PCR cloning and detection of point mutations in the eburicol 14α-demethylase (CYP51) gene from Erysiphe graminis f. sp. hordei, a "recalcitrant" fungus
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作者:
Délye, C
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机构:Inst Natl Rech Agron, Unite Rech Integrees Vigne, F-33883 Villenave Dornon, France
Délye, C
Bousset, L
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机构:Inst Natl Rech Agron, Unite Rech Integrees Vigne, F-33883 Villenave Dornon, France
Bousset, L
Corio-Costet, MF
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机构:Inst Natl Rech Agron, Unite Rech Integrees Vigne, F-33883 Villenave Dornon, France
Corio-Costet, MF
机构:
[1] Inst Natl Rech Agron, Unite Rech Integrees Vigne, F-33883 Villenave Dornon, France
[2] INRA, Lab Pathol Vegetale, F-78850 Thiverval Grignon, France
Molecular studies of some micro-organisms are hampered by the difficulty of obtaining sufficient amounts of nucleic acids. A cloning strategy based on PCR has therefore been used to clone the eburicol 14 alpha-demethylase (CYP51) gene of the obligate fungus Erysiphe graminis f. sp. hordei (Egh) using minute amounts of,genomic DNA. The CYP51 gene encodes the enzymatic target of a major group of fungicides. Sequencing CYP51 from different Egh isolates revealed the occurrence of two alleles for this gene.,An allele-specific PCR assay was developed to detect each CYP51 allele.