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Growth, Differentiation and Sexuality

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unit (an individual colony) is advantageous in<br />

competitive environments. In a confrontation<br />

between the cord-forming wood decomposers<br />

H. fasciculare <strong>and</strong> Steccherinum fimbriatum, one<br />

species eventually replaced the other. Which<br />

species eventually dominated over the other was<br />

strongly influenced by inoculum size (Dowson<br />

et al. 1988). In confrontations between a competitor<br />

<strong>and</strong> colonies from the same isolate, but of<br />

different sizes, larger colonies had a higher success<br />

rate than smaller ones (Holmer <strong>and</strong> Stenlid 1993).<br />

These data from basidiomycete species suggest<br />

that, in ascomycete species, too, the capacity of<br />

conidial germlings or colonies of like genotype to<br />

undergo anastomosis to generate a larger colony<br />

may provide a competitive advantage.<br />

VII. Conclusion<br />

Anastomosis captured the imagination of early<br />

mycologists, <strong>and</strong> numerous studies describing<br />

the morphology of hyphal fusion in ascomycete<br />

<strong>and</strong> basidiomycete species have been published.<br />

However, work describing mutant phenotypes<br />

or the molecular function of genes <strong>and</strong> proteins<br />

required for anastomosis in filamentous fungi has<br />

largely been ignored. Advances in cell biology<br />

techniques <strong>and</strong> live cell imaging of the hyphal<br />

fusion process will hopefully lead to an increased<br />

awareness <strong>and</strong> interest in this important aspect of<br />

filamentous fungal biology. In addition, advances<br />

in molecular <strong>and</strong> genetic tractability of a variety of<br />

filamentous fungi, <strong>and</strong> the availability of genome<br />

sequences will lead to in-depth comparative<br />

analyses that will, hopefully, begin to reveal the<br />

rich tapestry of inter- <strong>and</strong> intrahyphal communication<br />

that accompanies both developmental<br />

<strong>and</strong> morphogenetic processes. Many questions<br />

regarding the mechanism <strong>and</strong> function of hyphal<br />

anastomosis remain unanswered. What are the<br />

diffusible chemotropic molecules responsible<br />

for causing fusion-competent hyphae to grow<br />

toward each other, <strong>and</strong> how do they regulate<br />

Spitzenkörper behavior? Is the signal transduction<br />

machinery involved in regulating hyphal homing<br />

<strong>and</strong> fusion between conidial germlings the same<br />

or different to that involved in homing <strong>and</strong> fusion<br />

between hyphae in the colony interior? How<br />

similar or different are the signaling <strong>and</strong> fusion<br />

machineries involved in vegetative stages vis-à-vis<br />

those involved in sexual stages of the life cycle?<br />

Anastomosis in Filamentous Fungi 135<br />

Finally, what selective advantage maintains the<br />

capacity of germlings <strong>and</strong> hyphae to undergo<br />

anastomosis, <strong>and</strong> under what conditions?<br />

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