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Wednesday, September 4, 2013

Coprinopsis cinerea mushroom

Coprinopsis cinereaCoprinopsis cinerea
General Description
gray shag

Coprinus cinereus is a multicellular basidiomycete with a typical mushroom form that undergoes a complete sexual cycle. Unlike most mushrooms, C. cinereus can complete its entire life cycle (2 weeks) in the laboratory. Its easy cultivation on simple defined media permits extensive genetic and molecular analysis. Spores of each mating type produce a monokaryotic mycelium. The fusion of compatible hyphae establishes a dikaryotic mycelium that forms a fruiting body  a miniature mushroom with three distinct tissues gill, stalk, and cap. The primordium grows and the basidial cells of the hymenial layers in the gills initiate and complete nuclear fusion, meiosis, and haploid basidiospore formation. Spore maturation and active discharge from the cap are accompanied by elongation of the stalk and auto digestion of the remaining gill tissue.
Significance

Genomic analysis will reveal whether the genes responsible for the multicellularity of Coprinus cinereus are the progenitors of those in other multicellular organisms e.g., nuclear receptors) or are innovations restricted to the fungal kingdom. Coprinus cinereus is a higher fungus (Agaricales) comprised of many cell types and, therefore, provides a window on the development of multicellularity within a single kingdom. The cells of this organism undergo coordinated developmental events not observed in unicellular fungi, including secondary and tertiary gill formation, cap expansion and autodigestion, active spore discharge, and stalk elongation, phototropism, and gravitropism.

Genome Facts
http://www.genetics.org/content/172/2/873.full.pdf

The haploid genome size of C. cinereus is estimated at 37.5 Mb. The 13 chromosomes range in size from 1-5 Mb. Over 100 markers affecting mating type, hyphal growth, fruit body morphogenesis, and DNA repair have been assigned to 10 linkage groups. Coprinus cinereus is easily transformed by DNA, and targeted gene disruption is achieved in some instances. Both RFLP and RAPD markers are widely utilized. Duplicated genes frequently become methylated at CpG dinucleotides. Chromosome-specific cosmid libraries have been prepared for 8 of the 13 chromosomes. Both commercially prepared cDNA libraries and a cDNA library suitable for yeast two-hybrid screens are available. A partial contig map of the smallest chromosome (~1 Mb) has been assembled and its sequence is currently being determined.

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