Barley stripe disease pathogenic gene pgsln and application thereof
A disease-causing gene and disease-causing technology, applied in the fields of application, genetic engineering, plant gene improvement, etc., can solve the problems such as the report of pgsln gene and function of barley stripe disease, and achieve the effect of efficient breeding
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Embodiment 1
[0052] The present embodiment provides a barley stripe disease pathogenic gene pgsln, the gene full-length sequence such as the sequence table SEQID NO: 1 and figure 1 with Figure 19 shown.
Embodiment 2
[0054] This embodiment provides a method for cloning the pgsln gene, the causative gene of barley streak disease, and its gene function verification method, comprising the following steps:
[0055] 1. Cloning and sequence analysis of pgsln gene
[0056] Carry out single spore isolation to barley streak WT bacterial strain, mycelia plate culture is in PDA medium, culture temperature 23-25 ℃, mycelia liquid culture is in PD medium, 23-25 ℃, 180rpm. Mycelia were cultured for DNA extraction, RNA extraction and protoplast preparation. The sequence of Saccharomyces cerevisiae sln (GenBank ID: NP EDV09625) was homologously compared with the results of barley streak WT genome sequencing (to be published), and the homologous sequence of sln was found, which was named pgsln, and the pgsln gene sequence was homologous Source clones, PCR amplification using cDNA and DNA as templates, and primer pair pgsln-F1 / pgsln-R1 (see Table 1) as primers to amplify the target fragment, the produc...
Embodiment 3
[0084] The present embodiment provides the application of a kind of barley stripe disease pathogenic gene pgsln gene in regulating mycelial growth rate, and the verification of this application comprises the following steps:
[0085] 1. Cloning and sequence analysis of pgsln gene
[0086] Single spores were isolated from the WT strain of barley stripe disease, and the mycelia were cultured on PDA medium at a culture temperature of 23°C, and the mycelium liquid was cultured on PD medium at 23°C and 180rpm. The mycelia were cultured for DNA extraction, RNA extraction and protoplast preparation. The sequence of Saccharomyces cerevisiae sln (GenBank ID: NP EDV09625) was homologously compared with the sequencing results of barley stripe disease WT genome, and the homologous sequence of sln was found, which was named pgsln, and the pgsln gene sequence was homologously cloned by PCR The amplification uses cDNA and DNA as templates, and the primer pair pgsln-F1 / pgsln-R1 (see Table 1)...
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