trp12D63, leu2 D, ura3-52) [S1]. The tpkw strains were gifts from J. Broach. The strains YNP2 and PSY1201 were gifts from P. Silver. All of the cultures were performed at 30C in YNBmedium supple-mented by the required amino acids. Plasmid Constructions In all of the constructions, we used pAMG as a template [S2], and the sequences of oligonucleotides we used are shown in Table S1. An intermediary plasmid called pO1wasmade in order to facilitate further constructions. This plasmid is derived from pAMG and con-tains the ATG, a small polylinker (SalI, BamHI, and PstI), and the sequence of MSN2 from 1723 to the end and the sequence of GFP. The MSN2-GFP open reading frame (ORF), cut out by SalI and HindIII, has been replaced by the SalI-HindIII-...
<p>A–C. Schematics of PCR reactions used to confirm strains. See <a href="http://www.plosone.org/art...
We have extended the technique of PCR-directed recombination in Saccharomyces cerevisiae to develop ...
<p>Sequence of oligonucleotides used to construct plasmids and yeast strains.</p
Yeast Strains. Saccharomyces cerevisiae strains were grown in standard yeast extract– peptone–dextro...
table, Table 5). Promoter insertions, C-terminal tags, and deletions were generated using PCR and re...
Yeast strains used in this study are listed in Table S1. Strain JRY3 was constructed by replacement ...
∆PLD82a of the W303 background was a kind gift from Susan Lindquist (Nathan and Lindquist, 1995) and...
Yeast strains used in all experiments of this study are listed in Table S6. The wild type BY4741 str...
Yeast strains and plasmids The bem1::URA3 [1], rsr1::HIS3 [2] and bud8::TRP1 (previously bud8-∆1) [3...
All S. pombe strains used are listed in Table S1. Deletion and tagging to produce 5FLAG fusion prote...
To make the pre3∆LS-T1A (β1∆LS-T1A) strain MHY2267, Quikchange mutagenesis (Stratagene) was used to ...
All plasmids were constructed by PCR amplification of the respective DNA. Detailed information about...
a<p>NCYC, National Collection of Yeast Cultures.</p><p>doi:10.1371/journal.pone.0104204.t001</p
<p>The coding sequence for full length wild type SIRT6 and the H133W mutant was PCR-amplified and cl...
S. cerevisiae strains used in this study are related to S288c and are listed in Table S1. Standard m...
<p>A–C. Schematics of PCR reactions used to confirm strains. See <a href="http://www.plosone.org/art...
We have extended the technique of PCR-directed recombination in Saccharomyces cerevisiae to develop ...
<p>Sequence of oligonucleotides used to construct plasmids and yeast strains.</p
Yeast Strains. Saccharomyces cerevisiae strains were grown in standard yeast extract– peptone–dextro...
table, Table 5). Promoter insertions, C-terminal tags, and deletions were generated using PCR and re...
Yeast strains used in this study are listed in Table S1. Strain JRY3 was constructed by replacement ...
∆PLD82a of the W303 background was a kind gift from Susan Lindquist (Nathan and Lindquist, 1995) and...
Yeast strains used in all experiments of this study are listed in Table S6. The wild type BY4741 str...
Yeast strains and plasmids The bem1::URA3 [1], rsr1::HIS3 [2] and bud8::TRP1 (previously bud8-∆1) [3...
All S. pombe strains used are listed in Table S1. Deletion and tagging to produce 5FLAG fusion prote...
To make the pre3∆LS-T1A (β1∆LS-T1A) strain MHY2267, Quikchange mutagenesis (Stratagene) was used to ...
All plasmids were constructed by PCR amplification of the respective DNA. Detailed information about...
a<p>NCYC, National Collection of Yeast Cultures.</p><p>doi:10.1371/journal.pone.0104204.t001</p
<p>The coding sequence for full length wild type SIRT6 and the H133W mutant was PCR-amplified and cl...
S. cerevisiae strains used in this study are related to S288c and are listed in Table S1. Standard m...
<p>A–C. Schematics of PCR reactions used to confirm strains. See <a href="http://www.plosone.org/art...
We have extended the technique of PCR-directed recombination in Saccharomyces cerevisiae to develop ...
<p>Sequence of oligonucleotides used to construct plasmids and yeast strains.</p