Figures (7)  Tables (2)
    • Figure 1. 

      Relative expression of CmPDS after transient silencing, as determined by RT-qPCR. Different lowercase letters indicate significant differences between different treatments at the same time (p < 0.05).

    • Figure 2. 

      Process for genetic transformation of C. morifolium. (a) Preculture. (b) Coculture. (c) Screening and cultivation. (d) Albino plant. (e) Interalbino plant. (f) Negative control plant.

    • Figure 3. 

      Sequence alignment of CmPDS from transgenic plants along with the WT and the negative control plants.

    • Figure 4. 

      Relative expression of CmTGA1 after transient silencing, as determined by RT-qPCR. Different lowercase letters indicate significant differences between different treatments at the same time (p < 0.05).

    • Figure 5. 

      Process for genetic transformation of C. morifolium. (a) Preculture. (b) Coculture. (c) Delayed cultivation. (d) Screening and cultivation (the red box highlights a resistant bud). (e) Transgenic plant.

    • Figure 6. 

      Sequence alignment of CmTGA1 from transgenic plants compared to the WT.

    • Figure 7. 

      Expression of CmPR1, CmPR2 and CmPR5 genes in WT and CmTGA1 lines after inoculation with P. horiana. (a) Expression of CmPR1. (b) Expression of CmPR2. (c) Expression of CmPR5. Analysis of significant differences was performed using Student's t-test (**, p < 0.01).

    • Primer
      name
      Primer sequence
      PDST1-BsFATATATGGTCTCGATTGTGCCTGCACCATTGAATGGGTT
      PDST1-F0TGTGCCTGCACCATTGAATGGGTTTTAGAGCTAGAAATAGC
      PDST2-R0AACTTGGCTTGCAAAGTCTCTCCAATCTCTTAGTCGACTCTAC
      PDST2-BsRATTATTGGTCTCGAAACTTGGCTTGCAAAGTCTCTCCAA
      TGA1T1-BsFATATATGGTCTCGATTGAAGCTAACCCTAATAGAAGGTT
      TGA1T1-F0TGAAGCTAACCCTAATAGAAGGTTTTAGAGCTAGAAATAGC
      TGA1T2-R0AACGAATAAAGCTTGTTCGAATCAATCTCTTAGTCGACTCTAC
      TGA1T2-BsRATTATTGGTCTCGAAACGAATAAAGCTTGTTCGAATCAA
      PDS-TFGTACAGAACCTGTTTGGAGAGTTA
      PDS-TRCTTCCGGCAAAAGAAGCTTCAGAA
      TGA1-TFATGAGCATCCTTGAAACAACATTC
      TGA1-TRTCATAGTGTTTGAGTTGCCATCAT

      Table 1. 

      Primers used for mutant identification.

    • Primer namePrimer sequence
      PR1-FCCTTAAACCCAATCTCACAATG
      PR1-RTGAGTGCGTTGGTGGAGTT
      PR2-FTCGACTGACATAAGGCACATAACGC
      PR2-RGCTTCCATAACCTCCATCTCCTTCG
      PR5-FCCAATGGAGTTTAGCCCCGT
      PR5-RGTCCACAACTACCACGCTCA
      Actin-FTCCGTTGCCCTGAGGTTCT
      Actin-RGATTTCCTTGCTCATCCTGTCA

      Table 2. 

      Primers used for RT-PCR.