Comprehensive functional analysis of protein kinase C of filamentous fungi
| Project/Area Number |
23380048
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| Research Category |
Grant-in-Aid for Scientific Research (B)
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| Allocation Type | Single-year Grants |
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| Section | 一般 |
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| Research Field |
Applied microbiology
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| Research Institution | The University of Tokyo |
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Principal Investigator |
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| Project Period (FY) |
2011-04-01 – 2015-03-31
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| Project Status |
Completed (Fiscal Year 2014)
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| Budget Amount *help |
¥18,720,000 (Direct Cost: ¥14,400,000、Indirect Cost: ¥4,320,000)
Fiscal Year 2013: ¥5,070,000 (Direct Cost: ¥3,900,000、Indirect Cost: ¥1,170,000)
Fiscal Year 2012: ¥4,810,000 (Direct Cost: ¥3,700,000、Indirect Cost: ¥1,110,000)
Fiscal Year 2011: ¥8,840,000 (Direct Cost: ¥6,800,000、Indirect Cost: ¥2,040,000)
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| Keywords | バイオテクノロジー / 糸状菌 / PKC / 細胞壁 / 微生物 |
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| Outline of Final Research Achievements |
The functions of protein kinase C (PKC) in filamentous fungi remain largely unknown. Aspergillus nidulans is one of the model filamentous fungus and there is a PKC-encoding gene, pkcA, in its genome. In our previous study, we showed that pkcA is essential for the growth of A. nidulans. In this study, to clarify the function of PkcA, we constructed pkcA-ts mutant in which the activity of PkcA was temperature sensitive and R429A mutant that produces an activated form of PkcA under the alcA promoter of A. nidulans. We performed transcriptome analysis using these mutants and identified genes whose expression changed in response to the changes of the PkcA activity. Genes related to cell wall synthesis, cell polarization, Ca2+ signal transduction, and a mycotoxin, sterigmatocystin, synthesis were included in these genes. We analyzed the regulation mechanisms of the gene expression by PkcA and clarified them.
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Report
(4 results)
Research Products
(9 results)
