Structure of the octopine synthase upstream activator sequence.
- 1 April 1988
- journal article
- research article
- Published by Proceedings of the National Academy of Sciences in Proceedings of the National Academy of Sciences
- Vol. 85 (8) , 2553-2557
- https://doi.org/10.1073/pnas.85.8.2553
Abstract
We have identified a transcriptional activating element within the 5'' flanking sequence of the Agrobacterium tumefaciens octopine synthase (ocs) gene that is necessary for ocs expression in transformed tobacco calli. This element is located between 333 and 116 base pairs upstream from the transcription initiation site and functions independent of orientation when placed upstream of the ocs gene. It does not function in either orientation when placed downstream of the gene, nor can it activate its promoter when separated by a distance of 608 base pairs. Deletion analysis indicates that sequences essential for activator function are localized between 222 and 177 base pairs upstream of the transcription initiation site. Another region, located between 333 and 249 base pairs upstream of the transcription initiation site, does not as a monomer activate the ocs promoter, but it can as a dimer.This publication has 18 references indexed in Scilit:
- A Simple and General Method for Transferring Genes into PlantsScience, 1985
- Genetic properties and chromatin structure of the yeast gal regulatory element: an enhancer-like sequence.Proceedings of the National Academy of Sciences, 1984
- Upstream activation sites of the CYC1 gene of Saccharomyces cerevisiae are active when inverted but not when placed downstream of the "TATA box".Proceedings of the National Academy of Sciences, 1984
- Nucleotide sequence of the T-DNA region from theA grobacterium tumefaciens octopine Ti plasmid pTi15955Plant Molecular Biology, 1983
- The opine synthase genes carried by Ti plasmids contain all signals necessary for expression in plants.The EMBO Journal, 1983
- Genetic analysis of crown gall: Fine structure map of the T-DNA by site-directed mutagenesisCell, 1981
- Mendelian transcmission of genes introduced into plants by the Ti plasmids of Agrobacterium tumefaciensMolecular Genetics and Genomics, 1981
- Broad host range DNA cloning system for gram-negative bacteria: construction of a gene bank of Rhizobium meliloti.Proceedings of the National Academy of Sciences, 1980
- A rapid micro scale method for the detection of lysopine and nopaline dehydrogenase activitiesBiochimica et Biophysica Acta (BBA) - Enzymology, 1978
- A Rapid and Sensitive Method for the Quantitation of Microgram Quantities of Protein Utilizing the Principle of Protein-Dye BindingAnalytical Biochemistry, 1976