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Far upstream activating promoter regions are responsible for expression of the BnC1 cruciferin gene from Brassica napus
Authors:Pierre Bilodeau  Jean-G. Lafontaine  Guy Bellemare
Affiliation:(1) Departement de Biochimie, Faculté des Sciences et de Génie, Université Laval, G1K 7P4 Québec (Québec), Canada;(2) Département de Biologie, Faculté des Sciences et de Génie, Université Laval, G1K 7P4 Québec (Québec), Canada;(3) Present address: Division of Plant industry, CSIRO, GPO Box 1600, 2601 Canberra, ACT, Australia
Abstract:Summary Cruciferin is the major seed storage protein in Brassica napus. As much as 1.9 kbp of the BnC1 cruciferin gene promoter have been sequenced and analyzed. Promoter fragments with 5prime deletions from –2500 to –v202 were fused with the ß-glucuronidase reporter gene and used for Nicotiana tabacum transformation. ß-glucuronidase could be specifically expressed in transgenic tobacco seeds under the control of the BnC1 promoter and regulatory elements were found to be dispersed over 1903 bp. An almost 5-fold increase in ß-glucuronidase expression was obtained when the promoter length was increased from –379 to –498, and another 10-fold increase was observed when sequences between –1266 and –1903 were added. Histochemical analysis shows that the region between –844 and –1266 directs the expression of the chimeric gene specifically to the root apical meristem.Abbreviations GUS ß-glucuronidase - MU 4-methyl umbelliferone - MUG 4-methyl-umbelliferyl-ß-D-glucuronide - X-gluc 5-bromo-4-chloro-3-indolyl-ß-D-glucuronide
Keywords:ß  -glucuronidase  Embryo  Promoter  Seed-storage proteins  Transgenic plant
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