Nitric oxide synthase is induced in sporulation of Physarum polycephalum

  1. Georg Golderer,
  2. Ernst R. Werner,
  3. Stefan Leitner,
  4. Peter Gröbner, and
  5. Gabriele Werner-Felmayer1
  1. Institute of Medical Chemistry and Biochemistry, University of Innsbruck, A-6020 Innsbruck, Austria

Abstract

The myxomycete Physarum polycephalum expresses a calcium-independent nitric oxide (NO) synthase (NOS) resembling the inducible NOS isoenzyme in mammals. We have now cloned and sequenced this, the first nonanimal NOS to be identified, showing that it shares < 39% amino acid identity with known NOSs but contains conserved binding motifs for all NOS cofactors. It lacks the sequence insert responsible for calcium dependence in the calcium-dependent NOS isoenzymes. NOS expression was strongly up-regulated inPhysarum macroplasmodia during the 5-day starvation period needed to induce sporulation competence. Induction of both NOS and sporulation competence were inhibited by glucose, a growth signal and known repressor of sporulation, and byl-N6–(1-iminoethyl)-lysine (NIL), an inhibitor of inducible NOS. Sporulation, which is triggered after the starvation period by light exposure, was also prevented by 1H-[1,2,4]oxadiazolo-[4,3-a]quinoxalin-1-one (ODQ), an inhibitor of NO-sensitive guanylate cyclase. In addition, also expression oflig1, a sporulation-specific gene, was strongly attenuated by NIL or ODQ. 8-Bromo-cGMP, added 2 h before the light exposure, restored the capacity of NIL-treated macroplasmodia to express lig1 and to sporulate. This indicates that the second messenger used for NO signaling in sporulation of Physarum is cGMP and links this signaling pathway to expression of lig1.

Keywords

Footnotes

  • 1 Corresponding author.

  • E-MAIL gabriele.werner-felmayer{at}uibk.ac.at; FAX 43-512-507-2865.

  • Article and publication are at www.genesdev.org/cgi/doi/10.1101/gad.890501.

    • Received December 6, 2000.
    • Accepted March 9, 2001.
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