ライフサイエンスコーパス: S. cerevisiae

1 S. cerevisiae GAL genes thus encode a regulatory program

2 S. cerevisiae Hop1 and Red1 are essential structural com

3 S. cerevisiae is found in multiple environments-one of w

4 S. cerevisiae Sir1, enriched at the silencers of HMLalph

5 S. cerevisiae was grown in YNB media, containing randomi

6 Analyses of over 1000 S. cerevisiae isolates are providing rich resources to b

7 ese sequences along with a collection of 158 S. cerevisiae strains.

8 Here 2 S. cerevisiae GCR assays were used to screen a targeted

9 acterising 1,068 and 970 polymorphisms in 34 S. cerevisiae and 26 S. paradoxus strains respectively.

10 n unexpected resistance to cytotoxicity by a S. cerevisiae mutant with ablated post-transfer editing

11 Here we identified the mRNA targets of a S. cerevisiae PUF protein, Puf5p, by ultraviolet-crossli

12 to analyze pheno-metabolomic diversity of a S. cerevisiae strain collection with different origins.

13 In this regard, analysis of a S. cerevisiae transcriptional regulatory network using o

14 This process allows S. cerevisiae to adapt on a physiological timescale, but

15 cluding Kluyveromyces lactis and alternative S. cerevisiae strains.

16 Surprisingly, although S. cerevisiae Hop1, a component of synaptonemal complex

17 SID showed clear differences among S. cerevisiae populations in grape fermentation samples,

18 Untargeted metabolomics analysis of an S. cerevisiae deletion mutant of YDR109C revealed ribulo

19 aromyces cerevisiae exopolyphosphatase 1 and S. cerevisiae inorganic pyrophosphatase 1, followed by c

20 The binary culture of L. plantarum AFI5 and S. cerevisiae AYI7 had the best effect on the bioavailab

21 to TORC1 may differ between C. albicans and S. cerevisiae The converse direction of signaling from T

22 ll cycle in HeLa (human cervical cancer) and S. cerevisiae cells.

23 monitor antimicrobial effects on E. coli and S. cerevisiae.

24 enes for two model organisms (C. elegans and S. cerevisiae) using the GenAge database as ground truth

25 n of Arabidopsis, mammalian, C. elegans, and S. cerevisiae RBPs reveals a common set of proteins with

26 vity relationships in both P. falciparum and S. cerevisiae.

27 he luminal domains of S. cerevisiae Gpi8 and S. cerevisiae Gpi16 do not interact directly, nor do the

28 ic nucleosome assembly between K. lactis and S. cerevisiae, we determined the structure of a K. lacti

29 organisms--H. sapiens, D. melanogaster, and S. cerevisiae--and show that, as compared to other annot

30 ct DNA sequence-dependencies of metazoan and S. cerevisiae initiators in origin recognition and suppo

31 indicate that APA mechanisms in S. pombe and S. cerevisiae are largely different: S. pombe has many o

32 on some key differences between S. pombe and S. cerevisiae is included for readers with some familiar

33 endocytic protein abundance in S. pombe and S. cerevisiae is more similar than previously thought, m

34 consistent differences between in vitro and S. cerevisiae (in vivo) Cas9 cleavage specificity profil

35 also associated with a higher level of anti-S. cerevisiae antibodies.

36 activity, MBL2 and NOD2 polymorphisms, anti-S. cerevisiae antibody levels and clinical Crohn's disea

37 However, the anti-S. cerevisiae Ab levels showed a significant inverse cor

38 mily chromatin remodeling complexes, such as S. cerevisiae RSC, slide and eject nucleosomes to regula

39 SEC23B encodes Sec23 homolog B (S. cerevisiae), a component of coat protein complex II (

40 kinetochore composition vary greatly between S. cerevisiae (point centromere) and other eukaryotes (r

41 th corresponding experimental data from both S. cerevisiae and human cells and provides a quantitativ

42 ates supporting significant activity of both S. cerevisiae and E. coli HADs includes 28 common metabo

43 imination against non-protein amino acids by S. cerevisiae PheRS and support a non-canonical role for

44 E. coli, and S. enterica) and a yeast cell (S. cerevisiae), ranging in size from 1 to 6.3 mum, in a

45 luminal domain of Saccharomyces cerevisiae (S. cerevisiae) Gpi8 using different expression systems,

46 This resource will help clarify S. cerevisiae biological processes by furthering studies

47 A large percentage of clinical S. cerevisiae isolates are heterozygous across many nucl

48 (MDSet) in interaction networks of E. coli, S. cerevisiae and H. sapiens, defined as subsets of prot

49 When combined, S. cerevisiae GAL coding regions gave rise to profound g

50 we show that seven evolutionarily conserved S. cerevisiae proteins (actin, formin, profilin, tropomy

51 NifX as purified from aerobically cultured S. cerevisiae coexpressing M. thermautotrophicus NifB wi

52 in the extreme sensitivity of Mag1-deficient S. cerevisiae toward alkylation damage.

53 +) can support growth of polyamine-deficient S. cerevisiae mutants.

54 size differences among APA isoforms than did S. cerevisiae PASs in different locations of gene are su

55 h quality genome sequences from 11 different S. cerevisiae strains and stored in the SGD.

56 ces cerevisiae First, analysis of 36 diverse S. cerevisiae isolates revealed evidence of numerous pas

57 iginated from three lineages of domesticated S. cerevisiae, including the major wine-making lineage a

58 t the detailed characterization of the eight S. cerevisiae enzymes and show that they carry a total o

59 Here we use an engineered S. cerevisiae BY4742 strain, containing an established h

60 nrelated to those observed in the equivalent S. cerevisiae mutants, and the CnHal3b-deficient strain

61 Like other eukaryotes, S. cerevisiae undergoes a dramatic reprogramming of gene

62 For S. cerevisiae, we used a metagenomics assembly approach

63 " A. thaliana query genes, and about 20% for S. cerevisiae, as lacking a syntenic homolog because of

64 ofmeister series, as observed previously for S. cerevisiae.

65 (TSSs) at a single-nucleotide resolution for S. cerevisiae grown in nine different conditions using n

66 Additionally, we argue that for S. cerevisiae the "volume increment" is not added from b

67 and the Nup133 N-terminal domain, both from S. cerevisiae.

68 By applying our methods to data from S. cerevisiae and mouse embryonic stem cells, we find th

69 kluyveri, a yeast species that diverged from S. cerevisiae more than 100 million years ago.

70 pigenetic states in fungi that diverged from S. cerevisiae ~200 million years ago, and in which gluco

71 ochemical studies of RNA bound exosomes from S. cerevisiae revealed that the Exo9 central channel gui

72 eading frame in Ribo-Seq data generated from S. cerevisiae and mouse embryonic stem cells.

73 f seven galactose (GAL) metabolic genes from S. cerevisiae, when introduced together into S. bayanus,

74 f the UBL domain of the WDR12 homologue from S. cerevisiae at 1.7 A resolution and demonstrate that h

75 uctures of intact Drs2p-Cdc50p isolated from S. cerevisiae in apo form and in the PI4P-activated form

76 the ubiquitin-bound structure of Rpn11 from S. cerevisiae and the mechanisms for mechanochemical cou

77 - and six-gene pathways by VEGAS to generate S. cerevisiae cells synthesizing beta-carotene and viola

78 ic forms in the heterologous expression host S. cerevisiae where we were able to apply yeast genetic

79 However, S. cerevisiae uses a chemically inefficient pathway for

80 We identified S. cerevisiae Mps2 as the outer nuclear membrane protein

81 a metagenomics assembly approach to identify S. cerevisiae scaffolds from pulque, and performed phylo

82 ol can be successfully exploited to identify S. cerevisiae strains in any kind of complex samples.

83 In S. cerevisiae, less Pho2-dependent Pho4 orthologs induce

84 In S. cerevisiae, replication origins occupy characteristic

85 In S. cerevisiae, the phosphate starvation (PHO) responsive

86 In S. cerevisiae, there was no evidence for a dominant-nega

87 In S. cerevisiae, we account for 89% of the variance in gro

88 atures in mammalian interphase, is absent in S. cerevisiae, suggesting alternative mechanisms of barr

89 in efficiency under loss of Rat1 activity in S. cerevisiae, demonstrating that both reduced licencing

90 lation are the main drivers of adaptation in S. cerevisiae populations in the human gut.

91 mammalian cells, and functional analysis in S. cerevisiae.

92 redate the sub-functionalization apparent in S. cerevisiae after the genome duplication.

93 technique for visualization of the areas in S. cerevisiae cells which contain higher amount of calci

94 egregated even within single mother cells in S. cerevisiae.

95 or producing fatty acid-derived chemicals in S. cerevisiae.

96 sembly, producing a functional chromosome in S. cerevisiae.

97 promoter scanning across promoter classes in S. cerevisiae, we perturb Pol II catalytic activity and

98 Our data suggest that eccDNAs are common in S. cerevisiae, where they might contribute substantially

99 ls of DNA replication have been developed in S. cerevisiae.

100 of submitochondrial protein distribution in S. cerevisiae.

101 le for loss of transcription around a DSB in S. cerevisiae.

102 sential for the normal functions of eEF1A in S. cerevisiae However, eEF1A glutaminylation slightly re

103 bolism in E. coli and the Crabtree effect in S. cerevisiae, meaning that energy metabolism is suffici

104 be established and efficiently engineered in S. cerevisiae, highlighting the potential for natural pr

105 The results suggest that ES7 in S. cerevisiae could play a role analogous to the multi-s

106 Complementation experiments in S. cerevisiae provide evidence for the ability of SiPHT1

107 Pah1 expressed in S. cerevisiae or Escherichia coli was not degraded by th

108 Consistently, when expressed in S. cerevisiae, they poorly reproduced the Ppz1-regulator

109 reduces the levels of gfp mRNA expression in S. cerevisiae cells, with a concomitant decrease in gree

110 ne regulation for 5 transcription factors in S. cerevisiae.

111 HEM15 encoding the enzyme ferrochelatase in S. cerevisiae and performed a genetic suppressor screen.

112 Consistent with findings in S. cerevisiae, MoGlo3 is localized to the Golgi, and tha

113 capitulate wild-type function and fitness in S. cerevisiae We also find that the electrostatic charge

114 and compared them to those already found in S. cerevisiae We observed common features between the tw

115 aintains cohesin on chromosomes during G1 in S. cerevisiae cells.

116 II transcription, with about 10% of genes in S. cerevisiae dependent on SAGA.

117 The CgSTE11 homolog in S. cerevisiae plays crucial roles in various mitogen-act

118 s nonacetylatable Smc3 mutants are lethal in S. cerevisiae, they are not in S. pombe We show that the

119 that involves nascent transcript mapping in S. cerevisiae strains containing foreign yeast DNA.

120 tions to rewire central carbon metabolism in S. cerevisiae, enabling biosynthesis of cytosolic acetyl

121 Using fast DNA tracking microscopy in S. cerevisiae cells and improved analysis of mean square

122 tes the deposition of these modifications in S. cerevisiae under conditions of replicative stress.

123 ASC1 mutants in S. cerevisiae display compromised translation of specifi

124 and repair outcomes in histone H2 mutants in S. cerevisiae.

125 The 390Q mutation in S. cerevisiae TUB2 did not affect growth under basal con

126 C1 to the PHO regulon previously observed in S. cerevisiae was genetically shown in C. albicans using

127 at the HML and HMR loci than was observed in S. cerevisiae.

128 an short ones, a feature that is opposite in S. cerevisiae Differences in PAS placement between conve

129 o the DNA sequence-specificity of origins in S. cerevisiae and Orc4 alpha-helix mutations change geno

130 ase(s) responsible for activating the PDC in S. cerevisiae has not been conclusively defined.

131 Functional genomic analysis was performed in S. cerevisiae and zebrafish.

132 Our data show that pH in S. cerevisiae changes over several time scales, and that

133 induces three times as many genes as Pho4 in S. cerevisiae does.

134 fine Ptc6p as the primary PDC phosphatase in S. cerevisiae Our analyses further suggest additional su

135 etion mutants of kinases and phosphatases in S. cerevisiae we show that epistatic NEMs can point to m

136 an, i.e., the major carbohydrates present in S. cerevisiae, and principal components analysis reveale

137 nd screen for increased L-DOPA production in S. cerevisiae using FACS enrichment of an enzyme-coupled

138 ic, antifungal and anticancer properties, in S. cerevisiae.

139 fy ~600 putative multifunctional proteins in S. cerevisiae.

140 ngineering, and expression quantification in S. cerevisiae.

141 We addressed this question in S. cerevisiae, where tropomyosins (Tpm1 and Tpm2), profi

142 Here, we studied these reactions in S. cerevisiae CytcO, which serves as a model of the mamm

143 proteins are known from previous research in S. cerevisiae and S. pombe to play roles in the cell cyc

144 and 5-fold titer increases, respectively, in S. cerevisiae, while not affecting growth, which was in

145 erase and H3K4 demethylase, respectively, in S. cerevisiae.

146 a non-natural mcm(5) isoC ribonucleoside in S. cerevisiae total tRNA hydrolysate by higher-energy co

147 e addressed this in vivo, analyzing RNAPI in S. cerevisiae.

148 r genes (25S rDNA, ARX1, CTT1, and RPL30) in S. cerevisiae under normal and stressed conditions.

149 iction tools to screen intronic sequences in S. cerevisiae and 36 other fungi.

150 likely to contribute to glucose signaling in S. cerevisiae on the level of ScHxk2-S15 phosphorylation

151 We observed phenotypic similarity in S. cerevisiae genetic interaction data between mitochond

152 it is a key regulator of meiotic splicing in S. cerevisiae.

153 titutive expression of the nanobody suite in S. cerevisiae detect accessible and obstructed surfaces

154 omosomal reshuffling, with a higher tempo in S. cerevisiae.

155 nificantly better conserved in human than in S. cerevisiae.

156 We provide evidence that in S. cerevisiae Cdc3 guanidinium occupies the site of a 'm

157 ssue, Deng et al. (2015) demonstrate that in S. cerevisiae RPA and Mre11-Sae2 cooperate to prevent th

158 We show here that in S. cerevisiae, both mechanisms exist and that each requi

159 dinately suppress pervasive transcription in S. cerevisiae and murine embryonic stem cells (mESCs).

160 unidirectional nature of lysine transport in S. cerevisiae by the extraordinary kinetics of Lyp1 and

161 compared with the APOL1 nonrisk variants in S. cerevisiae, including impairment of vacuole acidifica

162 Prior to pathway assembly by VEGAS in S. cerevisiae, each gene is assigned an appropriate pair

163 Working in S. cerevisiae, and to study the assembly of these two es

164 r-brewing yeasts, have inherited inactivated S. cerevisiae alleles of critical phenolic off-flavour g

165 do they form a disulfide bond in the intact S. cerevisiae GPIT.

166 we have transferred human fragile zones into S. cerevisiae in the context of a genetic assay to under

167 ification and characterization of the 89-kDa S. cerevisiae Sen1 helicase domain (Sen1-HD) produced in

168 is a powerful tool for mRNA imaging in live S. cerevisiae with high spatial-temporal resolution and

169 ution of fitness consequences versus matched S. cerevisiae hemizygous diploids.

170 set of the random 5' UTRs as well as native S. cerevisiae 5' UTRs.

171 o create hybrids such that each nonessential S. cerevisiae allele is deleted.

172 is consistent with a genome-wide analysis of S. cerevisiae, which reveals that under favourable growt

173 bly system), exploits the native capacity of S. cerevisiae to perform homologous recombination and ef

174 In the case of S. cerevisiae, the OD600 method failed to distinguish be

175 cation concentrations in the yeast cells of S. cerevisiae.

176 light into the holistic characterization of S. cerevisiae pheno-metabolome in must fermentative cond

177 by the construction and characterization of S. cerevisiae strains whose growth depended on two nonna

178 mainly formed and degraded in the cytosol of S. cerevisiae cells in a process that couples D-2HG meta

179 ined the role of TFIID by rapid depletion of S. cerevisiae TFIID subunits and measurement of changes

180 with insect cell expressed luminal domain of S. cerevisiae Gpi16.

181 We determined that the tandem SH2 domain of S. cerevisiae Spt6 binds the linker region of the RNA po

182 T, our data show that the luminal domains of S. cerevisiae Gpi8 and S. cerevisiae Gpi16 do not intera

183 g that deletion of the activation domains of S. cerevisiae Med2 and Med3, as well as C. dubliniensis

184 ed in-line during fed-batch fermentations of S. cerevisiae.

185 Remarkably, hundreds of S. cerevisiae mRNAs that contain ribosome stall sequence

186 of-principle, we explore the interactions of S. cerevisiae Proliferating Cell Nuclear Antigen (yPCNA)

187 significantly alter the fitness landscape of S. cerevisiae We therefore provide evidence that transpo

188 effects on mRNA recruitment of a library of S. cerevisiae eIF3 functional variants spanning its 5 es

189 a previously unappreciated wild lifestyle of S. cerevisiae outside the restrictions of human environm

190 s dominula social wasps favors the mating of S. cerevisiae strains among themselves and with S. parad

191 within the TOR growth-signalling network of S. cerevisiae and, more generally, excised spliceosomal

192 troscopies, we show here that G-overhangs of S. cerevisiae form distinct Hoogsteen pairing-based seco

193 ively high frequency, in cell populations of S. cerevisiae.

194 ogether, our results unveil the potential of S. cerevisiae to study hBRAFV600E, to populate the netwo

195 The preparation of S. cerevisiae cells for superresolution imaging takes 2-

196 vestigated the evolutionary relationships of S. cerevisiae and Z. mobilis, two of the major microbial

197 ff-line 2D LC-MS/MS analysis (HILIC-RPLC) of S. cerevisiae whole cell lysate has been used to acquire

198 Off-line 2D LC-MS/MS analysis (SCX-RPLC) of S. cerevisiae whole cell lysate was used to generate a r

199 idy is well tolerated in the wild strains of S. cerevisiae that we studied and that the group of gene

200 n natural variants and laboratory strains of S. cerevisiae, we evaluated the karyotype and gene expre

201 y was frequently observed in wild strains of S. cerevisiae.

202 c electron microscopy (cryo-EM) structure of S. cerevisiae CIV in a III(2)IV(2) SC at 3.3 angstrom re

203 sent a cryo-electron microscopy structure of S. cerevisiae Hrd1 in complex with its endoplasmic retic

204 A 3.9 angstrom structure of S. cerevisiae ORC-Cdc6-Cdt1-Mcm2-7 (OCCM) bound to origi

205 the transcriptome and chromatin structure of S. cerevisiae upon quiescence entry.

206 and compared it with published structures of S. cerevisiae CBF3.

207 derivatives, but the endogenous substrate of S. cerevisiae Ydr109c and human FGGY has remained unknow

208 ustrated by the finding that YMR291W/TDA1 of S. cerevisiae and the homologous KLLA0A09713 gene of Klu

209 ology by analyzing the N- and C-terminome of S. cerevisiae, identifying 2190 N-termini and 1562 C-ter

210 isiae; inoculum size and inoculation time of S. cerevisiae; fermentation time and temperature) result

211 tage relative to S. bayanus; transgenesis of S. cerevisiae GAL promoter alleles or GAL coding regions

212 n and mass spectrometry analyses, the use of S. cerevisiae as a model system, and the assessment of c

213 aboratory strains nor in natural variants of S. cerevisiae.

214 wild populations have had a strong impact on S. cerevisiae population structure.

215 effects of amphotericin-B and miconazole on S. cerevisiae through the device's time-dependent freque

216 ified as Cdc14 interactors in C. albicans or S. cerevisiae.

217 hologs identified in mammals, C. elegans, or S. cerevisiae in addition to 595 novel candidate RBPs.

218 testine of social wasps hosts highly outbred S. cerevisiae strains as well as a rare S. cerevisiaexS.

219 C. elegans dauer larvae and stationary phase S. cerevisiae require elevated amounts of the disacchari

220 constituted retrotranslocation with purified S. cerevisiae proteins, using proteoliposomes containing

221 er suggest additional substrates for related S. cerevisiae phosphatases and describe the overall phos

222 Our findings reveal that IZP-resistant S. cerevisiae clones carry mutations in genes involved i

223 verge quantitatively from its highly similar S. cerevisiae ortholog Ded1p.

224 ntified Ptc6p as the primary-and likely sole-S. cerevisiae PDC phosphatase, closing a key knowledge g

225 n integrated database covering four species (S. cerevisiae, C. elegans, D. melanogaster and H. sapien

226 enylation sites (PASs) in two yeast species, S. cerevisiae and S. pombe Although >80% of the mRNA gen

227 to produce bioactive yields that allow spent S. cerevisiae growth media to have antibacterial action

228 By harnessing this experimental system, S. cerevisiae is used to (i) determine the genetic inter

229 Interestingly, BII specifically targeted S. cerevisiae, whereas BL6 more effectively inhibited E.

230 itochondrial genome from a parent other than S. cerevisiae, which recent functional studies suggest c

231 be appears to have evolved less rapidly than S. cerevisiae so that it retains more characteristics of

232 Our results demonstrate that S. cerevisiae Replication Factor C (yRFC) can load yPCNA

233 This work demonstrates that S. cerevisiae can be engineered to perform the complex b

234 We show here that S. cerevisiae also acquires mutations in a gene encoding

235 Here, we report that S. cerevisiae cells regulate carbon and nitrogen metabol

236 Here, we show that S. cerevisiae actively forms the D enantiomer of 2HG.

237 Here we show that S. cerevisiae CMG tracks with force while encircling dou

238 Here we show that S. cerevisiae eIF4A and Ded1p directly interact with eac

239 We further show that S. cerevisiae experiences homologous metabolic constrain

240 Previously, we have shown that S. cerevisiae broadly re-configures the nutrient transpo

241 inase remains unclear, but we speculate that S. cerevisiae Ydr109c and human FGGY could act as metabo

242 This analysis suggests that S. cerevisiae from pulque is most closely related to Asi

243 Accordingly, the S. cerevisiae genome encodes two homologs of the human D

244 nd-specific nucleotide resolution across the S. cerevisiae and human genomes-and use the meiotic Spo1

245 G1 varies greatly around origins across the S. cerevisiae genome, and nucleosome occupancy around or

246 /- 20.1 nmol*min(-1)*mg(-1)) that allows the S. cerevisiae strain to show significant growth with xyl

247 r strains and found that ale strains and the S. cerevisiae portion of allotetraploid lager strains we

248 eins and protein complexes implicated by the S. cerevisiae eGIS genes revealed a significant enrichme

249 alization of leading-strand synthesis by the S. cerevisiae replisome at the single-molecule level.

250 In one, we disrupted the S. cerevisiae INO80 protein interaction network by isola

251 ometry (GC/TOF-MS), here used to examine the S. cerevisiae metabolome.

252 Furthermore, the ADH-Nafion bonding for the S. cerevisiae strain was confirmed to be 3 times higher

253 onstitute the 34 proteins needed to form the S. cerevisiae replisome and show how changing local conc

254 nal properties of an 81-residue IDR from the S. cerevisiae transcription factor Ash1.

255 In the S. cerevisiae protein-protein interaction network, the h

256 Insertion of Ty1 elements into the S. cerevisiae genome, which occurs upstream of genes tra

257 the previously determined cryo-EM map of the S. cerevisiae CCAN-Cenp-ANuc complex.

258 reveals new detail about the folding of the S. cerevisiae genome.

259 However, colocalization of the S. cerevisiae mispair recognition proteins with the repl

260 tion drives the polarized orientation of the S. cerevisiae mitotic spindle and primes the invariant i

261 Here we report the structure of the S. cerevisiae Pol II-Rad26 complex solved by cryo-electr

262 We report a cryo-EM structure of the S. cerevisiae RNase MRP holoenzyme solved to 3.0 angstro

263 th efficient mating with cells producing the S. cerevisiae pheromone and near-perfect discrimination

264 d mating efficiency with cells producing the S. cerevisiae pheromone, resulting in low fitness.

265 Here we show that the S. cerevisiae Atg19, Atg34 and the human p62, Optineurin

266 The data indicate that the S. cerevisiae CytcO uses the D pathway for proton uptake

267 and cyclic versions of peptides bind to the S. cerevisiae AAA+ ATPase Vps4 with similar affinities,

268 h shares 25 and 19% sequence identity to the S. cerevisiae and Homo sapiens orthologs of Usb1, respec

269 shed by mating Saccharomyces uvarum with the S. cerevisiae deletion collection to create hybrids such

270 share almost no sequence similarity with the S. cerevisiae homolog.

271 : three co-inoculated with L. thermotolerans:S. cerevisiae, at the ratio of 50:1, 20:1 and 5:1 respec

272 We identified three S. cerevisiae strains that lack endogenous 2mu plasmids

273 tonin during the fermentation process: three S. cerevisiae strains and the two non-Saccharomyces.

274 In contrast to S. cerevisiae SIR1's partially dispensable role in silen

275 t least one additional transporter native to S. cerevisiae (Pdr12).

276 Today, S. cerevisiae strains residing in vineyards around the w

277 Then, using transcriptome data from tolerant S. cerevisiae strain NRRL Y-50049 and a wild-type intole

278 ucose supplemented with galactose, wild-type S. cerevisiae repressed GAL gene expression and had a ro

279 Using S. cerevisiae proteins, we identified sequence and struc

280 stitution of Pol epsilon-dependent MMR using S. cerevisiae proteins.

281 ation of conditions (cell ratio of H. uvarum/S. cerevisiae; inoculum size and inoculation time of S.

282 rly sensitive to transcript folding, as were S. cerevisiae RNAPII and RNAPIII.

283 When S. cerevisiae grows on a nonfermentable carbon source, i

284 translocations and transpositions), whereas S. cerevisiae accumulates unbalanced rearrangements (nov

285 ion studies performed by Hose et al. on wild S. cerevisiae strains.

286 ns (which last shared a common ancestor with S. cerevisiae some 300 million years ago), we show that

287 Compared with S. cerevisiae, C. glabrata exhibits higher innate tolera

288 hensive gene dispensability comparisons with S. cerevisiae predicted diverged dispensability at 12% o

289 formation were faster in wort fermented with S. cerevisiae than with S. pastorianus.

290 ent was higher than in ciders fermented with S. cerevisiae.

291 Hybrids with S. cerevisiae contributions originated from three lineag

292 nce variation and allelic differences within S. cerevisiae.

293 ce that the GAL lncRNAs in the budding yeast S. cerevisiae promote transcriptional induction in trans

294 s up to 250 kb from complex genomes in yeast S. cerevisiae has been developed more than a decade ago.

295 namely >700 export substrates from the yeast S. cerevisiae, approximately 1000 from Xenopus oocytes a

296 focus on two metabolic enzymes of the yeast S. cerevisiae, neutral trehalase (Nth1) and glycogen pho

297 exemplified for the cell cycle in the yeast S. cerevisiae.

298 e application of a commercial brewing yeast (S. cerevisiae Nottingham Ale), entrapped into chitosan-c

299 CCS1, the budding yeast (S. cerevisiae) Cu chaperone for Cu-zinc (Zn) superoxide

300 ncrease upon Puf3 deletion in budding yeast (S. cerevisiae) suggests that the output of the RNA regul