Internal reference genes and their primers and applications in the growth and infection stages of Phytophthora litchie
A technology of litchi frost blight and internal reference genes, applied in the fields of application, microbes, genetic engineering, etc., can solve the problems hindering the molecular biology research of litchi frost blight
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Embodiment 1
[0026] First, by analyzing the transcriptome of P. litchi, we obtained 942 genes with relatively stable expression in the transcriptome data of P. litchi. Further, we screened 4 genes with higher expression levels among these 942 genes. Mold genes (PlACTIN, PLGAPDH, PlrpS5, and Pl006400, whose nucleotide sequences are shown in sequence as SEQ ID NO.1, SEQ ID NO.2, SEQ ID NO.3, and SEQ ID NO.4) were further verified by real-time fluorescence Quantitative PCR method was used to measure the expression level changes of these genes in the stages of germination and infection of Pythora peronospora litchi, sporangia, zoospores, restospores, and restospores, and to compare the expression stability of selected genes. details as follows:
[0027] 1. Cultivation of Phytophthora peronosa of litchi. Inoculate P. litchi on carrot solid medium and culture at 28°C for one week until the culture dish is covered.
[0028] 2. Collect the samples of mycelia, sporangia, zoospores, restospores, a...
Embodiment 2
[0056] According to the method of the embodiment of the present invention 1, take P1006400 as internal reference gene, carried out transcript level analysis to Lychee downy mildew PlrpL13, the result is as follows Figure 9 As shown, the expression level of PlrpL13 gene was relatively high in the germination stage of P. litchi peronospora mycelia, sporangia, zoospores, restospores and restospores, but not in the infection stage.
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