S. cerevisiae
Proton transfer pathways in the mitochondrial S cerevisiae cytochrome c oxidase
... the S. cerevisiae CytcO Ser382 residue, was modified, showed that this residue is not important for proton conduction, but only results in a small increase in the midpoint potential of heme a 33 ...
9
Anti-CRISPR-based biosensors in the yeast S. cerevisiae
... We evaluated the functions of these three anti-CRISPR proteins in the yeast S. cerevisiae. Each of them acted on a yeast codon-optimized version of dSpCas9 (fused to a nuclear localization sequence–NLS) ...
14
Structural constraints revealed in consistent nucleosome positions in the genome of S. cerevisiae
... described above. We implemented this concept (’sym- metry of DNA curvature’) in a suitably adjusted method (SymCurv), which permits us to attribute a symmetry of curvature score to each nucleotide on a given DNA sequence ...
14
Understanding crossover control using A. thaliana and S. cerevisiae
... The central unanswered question regarding interference is how it is achieved within the cell. The answer to this question has been elusive partly because traditional genetic screens designed to discover interference ...
243
Identification of new cell size control genes in S. cerevisiae
... Cell size homeostasis is a conserved attribute in many eukaryotic species involving a tight regulation between the processes of growth and proliferation. In budding yeast S. cerevisiae, growth to a “ ...
13
Histone chaperones and the Rrm3p helicase regulate flocculation in S. cerevisiae
... Several histone chaperones are involved in the epige- netic transmission and maintenance chromatin structure in S. cerevisiae [14, 15]. The histone chaperones ASF1 and FACT are involved in both the ...
14
Farnesol inhibits translation to limit growth and filamentation in C. albicans and S. cerevisiae.
... eIF2B regulation plays a critical role in reprograming gene expression as part of the response to stress across different eukaryotic cells [23]. For instance, eIF2 phosphor- ylation by eIF2 α kinases, like Gcn2p in ...
11
Temperature-dependent regulation of upstream open reading frame translation in S. cerevisiae
... 90 s, followed by annealing at 37 ...the S. cerevisiae rRNA database using Bowtie ...the S. cerevisiae genome or to the FASTA file made from the reporter sequence (pR AUG F- F UUG ) to ...
27
Specialization of B-type cyclins for mitosis or meiosis in S. cerevisiae.
... General effects of clb mutations on sporulation: The various viable homozygous clb mutants were sporulated, and the proportion of vegetative cells, lysed cells, tet- rad[r] ...
7
Mutations Synthetically Lethal with cep1 Target S. cerevisiae Kinetochore Components
... Four of the five mutations synergistically increased the loss rate of marker chromosomes carrying a centromere lacking the CP1 binding site, suggesting that the cep1 synthetic lethality [r] ...
13
THE ROLE OF S. CEREVISIAE CELL DIVISION CYCLE GENES IN NUCLEAR FUSION
... Forty temperature-sensitive cell division cycle (cdc) mutants of Sac- charomyces cerevisiae were examined for their ability to complete nuclear fusion during conjugat[r] ...
10
THE SELECTION OF S. CEREVISIAE MUTANTS DEFECTIVE IN THE START EVENT OF CELL DIVISION
... Therefore, if we adopt the four demon- strated properties at the restrictive temperature of cdc28-I, the charter member of the Class-I start mutants, as a set of standar[r] ...
17
Rpl22 is required for IME1 mRNA translation and meiotic induction in S. cerevisiae
... Similar to a previous report [ 18 ], Rpl22A and/or Rpl22B function is not required for mitotic cell division in rich medium although the doubling times for the rpl22A∆ and rpl22∆ d[r] ...
14
ALTERED FIDELITY OF MITOTIC CHROMOSOME TRANSMISSION IN CELL CYCLE MUTANTS OF S. CEREVISIAE
... The increase in chromosome loss and/or recombination is likely to be due to the deficiency of functional gene product rather than to an aberrant function of the [r] ...
15
Ste7 variants that promote pathway specificity in S. cerevisiae
... 194 S might be a more potent activator of Kss1 than wild-type ...194 S some how involves Hog1 or Mpk1 in the promotion of filamentation specific reporter gene ...194 S (Table ...194 S strain ...
186
MUTANTS OF S. CEREVISIAE DEFECTIVE IN THE MAINTENANCE OF MINICHROMOSOMES
... T h e specific class may include mutants that d o not initiate DNA replication effec- tively at specific ARSs present on the minichromosomes; the nonspecific clas[r] ...
21
MAPPING CDC MUTATIONS IN THE YEAST S. Cerevisiae BY RAD52-MEDIATED CHROMOSOME LOSS
... T h e chromosome loss-mapping method used here is based on the finding that diploids homozygous for rad52 lose chromosomes spontaneously and that the frequency of l[r] ...
17
Functional expression and evaluation of heterologous phosphoketolases in Saccharomyces cerevisiae
... Single deletions of S. cerevisiae genes GPP1 and GPP2 were performed according to PCR-mediated seamless gene deletion principle of Akada et al. (2006). 500 bp recognition sequences up- and downstream of the ...
13
Respiratory mutants of Chlamydomonas
... in S. cerevisiae (Luttik et ...from S. cerevisiae (de Vries and Grivell, 1988), it has been suggested that the FAD prosthetic group acts as the redox centre in these ...
231
Lists in a Lighthouse
... S. cerevisiae Yap5. The regulatory functions of the low iron-sensing transcriptional activators Aft1/Aft2 are also complemented by a high iron-sensing transcriptional activator named Yap5. Under high iron ...
258