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Open AccessJournal ArticleDOI

Fruiting body development in Coprinus cinereus: regulated expression of two galectins secreted by a non-classical pathway.

TLDR
Heterologous expression of Cgl2 in Saccharomyces cerevisiae indicated that secretion of this protein occurred independently of the classical secretory pathway, and two fungal galectins, Cgl1 and cgl2, are differentially regulated during fruiting body formation.
Abstract
Fruiting body formation in the basidiomycete Coprinus cinereus is a developmental process that occurs as a response of the mycelium to external stimuli. First, localized, highly branched hyphal structures (knots) are formed as a reaction to nutritional depletion. Hyphal-knot formation is repressed by light; however, light signals are essential for the development of the hyphal knot into an embryonic fruiting body (primordium) as well as karyogamy, meiosis and fruiting body maturation. The role of the different environmental signals in the initial phases of fruiting body development was analysed. It was observed that two fungal galectins, Cgl1 and Cgl2, are differentially regulated during fruiting body formation. cgl2 expression initiated in early stages of fruiting body development (hyphal knot formation) and was maintained until maturation of the fruiting body, whereas cgl1 was specifically expressed in primordia and mature fruiting bodies. Immunofluorescence and immuno-electron microscopy studies detected galectins within specific fruiting body tissues. They localized in the extracellular matrix and the cell wall but also in membrane-bound bodies in the cytoplasm. Heterologous expression of Cgl2 in Saccharomyces cerevisiae indicated that secretion of this protein occurred independently of the classical secretory pathway.

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Journal ArticleDOI

Galectinomics: finding themes in complexity.

TL;DR: Although the identification of many novel galectin relatives in widely divergent organisms has added significantly to the size and complexity of this intriguing protein family, several common themes arise, which suggest promising new research targets.
Journal ArticleDOI

Fruiting body production in Basidiomycetes.

TL;DR: A better understanding of the developmental processes underlying fruiting in these model organisms is expected to help mushroom cultivation of other basidiomycetes in the future.
Journal ArticleDOI

Identification of genes in the bW/bE regulatory cascade in Ustilago maydis

TL;DR: It is demonstrated that in one of the early upregulated genes, the promoter can be bound by a bW/bE fusion protein in vitro, suggesting a connection to the mating process.
Journal ArticleDOI

The laccase multi-gene family in Coprinopsis cinerea has seventeen different members that divide into two distinct subfamilies.

TL;DR: Overexpression of the 17 non-allelic laccase genes under the control of a constitutive promoter identified nine active enzymes from subfamily 1, and Lcc15 is expected to be non-functional in lacc enzyme activity due to an internal deletion of about 150 amino acids.
References
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Journal ArticleDOI

Cleavage of Structural Proteins during the Assembly of the Head of Bacteriophage T4

TL;DR: Using an improved method of gel electrophoresis, many hitherto unknown proteins have been found in bacteriophage T4 and some of these have been identified with specific gene products.
Journal Article

Cleavage of structural proteins during the assemble of the head of bacterio-phage T4

U. K. Laemmli
- 01 Jan 1970 - 
TL;DR: Using an improved method of gel electrophoresis, many hitherto unknown proteins have been found in bacteriophage T4 and some of these have been identified with specific gene products as mentioned in this paper.
Journal ArticleDOI

Single-step method of RNA isolation by acid guanidinium thiocyanate-phenol-chloroform extraction

TL;DR: A new method of total RNA isolation by a single extraction with an acid guanidinium thiocyanate-phenol-chloroform mixture is described, providing a pure preparation of undegraded RNA in high yield and can be completed within 4 h.
Journal ArticleDOI

Transformation of intact yeast cells treated with alkali cations.

TL;DR: The transformation efficiency with Cs+ or Li+ was comparable with that of conventional protoplast methods for a plasmid containing ars1, although not for plasmids containing a 2 microns origin replication.
Journal ArticleDOI

Transformation of intact yeast cells treated with alkali cations or thiol compounds

TL;DR: The transformation efficiency with Cs+ or Li+ was comparable with that of conventional protoplast methods for a plasmid containing ars1, although not for plasmids containing a 2 microns origin replication.
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