通过异常多聚腺苷酸化信号介导异常的 mRNA 加工。总 RNA 的 Northern blot 和 RT-PCR 分析显示截短的转录本,表明提前多聚腺苷酸化。通过定点突变去除一个潜在的多聚腺苷酸化上游元件,导致瞬时表达在 Nicotiana benthamiana 叶片中的 NaVCP 表达增加。此外,从转基因 NaVCP 马铃薯植物的截短 cDNA 和瞬时转染的 N. benthamiana 克隆,使我们能够鉴定至少十种不同的截短转录本,这些转录本是由于全长 NaVCP 转录本的提前多聚腺苷酸化而产生的。使用瞬时转染植物的 cDNA 样本进行实时 PCR 分析的比较研究表明,与瞬时转染植物中编码诺如病毒衣壳蛋白(一种相关的属 I 型诺如病毒)的基因相比,NaVCP 的全长转录本的积累较低。这些发现为转基因组植物中由异常多聚腺苷酸化信号介导的 NaVCP 表达受损提供了证据,并证明需要严格搜索潜在的多聚腺苷酸化信号,以提高植物中转基因的表达。

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