2002
DOI: 10.1023/a:1016313924844
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Abstract: To attain high transgene expression in petal tissue of ray florets of chrysanthemum an endogenous ubiquitin extension protein (UEP1) promoter was cloned and tested with the beta-glucuronidase (GUS) reporter gene. Expression levels were compared with four heterologous promoters: chalcone synthase (chs-A) and zinc finger transcription factor (EPF2-5) from petunia, eceriferum (CER6) from Arabidopsis and multicystatin (PMC) from potato. The comparison of the expression levels of the different constructs in ray flo… Show more

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Cited by 29 publications
(5 citation statements)
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“…Mounting evidence suggests that numerous cis-elements play a vital role in specifying the tissue expression patterns of plant genes 50,51 . To understand what drives the expression of SlOFP20 in the pollen, a 2000-bp region upstream of the SlOFP20 start codon was submitted to a public database (http://www.dna.affrc.go.jp/PLACE) to analyze cis-acting elements to determine whether pollen development-associated elements were present in the promoter.…”
Section: Resultsmentioning
confidence: 99%
“…Mounting evidence suggests that numerous cis-elements play a vital role in specifying the tissue expression patterns of plant genes 50,51 . To understand what drives the expression of SlOFP20 in the pollen, a 2000-bp region upstream of the SlOFP20 start codon was submitted to a public database (http://www.dna.affrc.go.jp/PLACE) to analyze cis-acting elements to determine whether pollen development-associated elements were present in the promoter.…”
Section: Resultsmentioning
confidence: 99%
“…To date, many cis-elements have been reported for their critical roles in determining the tissue-specific expression profiles of plant genes 38 39 . In this study, a 1534-bp region upstream of the SlGLO1 start codon was analyzed to identify cis-acting elements, using the information in two public databases ( http://www.dna.affrc.go.jp/PLACE and http://intra.psb.ugent.be:8080/ Plant CARE).…”
Section: Resultsmentioning
confidence: 99%
“…Genomic DNA was extracted from silica gel-dried or fresh leaves with a Plant Genome Extraction Kit (Tiangen Biotech, China) following the manufacturer’s protocol. For better phylogenetic resolution, we utilized nrITS and seven low-copy nuclear genes, AGO1 ( ARGONAUTE 1 ; Zhang et al, 2015 ), BRC1 ( BRANCHED1 ; Zhou et al, 2012 ; Wang M. et al, 2019 ), CDS (chrysanthemyl diphosphate synthase gene; Rivera et al, 2001 ; Liu et al, 2012a ), F3’H (flavonoid3′-hydroxylase gene; Zhao et al, 2013 ), LFY ( LEAFY ; Ma et al, 2016 ), NAM ( No Apical Meristem ; Sha et al, 2017 ) and UEP1 (gene of ubiquitin extension protein; Annadana et al, 2002 ). Polymorphic regions mostly covering introns and 5′UTRs of five of the six genes were amplified using conserved primer pairs that were developed according to sequences acquired from GenBank ( Table 1 ).…”
Section: Methodsmentioning
confidence: 99%