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Authentic seed-specific activity of the Perilla oleosin 19 gene promoter in transgenic Arabidopsis
Authors:Kyoung-Ji Chung  Seon-Kap Hwang  Bum-Soo Hahn  Kyung-Hwan Kim  Jong-Bum Kim  Yong-Hwan Kim  Joo-Sung Yang  Sun-Hwa Ha
Affiliation:(1) National Institute of Agricultural Biotechnology, RDA, 225 Seodun-dong, Suwon, 441-707, South Korea;(2) Department of Genetic Engineering, Sungkyunkwan University, Suwon, 440-746, South Korea;(3) Institute of Biological Chemistry, Washington State University, Pullman, WA 99164, USA
Abstract:The Perilla (Perilla frutescens L. cv. Okdong) oleosin gene, PfOle19, produces a 19-kDa protein that is highly expressed only in seeds. The activity of the −2,015 bp 5′-upstream promoter region of this gene was investigated in transgenic Arabidopsis plants using the fusion reporter constructs of enhanced green fluorescent protein (EGFP) and β-glucuronidase (GUS). The PfOle19 promoter directs Egfp expression in developing siliques, but not in leaves, stems or roots. In the transgenic Arabidopsis, EGFP fluorescence and histochemical GUS staining were restricted to early seedlings, indehiscent siliques and mature seeds. Progressive 5′-deletions up to the −963 bp position of the PfOle19 promoter increases the spatial control of the gene expression in seeds, but reduces its quantitative levels of expression. Moreover, the activity of the PfOle19 promoter in mature seeds is 4- and 5-fold greater than that of the cauliflower mosaic virus 35S promoter in terms of both EGFP intensity and fluorometric GUS activity, respectively.
Keywords:Arabidopsis   Oleosin   Perilla (Perilla frutescens L.)  Promoter  Seed-specific
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