Mutagenesis via Insertional or Restriction Enzyme-Mediated Integration (REMI) as a Tool to Tag Pathogenicity Related Genes in Plant Pathogenic Fungi
- 1 July 1999
- journal article
- review article
- Published by Walter de Gruyter GmbH in Biological Chemistry
- Vol. 380 (7-8) , 855-864
- https://doi.org/10.1515/bc.1999.105
Abstract
Random insertional mutagenesis is a powerful tool to investigate the molecular basis of most genetically determined processes, for example in pathogenic fungi. An improved version of this method is the insertional mutagenesis via restriction enzyme mediated integration (REMI). Transformation efficiency and mode of vector integration are species dependent and further influenced by vector conformation, restriction enzyme activity, and transformation protocol. An overview is given, covering the mutants and already identified genes obtained after REMI mutagenesis. An outlook describes the future developments in the field.Keywords
This publication has 39 references indexed in Scilit:
- Identification of Pathogenicity Mutants of the Rice Blast Fungus Magnaporthe grisea by Insertional MutagenesisMolecular Plant-Microbe Interactions®, 1999
- Insertional mutagenesis of pathogenic fungiCurrent Opinion in Microbiology, 1998
- Transformation-Mediated Developmental Mutants ofGlomerella graminicola (Colletotrichum graminicola)Fungal Genetics and Biology, 1998
- clk1, a Serine/Threonine Protein Kinase-Encoding Gene, Is Involved in Pathogenicity ofColletotrichum lindemuthianumon Common BeanMolecular Plant-Microbe Interactions®, 1998
- Restriction enzyme-mediated DNA integration in Coprinus cinereusMolecular Genetics and Genomics, 1997
- AAL-Toxin-Deficient Mutants of Alternaria alternata Tomato Pathotype by Restriction Enzyme-Mediated IntegrationPhytopathology®, 1997
- Trapping Developmental Promoters inDictyosteliumPlasmid, 1995
- Tagging pathogenicity genes inUstilago maydis by restriction enzyme-mediated integration (REMI)Molecular Genetics and Genomics, 1995
- Regulated expression of endonuclease EcoRI in Saccharomyces cerevisiae: nuclear entry and biological consequences.Proceedings of the National Academy of Sciences, 1985
- Efficient transformation of Neurospora crassa by utilizing hybrid plasmid DNAProceedings of the National Academy of Sciences, 1979