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

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

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

7 STU2 encodes a component of the spindle pole body.

8 r3p-GFP was found at the nuclear side of 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 Most components of the MEN localize to spindle pole bodies.

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

18 bundles of cytoplasmic microtubules from the spindle pole bodies.

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

20 ble microtubules were observed unattached to spindle pole bodies.

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

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

23 P), to intranuclear spindle microtubules and spindle pole bodies.

24 tation of sister centromeres toward opposite spindle pole bodies.

25 clb4 mad2 cells accumulated with unseparated spindle pole bodies.

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

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

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

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

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

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

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

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

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

35 Plo1p localizes to the spindle pole bodies and spindles of mitotic cells and al

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

73 The yeast Xgrip109 homologue, Spc98, is a spindle-pole body component that interacts with gamma tu

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

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

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

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

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

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

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

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

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

83 binds Mps1p, a protein kinase essential for spindle pole body duplication and mitotic checkpoint reg

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

85 Spindle pole body duplication begins in G1 and continues

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

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

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

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

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

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

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

93 function necessary for the initiation of the spindle pole body duplication.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

109 ue to lack of nimQMCM2 continue to replicate spindle pole bodies in the absence of DNA replication an

110 d with intranuclear spindle microtubules and spindle pole bodies in vivo.

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

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

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

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

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

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

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

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

119 absence of Taz1, telomere clustering at the spindle pole bodies is disrupted, meiotic recombination

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

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

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

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

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

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

126 ulum excluded from the region containing the spindle-pole body, mitotic Golgi appeared to be disperse

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

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

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

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

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

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

133 The spindle pole body of the budding yeast Saccharomyces cer

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

164 11 mutation in the Schizosaccharomyces pombe spindle pole body (SPB) component Cut12 both suppresses

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

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

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

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

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

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

171 he Mps1p protein kinase is critical for both spindle pole body (SPB) duplication and the mitotic spin

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

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

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

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

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

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

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

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

180 The spindle pole body (SPB) in Saccharomyces cerevisiae func

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

197 8 kinesin in CDH1-m11 cells does not promote spindle pole body (SPB) separation.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

224 a component of the Saccharomyces cerevisiae spindle pole body (SPB).

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

247 ning and electron microscopy showed that the spindle pole bodies (SPBs) either failed to complete nor

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

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

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

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

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

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

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

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

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

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

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

259 During fission yeast mitosis, the duplicated spindle pole bodies (SPBs) nucleate microtubule arrays t

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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