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1 subunits, Spt16 and Pob3, and functions as a histone chaperone.
2 terodimer of Spt16 and Pob3, is an essential histone chaperone.
3 lso find TONSL-MMS22L to function as a H3-H4 histone chaperone.
4 at1) catalytic subunit and the Hat2 (rbap46) histone chaperone.
5 leosome assembly in vitro and is therefore a histone chaperone.
6 eposition, identifying NASP(SIM3) as a CenH3 histone chaperone.
7 (Nap proteins) represent a distinct class of histone chaperone.
8 ulated protein APLF as a DNA-damage-specific histone chaperone.
9  to histone H3 and perform the function of a histone chaperone.
10 matin disassembly and reassembly mediated by histone chaperones.
11 otetramers is a common feature of NAP-1 fold histone chaperones.
12 ructurally related, evolutionarily conserved histone chaperones.
13 cked histones accompanying a decline in four histone chaperones.
14 d action of ATP-dependent motor proteins and histone chaperones.
15 emonstrate roles in VSG ES silencing for two histone chaperones.
16 P) is a human homolog of the N1/N2 family of histone chaperones.
17 mulate high levels of endogenous histones on histone chaperones.
18 sic factors such as chromatin remodelers and histone chaperones.
19 nal factors such as chromatin remodelers and histone chaperones.
20 ion and has overlapping functions with known histone chaperones.
21 of this region and mediate interactions with histone chaperones.
22 ent by H2A-H2B dimers without any additional histone chaperones.
23  cycle regulation defective homolog A (HIRA) histone chaperone accounts for these effects.
24    We further demonstrate that APLF exhibits histone chaperone activities in a manner that is depende
25 e early steps of gene activation through its histone chaperone activities that serve to open the chro
26 found that SART3 has previously unrecognized histone chaperone activities.
27  which couples transcription elongation with histone chaperone activity and the regulation of H3 lysi
28 d ES derepression is a direct consequence of histone chaperone activity by FACT at the G2/M cell cycl
29 lecular interactions negatively regulate Npm histone chaperone activity in vitro.
30 modynamic explanation for the specific H3-H4 histone chaperone activity of CAF-1.
31                    Nucleolin, a protein with histone chaperone activity, interacts with RAD50 via its
32 ry, and in the absence of both Dpb3 and Mcm2 histone chaperone activity, nucleosomes did not remember
33 ence the oncogenic effect of SET/TAF-Ibeta's histone chaperone activity.
34 ge or transcription events trigger transient histone chaperone activity.
35 osely related ASF1b and does not require its histone chaperone activity.
36 ally binds to the H2A-H2B dimer and exhibits histone chaperone activity.
37 nd the molecular details of this PPIase with histone chaperoning activity, we have solved the crystal
38                                              Histone chaperones affect chromatin structure and gene e
39              Via altering DNA accessibility, histone chaperones affect the transcriptional competence
40                   In this study, we show the histone chaperone and epigenetic regulator CHAF1A functi
41                 Here we demonstrate that the histone chaperone and transcription elongation factor Sp
42            Thus, in addition to serving as a histone chaperone and transcription elongation factor, S
43 gs establish a hitherto unknown link between histone chaperones and abiotic stress response in plants
44 tin assembly involves the combined action of histone chaperones and ATP-dependent motor proteins.
45 that alter nucleosome configurations such as histone chaperones and chromatin remodeling complexes.
46 eome, with emphasis on its interactions with histone chaperones and components of the replication for
47                        Moreover, we examined histone chaperones and found that the FACT complex recog
48  acetylation, chromatin remodelling enzymes, histone chaperones and histone turnover.
49  underscore the dynamic interactions between histone chaperones and nucleosomes.
50  homology structure is common to these three histone chaperones and reports that Pob3 and Rtt106 doub
51 ignificant discoveries regarding the role of histone chaperones and specifically FACT have come over
52 itment of a cascade of regulators, including histone chaperones and the histone-acetyltransferase gen
53 e discuss our current knowledge of the known histone chaperones and their histone partners, focusing
54                            The role of these histone chaperones and Yta7 differed markedly among the
55 in showed strong PPIase activity, no role in histone chaperoning and revealed a monomeric five-beta p
56 es interaction with HJURP (a CENP-A-specific histone chaperone) and abrogates localization of CENP-A
57 stant nucleosomes is dependent upon the FACT histone chaperone, and FACT is recruited to these region
58 ces cerevisiae, Fpr4 has been described as a histone chaperone, and is in addition implicated in epig
59 reaction that has remained elusive for other histone chaperones, and it advances our understanding of
60 d nucleophosmin are previously characterized histone chaperones, and TAP/p32 has no known function in
61 sized H3-H4 is directly transferred from the histone chaperone anti-silencing factor 1 (Asf1) to chro
62                               The ability of histone chaperone Anti-silencing factor 1 (Asf1) to dire
63                                          The histone chaperone anti-silencing factor 1a (ASF1a) inter
64  The CBP bromodomain also interacts with the histone chaperone anti-silencing function 1 (ASF1) via a
65                                              Histone chaperone, anti-silencing function-1 A (ASF1A),
66                                              Histone chaperones are a diverse class of proteins that
67                                              Histone chaperones are a non-catalytic group of proteins
68 tantly, sequence-based predictions show that histone chaperones are highly enriched in intrinsically
69                                              Histone chaperones are proteins that interact with histo
70                                              Histone chaperones are responsible for binding the highl
71 ork sheds further light on the importance of histone chaperones as general regulators of transcriptio
72                        Recent works identify histone chaperones as key regulators of damaged chromati
73 lator of cell fate during tumorigenesis, and histone chaperones as valuable therapeutic targets for i
74   However, this is just one function of this histone chaperone, as FACT also functions in DNA replica
75  Newly synthesized histones H3-H4 first bind histone chaperone Asf1 and are then transferred to other
76 s75-H3-H4 interaction is compatible with the histone chaperone Asf1 and deduce a structural model of
77 cordingly, the association of H3/H4 with the histone chaperone ASF1 and importin 4 is disrupted and t
78                                          The histone chaperone Asf1 and the checkpoint kinase Rad53 a
79                    Indeed, yeast lacking the histone chaperone Asf1 or acetylation of histone H3 on l
80 g a slowly repaired DSB does not require the histone chaperone Asf1 to resume cell cycle progression
81             Here, we show that yeast lacking histone chaperone Asf1 undergo reproducible rDNA repeat
82 es encoding homologs of the highly conserved histone chaperone Asf1, however, little is known of thei
83 acetyltransferase (HAT) that associates with histone chaperones Asf1 and Vps75 to acetylate H3K56, H3
84                           During S phase the histone chaperones Asf1, CAF-1, and Rtt106 coordinate to
85 ein-1 (UBN1) and CABIN1, cooperates with the histone chaperone ASF1a to mediate H3.3-specific binding
86 RA, UBN1, and CABIN1 and cooperates with the histone chaperone ASF1a to specifically bind and deposit
87                                          The histone chaperones ASF1A in humans and Asf1 in Drosophil
88 histone fold domains of H3 and H4 and/or the histone chaperone Asf1b are important for Importin-histo
89 SV DNA replication proteins and the cellular histone chaperone Asf1b, a protein that regulates the pr
90  on these data, we propose a model for HAT-B/histone chaperone assembly and acetylation of H3-H4 comp
91                           Additionally, NAP1 histone chaperones, ATP-dependent chromatin remodeling f
92                                              Histone chaperones bind specific histones to mediate the
93 hila CAL1, an evolutionarily distinct CENP-A histone chaperone, binds both CENP-A and the centromere
94 or acetylation of H3K56 in vivo, whereas the histone chaperone CAF-1 (chromatin assembly factor 1) in
95 RISPR and shRNA screening, we identified the histone chaperone CAF-1 as a critical component for Cd4
96           H3.1-H4 molecules are assembled by histone chaperone CAF-1 in a replication-coupled process
97 t the interaction between histone H3-H4 with histone chaperone CAF-1 or Rtt106 increases in cells lac
98            Together, our findings reveal the histone chaperone CAF-1 to be a novel regulator of somat
99 ucleosome assembly shaped by the replication histone chaperone CAF-I.
100 ted Src identified the replication-dependent histone chaperone CAF1 as an important factor for Src-me
101 ing Hat1, Hat2, and a histone H3-H4 specific histone chaperone called Hif1 (NASP).
102 irected recruitment of a generally expressed histone chaperone can lead to tissue-restricted changes
103                                              Histone chaperones can also participate in the distribut
104 ow that OsNAPL6 is a nuclear-localized H3/H4 histone chaperone capable of assembling a nucleosome-lik
105                                      It is a histone chaperone capable of reassembling nucleosomes, a
106 embers, the cohesin component Rad21, and the histone chaperone CHAF1A (CAF-1 p150).
107                                              Histone chaperones (Chaf1a/b), sumoylation factors (Sumo
108                                          The histone chaperone Chromatin Assembly Factor 1 (CAF-1) de
109                        Here we show that the histone chaperone Chromatin Assembly Factor 1 (CAF-1), w
110                How histone modifications and histone chaperones collaborate to reassemble nucleosomes
111                                We describe a histone chaperone complex containing Asf1 and HIRA that
112                                     The HIRA histone chaperone complex deposits histone H3.3 into nuc
113 roaches revealed that HP1 interacts with the histone chaperone complex FACT (facilitates chromatin tr
114 ve-cell imaging to reveal a key role for the histone chaperone complex FACT (SPT16 and SSRP1) in gove
115 hey displayed phenotypes similar to those of histone chaperone complex FACT mutants, including an inc
116  of histone methylation was dependent on the histone chaperone complex FACT.
117 ing RNA processing complex RIXC and with the histone chaperone complex FACT.
118  evolutionarily conserved H2A.Z via the SWR1 histone chaperone complex has been extensively studied,
119 vel role for the replication-independent HIR histone chaperone complex in fungal morphogenesis.
120                                The ATRX-DAXX histone chaperone complex incorporates the histone varia
121                                     The HIRA histone chaperone complex is composed of the proteins HI
122 ACT (facilitates chromatin transcription), a histone chaperone complex predominantly expressed in und
123 omatin assembly factor 1 (CAF1), a conserved histone chaperone complex that deposits H3-H4 during DNA
124   The mammalian HIRA/UBN1/ASF1a complex is a histone chaperone complex that is conserved from yeast (
125 o histone gene regulatory regions by the HIR histone chaperone complex to ensure S-phase-specific exp
126 icative stress caused by defects in the ATRX-histone chaperone complex, and that induced by MYCN-medi
127                                     The HIRA histone chaperone complex, composed of HIRA, ubinuclein-
128 e facilitates chromatin transcription (FACT) histone chaperone complex.
129 omatin incorporation is mediated by the HUCA histone chaperone complex.
130 and DAXX, which encode components of an H3.3 histone chaperone complex.
131 ion together as a multiprotein H3.3-specific histone chaperone complex.
132                                     Specific histone chaperone complexes control the correct depositi
133  studies suggested that feedback mediated by histone chaperone complexes plays a pivotal role in regu
134 ndothelial gene regulation and indicate that histone chaperones could be new targets for angiogenesis
135 hromatin transcription), is categorized as a histone chaperone critical for nucleosome reorganization
136 ociated function of PTEN in complex with the histone chaperone DAXX and the histone variant H3.3.
137             Here, we analyze the role of the histone chaperone DAXX in the regulation of H3.3 incorpo
138 mediated ALT suppression is dependent on the histone chaperone DAXX.
139 stering is not disrupted by loss of the HIRA histone chaperone, despite high levels of expression, an
140 emodeling complex, and ASF1, which encodes a histone chaperone, distinct sets of gene promoters carry
141  that shows preference for AT-rich DNA and a histone chaperone domain that promotes specific loading
142                   The replication-associated histone chaperones Dpb3 and Mcm2 were essential for nucl
143        Finally, we discuss the importance of histone chaperones during development and describe how m
144 the FACT chromatin reorganizer, and the Asf1 histone chaperone each required for nucleosome eviction
145                                  ATPases and histone chaperones facilitate RNA polymerase II (pol II)
146 ied Spt16 and SSRP1, subunits of the H2A-H2B histone chaperone facilitates chromatin transcription (F
147 us laevis egg extract identified the dimeric histone chaperone facilitates chromatin transcription (F
148 esin in chromosome organization requires the histone chaperone FACT ('facilitates chromatin transcrip
149 f the tetranucleosomal unit is attenuated by histone chaperone FACT (facilitates chromatin transcript
150                                          The histone chaperone FACT (facilitates chromatin transcript
151                          The subunits of the histone chaperone FACT (facilitates chromatin transcript
152 ubsequent replisome progression requires the histone chaperone FACT (facilitates chromatin transcript
153                      In yeast, the essential histone chaperone FACT (FAcilitates Chromatin Transcript
154  residue is part of the binding site for the histone chaperone FACT (facilitator of chromatin transcr
155                                          The histone chaperone FACT and histone H2B ubiquitination (H
156                                              Histone chaperone FACT binds rapidly to the same regions
157                                          The histone chaperone FACT is an essential and abundant hete
158                                          The histone chaperone FACT is upregulated during mammary tum
159                             We show that the histone chaperone FACT specifically binds UIF, but not R
160 o-be fertilized germ cells by recruiting the histone chaperone FACT, displacing histones, and initiat
161 d displayed a synthetic interaction with the histone chaperone FACT.
162 merase II (RNA Pol II) elongation-associated histone chaperones FACT and Spt6 both contribute to rest
163 ome and in H2A/H2B dimers complexed with the histone chaperone, FACT, suggesting that SAGA could targ
164 ciates with RNAPII and collaborates with the histone chaperone, FACT, which facilitates RNAPII elonga
165 d is required for normal localization of the histone chaperone, FACT.
166  suggesting that IDRs are often critical for histone chaperone function and play key roles in chromat
167 that this process is contingent on ATRX/DAXX histone chaperone function, independently of telomere le
168                                              Histone chaperones function in chromatin assembly and di
169  hypothesis that histone pre-acetylation and histone chaperones function together to drive preferenti
170 o neurons can be achieved by knocking down a histone chaperone gene and ectopic expression of a termi
171                            Multiple involved histone chaperones have been identified, but how nucleos
172                     In addition, loss of the histone chaperone Hif1p, when combined with an allele of
173              We investigated the role of the histone chaperone HIRA (histone cell cycle regulation-de
174                                          The histone chaperone HIRA complex, consisting of histone ce
175                                              Histone chaperone HIRA deposits variant histone H3.3 and
176                                          The histone chaperone HIRA is involved in depositing histone
177 ong with histone H4, at genic regions by the histone chaperone HIRA, whereas H3.1 is assembled into n
178    Our results for the first time decipher a histone chaperone (HIRA)-dependent molecular mechanism i
179 rowth factor receptor 1) is dependent on the histone chaperone, HIRA (histone cell cycle regulation-d
180  H3.3-dependent interaction of PRC2 with the histone chaperone, Hira, and that Hira localization to c
181 lation suppresses the interaction of H3 with histone chaperones, histone exchange over coding regions
182   New CENP-A recruitment requires the CENP-A histone chaperone HJURP.
183 s in early G(1) phase by the CENP-A-specific histone chaperone Holliday junction recognition protein
184 e have assessed the global roles of the HIRA histone chaperone in Schizosaccharomyces pombe.
185      Prior work showed an importance of FACT histone chaperone in such process.
186 e additional evidence that it functions as a histone chaperone in vivo.
187 ecting chromatin dynamics, the role of plant histone chaperones in abiotic stress response and adapta
188 in H3.3 deposition and emphasize the role of histone chaperones in adjusting genome expression.
189      This review focuses on the roles of the histone chaperones in assembling and disassembling chrom
190                           The two NAP-1 fold histone chaperones in budding yeast, Vps75 and Nap1, hav
191 ate the molecular roles of the Hif1 and Asf1 histone chaperones in HAT-B histone binding and acetyltr
192 ly, these findings define the involvement of histone chaperones in poly(ADP-ribose)-regulated DNA rep
193 motor proteins, such as ISWI, cooperate with histone chaperones in the assembly and remodeling of chr
194 that much more H4 and H3 were bound to these histone chaperones in the case of the H4 mutants than in
195 e for binding of free histone by specialized histone chaperones in vivo.
196 y the SWR-C complex, which relies on several histone chaperones including Nap1 and Chz1 to deliver H2
197                                              Histone chaperones, including the FACT (facilitates chro
198       Inhibiting topoisomerases or depleting histone chaperones increased unwrapping, whereas inhibit
199 also associated with HIRA, the H3.3-specific histone chaperone, independent of BRD4 and P-TEFb.
200 eased levels of damage and that Asf1 plays a histone chaperone-independent role in facilitating compl
201 hat the Xnp chromatin remodeler and the Hira histone chaperone independently bind nucleosome-depleted
202                        Strikingly, NAP1-like histone chaperones interact with CSB and greatly enhance
203  assembly in part through regulating histone-histone chaperone interactions.
204  also show reduced binding of H3 to CAF-1, a histone chaperone involved in RC nucleosome assembly.
205                    Spt6 is a multifunctional histone chaperone involved in the maintenance of chromat
206                                    Nap1 is a histone chaperone involved in the nuclear import of H2A-
207  transcription), an evolutionarily conserved histone chaperone involved in transcription and other DN
208                                    Recently, histone chaperones, involved in the assembly and disasse
209                               Thus, the HIRA histone chaperone is required to maintain the protective
210               The assembly of nucleosomes by histone chaperones is an important component of transcri
211                  The nucleoplasmin family of histone chaperones is identified by a pentamer-forming d
212 f H3-H4 from the Asf1-H3-H4 complex to other histone chaperones is regulated by a conserved E3 ligase
213                                          The histone chaperone known as 'facilitates chromatin transc
214                                              Histone chaperones, like nucleosome assembly protein 1 (
215 g that the TD/RS interface may operate as a "histone chaperone-like platform."
216 rogramming event requires the removal of the histone chaperone LIN-53 (RbAp46/48 in humans), a compon
217            The tetramerisation of NAP-1 fold histone chaperones may act to shield acidic surfaces in
218 3-H4)2 tetrasome to form the nucleosome by a histone chaperone mechanism.
219 ied chromatin assembly system containing the histone chaperone NAP1 and the ATP-dependent motor prote
220 investigated nucleosome assembly mediated by histone chaperone Nap1 and the effects of CpG methylatio
221 DNA binding, and the interaction between the histone chaperone Nap1 and the histone H2A-H2B heterodim
222                            We found that the histone chaperone Nap1 efficiently promotes disassembly
223 evealing an unexpected mechanism used by the histone chaperone Nap1 to prevent aberrant chromatin for
224        SART3, but not the well-characterized histone chaperone Nap1, enhances Usp15 binding to ubH2B
225 ependent nucleosome eviction mediated by the histone chaperone Nap1.
226          The ATR checkpoint pathway causes a histone chaperone normally associated with the replicati
227 biochemical fractionation, we identified the histone chaperone nucleoplasmin (Npm2) as a putative nuc
228 position histones H2A/H2A.X-F and H4 and the histone chaperone nucleoplasmin on a conserved motif (GR
229                We found that the cytoplasmic histone chaperone nucleosome assembly protein 1 (Nap1) a
230 emodels structure of chromatin (RSC) and the histone chaperone nucleosome assembly protein 1 (NAP1).
231 tudies reveal the mechanism of action of the histone chaperone nucleosome assembly protein 1 (Nap1).
232                                     The FACT histone chaperone/nucleosome reorganization factor plays
233 ress-responsive putative rice (Oryza sativa) histone chaperone of the NAP superfamily: OsNAPL6.
234  is homologous to the motif conserved in the histone chaperones of the NAP1L family (NAP1L motif).
235               These results suggest that the histone chaperone OsNAPL6 may serve a regulatory role in
236                                Although most histone chaperones perform these common functions, recen
237                                              Histone chaperones physically interact with histones to
238                                   NAP-1 fold histone chaperones play an important role in escorting h
239 including the roles of chromatin remodelers, histone chaperones, post-translational modifications of
240 eacetylation and suggest that HP1-associated histone chaperone promotes nucleosome occupancy to assem
241  using chicken erythrocyte core histones and histone chaperone protein Nap1 under constant low force.
242                                          The histone chaperone protein RBBP4, has previously been sho
243                                    Different histone chaperone proteins mediate the storage and chrom
244 ish a potentially generalizable mechanism of histone chaperone regulation via dynamic and specific in
245                                              Histone chaperones represent a structurally and function
246 to be a cell-cycle-regulated CENP-A-specific histone chaperone required for centromeric chromatin ass
247   Chromatin assembly factor 1 (CAF-1) is the histone chaperone responsible for histone (H3-H4)2 depos
248    Nucleoplasmin (Npm) is a highly conserved histone chaperone responsible for the maternal storage a
249  recent structural studies of many different histone chaperones reveal that there are few commonaliti
250                                          The histone chaperone Rtt106 binds histone H3 acetylated at
251             In Saccharomyces cerevisiae, the histone chaperone Rtt106 binds newly synthesized histone
252             In Saccharomyces cerevisiae, the histone chaperone Rtt106 contributes to the deposition o
253                                    The yeast histone chaperone Rtt106 is involved in de novo assembly
254 the small subunit of FACT and in the related histone chaperone Rtt106, although Spt16-M is distinguis
255 ctions with the genes encoding two different histone chaperones, Rtt106 and CAF-I.
256 specific histone H3 variant is Cse4, and the histone chaperone Scm3 functions as a Cse4-specific nucl
257 ly after completion of repair, suggests that histone chaperones sequester the repair complex for oxid
258    H2B S6ph impairs chromatin binding of the histone chaperone SET (I2PP2A), which is important for m
259                  This study reveals that the histone chaperone SET/TAF-Ibeta interacts with cytochrom
260 PROTEIN (NASP) and Schizosaccharomyces pombe histone chaperone Sim3 is a soluble nuclear protein that
261                           DAXX is a metazoan histone chaperone specific to the evolutionarily conserv
262 hich resulted from attenuated recruitment of histone chaperone SPT-16 following anthracycline exposur
263 rms a complex with ANXA2 that interacts with histone chaperone SPT6 and histone demethylase KDM6A.
264                     Here, we report that the histone chaperone Spt6 counteracts H3K27me3, an epigenet
265 cetylation can be altered by factors such as histone chaperones, subunit proteins or external stimulu
266  is regulated by numerous factors, including histone chaperones such as nucleosome assembly protein 1
267                                        Other histone chaperones, such as Vps75, that also bind histon
268 romatin assembly factor 1 (CAF-1) is a H3-H4 histone chaperone that associates with the replisome and
269                           Nucleoplasmin is a histone chaperone that consists of a pentameric N-termin
270 protein complex, an evolutionarily conserved histone chaperone that deposits histone H3-H4 proteins o
271 ons to reorganize nucleosomes by acting as a histone chaperone that destabilizes and restores nucleos
272                                   Vps75 is a histone chaperone that has been historically characteriz
273 cts with Asf1 (anti-silencing function 1), a histone chaperone that has been reported to be involved
274 ow focus on the dynamic features of the DAXX histone chaperone that have been elusive from previous s
275                   Spt6 is a highly conserved histone chaperone that interacts directly with both RNA
276                                   Chz1p is a histone chaperone that interacts physically and function
277 chromatin assembly factor 1 (CAF-1), another histone chaperone that is critical for the deposition of
278 omatin assembly complex-1 (CAF-1) complex, a histone chaperone that is required for nucleosome assemb
279  during DSB repair was dependent on the HIRA histone chaperone that is specific to the replication-in
280 T (facilitates chromatin transcription) is a histone chaperone that promotes chromatin recovery durin
281 6 is a transcriptional elongation factor and histone chaperone that reassembles transcribed chromatin
282           Nucleoplasmin (NP) is a pentameric histone chaperone that regulates the condensation state
283 otein (NAP) family represents a key group of histone chaperones that are essential for cell viability
284                 sNASP and ASF1 are conserved histone chaperones that interact with histones H3 and H4
285 he RSC chromatin-remodeling complex, various histone chaperones [the histone regulatory (HIR) complex
286 Drosophila nucleoplasmin-like protein (dNLP) histone chaperone, the imitation switch (ISWI) ATP-drive
287 nsically disordered regions are common among histone chaperones, their roles in histone binding and c
288 tails of virus reprogramming of an antiviral histone chaperone to promote viral latency and cellular
289        Cells use specific mechanisms such as histone chaperones to abrogate the inherent barrier that
290 w that metastasis-inducing pathways regulate histone chaperones to reduce canonical histone incorpora
291 y in vivo requires assembly factors, such as histone chaperones, to bind to histones and mediate thei
292 9 acetyltransferase activity also requires a histone chaperone, vacuolar protein sorting 75 (Vps75),
293       Rtt109 associates with the NAP1 family histone chaperone Vps75 and stimulates histone acetylati
294                                          The histone chaperone Vps75 forms a complex with, and stimul
295                                          The histone chaperone Vps75 presents the remarkable property
296 ivity require association with either of two histone chaperones, Vps75 or Asf1.
297            In addition, nucleolin, a classic histone chaperone, was demonstrated to physically bind t
298                                              Histone chaperones, which are proteins that escort histo
299 t and deposition of CenH3 must be ensured by histone chaperones, which handle the non-nucleosomal Cen
300  proteins through the level of saturation of histone chaperones with histone.

 
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