<oai_dc:dc xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:oai_dc="http://www.openarchives.org/OAI/2.0/oai_dc/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/ http://www.openarchives.org/OAI/2.0/oai_dc.xsd">
  <dc:creator>Toulmay A</dc:creator>
  <dc:creator>Schneiter R</dc:creator>
  <dc:date>2006</dc:date>
  <dc:description xmlns:ns0="xml" ns0:lang="en">The introduction of defined mutations into open reading frames (ORF) or non-translated regions of the genome is important to study of the structure-function relationship of amino acid residues in proteins or that of sequence motifs at the genome level. We describe a simple two-step method for the introduction of defined single or multiple point mutations into the genome of Saccharomyces cerevisiae. This method circumvents the need for plasmid-based mutagenesis and thus ensures homogenous expression of the gene of interest within the cell population. It is based on the introduction of a selectable marker downstream of the gene of interest. This marker is then amplified with a gene-specific primer that harbours the desired point mutation, creating a selectable marker-tagged mutant version of the gene of interest. The mutant fragment is then integrated into the genome of a wild-type strain through homologous recombination. Successive rounds of amplification of the mutant loci with primers that introduce additional point mutations upstream of existing mutations will generate multiple defined mutations within a single gene. As a proof of principle, we have employed this method to generate a temperature-sensitive mutant version of the plasma membrane ATPase, pma1-7, which bears two point mutations (Pro434Ala and Gly789Ser). Phenotypic analysis of a pma1-7 haploid strain indicates that this allele has the same characteristics as the original pma1-7 allele. It confers a temperature-sensitive growth phenotype and the newly synthesized Pma1-7 protein is unstable and rapidly degraded.</dc:description>
  <dc:identifier>https://sonar.ch/global/documents/138770</dc:identifier>
  <dc:language>eng</dc:language>
  <dc:relation>info:eu-repo/semantics/altIdentifier/doi/10.1002/yea.1397</dc:relation>
  <dc:relation>info:eu-repo/semantics/altIdentifier/pmid/16921548</dc:relation>
  <dc:source>Yeast (Chichester, England). - 2006</dc:source>
  <dc:subject xmlns:ns1="xml" ns1:lang="en">Alleles</dc:subject>
  <dc:subject xmlns:ns2="xml" ns2:lang="en">Genome, Fungal</dc:subject>
  <dc:subject xmlns:ns3="xml" ns3:lang="en">Mutagenesis, Site-Directed</dc:subject>
  <dc:subject xmlns:ns4="xml" ns4:lang="en">Point Mutation</dc:subject>
  <dc:subject xmlns:ns5="xml" ns5:lang="en">Polymerase Chain Reaction</dc:subject>
  <dc:subject xmlns:ns6="xml" ns6:lang="en">Proton-Translocating ATPases</dc:subject>
  <dc:subject xmlns:ns7="xml" ns7:lang="en">Recombination, Genetic</dc:subject>
  <dc:subject xmlns:ns8="xml" ns8:lang="en">Saccharomyces cerevisiae</dc:subject>
  <dc:subject xmlns:ns9="xml" ns9:lang="en">Saccharomyces cerevisiae Proteins</dc:subject>
  <dc:title xmlns:ns10="xml" ns10:lang="en">A two-step method for the introduction of single or multiple defined point mutations into the genome of Saccharomyces cerevisiae.</dc:title>
  <dc:type>http://purl.org/coar/resource_type/c_6501</dc:type>
</oai_dc:dc>
