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Book of Abstracts (PDF) - International Mycological Association

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IMC7 Tuesday August 13th Lectures<br />

196 - Examining the relationship between nonself<br />

recognition, heterokaryon incompatibility and hyphal<br />

fusion in Neurospora crassa<br />

N.L. Glass 1* , Q. Xiang 1 , S. Sarkar 1 , D.J. Jacobson 1 & N.D.<br />

Read 2<br />

1 Plant and Microbial Biology Department, University <strong>of</strong><br />

California, Berkeley, CA, 94720-3102, U.S.A. - 2 Institute <strong>of</strong><br />

Cell and Molecular Biology, University <strong>of</strong> Edinburg,<br />

Edinburgh, EH9 EJH, U.K. - E-mail:<br />

Lglass@uclink.berkeley.edu<br />

Filamentous fungi grow by tip extension, branching and<br />

hyphal fusion to form a hyphal network. Filamentous fungi<br />

can also undergo hyphal fusion between individuals to<br />

make vegetative heterokaryons. Recognition <strong>of</strong> nonself in<br />

such heterokaryons is mediated by genetic differences at<br />

het loci. Heterokaryons or transformants that contain<br />

alternative het alleles show severe growth inhibition,<br />

conidiation suppression and death. We use Neurospora<br />

crassa to study the molecular mechanism <strong>of</strong> hyphal fusion<br />

and the consequences <strong>of</strong> fusion between het incompatible<br />

individuals. Live cell imaging <strong>of</strong> hyphal anastomoses<br />

showed a self-signaling phenomenon which initiates the<br />

multi-stage process <strong>of</strong> fusion. We identified four mutants<br />

that fail to undergo hyphal fusion. Two mutations are in<br />

genes encoding signal transduction components; these<br />

mutants also suppress heterokaryon incompatibility<br />

mediated by the mat locus. Nonself recognition during<br />

heterokaryon incompatibility has been shown to be<br />

mediated by the formation <strong>of</strong> a HET heterocomplex.<br />

Suppressor analyses identified two additional loci that are<br />

required for mediating heterokaryon incompatibility. One<br />

<strong>of</strong> these mutants suppresses heterokaryon incompatibility<br />

at both the mat and het-c locus. By these analyses, we hope<br />

to shed light on nonself recognition mechanisms in<br />

filamentous fungi that underlie heterokaryon<br />

incompatibility and explore its relationship to the hyphal<br />

fusion process.<br />

197 - Somatic incompatibility in basidiomycetes.<br />

Genetic analysis in Heterobasidion<br />

J. Stenlid * , Å. Olson, N. Högberg & M. Lind<br />

Dept Forest Mycology and Pathology, Swedish University<br />

<strong>of</strong> Agricultural Sciences, Box 7026, S-750 07 Uppsala,<br />

Sweden. - E-mail: Jan.stenlid@mykopat.slu.se<br />

In basidiomycetes, intraspecific recognition <strong>of</strong> self and<br />

non-self is mediated through the somatic incompatibility<br />

(SI) system (similar to the vegetative compatibility system<br />

in ascomycetes). It is expressed in the vegetative phase <strong>of</strong><br />

growth both in homokaryons and in heterokaryons when<br />

dissimilar genotypes meet. In the homokaryotic stage, the<br />

system can be overridden by mating. SI involves postfusion<br />

cell death, and depending on the species involved,<br />

activation <strong>of</strong> phenol oxidases, melanin production,<br />

formation <strong>of</strong> clear zones <strong>of</strong> collapsed aerial hyphae, hyphal<br />

knot cells or dense so called barrages. The genetic control<br />

<strong>of</strong> SI has been studied in less than ten species. In members<br />

<strong>of</strong> the genus Phellinus, SI was under control <strong>of</strong> one major<br />

gene, while 3-4 genetic loci have been implied in<br />

Heterobasidion, Collybia and Pleurotus. In this<br />

presentation we describe a QTL approach to characterise<br />

the genetic and molecular background to SI in<br />

Heterobasidion annosum. A genetic map was constructed<br />

using AFLP markers for a cross between a S and a P<br />

homokaryon <strong>of</strong> H. annosum. Siblings were mated with the<br />

parent mycelia and resulting heterokaryons, differing in<br />

one sib-related nucleus, were paired in all combinations.<br />

Putative loci for SI were mapped based on the<br />

incompatibility reactions. Implications for future work will<br />

be discussed.<br />

198 - Overview <strong>of</strong> fungal lignin degradation<br />

C.A. Reddy<br />

Dept. <strong>of</strong> Microbiology & Molecular Genetics, Michigan<br />

State University, East Lansing, MI 48824-4320, U.S.A. - Email:<br />

reddy@msu.edu<br />

Lignocellulose, a major component <strong>of</strong> woody biomass, is<br />

the most abundant renewable organic material in the<br />

biosphere and has important applications as a resource for<br />

producing pulp and paper, animal feeds, and industrial<br />

chemicals. Lignin, which limits access <strong>of</strong> microbial<br />

enzymes to cellulose and hemicellulose in woody<br />

materials, is a key limiting factor not only in the efficient<br />

conversion <strong>of</strong> the latter to useful materials but also in<br />

global carbon cycling. White-rot basidiomycetes are<br />

efficient lignin degraders in natures and produce one or<br />

more <strong>of</strong> three major classes <strong>of</strong> lignin-modifying enzymes<br />

(LMEs) designated: laccases, lignin peroxidases (LiPs),<br />

and manganese peroxidases (MnPs). LMEs are<br />

extracellular, non-specific, metalloenzymes and catalyze<br />

radical-mediated oxidative degradation reactions.<br />

Cumulative evidence indicates that a large number <strong>of</strong><br />

isoenzymes <strong>of</strong> LiPs, MnPs, and laccases are produced by<br />

various ligninolytic fungi and that different isoenzymes<br />

appear to be encoded by individual genes which are<br />

distributed on multiple chromosomes. Regulation <strong>of</strong><br />

production <strong>of</strong> LMEs appears to be subject to complex<br />

interplay <strong>of</strong> nutritional, environmental, temporal, and<br />

genetic factors. An overview <strong>of</strong> the studies on the<br />

physiology and molecular biology <strong>of</strong> LMEs as well as<br />

applications <strong>of</strong> ligninolytic fungi for bioremediation <strong>of</strong><br />

priority environmental pollutants will be presented.<br />

<strong>Book</strong> <strong>of</strong> <strong>Abstracts</strong> 63

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