In 2015, researchers from the California Institute of Technology and Princeton University found that the Watts and Strogatz model explains fat-metabolism communication models in budding yeast.
42.
Thus, in evolution, the FYVE-domain-containing phosphoinositide kinases retain several aspects of the structural organization, enzyme activity and protein interactions from budding yeast.
43.
The budding yeast " Saccharomyces cerevisiae " encodes an ortholog of the Bloom syndrome ( BLM ) protein that is designated Sgs1 ( Small growth suppressor 1 ).
44.
Table 1 provides gene names and chromosomal locations for the various subunits of Pol? in humans, mice, budding yeast ( " S . pombe " ).
45.
In the budding yeast, initial cell cycle entry is controlled by two regulatory complexes, SBF ( SCB-binding factor ) and MBF ( MCB-binding factor ).
46.
In budding yeasts, the centromere region is relatively small ( about 125 bp DNA ) and contains two highly conserved DNA sequences that serve as binding sites for essential kinetochore proteins.
47.
In the budding yeast " Sacharomyces cerevisiae ", the meiotic defects in recombination and chromosome disjunction of " spo11 " mutants are alleviated by X-irradiation.
48.
Budding yeast Cdc5 is required in meiosis I for the removal of cohesins from chromosome arms, for the co-orientation of homologous chromosomes, and for the resolution of crossovers.
49.
The DMC1 gene and protein were discovered in the budding yeast S . cerevisiae by Douglas Bishop when he was a postdoctoral fellow in the laboratory of Nancy Kleckner at Harvard University.
50.
In the budding yeast, the G1 phase is particularly extended, and cytokinesis ( daughter-cell segregation ) does not happen until a new S ( Synthetic ) phase is launched.
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