2009
DOI: 10.1016/j.jbiotec.2009.03.009
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Construction vascular-specific expression bi-directional promoters in plants

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Cited by 14 publications
(12 citation statements)
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“…Moreover, the study showed that a cauliflower mosaic virus (CaMV) 35S minimal promoter could be bipolarized not only by fusion with another copy of the 35S minimal promoter in the reverse orientation, but also by fusion with an unrelated minimal promoter ( At SAGmini) derived from a senescence-specific gene. Two reporter genes were expressed successfully in transgenic tobacco using an artificial BD PRO constructed from a 35S mini promoter fused to a natural polar promoter [11, 12]. The BD PROs in the intergenic regions between the cab1 and cab2 , At5g06280 and At5g06290 genes in Arabidopsis thaliana and the Ocpi1 and Ocpi2 genes in rice, and the CaTin1 and CaTin1-2 genes in hot pepper cultivar Bugang have been investigated [1316].…”
Section: Introductionmentioning
confidence: 99%
“…Moreover, the study showed that a cauliflower mosaic virus (CaMV) 35S minimal promoter could be bipolarized not only by fusion with another copy of the 35S minimal promoter in the reverse orientation, but also by fusion with an unrelated minimal promoter ( At SAGmini) derived from a senescence-specific gene. Two reporter genes were expressed successfully in transgenic tobacco using an artificial BD PRO constructed from a 35S mini promoter fused to a natural polar promoter [11, 12]. The BD PROs in the intergenic regions between the cab1 and cab2 , At5g06280 and At5g06290 genes in Arabidopsis thaliana and the Ocpi1 and Ocpi2 genes in rice, and the CaTin1 and CaTin1-2 genes in hot pepper cultivar Bugang have been investigated [1316].…”
Section: Introductionmentioning
confidence: 99%
“…This strategy was based on the hypothesis that, for many promoters, only the core promoter sequence needs to be oriented with respect to the coding sequence of the gene to ensure transcription in the correct direction, while the upstream promoter elements can be present in either orientation (Peremarti et al 2010). Previously, several studies also employed the same or a similar strategy to produce chimeric bidirectional promoters from unidirectional ones (Barfield and Pua 1991;Xie et al 2001;Li et al 2004;Chaturvedi et al 2006;Lv et al 2009), which provides precedence for the biotechnological application of this hypothesis.…”
Section: Resultsmentioning
confidence: 99%
“…TCGTCCATGCCGAGAGTGAT GFP gene specific primer for RT-PCR and qRT-PCR Qgus1 ATCCGGTCAGTGGCAGTGAAGG GUS gene specific primer for RT-PCR and qRT-PCR Qgus2 CAGCGTAAGGGTAATGCGAG GUS gene specific primer for RT-PCR and qRT-PCR * The added restriction sites are underlined (Zheng et al 2007), pBI121 (for CaMV 35S promoter and NOS-T) (Clontech, USA) and pBIGG (for GFP gene) (kindly provided by Song X; Lv et al 2009) with the following sequence-specific primers: P985-1/ P985-2, 35S1/35S2, NOS1/NOS2 and GFP1/GFP2, respectively (Table 1). The amplified CaMV 35S promoter and the GFP gene were digested with BamHI and joined by ligation with T4 DNA Ligase (Promega, Madison, WI, USA).…”
Section: Vector Constructionmentioning
confidence: 99%
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“…It activated transcription simultaneously in both directions at comparable levels. Recently, Lv et al (2009) have constructed bidirectional promoters by fusing CaMV35S minimal promoter to 5′ end of either grp1.8 or 4Cl1 promtoer. The regulatory complexities in cis and trans-regulatory mechanisms and technological advances for the development of synthetic promoters have been reviewed by Venter (2007).…”
Section: Inducible Promotersmentioning
confidence: 99%