Scientia Agricultura Sinica ›› 2023, Vol. 56 ›› Issue (19): 3747-3758.doi: 10.3864/j.issn.0578-1752.2023.19.004

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• SPECIAL FOCUS: GENE FUNCTION AND BREEDING IN COTTON • Previous Articles     Next Articles

Cloning and Functional Characterization of GhCPR5 in Disease Resistance of Gossypium hirsutum

XU FuChun1,2(), ZHAO JingRuo2(), ZHANG ZhenNan2, HU GaiYuan2, LONG Lu2()   

  1. 1 Changzhi Medical College, Changzhi 046000, Shanxi
    2 School of Life Sciences, Henan University/National Key Laboratory of Cotton Bio-Breeding and Integrated Utilization, Kaifeng 475000, Henan
  • Received:2023-05-05 Accepted:2023-06-12 Online:2023-10-01 Published:2023-10-08
  • Contact: LONG Lu

Abstract:

【Objective】This study on the function and mechanism of GhCPR5 in response to Verticillium dahliae (V. dahliae) and Botrytis cinerea (B. cinerea) in cotton analysed nucleotide sequence, protein structure, expression pattern, and biological function to provide a theoretical basis and genetic resources for cotton disease resistance and breeding mechanism research. 【Method】GhCPR5 was identified from the unpublished transcriptome data of cotton responses to V. dahliae infection. The full-length coding sequence of GhCPR5 was amplified from upland cotton TM-1. The conserved domain, protein structure, and phylogenetic relationship of GhCPR5 and homologous genes were analysed using bioinformatics techniques. Real-time fluorescence quantitative PCR (qPCR) was used to analyse the GhCPR5 expression patterns in cotton roots, stems, leaves, ovules, fibres, and petals, and the induced expression of GhCPR5 by V. dahliae infection. The silencing fragments of GhCPR5 were amplified and inserted into the VIGS vector to generate the gene silencing construct TRV:CPR5. GhCPR5-silencing plants were created via Agrobacterium-mediated transformation methods. RT-PCR and qPCR were used to analyse the silencing efficiency of GhCPR5 in TRV:CPR5 plants. TRV:00 and TRV:CPR5 plants were inoculated with V. dahliae and B. cinerea, respectively, to analyse the difference in resistance in TRV:00 and TRV:CPR5 plants in response to pathogens. To analyse defence signal pathways involving GhCPR5, the expression levels of defence-related genes in TRV:00 and TRV:CPR5 plants were detected by qPCR. 【Result】The GhCPR5 cloned from G. hirsutum TM-1 is 1 683 bp long and encodes a 560 amino acid protein. The relative molecular weight and isoelectric point of GhCPR5 are 62.883 kDa and 9.01, respectively. Multiple-sequence alignment and phylogenetic analysis showed that GhCPR5 is highly homologous with the CPR5 of Durio zibethinus and Theobroma cacao. Furthermore, the C-terminals of GhCPR5 and CPR5 of other species are highly conserved and contain 4-5 transmembrane domains. The GhCPR5 expression level was induced by V. dahliae infection and is highest in leaves and lowest in stems. Under normal conditions, no significant developmental differences were observed between the GhCPR5-silencing plants, TRV:CPR5, and the TRV:00 control plants. After inoculation with V. dahliae, the rate of disease and the disease index of TRV:CPR5 plants were significantly higher than those of the control plants. Analysis of detached leaves inoculated with V. dahliae and B. cinerea and lactophenol-trypan blue staining showed that the lesions on the leaves of TRV:CPR5 plants were much bigger than those of TRV:00 plants, indicating that silencing GhCPR5 made cotton less resistant to V. dahliae and B. cinerea. In addition, the JAZ1 expression levels in TRV:CPR5 plants were significantly higher than in TRV:00 plants, whereas the PR3, PR4, and PR5 expression levels were markedly lower in TRV:CPR5 plants. 【Conclusion】GhCPR5 positively regulates cotton disease resistance; the downregulated expression of GhCPR5 significantly reduced cotton resistance to V. dahliae and B. cinerea.

Key words: cotton, disease resistance protein, Verticillium dahliae, Botrytis cinerea, gene expression

Table 1

Primers used in this study"

引物名称Primer name 引物序列Primer sequence (5′-3′)
VIGS-GhCPR5-F CGGGGTACCGATGTTGATCGGCCTTCTGT
VIGS-GhCPR5-R CGCGGATCCGCAACTCAGCCTGTCCTGT
qRT-GhCPR5-F TCTGTGGTTTGGCTGGGAAGT
qRT-GhCPR5-R GGCATAAGACCGCACAATAAGG
qRT-JAZ1-F AGCCTCAAAAAGGAAGACCTCAAAC
qRT-JAZ1-R TGGCTGCTCAATCACCATAGTAATC
qRT-JAZ3-F TGATTTTGCTCAAGGAGATAACGCT
qRT-JAZ3-R TGATTGCCTACTCGTTGCCTGT
qRT-NPR1-F CTAGCTTGCGGAGGGATTGATACC
qRT-NPR1-R GAGATGGCTGACCTGTCAAACTGC
qRT-PR3-F ACTCCACAATCACCGAAGCCAT
qRT-PR3-R GCATTCCAACCCTTACCACATTC
qRT-PR4-F CAGGAGAAGGAGCGACTGTGA
qRT-PR4-R TCCCACATCCAAATCTAACCC
qRT-PR5-F AAGGAGTCCACCACAATCACCG
qRT-PR5-R CTGGCACTGCTATGGCTCGTAT

Fig. 1

Protein sequence analysis of GhCPR5 in cotton A: Alignment of the amino acids of GhCPR5 with homologous in Arabidopsis thaliana. AT5G64930: AtCPR5, Gh_A02G1287/Gh_D03G0427: GhCPR5 on A and D genomes in upland cotton; CPR5: amplified sequence of GhCPR5. B: Phylogenetic tree of GhCPR5 and CPR5 of other plant species. Dz: Durio zibethinus, XP_022739926, Tc: Theobroma cacao, XP_007048101, Me: Manihot esculenta, XP_021633464, Cs: Camellia sinensis, XP_028102180, At: Arabidopsis thaliana, AT5G64930, Sb: Sorghum bicolor, XP_002454622, Zm: Zea mays, NP_001146273, Os: Oryza sativa, XP_015643035, Vv: Vitis vinifera, XP_002280314, Pt: Populus trichocarpa, XP_006380467, Hs: Hibiscus syriacus, XP_039044948, Gm: Glycine max, XP_006581733. C: Prediction of the transmembrane domains (TMs) of GhCPR5 protein"

Fig. 2

Expression pattern of GhCPR5 in cotton A: Expression patterns of GhCPR5 in different tissues of cotton; B: The expression level of GhCPR5 after V. dahliae inoculation. * and **: Significant differences and extremely significant differences at P<0.05 and P<0.01. The same as below"

Fig. 3

Creating GhCPR5 silencing plants by VIGS technique in cotton A: Albino phenotype of TRV:CLA plants; B: Phenotypic analysis of control plants TRV:00 and GhCPR5 gene silencing plants TRV:CPR5; C: RT-PCR and qRT-PCR analysis of the silencing efficiency of GhCPR5"

Fig. 4

The analysis disease resistance of TRV:00 and TRV:CPR5 plants A: The disease symptoms of TRV:00 and TRV:CPR5 plants on day 9 after infected by V. dahliae; B: Photos of the cross section of stems of TRV:00 and TRV:CPR5 plants after infected for 9 days by V. dahliae; C: Fungal recovery assays of TRV:00 and TRV:CPR5 plants on day 9 after infected by V. dahliae; D: The calculation of diseased plant percentage of TRV:00 and TRV:CPR5 plants in different days following V. dahliae inoculation; E: Disease index statistics of TRV:00 and TRV:CPR5 plants after V. dahliae inoculation"

Fig. 5

The resistance assay of TRV:00 and TRV:CPR5 leaves to different pathogens A: The lesion expansion of V. dahliae on TRV:00 and TRV:CPR5 leaves at 3 d; B: The calculation of the lesion size on detached leaves of TRV:00 and TRV:CPR5 generated by V. dahliae infection; C: Trypan blue staining of the hyphae and dead cells on TRV:00 and TRV:CPR5 leaves after inoculation of V. dahliae; D: Phenotypic analysis of TRV:00 and TRV:CPR5 detached leaves after inoculation with B. cinerea; E: The calculation of lesion size on TRV:00 and TRV:CPR5 detached leaves after inoculation with B. cinerea for 4 d; F: Trypan blue staining of the hyphae and dead cells on TRV:00 and TRV:CPR5 leaves after inoculation of B. cinerea"

Fig. 6

Expression analyze of defense-related genes in TRV:00 and TRV:CPR5 plants by qRT-PCR"

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