Cloning and transcriptional profiling of PsNCS1 from Puccinia striiformis f.sp. Tritici
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Supported by the Industry projects from Ministry of Agriculture of China (200903035-2), the National Basic Research Program of China (2006CB100203), the Special Capital for the Construction of Modern Agriculture Technical System of China, the 111 Project from Ministry of Education of China (No.B07049), Science and Technology Research Key Project, the Ministry of Education of China (107104) and the Program for Excellent Young Scholars in Northwest A&F University

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    Abstract:

    Abstract: [Objective] We cloned PsNCS1 encoding neuronal calcium sensor from Pst and analyzed its transcriptional profile. [Methods] A full-length cDNA of PsNCS1 was cloned by using RT-PCR in combination with cDNA library screening, the sequence was analyzed with different bioinformatic tools and the gene expression pattern was characterized via real-time RT-PCR. [Results] PsNCS1 (Genbank accession no. GU134621) encoded 190 amino acids, with a molecular weight of 22.17 KDa and a pI of 4.96. PsNCS1 contained four conserved EF-hand domains and was N-terminally myristoylated. Phylogenetic analysis indicated that PsNCS1 was highly similar to the NCS from Basidiomycetes and the highest similarity was with that from Puccinia graminis (96%). Real-time RT-PCR analysis indicated the amount of PsNCS1 transcripts of urediospores and of germinated urediospores were doubled or more comparing with those of fungal bodies at other different developmental stages. [Conclusion] PsNCS1 might be involved in the process of urediospore formation and germ tube elongation. The present results may provide basic data for further analysis of the role of PsCNS1 in pathogenesis process and calcium signaling.

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Jun Guo, Hong Zhang, Ke Ding, Xiwei Dai, Yueying Chen, Yinghui Duan, Lili Huang, Zhensheng Kang. Cloning and transcriptional profiling of PsNCS1 from Puccinia striiformis f. sp. Tritici. [J]. Acta Microbiologica Sinica, 2010, 50(7): 963-969

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  • Received:December 26,2009
  • Revised:February 08,2010
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