Genetics - Theses

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Type: PhD thesis × Subject: Genetic regulation × Subject: Aspergillus -- Genetics. ×

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    Molecular characterisation of the structure and regulation of the gatA, lamA and lamB genes of Aspergillus nidulans
    Richardson, Imogen Barbara. (University of Melbourne, 1991)
    The amdR gene of Aspergillus nidulans controls the expression of structural genes needed for utilisation of omega amino acids and lactams. To understand this regulation the regulatory protein and the genes it controls need to be analysed. This thesis presents work on the structure and regulation of three genes of the amdR regulon, the gatA, lamA and lamB genes. The full sequence and structure of the gatA and lamB genes and the 5' sequence and structure of the lamA gene has been determined. Structural features of these are discussed in relation to other filamentous fungal genes. The gatA gene encodes a gamma-amino butyric acid transaminase and shows homology to the equivalent genes from Saccharomyces cerevisiae and Escherichia coli. The lamA promoter has been found to contain two unusual features: a potential Initiator element at the startpoint of transcription and a downstream TATA element. All three of these genes are under the control of the positive regulatory gene, amdR. Binding sites for the amdR protein in the 5' of gatA and between the divergently transcribed lamA and lamB genes have been identified by comparison with the known amdR protein binding region of the coregulated amdS gene. Analysis of the function of these sequences indicates that there is one major binding site in the gatA promoter and between the divergently transcribed lamA and lamB genes. Comparison of these functional sequences and the previously identified site in amdS with the non-functional sites indicates certain bases within the binding sequence which may be important for efficient binding. Three CCAAT factor binding sequences have been found in the gatA and lam promoters. Two of these sequences are closely associated with functional amdR protein binding sites as has also been shown by others to be the case for amdS.
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    Use of gene transfer to study amdS regulation in Aspergillus nidulans
    Littlejohn, Timothy Graham. (University of Melbourne, 1989)
    Expression of the amdS gene of Aspergillus nidulans is regulated by a number of different regulatory genes and coeffectors. In vivo generated cis mutants permitted initial identification of regions 5' to the amdS gene involved in regulation by some of these regulatory genes. In this study, an amdS-lacZ fusion gene was used to follow the regulatory consequences of in vitro generated mutants of the amdS controlling region. Numerous deletion, inversion, insertion and oligonucleotide based mutants were constructed and introduced into A. nidulans using a gene transfer (transformation) technique. Three approaches for the production of transformants suitable for regulatory analysis were assessed; cotransformation, single copy integrations at the argB locus, and gene replacements. A single region of the amdS controlling region was found to be responsible for amdR mediated regulation of amdS, The sequence of the 5' regions of three coregulated genes, gatA, lamA and lamB, revealed that these genes shared this sequence in common. A mutant amdR allele, amdR104c, regulated amdS expression from the same location as the wildtype product. Three regions 5' to amdS were found to be involved in facB mediated regulation of amdS; their action were seen to be synergistic under some circumstances. No homology was found between them, or with the 5' regions of other genes under facB control. A mutant facB allele, facB88, resulted in altered regulation of amdS. Insertion mutants indicated that the wild type products of the amdR and facB genes could regulate amdS when their site(s) of action were moved 5' by several hundred base pairs, and that the products of the mutant alleles showed different responses. In addition, a region 5' to amdS with homology to eukaryotic CCAAT boxes was shown to be required for establishing basal amdS expression. Titration analysis, an in vivo DNA-regulatory product binding assay, was used to show that the same sequences required for amdR mediated expression titrated the amdR product. Individual sites of action of the facB gene product were not seen to titrate the facB gene product, however.