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  • 1990-1994  (2)
  • 1
    ISSN: 1432-0983
    Keywords: Mitochondrial DNA ; Fungi ; Basidiomycete ; Schizophyllum
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Summary Mitochondrial DNA (mtDNA) found in the basidiomycete Schizophyllum commune (strain 4–40) is a circular molecule 49.75 kbp in lenght. A physical map containing 61 restriction sites revealed no repeat structures. Cloned genes from Neurospora crassa, Aspergillus nidulans, and Saccharomyces cerevisiae were used in Southern hybridizations to locate nine mitochondrial genes, including a possible pseudogene of ATPase 9, on the restriction map. A probe from a functional ATPase 9 gene identified homologous fragments only in the nuclear genome of S. commune. Restriction fragment length polymorphisms (RFLPs) between mtDNA isolated from different strains of S. commune were used to show that mitochondria do not migrate with nuclei during dikaryosis.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1617-4623
    Keywords: Schizophyllum commune ; Homeodomain ; Homeobox ; Mating type
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract The Aα mating-type locus is one of four master regulatory loci controlling sexual development in Schizophyllum commune. The Aα locus contains two homeobox genes, Y and Z, encoding two homeodomain-related proteins, Y and Z, Y and Z are each multi-allelic genes. When haploid strains form fusion cells, only particular combinations of Y and Z alleles activate Aα-regulated sexual development. The role of the putative homeodomain was examined in several Y and Z alleles by site-directed mutagenesis of regions critical to secondary structure and function of homeodomains. Mutations of the Z homeobox do not affect the function of Z proteins in Aα-activated development, but mutations of Yhomeoboxes destroy the ability of Y proteins to activate development. We conclude that only one of two Aα homeodomain-related regulators relies upon the homeodomain motif to effect gene expression in sexual development. This conclusion affords a refinement of our working hypothesis for the mechanism by which Aα proteins may regulate target gene expression. On the basis of our results with the Z protein, we speculate that the DNA-binding motifs of some transcriptional regulators may be lost or modified during evolution once these regulators have been recruited to participate in complexes with other DNA-binding proteins.
    Type of Medium: Electronic Resource
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