ライフサイエンスコーパス: spindle pole body

1 ituated in proximity to one of the two SPBs (spindle pole bodies).

2 this function involves association with the spindle pole body.

3 ub2p/Bfa1p are located on the daughter-bound spindle pole body.

4 s to interact with Bbp1p, a component of the spindle pole body.

5 STU2 encodes a component of the spindle pole body.

6 r3p-GFP was found at the nuclear side of the spindle pole body.

7 e gammaTuRC and anchors the gammaTuRC to the spindle pole body.

8 l early mitosis when they co-localize at the spindle pole body.

9 DNA replication but unable to duplicate the spindle pole body.

10 identify a unique link between NuA4 and the spindle pole body.

11 hat tethers the gamma-tubulin complex to the spindle pole body.

12 this domain alone is able to localize to the spindle pole body.

13 uch as nuclear pore complexes (NPCs) and the spindle pole body.

14 nship between nuclear pore complexes and the spindle pole body.

15 se, FgCdc14-GFP localized to the nucleus and spindle-pole-body.

16 clb4 mad2 cells accumulated with unseparated spindle pole bodies.

17 tach to spindles emanating from the opposite spindle pole bodies.

18 f the nucleus or coalescence of the parental spindle pole bodies.

19 bundles of cytoplasmic microtubules from the spindle pole bodies.

20 recent birth scar, not with asymmetry in the spindle pole bodies.

21 ble microtubules were observed unattached to spindle pole bodies.

22 induce lethality in mutants defective in the spindle pole bodies.

23 quently localizes to the mitotic spindle and spindle pole bodies.

24 Most components of the MEN localize to spindle pole bodies.

25 the speed and acceleration of two separating spindle pole bodies.

26 tation of sister centromeres toward opposite spindle pole bodies.

27 ulation in diploid Saccharomyces cerevisiae, spindle pole bodies acquire the so-called meiotic plaque

28 ughout the cell, becomes concentrated at the spindle pole bodies after the meiosis I division, and at

29 h Cdc2 protein kinase activity and separated spindle pole bodies, an arrest state similar to that obs

30 antibodies shows that CaCse4p localizes near spindle pole bodies, analogous to the localization patte

31 have reduced amounts of gamma-tubulin at the spindle pole bodies and nucleation of spindle microtubul

32 rt of anaphase, GFP-Glc7p accumulated at the spindle pole bodies and remained there until cytokinesis

33 the nucleus in G2 and is mobilized onto the spindle pole bodies and spindle midzone at anaphase onse

34 ired for self-association and for binding to spindle pole bodies and that this domain is essential fo

35 ation is required for proper localization at spindle pole bodies and the cell division site, E3 ligas

36 During metaphase, KRIT1 is located on spindle pole bodies and the mitotic spindle.

37 ase transition and a fraction remains at the spindle pole bodies and the spindle midzone in anaphase

38 alization along aMTs, with enrichment at the spindle pole body and aMT plus ends.

39 stent with aggregation of centromeres at the spindle pole body and compartmentalization of individual

40 nase that is required for duplication of the spindle pole body and for the spindle assembly checkpoin

41 f19-HAp localizes to the nuclear face of the spindle pole body and genetically interacts with a spind

42 enesis, the temporal appearance of different spindle pole body and spindle structures, the cell cycle

43 work (MEN) driven by interaction between the spindle pole body and the bud cortex.

44 hree of these locations, the hyphal tip, the spindle pole body and the nucleus, correlate with previo

45 usion protein to the cytoplasmic side of the spindle pole body and used a kar9 mutant to show that ce

46 tion of the mitochondria was tethered to the spindle-pole bodies and moved to the cellular ends durin

47 a forespore membrane (FSM) initiates at each spindle-pole body and extends to form the spore envelope

48 e gamma-tubulin complex to both centrosomal (spindle pole body) and non-centrosomal sites.

49 ins Mpc70p localizes to only two of the four spindle pole bodies, and these are always nonsisters.

50 ulation of Nuf1p/Spc110p, a component of the spindle pole body, and in bud growth, by binding Myo2p,

51 tein markers to examine the dynamics of MTs, spindle pole body, and the nuclear envelope in living ce

52 perhaps by altering its localization to the spindle pole body, and, thus, that gamma-tubulin plays a

53 iae, vesicles transported to the vicinity of spindle pole bodies are fused to each other to generate

54 The paper also focuses attention on the two spindle pole bodies as potential sites for regulation of

55 I1, involved in the duplication of the yeast spindle pole body, as a critical regulator of centriole

56 the first evidence that the nuclear envelope spindle pole body assembly component Mps3p performs a fu

57 times in contractile rings and 7500 times in spindle pole bodies at certain times in the cell cycle.

58 ecause TINA is modified and localizes to the spindle pole bodies at mitosis, and lack of TINA causes

59 d chromatin was observed to segregate to the spindle pole bodies at rates greater than centromere to

60 re, we show that Sid2p is a component of the spindle pole body at all stages of the cell cycle and lo

61 e1, cytoplasmic microtubules detach from the spindle pole body at high rates.

62 C-terminal coiled-coil domains localized to spindle pole bodies but not along spindle microtubules.

63 e An-Nup84-120 complex locates to the NE and spindle pole bodies but, unlike vertebrate cells, does n

64 Thus, Sid2p, a component of the spindle pole body, by virtue of its transient localizati

65 mplicated three of these genes in centrosome/spindle pole body, centromere, and cohesion function.

66 yces cerevisiae, the cytoplasmic face of the spindle pole body changes from a site of microtubule ini

67 w that the localization of Spc72p within the spindle pole body changes throughout the cell cycle and

68 dosage of SPO21 leaves only two of the four spindle pole bodies competent to generate membranes.

69 The spindle pole body component Kar1p has a function in nucl

70 Interestingly, the meiosis-specific spindle pole body component Mpc54p, which is known to be

71 novel insights into the mechanism by which a spindle pole body component, when mutated, contributes t

72 sickened by the mutation of genes coding for spindle pole body components and that spo7Delta was synt

73 leading to changes in nuclear shape, loss of spindle pole body components from the nuclear envelope,

74 In spo7Delta cells, the spindle pole body defect of mps3 mutants was exacerbated

75 In some of these cells, the spindle pole body did not interact with the bud or the n

76 Our data can be explained by conservative spindle pole body distribution in which the two newly sy

77 ding of the recombinant Tub4p complex to the spindle pole body docking protein Spc110p affects its nu

78 f microtubule-organizing activity to the the spindle pole body, driven by the novel coiled-coil prote

79 Mps3p is required for spindle pole body duplication and for a variety of other

80 lope SUN domain protein that is required for spindle pole body duplication and for sister chromatid c

81 Key steps in spindle pole body duplication are the sequential recruit

82 Spindle pole body duplication begins in G1 and continues

83 nsertion into the nuclear membrane or affect spindle pole body duplication by altering the nuclear en

84 ly, suggesting that under certain conditions spindle pole body duplication can occur via an Mps3p-ind

85 report that overexpression of NDC1 leads to spindle pole body duplication defects indistinguishable

86 quisitely sensitive to altered dosage of the spindle pole body duplication gene, NDC1.

87 o shown that germ tubes can evaginate before spindle pole body duplication, chitin ring formation, an

88 Defects in microtubule polymerization, spindle pole body duplication, microtubule motors, and k

89 Although kic1 mutants were not defective for spindle pole body duplication, they exhibited a variety

90 stress response; (2) ESCRT factors regulate spindle-pole-body duplication; and (3) a membrane-protei

91 stral microtubule organizing capacity of the spindle pole bodies during metaphase.

92 and found that Mob1p first localized to the spindle pole bodies during mid-anaphase and then localiz

93 observed that the asymmetric behavior of the spindle pole bodies during spindle assembly was lost in

94 to the nuclear envelope near the site of the spindle pole body during interphase.

95 Targeting to the spindle pole body during mitosis depends on Sid4 and Cdc

96 e strengths of microtubule attachment to the spindle pole body during these stages of the cell cycle.

97 calization and roles for Hei10 in centrosome/spindle pole body dynamics and associated nuclear traffi

98 in sealing the nuclear envelope in mammals, spindle pole body dynamics in fission yeast, and surveil

99 visiae, entry into S phase and separation of spindle pole bodies each require CDC4 and CDC34, which e

100 clear pore complexes either compete with the spindle pole body for insertion into the nuclear membran

101 a diffusion based mechanism, centred on the spindle pole body, for the coordination of DNA replicati

102 ng that nuclear membrane composition affects spindle pole body function.

103 ing protein, with additional uncharacterized spindle pole body functions.

104 MEN genes CDC5, CDC14, CDC15, and DBF2, and spindle pole body gene NUD1 but was independent of MYO1.

105 evidence that microtubule nucleators at the spindle pole body help coordinate cytokinetic furrow for

106 in humans, basal bodies in green algae, and spindle pole bodies in yeast.

107 r many years that centromeres cluster at the spindle pole body in fission yeast.

108 anized in the nuclear envelope, known as the spindle pole body in yeast (analogous to the centrosome

109 ls, with significant colocalization with the spindle pole body in zygotes.

110 us and the nucleus-associated organelle, the spindle pole body, in a NIMA-dependent manner.

111 ontrast to its important role at the central spindle pole body, in none of these cases is it clear th

112 vpr-expressing yeast cells, suggesting that spindle pole body integrity was perturbed.

113 This functional change in the spindle pole body involves the expansion and modificatio

114 plasmid with Kip1p in close proximity to the spindle pole body is reminiscent of that of a CEN report

115 that the relocalization of Spc72p within the spindle pole body is the 'landmark' event in the pheromo

116 ligase, but a direct (SCF) connection to the spindle pole body is unknown.

117 m1p was not required for Kar9p's cortical or spindle pole body localization.

118 charged surface patch that is implicated in spindle pole body localization.

119 in G1 and continues during early S-phase as spindle pole bodies mature and start to separate.

120 mponents of the gamma-tubulin complex to non-spindle pole body MTOCs and physically interacts with th

121 required for microtubule nucleation from non-spindle pole body MTOCs in fission yeast.

122 mponents of the gamma-tubulin complex to non-spindle pole body MTOCs.

123 ovel antiparallel bundle associated with the spindle pole body, named Q-MT bundle.

124 ly by ensuring the functionality of all four spindle pole bodies of a cell during meiosis II.

125 n which the two newly synthesized meiosis II spindle pole bodies of MPC70/mpc70 strains lack Mpc70p.

126 The spindle pole body of the budding yeast Saccharomyces cer

127 wo new papers report the localisation at the spindle pole body of the Cdc14 released in early anaphas

128 e that TINA is specifically localized to the spindle pole bodies only during mitosis in a microtubule

129 by inactivating centromere attachment to the spindle pole body or changing the position of ribosomal

130 of mononucleate meiotic cells but not to the spindle pole body or prospore membrane.

131 microtubule-organizing center (known as the spindle pole body or SPB) and the meiotic spindle.

132 spindle assembly and elongation, interphase spindle pole body positioning, and epithelial cell reorg

133 minal region with similarity to the S. pombe spindle pole body protein Sad1 and to two predicted mamm

134 a green fluorescent protein tag fused to the spindle pole body protein Spc42p.

135 proteins, Slk19p and Okp1p, but not with the spindle pole body protein, Spc42p.

136 In particular, two spindle pole body proteins, sad1p and the polo kinase pl

137 yces cerevisiae, the cytoplasmic face of the spindle pole body, referred to as the meiosis II outer p

138 Vik1p localizes to the spindle-pole body region in a Kar3p-dependent manner.

139 At this time, centromeres and spindle pole bodies relocate to the bud neck, explaining

140 consequence, there is a loss of asymmetry in spindle pole body segregation into the bud.

141 netic nodes around the equator 10 min before spindle pole body separation (cell-cycle time, -10 min)

142 ng the earliest stages of mitosis to mediate spindle pole body separation and formation of a bipolar

143 Bilobed nuclei appeared predominantly after spindle pole body separation, suggesting that nuclear en

144 More than 90 min prior to separation of the spindle pole bodies (SPB), the anillin-like protein (Mid

145 ere we describe how scaffolding the MEN onto spindle pole bodies (SPB-centrosome equivalent) allows t

146 ast, spindle orientation begins with the old spindle pole body (SPB) (from the preceding cell cycle)

147 function is required for duplication of the spindle pole body (SPB) [12], the centrosome-equivalent

148 Both Alp4 and Alp6 localize to the spindle pole body (SPB) and also to the equatorial MTOC.

149 The asymmetric localization of Kar9p to one spindle pole body (SPB) and microtubule (MT) plus ends r

150 Both Alp7 and Alp14 colocalize to the spindle pole body (SPB) and mitotic spindles.

151 ges through the nuclear envelope (NE) at the spindle pole body (SPB) and other sites.

152 uter plaques (MOPs), form on each meiosis II spindle pole body (SPB) and serve as sites of membrane n

153 ing yeast polo kinase Cdc5p localizes to the spindle pole body (SPB) and to the bud-neck and plays mu

154 Mob1p localizes to the spindle pole body (SPB) and to the cell-division site du

155 , while cytoplasmic microtubules vanish, the spindle pole body (SPB) assembles a long and stable mono

156 ein or tubulin revealed that the nucleus and spindle pole body (SPB) became oriented and tethered to

157 equired for linking telomeres to the meiotic spindle pole body (SPB) but not for attachment of telome

158 ecular architecture of the core of the yeast spindle pole body (SPB) by Bayesian integrative structur

159 It is organized at the spindle pole body (SPB) by the scaffold proteins Sid4p a

160 11 mutation in the Schizosaccharomyces pombe spindle pole body (SPB) component Cut12 both suppresses

161 Mutations in the spindle pole body (SPB) component Cut12 suppress otherwi

162 In this state, Cdc14 targets the spindle pole body (SPB) component Spc110 to counterbalan

163 The yeast spindle pole body (SPB) component Spc110p (Nuf1p) underg

164 The fission yeast spindle pole body (SPB) comprises a cytoplasmic structur

165 The regulation and timing of spindle pole body (SPB) duplication and maturation in fi

166 ual-specificity protein kinase essential for spindle pole body (SPB) duplication and required for the

167 n essential protein kinase that has roles in spindle pole body (SPB) duplication and the spindle chec

168 ast MPS2 or the NDC1 gene leads to identical spindle pole body (SPB) duplication defects: The newly f

169 The earliest known step in yeast spindle pole body (SPB) duplication requires Cdc31p and

170 During spindle pole body (SPB) duplication, the new SPB is asse

171 DNA replication, bud growth initiation, and spindle pole body (SPB) duplication.

172 /regulatory particle (RP), causes failure of spindle pole body (SPB) duplication.

173 on network (SIN), which first appears at the spindle pole body (SPB) during mitosis.

174 Sid1p localizes asymmetrically to one spindle pole body (SPB) in anaphase.

175 en for mutations that increase stress on the spindle pole body (SPB) in Saccharomyces cerevisiae.

176 The fission yeast interphase spindle pole body (SPB) is a bipartite structure in whic

177 The spindle pole body (SPB) is a multiprotein complex that o

178 (Saccharomyces cerevisiae) the multilayered spindle pole body (SPB) is embedded in the nuclear envel

179 duplication of the Saccharomyces cerevisiae spindle pole body (SPB) is required for formation of a b

180 The yeast spindle pole body (SPB) is the functional equivalent of

181 The spindle pole body (SPB) is the major microtubule-organiz

182 The spindle pole body (SPB) is the microtubule organizing ce

183 The spindle pole body (SPB) is the microtubule organizing ce

184 The spindle pole body (SPB) is the sole site of microtubule

185 Sid2p that is required for Mob1p binding and spindle pole body (SPB) localization.

186 isiae, nuclear pore complexes (NPCs) and the spindle pole body (SPB) must assemble into an intact nuc

187 The budding yeast spindle pole body (SPB) not only organizes the astral an

188 The spindle pole body (SPB) of budding yeast duplicates once

189 The SIN is assembled at the spindle pole body (SPB) on the scaffold proteins Cdc11 a

190 Duplication of the Saccharomyces cerevisiae spindle pole body (SPB) once per cell cycle is essential

191 8 kinesin in CDH1-m11 cells does not promote spindle pole body (SPB) separation.

192 The Saccharomyces cerevisiae spindle pole body (SPB) serves as the sole microtubule-o

193 pecific component of the outer plaque of the spindle pole body (SPB) that is required for prospore me

194 triggers exit from mitosis, localize to the spindle pole body (SPB) that migrates into the daughter

195 ike Pcp1 regulates multiple functions of the spindle pole body (SPB) through recruiting two critical

196 known 76.4-kDa protein that localizes to the spindle pole body (SPB) throughout the cell cycle.

197 First, the initial movement of the spindle pole body (SPB) toward the emerging bud was defe

198 Saccharomyces cerevisiae, Kar9p directs one spindle pole body (SPB) toward the incipient daughter ce

199 Upon release, Cdc14p binds to the spindle pole body (SPB) via association with the Bfa1p-B

200 dc13 to the yeast centrosome equivalent, the spindle pole body (SPB), and disruption of this motif pr

201 om poorly characterized interphase MTOCs and spindle pole body (SPB), and during late anaphase from t

202 e yeast centrosome-equivalent organelle, the spindle pole body (SPB), and it is involved in multiple

203 in spindle orientation, the migration of the spindle pole body (SPB), became actin-independent if it

204 ation of Sad1, a protein associated with the spindle pole body (SPB), in dot mutants showed an elevat

205 on of the budding yeast centrosome, called a spindle pole body (SPB), in late S-phase and G2/M, but t

206 normally localizes to only the bud-directed spindle pole body (SPB), Kar9p-L304P-3GFP was mislocaliz

207 ubule organizing centre (MTOC), known as the spindle pole body (SPB), organizes the nuclear and cytop

208 t on a component of the yeast centrosome, or spindle pole body (SPB), that is required for SPB duplic

209 c29p, which are three core components of the spindle pole body (SPB), the nuclear envelope-associated

210 , Sfi1p, localizes to the half-bridge of the spindle pole body (SPB), where Cdc31p is also localized.

211 the MEN-activating zone in the bud, and the spindle pole body (SPB), where the components of the MEN

212 ing yeast, microtubules are organized by the spindle pole body (SPB), which is embedded in the nuclea

213 le, the correct localization of Cdc7p to the spindle pole body (SPB), which is normally lost in spg1

214 y of nuclear-associated MTOCs, including the spindle pole body (SPB)--the centrosomal equivalent.

215 ation initiation network (SIN), an essential spindle pole body (SPB)-associated kinase cascade, which

216 late anaphase when spindle elongation brings spindle pole body (SPB)-localized Spg1 into proximity wi

217 the recruitment of polo kinase (Plo1) to the spindle pole body (SPB).

218 ntially associate with the pre-existing, old spindle pole body (SPB).

219 e dot corresponds to the outer plaque of the spindle pole body (SPB).

220 ter side of the bud neck and to the daughter spindle pole body (SPB).

221 ions: the nuclear pore complex (NPC) and the spindle pole body (SPB).

222 Cs) such as the animal centrosome and fungal spindle pole body (SPB).

223 iciently suppresses cyclin B-Cdc2 around the spindle pole body (SPB).

224 anchors the septum initiation network to the spindle pole body (SPB, centrosome equivalent) to contro

225 The spindle position checkpoint (SPOC) is a spindle pole body (SPB, equivalent of mammalian centroso

226 primes the invariant inheritance of the old spindle pole body (SPB, the yeast centrosome) by the bud

227 or EAP30, Dot2, negatively regulates meiotic spindle pole body (SPB, the yeast equivalent of centroso

228 kinase Mps1 has well-characterized roles in spindle pole body (SPB, yeast centrosome equivalent) dup

229 is thought to be controlled by the daughter spindle-pole body (SPB) through a regulatory pathway nam

230 The spindle-pole body (SPB), the yeast analog of the centros

231 nters (MTOCs; mammalian centrosome and yeast spindle pole body [SPB]) nucleate more astral microtubul

232 fective duplication of the yeast centrosome (spindle pole body [SPB]).

233 lication of the yeast centrosome (called the spindle pole body, SPB) is thought to occur through a se

234 MEN is a signaling cascade that localizes to spindle pole bodies (SPBs) and activates the phosphatase

235 targeting the catalytic activity of Cdc5p to spindle pole bodies (SPBs) and cytokinetic neck-filament

236 ke proteins present in centrosomes and yeast spindle pole bodies (SPBs) and have essential functions

237 Centrosomes and spindle pole bodies (SPBs) are membraneless organelles w

238 yces cerevisiae depends on a modification of spindle pole bodies (SPBs) at the onset of meiosis II th

239 spindles and found that only one of the two spindle pole bodies (SPBs) contains gamma-tubulin, altho

240 Yeast spindle pole bodies (SPBs) duplicate once per cell cycle

241 We find that Cdc15 is recruited to both spindle pole bodies (SPBs) during anaphase.

242 The Osw1 protein localizes to spindle pole bodies (SPBs) during meiotic nuclear divisi

243 Cdc7p [8] in fission yeast, localizes to the spindle pole bodies (SPBs) during mitosis.

244 One of the two spindle pole bodies (SPBs) failed to nucleate microtubul

245 Cdc5 also localizes to the spindle pole bodies (SPBs) from S phase until the end of

246 he outer and inner nuclear membranes and the spindle pole bodies (SPBs) fuse simultaneously and a thr

247 orA accumulates at nuclear envelope-embedded spindle pole bodies (SPBs) in a way that requires its ol

248 nt activation, S. pombe Dma1 concentrates at spindle pole bodies (SPBs) in an FHA-dependent manner an

249 (MTOCs), known as centrosomes in animals and spindle pole bodies (SPBs) in fungi, are important for t

250 First, Kar9 binds to spindle pole bodies (SPBs) in G(1) of the cell cycle.

251 Tts1 promotes insertion of spindle pole bodies (SPBs) in the NE at the onset of mit

252 Centrosomes, or spindle pole bodies (SPBs) in yeast, are vital mechanica

253 Whereas binding of MEN components to spindle pole bodies (SPBs) is necessary for MEN signalin

254 lizes to the mother cell and associates with spindle pole bodies (SPBs) located in the mother cell to

255 e two nuclei, whereas dynein accumulating at spindle pole bodies (SPBs) may pull MTs nucleated from t

256 on between nuclear pore complexes (NPCs) and spindle pole bodies (SPBs) revealed by our studies of th

257 enable nucleocytoplasmic transport, and the spindle pole bodies (SPBs) that mediate chromosome segre

258 elated proteins also bind to centrosomes and spindle pole bodies (SPBs) through proteins like the mam

259 Spg1, a Ras-like GTPase, localizes to the spindle pole bodies (SPBs) throughout the cell cycle.

260 ideally situated to inhibit MEN signaling at spindle pole bodies (SPBs) when anaphase spindle elongat

261 ation network) and measured their binding to spindle pole bodies (SPBs), the centrosome equivalent of

262 l unexpected structural modifications of the spindle pole bodies (SPBs), the yeast microtubule organi

263 Second, Ipl1 localizes to the spindle pole bodies (SPBs), where it blocks spindle asse

264 At mitosis NIMA-GFP locates to spindle pole bodies (SPBs), which contain Cdk1/cyclin B,

265 Polo-like kinase and SIN activator, Plo1, to spindle pole bodies (SPBs), while at the same time prolo

266 mine the subcellular localization of Bfa1 at spindle pole bodies (SPBs).

267 reviously unknown functions localised to the Spindle Pole Bodies (SPBs).

268 fa1 are asymmetrically localized to opposite spindle pole bodies (SPBs).

269 g of the Kar9 protein to only one of the two spindle pole bodies (SPBs).

270 (MTs) contribute to the outward movement the spindle pole bodies (SPBs).

271 chromosomes but nevertheless duplicate their spindle pole bodies (SPBs).

272 ganisms such as fungi, centrosomes [known as spindle pole bodies (SPBs)] are essential for cell divis

273 Here we show that yeast spindle pole bodies (SPBs, yeast centrosomes) differenti

274 Spg1, a Ras family GTPase that localizes to spindle-pole bodies (SPBs) throughout the cell cycle.

275 twork is active on one of the two anaphase B spindle-pole bodies (SPBs).

276 requires insertion of centrosomes (known as spindle pole bodies [SPBs]) into fenestrated regions of

277 Yeast centrosomes (called spindle pole bodies [SPBs]) remain cohesive for hours du

278 ches in the ability to scale the size of the spindle pole body, spindle and kinetochores.

279 nucleus with centromeres clustering near the spindle pole body, telomeres clustering into foci at the

280 ras-related GTPase, Tem1, is located on the spindle pole body that enters the daughter cell and acti

281 ct intracellular pools: a stable pool at the spindle pole body that is depleted during cell cycle pro

282 gs, Mud is found associated with the central spindle pole body that lies between the two spindles of

283 regulator of mitotic exit, is present on the spindle pole body that migrates into the bud during S ph

284 ell fluorescence microscopy demonstrated the spindle pole body that segregated into the daughter cell

285 Thus, the mutant failed to assign one spindle pole body the task of organizing astral microtub

286 ona fide aggresome that colocalizes with the spindle pole body (the yeast centrosome) in a microtubul

287 iations identified between components of the spindle pole body (the yeast centrosome).

288 two types of MTOCs exist in addition to the spindle pole body, the yeast centrosome equivalent.

289 tion because of dynamic microtubule bundles, spindle-pole bodies, the nuclear envelope, and passive c

290 Dma1p itself localizes to spindle pole bodies through interaction with Sid4p.

291 Alp16 localizes to the spindle pole body throughout the cell cycle and to the e

292 alize Duo1p to intranuclear microtubules and spindle pole bodies to provide a previously unrecognized

293 s extending from centromeres adjacent to the spindle pole body to telomeres that abut the nuclear env

294 ype region, from its natural location at the spindle-pole body to the immediate vicinity of the nucle

295 Schizosaccharomyces pombe harbors MTOCs at spindle pole bodies, transient MTOCs in the division pla

296 1 normally accumulates (bud neck, nucleolus, spindle pole body) were not occupied by one PP1 variant.

297 ex to the half bridge, a substructure of the spindle pole body, where it organizes microtubules.

298 d-type strains, Mpc70p localizes to all four spindle pole bodies, whereas in MPC70/mpc70 strains Mpc7

299 required to recruit the MEN kinase Cdc15 to spindle pole bodies, which is both necessary and suffici

300 tion of Nak1 causes removal of Nak1 from the spindle pole bodies, which may both relieve Nak1 inhibit