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  • Cantharidin  (1)
  • Microtubule-associated protein  (1)
  • 1
    ISSN: 0014-5793
    Keywords: CaScin kinase II (CKII) ; Calcineurin ; Microtubule-associated protein ; Phosphorylation/dephosphorylation ; Proline direct protein kinase (PDPK) ; Protein phosphatase 1 and 2A
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Biology , Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Molecular genetics and genomics 259 (1998), S. 523-531 
    ISSN: 1617-4623
    Keywords: Key words Calyculin A ; Cantharidin ; Neurospora crassa ; Okadaic acid ; Protein phosphatase 2A
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract Cantharidin and calyculin A, natural toxins that are inhibitors of protein phosphatases 1 and 2A (PP1 and PP2A, respectively), inhibit Neurospora crassa hyphal growth. When N. cassa was grown in the presence of either drug, abnormalities were observed at hyphal tips. In addition, both drugs induced an increase in hyphal branching. Cantharidin inhibited N. crassa hyphal growth in a temperature-dependent manner, as the effect of the drug was more pronounced at 34° C than at 25° C. In addition to the drug-mediated inhibition of phosphatase activity, a genetic approach was used to determine the phenotypic consequences of reduced PP2A activity. Two strains with subnormal PP2A activity were constructed. The first, in which the original pph-1 gene (encoding the PP2A catalytic subunit) was replaced with an ectopically integrated copy of pph-1, exhibited lower levels of pph-1 transcript, lower PP2A activity and increased sensitivity to cantharidin. Similarly, in a second strain, in which the pph-1 gene was cloned in an antisense orientation downstream of the inducible isocitrate lyase promoter, lower levels of pph-1 transcript, as well as of PP2A activity, and a reduction in hyphal growth were observed. The results of this study indicate that PP2A, and probably other Ser/Thr phosphatases, are involved in the regulation of hyphal growth in N. crassa.
    Type of Medium: Electronic Resource
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