2001
DOI: 10.1094/mpmi.2001.14.4.580
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Mutation of an Arginine Biosynthesis Gene Causes Reduced Pathogenicity in Fusarium oxysporum f. sp. melonis

Abstract: Restriction enzyme-mediated integration (REMI) mutagenesis was used to tag genes required for pathogenicity of Fusarium oxysporum f. sp. melonis. Of the 1,129 REMI transformants tested, 13 showed reduced pathogenicity on susceptible melon cultivars. One of the mutants, FMMP95-1, was an arginine auxotroph. Structural analysis of the tagged site in FMMP95-1 identified a gene, designated ARG1, which possibly encodes argininosuccinate lyase, catalyzing the last step for arginine biosynthesis. Complementation of FM… Show more

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Cited by 242 publications
(164 citation statements)
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“…Plasmid pPN82 (9.7 kb), for the constitutive expression of GFP, was prepared by sequentially ligating into pBluescriptII KSþ a 0.7-kb BamHI/ SalI fragment of enhanced GFP (EGFP) from pEGFP (Clontech), a 1.4-kb HindIII fragment of hph under the control of the trpC promoter from pCB1004 (Carroll et al, 1994), a 2.3-kb EcoRI/NcoI fragment of gpd promoter from pAN7-1 (Punt et al, 1987), and a 0.6-kb NotI/SacII fragment of trpC terminator from pII99 (Namiki et al, 2001). The gpd promoter fragment was prepared by digesting a PCR product amplified with primer set M13-reverse and pgpdNc using pAN7-1 as template.…”
Section: Preparation Of Enhanced Gfp Vectormentioning
confidence: 99%
“…Plasmid pPN82 (9.7 kb), for the constitutive expression of GFP, was prepared by sequentially ligating into pBluescriptII KSþ a 0.7-kb BamHI/ SalI fragment of enhanced GFP (EGFP) from pEGFP (Clontech), a 1.4-kb HindIII fragment of hph under the control of the trpC promoter from pCB1004 (Carroll et al, 1994), a 2.3-kb EcoRI/NcoI fragment of gpd promoter from pAN7-1 (Punt et al, 1987), and a 0.6-kb NotI/SacII fragment of trpC terminator from pII99 (Namiki et al, 2001). The gpd promoter fragment was prepared by digesting a PCR product amplified with primer set M13-reverse and pgpdNc using pAN7-1 as template.…”
Section: Preparation Of Enhanced Gfp Vectormentioning
confidence: 99%
“…For the transformation experiments using geneticin (Sigma-Aldrich) as the selective agent, we transferred each gene cassette of Co ATG26, including the short promoter and terminator regions of SCD1, into pII99 carrying a geneticin resistance gene (Namiki et al, 2001). The gene cassettes released from pBATG26FL, pBATG26DCAT, pBATG26DPBD, and pBATG26CAT were introduced into pII99, which resulted in pIIATG26FL, pIIATG26DCAT, pIIATG26DPBD, and pIIATG26CAT, respectively.…”
Section: Plasmid Constructsmentioning
confidence: 99%
“…No obstante, es conveniente reconocer que algunas cepas de F. oxysporum no poseen acción patogénica (Namiki et al, 2001) por lo que la patogenicidad específica del aislamiento obtenido en este estudio requiere de una caracterización detallada.…”
Section: Resultados Y Discusiónunclassified