ライフサイエンスコーパス: budding

1 ruption of Vps4 recruitment stalled membrane budding.

2 ment formation with minimal effects on virus budding.

3 roposed role of M2 in scission at the end of budding.

4 migration signatures characteristic of organ budding.

5 e main driving force for virion assembly and budding.

6 ving limited effects on total virus particle budding.

7 simultaneously and relatively rapidly after budding.

8 the membrane, triggering polymerization and budding.

9 s to virus assembly sites where they mediate budding.

10 ure Gag lattice formation and virus particle budding.

11 budding processes, from endocytosis to viral budding.

12 e been reported as important or essential in budding.

13 oylated and plays an important role in virus budding.

14 ma membrane, which is the site of alphavirus budding.

15 ndrial RNAs are affected by inhibition of NE budding.

16 critical mediators of viral trafficking and budding.

17 itin ligase via its WW domains to facilitate budding.

18 be palmitoylated and to positively regulate budding.

19 asm to the plasma membrane leading to virion budding.

20 ion, which may slow down or prevent membrane budding.

21 a process referred to nuclear envelope (NE) budding.

22 trafficked to the plasma membrane for virus budding.

23 ights, reported in the past, to asexual nest budding.

24 s of growth and morphogenesis in the stalked budding alphaproteobacterium Hyphomonas neptunium.

25 therto unknown function for Fgf20 in mammary budding and branching morphogenesis.

26 he presence of M2Y76A and mediated increased budding and filament formation even in the absence of M2

27 cation of the mRNAs bound to PUF proteins in budding and filamentous fungi and by computational analy

28 deness and sequentiality, as observed in the budding and fission yeast cell- cycle.

29 Micro-C XL maps of budding and fission yeast genomes capture both short-ran

30 Therefore, knowledge from the budding and fission yeast systems illuminates highly con

31 summary regarding the human gene homologs in budding and fission yeast, worm, fly, fish, mouse, and r

32 roles for Spt4 in controlling elongation in budding and fission yeast.

33 c and cytokinesis functions of Cdc14/Flp1 in budding and fission yeast.

34 lopments in studies of Cdc42 polarization in budding and fission yeasts and demonstrate that models d

35 We show that Mer2, identified so far only in budding and fission yeasts, is in fact evolutionarily co

36 rent antisense transcript landscapes between budding and fission yeasts.

37 The data suggest that influenza A virus budding and genome incorporation can occur independently

38 s a stable site of polarization that induces budding and inhibits formation of competing sites.

39 ast, which undergoes polarized growth during budding and mating, has been a useful model system to st

40 ijacked by many enveloped viruses to mediate budding and release.

41 cholesterol-dependent manner to cause virus budding and release.

42 ings and a potential relationship between NE budding and the NPC.

43 i membrane dispersal process that drives the budding and transport of secretory vesicles.

44 treatment of hepatocytes increases both VTV budding and VLDL secretion.

45 , to a process that is both endogenous (nest budding) and exogenous (loss of preferred habitat), resu

46 vitro basal crypt organoid proliferation and budding, and in vivo significantly reduced the number of

47 ocytosis, membranes transition among planar, budding, and vesicular topographies through nanoscale re

48 Vps17 can regulate early endosome fusion and budding as well as endocytosis.

49 hin the Alix-binding motif involved in virus budding, as major contributors to subtype-specific repli

50 was inhibited by LdSar1:T34N in an in vitro budding assay, indicating that GTP-bound LdSar1 is requi

51 igidity of the coat, allowing for successful budding at higher membrane tensions.

52 l for maintaining the correct polarity of LD budding at the nuclear envelope, restricting it to the o

53 An exception to this rule are budding bacteria, in which new offspring emerges de novo

54 ystem must overcome at the stage of membrane budding by an assembling protein coat.

55 nes, primarily localizes to the cytoplasm in budding cells.

56 atidylinositol-4-phosphate immediately after budding coincides with a burst of phosphatidylinositol-3

57 nkey virus (M-PMV) wild-type MA with its two budding deficient double mutants, that is, T41I/T78I and

58 The presence of HA and NP at the site of budding depends upon the coexpression of other viral pro

59 Late (L) budding domains of eVP40 recruit host proteins (e.g., Ts

60 s, whereas milk fat globules are released by budding, enwrapped by the plasma membrane.

61 Productive budding events required at least two additional Vps4 hex

62 y acquire their primary envelope not through budding from cellular membranes but by forming and exten

63 holesterol synthesis), viperin retards viral budding from infected cells.

64 endophilin B1 has been implicated in vesicle budding from intracellular organelles, including the tra

65 and VLDL secretion, we studied HCV particles budding from the ER en route to the Golgi compartment in

66 Moreover, Ldgp63-containing COPII vesicle budding from the ER was inhibited by LdSar1:T34N in an i

67 plasma membrane inner leaflet to facilitate budding from the host cell.

68 liana endosomes to measure cargo escape from budding ILVs.

69 RNA into the virus and forms the shell of a budding immature viral capsid.

70 Together with its role in HIV-1 entry and budding into host cells, the data herein indicate that H

71 tages of capsid formation, nuclear export by budding into the perinuclear space, tegument formation,

72 t interactions that promote or inhibit viral budding is warranted.

73 oleosin as the sole molecule responsible for budding-LD entering cytosol.

74 ary for oleosin targeting ER and moving onto budding LDs and extracting them to cytosol.

75 n endoplasmic reticulum (ER) and extracts ER-budding LDs to cytosol.

76 m of oleosin targeting ER-LDs and extracting budding LDs to the cytosol as well as reveal potential a

77 ed oleosin to enter the ER lumen and extract budding LDs to the ER lumen.

78 -type specific biological processes, such as budding, mating, mating type switch, consumption of nutr

79 This spontaneous budding mechanism gives key insights on cellular LD form

80 Recent studies indicate that NE budding might be an endogenous cellular process for the

81 Two models have been put forward: the budding model, based largely on structural data, and the

82 C. albicans budding mother cells were found to be nonadherent, which

83 ociated with activation of senescence, while budding of daughter cells was associated with senescence

84 Endophilins A1 and A2 promote the budding of endocytic vesicles from the plasma membrane,

85 mechanism of eHAV egress involving endosomal budding of HAV capsids into multivesicular bodies.

86 of M2-mediated membrane scission during the budding of influenza viruses.

87 RT-III executes membrane scission during the budding of intralumenal vesicles (ILVs) at endosomes.

88 cating that GTP-bound LdSar1 is required for budding of Ldgp63-containing COPII vesicles.

89 transport (ESCRT) machinery is necessary for budding of many enveloped viruses.

90 step in cellular-trafficking pathways is the budding of membranes by protein coats, which recent expe

91 ena such as perturbation growth, necking and budding of offspring droplets from a bulk body are obser

92 s that regulates segregation, packaging, and budding of peroxisomal importomer subcomplexes, thereby

93 f influenza virus proteins necessary for the budding of progeny virions needs to accumulate at budozo

94 oscopy and super-resolution imaging show the budding of syntaphilin cargos, which then share a ride o

95 ates that ILVs form individually from inward budding of the endosomal limiting membrane, plant ILVs f

96 (CME) involves nanoscale bending and inward budding of the plasma membrane, by which cells regulate

97 mammalian cells results in the formation and budding of virus-like particles (VLPs) which mimic the b

98 developmental biology continues to roll on, budding off more disciplines, while retaining its own id

99 ffectively prevents TF from participating in budding or being incorporated into virus particles.

100 droplets released by cells through membrane budding or exocytosis.

101 zomycotina, which are absent or divergent in budding or fission yeasts.

102 anching morphogenesis, new branches form by "budding" or "clefting." Cell migration, proliferation, r

103 cation, virion assembly, or virus egress via budding out of infected cells.

104 The model demonstrates that the axial budding pattern enhances mating probability at an early

105 robability at an early stage and the bipolar budding pattern improves colony development under nutrie

106 hment, not much is known about how different budding patterns give rise to different functions at the

107 virus-like particles (VLPs) which mimic the budding process and morphology of authentic, infectious

108 To complete the budding process, eVP40 utilizes its PPXY L-domain motif

109 ward identifying the machinery mediating the budding process, we performed comprehensive mutational a

110 Membrane scission is a crucial step in all budding processes, from endocytosis to viral budding.

111 f the ESCRT cargo would escape from a single budding profile in 5-20 ms and from three concatenated I

112 We also developed a cell-free COPII vesicle budding reaction that reconstitutes the capture of PC1 i

113 free coat protein complex II (COPII) vesicle budding reaction, that mutant TREM2 is exported efficien

114 ecular mechanisms of NC's involvement in HIV budding remain unclear.

115 n-selective channel and facilitator of viral budding, replacing the need for the ESCRT proteins that

116 to external growth cues, local growth-driven budding, self-sustaining elongation, and the triggering

117 as found to be biologically relevant for VLP budding since (i) small interfering RNA (siRNA) knockdow

118 VAP is recruited to retromer budding sites on endosomes via an interaction with the r

119 eassemble before arriving at plasma membrane budding sites.IMPORTANCE Hendra virus and Nipah virus ar

120 nging from receptor down-regulation to viral budding to cytokinesis.

121 nistic fungal pathogen Candida albicans from budding to hyphal growth has been implicated in its abil

122 athogen Candida albicans can transition from budding to hyphal growth, which promotes biofilm formati

123 at the same site on the plasma membrane for budding to occur.

124 ies connect defects in RNA export through NE budding to progressive loss of mitochondrial integrity a

125 This budding transition does not require any energy-consuming

126 docytosis and on syntenin-syndecan endosomal budding, upstream of ARF6 small GTPase and its effector

127 nd ECM dynamics have varied roles in driving budding versus clefting in different organs.

128 ol mediates M2 clustering to the neck of the budding virus to cause the necessary curvature for membr

129 vitro crypt organoid proliferation and crypt budding was abrogated by the Wnt inhibitor IWP2.

130 Membrane budding was associated with continuous, stochastic excha

131 e a portion of the host cell membrane during budding, which then constitutes part of the virus partic

132 ese results suggest a mechanism to delay ILV budding while cargoes undergo deubiquitination.

133 ated cargoes to trap them at the site of ILV budding while the cargoes undergo deubiquitination.

134 a Cdc42 GTPase-activating protein, prevents budding within the division site by inhibiting Cdc42 rep

135 In budding yeast (Saccharomyces cerevisiae) the multilayere

136 control of autophagic proteasome turnover in budding yeast (Saccharomyces cerevisiae).

137 gene expression output, we have conducted in budding yeast a large-scale measurement of the activity

138 Using budding yeast and human cell line model systems, we exam

139 In contrast, herein we analyze Hi-C data for budding yeast and identify 200-kb scale TADs, whose boun

140 ily of endocytic adaptors, including Syp1 in budding yeast and its mammalian orthologue, FCHo1.

141 in and regulate force, we purified SPBs from budding yeast and used laser trapping to manipulate sing

142 e role of mitochondria in this process using budding yeast as a model.

143 The interaction pattern of budding yeast as measured from genome-wide 3C studies ar

144 explored the extent of genomic robustness in budding yeast by genome wide dosage suppressor analysis

145 Dynein mediates spindle positioning in budding yeast by pulling on astral microtubules (MTs) fr

146 r to produce rejuvenated daughters, dividing budding yeast cells confine aging factors, including pro

147 Mating of budding yeast cells is a model system for studying cell-

148 elicase function of Dna2 in end resection in budding yeast cells lacking exonuclease 1.

149 in have shown that in response to pheromone, budding yeast cells undergo a rise of cytosolic Ca(2+) t

150 xpressed wild-type levels of mcm10-m2,3,4 in budding yeast cells, we observed a severe growth defect

151 severe growth and DNA replication defects in budding yeast cells, with diminished DDK phosphorylation

152 dicate aggregate activity observed in living budding yeast cells.

153 properties of formaldehyde-cross-linking in budding yeast cells.

154 One such locus is the budding yeast centromere, which is a paradigm for target

155 to argue that the small, highly constrained budding yeast chromosomes could not have these structure

156 a two-dimensional agent-based model to study budding yeast colonies with cell-type specific biologica

157 Purification of budding yeast condensin reveals that it occurs not only

158 report the finding of a new function for the budding yeast Cse4/CENP-A histone-fold domain interactin

159 In particular, budding yeast daughter cells are more vulnerable to stre

160 2017) have reconstituted rapid and regulated budding yeast DNA replication on naked and chromatinized

161 We used natural budding yeast DNA replication origins and synthetic DNA

162 The spindle pole body (SPB) of budding yeast duplicates once per cell cycle.

163 c cells because most prior studies have used budding yeast for RLS studies.

164 IN), we performed genome-wide screens in the budding yeast for yeast genes that cause CIN when overex

165 rm to multicellular filaments is crucial for budding yeast foraging and the pathogenesis of many fung

166 Budding yeast Fun30 and human SMARCAD1 are cell cycle-re

167 To examine whether budding yeast function at this limit of full ribosomal u

168 model (mC-SAC) to gain understanding of the budding yeast genome organization.

169 rates for UV-induced lesions throughout the budding yeast genome.

170 d two different strategies for size control: budding yeast has been proposed to use an inhibitor-dilu

171 Here we study budding yeast in dynamic environments of hyperosmotic st

172 mitochondrial carrier family protein Pic2 in budding yeast is a copper importer.

173 lucose-mediated repression of respiration in budding yeast is at least partly due to the low cellular

174 Heterochromatin formation in budding yeast is regulated by the silent information reg

175 One step in this assembly in budding yeast is the association of Cdc45 with the Mcm2-

176 to other eukaryotes with symmetric division, budding yeast keeps the nascent transcription rates of i

177 d here the forces that ensembles of purified budding yeast kinesin-5 Cin8 produce in microtubule glid

178 model of microtubule depolymerization by the budding yeast kinesin-8, Kip3.

179 iscussion, we will use the relatively simple budding yeast kinetochore as a model, and extrapolate in

180 he binding of Bub3-Bub1 and Mad1-Mad2 to the budding yeast kinetochore.

181 anisms of group formation in the unicellular budding yeast Kluyveromyces lactis.

182 is study, we find that Stu1 recruits Stu2 to budding yeast KTs, which promotes MT generation there.

183 Msp1 is a conserved AAA ATPase in budding yeast localized to mitochondria where it prevent

184 In budding yeast meiosis, homologous chromosomes become lin

185 Here we show that the budding yeast mismatch repair related MutLbeta complex,

186 Here, using the budding yeast model, we show that the abundant PP2A(Cdc5

187 The budding yeast Mre11-Rad50-Xrs2 (MRX) complex and Sae2 fu

188 Fluorescent labeling of budding yeast nucleoli with CDC14-GFP revealed that a sp

189 work defines spatial organization within the budding yeast nucleus, demonstrates the conserved role o

190 Boi1 and Boi2 (Boi1/2) are budding yeast plasma membrane proteins that function in

191 The budding yeast Polo-like kinase Cdc5 is a key regulator o

192 Microfluidic experiments on budding yeast populations in space-limited environments

193 is essential, we previously interrogated the budding yeast proteome to identify candidates that funct

194 ith our in vitro results, our experiments in budding yeast provide evidence that Rad52 inverse strand

195 Although budding yeast Rad51 has been extensively characterized i

196 Here we show that Y1F substitution in budding yeast resulted in a strong slow-growth phenotype

197 RCT domain protein Brc1, which is related to budding yeast Rtt107 and mammalian PTIP, plays an import

198 The budding yeast Saccharomyces cerevisiae is a long-standin

199 Under aerobic conditions, the budding yeast Saccharomyces cerevisiae metabolizes gluco

200 The budding yeast Saccharomyces cerevisiae stores iron in th

201 zed a set of strong, synthetic promoters for budding yeast Saccharomyces cerevisiae that are inducibl

202 this obstacle, we engineered strains of the budding yeast Saccharomyces cerevisiae that differ only

203 Ras1 is a small GTPase in the budding yeast Saccharomyces cerevisiae that regulates nu

204 rms multiple vital cellular functions in the budding yeast Saccharomyces cerevisiae These include reg

205 of nuclear microtubule (MT) dynamics in the budding yeast Saccharomyces cerevisiae This activity req

206 encing), for mapping hybrid-prone regions in budding yeast Saccharomyces cerevisiae Using this method

207 The alpha pheromone from the budding yeast Saccharomyces cerevisiae, a 13-residue pep

208 n Drosophila melanogaster, the cell cycle of budding yeast Saccharomyces cerevisiae, and the floral o

209 In the budding yeast Saccharomyces cerevisiae, ECM remodeling r

210 e, we report on experimental results for the budding yeast Saccharomyces cerevisiae, finding, surpris

211 In budding yeast Saccharomyces cerevisiae, the ten-subunit

212 P protein that is homologous to Glo3p of the budding yeast Saccharomyces cerevisiae.

213 in solution with purified proteins from the budding yeast Saccharomyces cerevisiae.

214 regulator dynamics during endocytosis in the budding yeast Saccharomyces cerevisiae.

215 ys a central role in zinc homeostasis in the budding yeast Saccharomyces cerevisiae.

216 assembly pathway produces the two species of budding yeast septin hetero-octamers: Cdc11/Shs1-Cdc12-C

217 Here, we investigate the role of the budding yeast Shu complex in promoting homologous recomb

218 This domain also exhibits homology with budding yeast Sld7.

219 e Arabidopsis RNaseIII enzyme resembling the budding yeast small interfering RNA (siRNA)-producing Dc

220 unctional similarities between Ppc89 and the budding yeast SPB scaffold Spc42, distribution of Sad1 t

221 expressed the human RAD52 gene (HsRAD52) in budding yeast strains lacking the endogenous RAD52 gene

222 maging and deep sequencing, we show that the budding yeast telomerase RNA (TLC1 RNA) is spatially seg

223 characterized in vivo system using data from budding yeast that have been synchronized in the cell cy

224 1 is a meiosis-specific MAP kinase (MAPK) in budding yeast that is required for spore formation.

225 lation, we carried out ribosome profiling in budding yeast to characterize 57 nonessential genes invo

226 f truncations and artificial dimerization in budding yeast to define the minimal CPC elements essenti

227 dics to investigate the adaptive response of budding yeast to temporally controlled H2O2 stress patte

228 For example, in the case of the budding yeast transcription factor Msn2, different stres

229 ehensive analysis of nucleosome positions as budding yeast transit through an ultradian cycle in whic

230 tubules assembled in vitro from mammalian or budding yeast tubulin.

231 In budding yeast, alignment of the anaphase spindle along t

232 ofore unknown biological responses to VPA in budding yeast, and highlight the broad spectrum of cellu

233 urveillance pathways were first described in budding yeast, and there are now high-resolution structu

234 its inhibitor Sic1 at the G1/S checkpoint in budding yeast, APC:Cdc20 and its inhibitor MCC at the mi

235 the oscillations of the anaphase spindle in budding yeast, but in A. gossypii, this system is not re

236 ons were also observed in vegetative diploid budding yeast, but their functional significance is unkn

237 In budding yeast, cell cycle progression and ribosome bioge

238 In budding yeast, cell size is thought to be controlled alm

239 In budding yeast, cell size primarily modulates the duratio

240 In budding yeast, centromere establishment begins with the

241 This mutant, when expressed in budding yeast, diminished cell growth and DNA replicatio

242 In budding yeast, dynein moves the mitotic spindle to the p

243 In budding yeast, each chromosome has a point centromere up

244 ere are two distinct TRAPP complexes, yet in budding yeast, four distinct TRAPP complexes have been r

245 Here we show that in budding yeast, Hsf1 basally associates with the chaperon

246 series of transcriptome sequencing data from budding yeast, in high temporal resolution over ca. 2.5

247 In budding yeast, it is required for the dynamicity of spin

248 We discovered that in budding yeast, kinetochore inactivation occurs by reduci

249 Here, we show that in budding yeast, mutations in the DEAD-box ATPase Dhh1 tha

250 In budding yeast, polarization is associated with a focus o

251 In budding yeast, proper execution of cytokinesis and cell

252 In budding yeast, Rph1 transcriptionally represses many DNA

253 single-probe FISH protocol termed sFISH for budding yeast, Saccharomyces cerevisiae using a single D

254 The budding yeast, Saccharomyces cerevisiae, harbors several

255 In budding yeast, selection of a bud site directs polarity

256 iptional splicing and splicing efficiency in budding yeast, suggesting that splicing is more efficien

257 his manuscript, using purified proteins from budding yeast, that Mcm10 directly interacts with the Mc

258 In budding yeast, the 3' end processing of mRNA and the cou

259 Here, we show that, in contrast to budding yeast, the horsetail movement is largely radiati

260 In budding yeast, the nuclear RNA surveillance system is ac

261 In budding yeast, the protein Gps1 plays a pivotal role in

262 In budding yeast, the scaffold Bem1 contributes to polarity

263 ng formation are well studied in fission and budding yeast, there is relatively poor understanding of

264 Using budding yeast, we demonstrate that global genotoxic dama

265 , bead-spring representation of chromatin in budding yeast, we find enrichment of protein-mediated, d

266 Here, this question is addressed in budding yeast, where during meiosis Spr3 and Spr28 repla

267 specific context of mating-type switching in budding yeast, which is a model system for homologous re

268 Budding yeast, which undergoes polarized growth during b

269 tial to fulfil recombinational DNA repair in budding yeast.

270 g numerous pathways that lack equivalents in budding yeast.

271 one of the two major osmosensing pathways in budding yeast.

272 two splicing isoforms of the same protein in budding yeast.

273 lance of defective nuclear pore complexes in budding yeast.

274 location and role in global transcription in budding yeast.

275 determinant of cell size in bacteria and in budding yeast.

276 CAT-tailing in nascent-chain degradation in budding yeast.

277 themes are beginning to emerge, primarily in budding yeast.

278 ons enriched on chromatin bearing a DSB from budding yeast.

279 We investigated this model in budding yeast.

280 CTD for transcription during mitosis in the budding yeast.

281 or of the unfolded protein response (UPR) in budding yeast.

282 ous genes were analyzed on a global scale in budding yeast.

283 shing PS and PE plasma membrane asymmetry in budding yeast.

284 ng and spindle alignment during metaphase in budding yeast.

285 arget for actin cable assembly regulation in budding yeast.

286 es an attractive and complementary system to budding yeast.

287 en attributed to the metalloprotease Wss1 in budding yeast.

288 s have not been implicated in respiration in budding yeast.

289 CDC) and the yeast metabolic cycle (YMC), in budding yeast.

290 at links mitotic entry to membrane growth in budding yeast.

291 and in enhancing promoter directionality in budding yeast.

292 sm for the emergence of copper resistance in budding yeast.

293 conformation and 3D nuclear organization in budding yeast.

294 e signal transduction and gene expression in budding yeast.

295 re immediate effect in the early anaphase of budding yeast.

296 at is called B55 in vertebrates and Cdc55 in budding yeast.

297 owth rate via the TORC2 signaling network in budding yeast.

298 larizes dynein-mediated spindle movements in budding yeast.

299 is play a major role in cell size control in budding yeast.

300 We used the budding yeasts Saccharomyces cerevisiae and Torulaspora