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Integrative and self-replicatingLcvectors and their transactivation capacity in maize callus protoplasts

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The regulatoryLcgene is a member of theRgene family of maize which amongst other transcriptional activators controls anthocyanin biosynthetic genes. The availability ofRlocus mutants which lack anthocyanin production in all tissues offers the possibility of studying cell lineage by introducing a chimericLcgene into defined cells and following cell autonomous anthocyanin production. For this purpose integrative and self-replicatingLcvectors were constructed. Integrative expression vectors contained the 2.4 kbpLccDNA with the entire 5′ leader fused to the constitutive cauliflower mosaic virus 35S promoter with and without the maize alcohol dehydrogenase 1 intron 1 or to the mesophyll specific phosphoenolpyruvate carboxylase promoter of maize. To enhance expression and to circumvent the necessity of stable integration, extrachromosomally replicating and expressing wheat dwarf virus-Lcconstructions were also designed. Both categories of expression vectors were tested in embryogenic callus-derived protoplasts of maize and were found to transactivate anthocyanin biosynthesis. Southern blot analysis indicated that the wheat dwarf virus-Lcconstructions were replicatin

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