Function of a calcium-dependent protein kinase gene Pscamk in Puccinia striiformis f. sp. tritici
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Supported by the Key Project of China National Programs for Fundamental Research and Development (2013CB127700),by the National Natural Science Foundation of China (31371889,31171795),by the 111 Project from the Ministry of Education of China (B07049),by the Program for New Century Excellent Talents in University (NCET-12-0471) and by the Fundamental Research Funds for the Central Universities of China (YQ2013001)

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    Abstract:

    Abstract:[Objective]To clone calcium-dependent protein kinase gene (camk) from Puccinia striiformis f. sp. tritici (Pst) and analyze its function.[Methods]The cDNA full-length of Pscamk was isolated by using reverse transcriptional-PCR (RT-PCR),and gene expression profile at different morphological stages was analyzed via quantitative real-time -PCR(qRT-PCR).Pst urediospores were treated with CaMK suppressor KN-93 and germination rate was investigated.[Results]A gene cDNA full-length with 1 620 bp was obtained and designated as Pscamk.qRT-PCR analysis showed Pscamk expression was highly induced in the early stages of Pst infection and reached the maximum at 6 h post inoculation (hpi) as 20. 74-fold as that in the control (0 hpi).With increasing of the concentration of CaMK suppressor KN-93,germination rate of Pst urediospores was gradually decreased. The germination rate was reduced to 8.02%,only 12% of the control,under 1.4 μmol/L KN-93 treatment at 10 h after incubation at 9 ℃.[Conclusion]Pscamk might play a role in germination and germ tube elongation of Pst urediospores.This study provides a basis for exploring pathogenesis of calcium signaling pathway during Pst infection.

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Juan Qin, Chuanming Huang, Fuxin He, Xiaoguo Zhu, Yang Zhang, Zhensheng Kang, Jun Guo. Function of a calcium-dependent protein kinase gene Pscamk in Puccinia striiformis f. sp. tritici. [J]. Acta Microbiologica Sinica, 2014, 54(11): 1296-1303

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History
  • Received:January 22,2014
  • Revised:April 07,2014
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  • Online: October 31,2014
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