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Science 5 June 1987: Vol. 236. no. 4806, pp. 1299 - 1302 DOI: 10.1126/science.236.4806.1299
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Articles
Duplication of CaMV 35S Promoter Sequences Creates a Strong Enhancer for Plant Genes
ROBERT KAY 1,
AMY CHAN 1,
MARK DALY 1, and
JOAN MCPHERSON 1
1 Department of Botany, University of British Columbia, Vancouver, British Columbia, Canada V6T 2B1.
A variant of the cauliflower mosaic virus 35S promoter with transcriptional activity approximately tenfold higher than that of the natural promoter was constructed by tandem duplication of 250 base pairs of upstream sequences. The duplicated region also acted as a strong enhancer of heterologous promoters, increasing the activity of an adjacent and divergently transcribed transferred DNA gene several hundredfold, and to a lesser extent, that of another transferred DNA gene from a remote downstream position. This optimized enhancer element should be very useful for obtaining high levels of expression of foreign genes in transgenic plants.
Submitted on November 3, 1986
Accepted on March 19, 1987
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258, 287-292
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275, 24701-24708
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J. Biol. Chem.
275, 31211-31218
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275, 34375-34381
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275, 36899-36909
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277, 2798-2803
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PNAS
98, 2047-2052
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PNAS
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Plant Physiology
128, 978-987
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