Start Date: Jun 29, 2007
End Date: Mar 17, 2010
Vegetative and sporulative cultures that have spontaneously segregated from a single wheat-biotype P. nodorum colony are isolated. The subtraction technique is used to enrich the differentially expressed gene sequences present in poly (A) RNAs of sporulative culture. The expression of specific genes in vegetative and sporulative samples is studied by Northern hybridization. Genetic transformation of vegetative culture is planned to study the gene(s) involved in asexual conidiation. In order to define the gene(s) responsible for sporulation in wheat-biotype P. nodorum, particular gene(s) are also silenced by the cloning of open reading frame (ORF) of the gene. The genes encoding the transcription factors responsible for asexual sporulation in wheat-biotype P. nodorum can be identified by using a knock-out procedure. All transcription factors gene sequences which can be identified in wheat-biotype P. nodorum will be used for gene knockouts to determine their roles in asexual sporulation in P. nodorum. The quantitative trait loci (QTL) associated with pathogen aggressiveness in wheat-biotype P. nodorum will be studied by a sexual crossing between two isolates with different aggressiveness levels and analyzing the segregation of molecular markers, functional genes and pathogen aggressiveness in their progeny. Polymorphisms in two parental isolates are detected with RAPD (Figure 1), RFLP, SSR, EST and AFLP techniques. The genetic linkage maps are analyzed and constructed with Joinmap 3.0 version software (www.biometris.nl). The segregation data of pathogen aggressiveness in the population are analyzed and the QTL mapping is produced by using an interval mapping method (MapQTL 5 software, www.biometris.nl). BSL-1 6/3/04.