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首页> 外文期刊>BMC Biotechnology >Switchgrass (Panicum virgatum L.) polyubiquitin gene (PvUbi1 and PvUbi2) promoters for use in plant transformation
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Switchgrass (Panicum virgatum L.) polyubiquitin gene (PvUbi1 and PvUbi2) promoters for use in plant transformation

机译:柳枝((Panicum virgatum L.)聚泛素基因(PvUbi1和PvUbi2)启动子用于植物转化

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Background The ubiquitin protein is present in all eukaryotic cells and promoters from ubiquitin genes are good candidates to regulate the constitutive expression of transgenes in plants. Therefore, two switchgrass ( Panicum virgatum L.) ubiquitin genes ( PvUbi1 and PvUbi2 ) were cloned and characterized. Reporter constructs were produced containing the isolated 5' upstream regulatory regions of the coding sequences (i.e. PvUbi1 and PvUbi2 promoters) fused to the uidA coding region ( GUS ) and tested for transient and stable expression in a variety of plant species and tissues. Results PvUbi1 consists of 607 bp containing cis -acting regulatory elements, a 5' untranslated region (UTR) containing a 93 bp non-coding exon and a 1291 bp intron, and a 918 bp open reading frame (ORF) that encodes four tandem, head -to-tail ubiquitin monomer repeats followed by a 191 bp 3' UTR. PvUbi2 consists of 692 bp containing cis -acting regulatory elements, a 5' UTR containing a 97 bp non-coding exon and a 1072 bp intron, a 1146 bp ORF that encodes five tandem ubiquitin monomer repeats and a 183 bp 3' UTR. PvUbi1 and PvUbi2 were expressed in all examined switchgrass tissues as measured by qRT-PCR. Using biolistic bombardment, PvUbi1 and PvUbi2 promoters showed strong expression in switchgrass and rice callus, equaling or surpassing the expression levels of the CaMV 35S, 2x35S, ZmUbi1 , and OsAct1 promoters. GUS staining following stable transformation in rice demonstrated that the PvUbi1 and PvUbi2 promoters drove expression in all examined tissues. When stably transformed into tobacco ( Nicotiana tabacum ), the PvUbi2+3 and PvUbi2+9 promoter fusion variants showed expression in vascular and reproductive tissues. Conclusions The PvUbi1 and PvUbi2 promoters drive expression in switchgrass, rice and tobacco and are strong constitutive promoter candidates that will be useful in genetic transformation of monocots and dicots.
机译:背景技术泛素蛋白存在于所有真核细胞中,来自泛素基因的启动子是调节植物中转基因组成型表达的良好候选者。因此,克隆并鉴定了两个柳枝((Panicum virgatum L.)的泛素基因(PvUbi1和PvUbi2)。产生了包含与uidA编码区(GUS)融合的编码序列的分离的5'上游调控区(即PvUbi1和PvUbi2启动子)的报告基因构建体,并测试了其在多种植物物种和组织中的瞬时和稳定表达。结果PvUbi1由607 bp的含有顺式作用的调控元件,5'非翻译区(UTR)以及93 bp的非编码外显子和1291 bp的内含子以及918 bp的开放阅读框(ORF)组成,编码四个串联序列,从头到尾的泛素单体重复序列,然后是191 bp的3'UTR。 PvUbi2由692 bp的顺式作用调节元件,5'的UTR,97 bp的非编码外显子和1072 bp的内含子,1146 bp的ORF组成,其编码5个串联泛素单体重复序列和183 bp的3'UTR。通过qRT-PCR测量,PvUbi1和PvUbi2在所有检查的柳枝tissue组织中表达。使用生物弹轰击,PvUbi1和PvUbi2启动子在柳枝and和水稻愈伤组织中显示出强表达,等于或超过CaMV 35S,2x35S,ZmUbi1和OsAct1启动子的表达水平。在水稻中稳定转化后的GUS染色表明,PvUbi1和PvUbi2启动子驱动了所有受检组织中的表达。当稳定转化到烟草(Nicotiana tabacum)中时,PvUbi2 + 3和PvUbi2 + 9启动子融合变体在血管和生殖组织中表达。结论PvUbi1和PvUbi2启动子可驱动柳枝,、水稻和烟草中的表达,并且是强大的组成型启动子候选物,可用于单子叶植物和双子叶植物的遗传转化。

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