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1.
Mol Ther ; 4(5): 398-406, 2001 Nov.
Article in English | MEDLINE | ID: mdl-11708876

ABSTRACT

Pseudotyped retroviral vectors combine the advantages of broad host range, high expression, stable chromosomal integration, and ease of preparation. These vectors greatly facilitate delivery into mammalian cells of sequences encoding individual peptide inhibitors-including those with therapeutic utility-and inhibitor libraries. However, retroviral vectors vary in behavior, particularly with respect to expression levels in different cell lines. Expression level is especially important in transdominant experiments because the concentration of an inhibitor (for example, an expressed peptide) is one of the key determinants in the degree of complex formation between the inhibitor and its target. Thus, inhibitor concentration should have an impact on the expressivity and/or penetrance of an induced phenotype. Here, we compare several retroviral vectors and human cell lines for relative expression levels using a green fluorescent protein reporter. We show for a subset of these lines that cellular protein concentrations produced by single-copy vectors range up to about 2 microM. We also examine other variables that contribute to expression level, such as the nature of the expressed protein's carboxy terminus. Finally, we test the effect of increased concentration on phenotype with a nine-amino-acid peptide derived from the human papilloma virus protein E7 which overcomes E7-mediated cell growth.


Subject(s)
Gene Expression , Genetic Therapy/methods , Genetic Vectors/genetics , Peptides/metabolism , Proteins/metabolism , Retroviridae/genetics , Animals , Blotting, Western , Cell Line , Cloning, Molecular , Cyclin-Dependent Kinase Inhibitor p16/metabolism , Flow Cytometry , Gene Library , Genes, Reporter/genetics , Green Fluorescent Proteins , Humans , Leukemia Virus, Murine/genetics , Luminescent Proteins/analysis , Luminescent Proteins/genetics , Mice , Oncogene Proteins, Viral/chemistry , Oncogene Proteins, Viral/genetics , Oncogene Proteins, Viral/metabolism , Peptide Fragments/chemistry , Peptide Fragments/genetics , Peptide Fragments/metabolism , Peptides/genetics , Phenotype , Protein Biosynthesis , Proteins/genetics , Retinoblastoma Protein/metabolism , Transduction, Genetic
2.
Genetics ; 151(4): 1287-97, 1999 Apr.
Article in English | MEDLINE | ID: mdl-10101157

ABSTRACT

Yeast fimbrin (Sac6p) is an actin filament-bundling protein that is lethal when overexpressed. To identify the basis for this lethality, we sought mutations that can suppress it. A total of 1326 suppressor mutations were isolated and analyzed. As the vast majority of mutations were expected to simply decrease the expression of Sac6p to tolerable levels, a rapid screen was devised to eliminate these mutations. A total of 1324 mutations were found to suppress by reducing levels of Sac6p in the cell. The remaining 2 mutations were both found to be in the actin gene and to make the novel changes G48V (act1-20) and K50E (act1-21). These mutations suppress the defect in cytoskeletal organization and cell morphology seen in ACT1 cells that overexpress SAC6. These findings indicate that the lethal phenotype caused by Sac6p overexpression is mediated through interaction with actin. Moreover, the altered residues lie in the region of actin previously implicated in the binding of Sac6p, and they result in a reduced affinity of actin for Sac6p. These results indicate that the two mutations most likely suppress by reducing the affinity of actin for Sac6p in vivo. This study suggests it should be possible to use this type of suppressor analysis to identify other pairs of physically interacting proteins and suggests that it may be possible to identify sites where such proteins interact with each other.


Subject(s)
Fungal Proteins/genetics , Membrane Glycoproteins/genetics , Microfilament Proteins , Saccharomyces cerevisiae/genetics , Actins/chemistry , Actins/genetics , Actins/metabolism , Alleles , Base Sequence , Binding Sites/genetics , DNA Primers/genetics , Fungal Proteins/metabolism , Gene Expression , Genome, Fungal , Membrane Glycoproteins/metabolism , Models, Molecular , Mutation , Phenotype , Protein Conformation , Saccharomyces cerevisiae/growth & development , Saccharomyces cerevisiae/metabolism , Suppression, Genetic
3.
Fungal Genet Biol ; 26(1): 19-32, 1999 Feb.
Article in English | MEDLINE | ID: mdl-10072317

ABSTRACT

A Galpha subunit-encoding gene (CGA1) was cloned from Cochliobolus heterostrophus, a heterothallic foliar pathogen of corn. The deduced amino acid sequence showed similarity to Galpha proteins from other filamentous fungi and suggested that CGA1 is a member of the Galphai class. cga1 mutants had reduced ability to form appressoria on glass surfaces and on corn leaves; mutants nevertheless caused lesions on corn plants like those of wild type. cga1 mutants were female sterile; sexual development was completely abolished when the mutant allele was homozygous in a cross. Ascospores produced in crosses heterozygous at Cga1 were all wild type. The signal transduction pathway represented by CGA1 appears to be involved in developmental pathways leading to either appressorium formation or mating; in sexual development CGA1 is required for both fertility and ascospore viability.


Subject(s)
Ascomycota/physiology , Fungal Proteins/physiology , GTP-Binding Proteins/physiology , Amino Acid Sequence , Ascomycota/chemistry , Ascomycota/pathogenicity , Fungal Proteins/classification , Fungal Proteins/genetics , GTP-Binding Proteins/classification , GTP-Binding Proteins/genetics , Molecular Sequence Data , Mutation , Pigmentation , Plant Leaves/microbiology , Polymerase Chain Reaction , Signal Transduction , Virulence , Zea mays/microbiology
4.
Mol Biol Cell ; 9(1): 89-101, 1998 Jan.
Article in English | MEDLINE | ID: mdl-9436993

ABSTRACT

A gene (NhKIN1) encoding a kinesin was cloned from Nectria haematococca genomic DNA by polymerase chain reaction amplification, using primers corresponding to conserved regions of known kinesin-encoding genes. Sequence analysis showed that NhKIN1 belongs to the subfamily of conventional kinesins and is distinct from any of the currently designated kinesin-related protein subfamilies. Deletion of NhKIN1 by transformation-mediated homologous recombination caused several dramatic phenotypes: a 50% reduction in colony growth rate, helical or wavy hyphae with reduced diameter, and subcellular abnormalities including withdrawal of mitochondria from the growing hyphal apex and reduction in the size of the Spitzenkörper, an apical aggregate of secretory vesicles. The effects on mitochondria and Spitzenkörper were not due to altered microtubule distribution, as microtubules were abundant throughout the length of hyphal tip cells of the mutant. The rate of spindle elongation during anaphase B of mitosis was reduced 11%, but the rate was not significantly different from that of wild type. This lack of a substantial mitotic phenotype is consistent with the primary role of the conventional kinesins in organelle motility rather than mitosis. Our results provide further evidence that the microtubule-based motility mechanism has a direct role in apical transport of secretory vesicles and the first evidence for its role in apical transport of mitochondria in a filamentous fungus. They also include a unique demonstration that a microtubule-based motor protein is essential for normal positioning of the Spitzenkörper, thus providing a new insight into the cellular basis for the aberrant hyphal morphology.


Subject(s)
Fungal Proteins/physiology , Kinesins/physiology , Organelles/physiology , Amino Acid Sequence , Biological Transport/genetics , Cell Division/genetics , Cloning, Molecular , Fungal Proteins/genetics , Gene Deletion , Hypocreales/growth & development , Kinesins/genetics , Mitosis/genetics , Molecular Sequence Data , Morphogenesis/genetics , Morphogenesis/physiology , Mutagenesis, Site-Directed , Organelles/genetics , Organelles/metabolism , Phenotype
5.
Genetics ; 147(4): 1635-42, 1997 Dec.
Article in English | MEDLINE | ID: mdl-9409826

ABSTRACT

Yeast fimbrin is encoded by the SAC6 gene, mutations of which suppress temperature-sensitive mutations in the actin gene (ACT1). To examine the mechanism of suppression, we have conducted a biochemical analysis of the interaction between various combinations of wild-type and mutant actin and Sac6 proteins. Previously, we showed that actin mutations that are suppressed by sac6 mutations encode proteins with a reduced affinity for wild-type Sac6p. In the present study, we have found that mutant Sac6 proteins bind more tightly to mutant actin than does wild-type Sac6p, and thus compensate for weakened interactions caused by the mutant actin. Remarkably, we have also found that mutant Sac6 proteins bind more tightly to wild-type actin than does wild-type Sac6p. This result indicates that suppression does not occur through the restoration of the original contact site, but rather through the formation of a novel contact site. This finding argues against suppression occurring through a "lock-and-key" mechanism and suggests a mechanism involving more global increases in affinity between the two proteins. We propose that the most common kind of suppressors involving interacting proteins will likely occur through this less specific mechanism.


Subject(s)
Actins/metabolism , Alleles , Arabidopsis Proteins , Membrane Glycoproteins/metabolism , Microfilament Proteins , Saccharomyces cerevisiae/metabolism , Actins/genetics , Binding Sites , Membrane Glycoproteins/genetics , Membrane Glycoproteins/isolation & purification , Mutagenesis , Saccharomyces cerevisiae/genetics
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