The Mis6 inner kinetochore subcomplex maintains CENP-A nucleosomes against centromeric non-coding transcription during mitosis

Hirai, Hayato; Shogaki, Yuki; Sato, Masamitsu

doi:10.1038/s42003-022-03786-y

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Published: 15 August 2022

The Mis6 inner kinetochore subcomplex maintains CENP-A nucleosomes against centromeric non-coding transcription during mitosis

Communications Biology volume 5, Article number: 818 (2022) Cite this article

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Abstract

Centromeres are established by nucleosomes containing the histone H3 variant CENP-A. CENP-A is recruited to centromeres by the Mis18–HJURP machinery. During mitosis, CENP-A recruitment ceases, implying the necessity of CENP-A maintenance at centromeres, although the exact underlying mechanism remains elusive. Herein, we show that the inner kinetochore protein Mis6 (CENP-I) and Mis15 (CENP-N) retain CENP-A during mitosis in fission yeast. Eliminating Mis6 or Mis15 during mitosis caused immediate loss of pre-existing CENP-A at centromeres. CENP-A loss occurred due to the transcriptional upregulation of non-coding RNAs at the central core region of centromeres, as confirmed by the observation RNA polymerase II inhibition preventing CENP-A loss from centromeres in the mis6 mutant. Thus, we concluded that the inner kinetochore complex containing Mis6–Mis15 blocks the indiscriminate transcription of non-coding RNAs at the core centromere, thereby retaining the epigenetic inheritance of CENP-A during mitosis.

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Introduction

Duplicated chromosomes must be equally distributed between daughter cells so that genetic information is adequately propagated to the progeny. The mitotic spindle attaches to the kinetochore, which is a macromolecular protein complex formed at the centromere, in order to equally separate sister chromatids to opposite spindle poles¹. In most eukaryotes, kinetochore assembly requires the deposition of CENP-A (Cnp1 in the fission yeast Schizosaccharomyces pombe), a centromere-specific variant of histone H3. In budding yeast, the centromere is composed of a 125-bp DNA sequence (called a point centromere), and a single histone octamer containing CENP-A is allocated to the centromere in addition to the usual H3-containing nucleosomes². In contrast, multiple CENP-A-containing nucleosomes are deposited to the regional centromere, which consists of a 35–110-kb central core region flanked by pericentric regions in fission yeast³, or megabases of repetitive DNA sequences in higher eukaryotes, including humans⁴.

Reduction of CENP-A levels at the centromere causes errors in chromosome segregation, which may result in aneuploidy, leading to cell death and birth defects⁵. Thus, the amount of CENP-A at the centromere is strictly regulated. Upon DNA replication, the number of nucleosomes containing CENP-A at the centromere is halved⁶, necessitating the replenishment of new CENP-A nucleosomes during the cell cycle especially prior to mitosis onset in order to assemble functional kinetochores. The timing of CENP-A deposition differs between organisms, occurring in the early G1 phase in humans as opposed to mainly in G2 in fission yeast^6,7.

Recruitment of CENP-A requires the Mis18 complex (Mis18BP1, Mis18α and Mis18β in humans⁸; Mis16, Mis18 and Mis19 (also known as Eic1 or Kis1) in fission yeast^9,10,11,12) as well as a chaperone HJURP (Holliday junction recognition protein; Scm3 in fission yeast)^13,14,15,16. The inner kinetochore protein Mis6 (CENP-I in human) has been discovered as a factor required for centromeric localisation of CENP-A¹⁷, and further studies have reported that Mis6 plays a role in the localisation of HJURP to centromeres^15,16. In budding yeast¹⁸, human cells¹⁹ and Drosophila cells²⁰, histone H3 within euchromatin undergoes dynamic turnover during the cell cycle, while CENP-A nucleosomes are generally immobile. Once recruited to centromeres, they appear neither disassembled nor replaced by new nucleosomes containing CENP-A or H3 during both mitotic cycles and meiosis in higher eukaryotes^6,21 implying the existence of machinery for CENP-A maintenance.

In various organisms, non-coding RNAs (ncRNAs) are transcribed at the central core region of centromeres²². When RNA polymerase II (RNAPII) progresses to the central core region of centromeric DNA to transcribe ncRNAs²³, some mechanisms may prevent the dissociation of CENP-A from the DNA. Transcription-coupled turnover of CENP-A has also been reported when transcription of the alphoid array is artificially enhanced by tethering the herpes virus VP16 activation domain to a human artificial chromosome²⁴. Furthermore, S. pombe Cnp1 (CENP-A) dispersed when ncRNA transcription at the central core region was upregulated in cells lacking the Mediator complex subunit Med20²⁵. These findings indicate that CENP-A needs to be maintained against the transcription of centromeric ncRNAs, even outside DNA replication.

While CENP-A maintenance at centromeres is necessary during the cell cycle, the underlying molecular mechanism remains elusive. Ubiquitylation of CENP-A was recently shown to contribute to CENP-A maintenance in human cells²⁶. Further, human kinetochore proteins CENP-C and CENP-N directly interact with CENP-A-containing nucleosomes in vitro^27,28. These interactions are required for the immobility of CENP-A-containing nucleosomes in human cells^29,30. Another study suggested that CENP-C and CENP-N do not contribute to CENP-A maintenance in human cells³¹. Taken together, whether these factors are required for CENP-A retention in vivo remains controversial. It was recently demonstrated that HJURP is necessary for CENP-A maintenance during DNA replication³². However, HJURP dissociates from centromeres in metaphase both in human cells^8,13,14 and in fission yeast^9,15,16, indicating that HJURP does not engage in CENP-A maintenance during metaphase. It was recently reported that the histone chaperone Spt6, which is known as a histone H3 recycler, also contributes to the recycling of pre-existing CENP-A during ncRNA transcription at centromeres in both Drosophila and human cells³³. However, whether more factors are involved in CENP-A maintenance remains unclear.

In this study, we demonstrate that the kinetochore protein Mis6 (CENP-I in human), which is required for centromere localisation of HJURP^15,16, contributes to maintenance of CENP-A during metaphase. We also found that Mis15 (CENP-N in human)³⁴ maintains CENP-A. We propose that the inner kinetochore subcomplex containing Mis6–Mis15 may counteract progression of RNAPII into core centromeres to prevent the reduction of CENP-A nucleosomes during metaphase.

Results

Cnp1 is not recruited to centromeres during metaphase

The Mis18 complex and Scm3 (HJURP) are loading factors for Cnp1 (CENP-A) conserved in fission yeast and higher eukaryotes, such as chickens and humans^{8,9,13,14,15,16}. Given that Cnp1 localisation is reduced in the mis6-302 temperature-sensitive mutant¹⁷ and overexpression of Mis6 partially rescues growth defects of the scm3 mutant³⁵, we first suspected that the kinetochore protein Mis6 (CENP-I) may have the potential to deposit Cnp1 even without HJURP. The Mis18 complex and Scm3 localise to kinetochores during interphase but are dispersed during mitosis, whereas Mis6 remains throughout the cell cycle^9,15,16,36. This suggests that Cnp1 could be recruited at any time, assuming that Mis6 would constantly serve as a Cnp1 loading factor without the help of HJURP.

To test this possibility, we examined the kinetics of Cnp1 localisation to centromeres using Cnp1-GFP strains (green fluorescent protein was tagged to the C-terminus of Cnp1, and the fusion gene was ectopically expressed under the adh21 promoter). Cnp1-GFP cells were arrested at G1, G2 and metaphase via cdc10-27, cdc25-22³⁷ and alp12-1828³⁸ mutations, respectively. Cnp1-GFP localised only to centromeres and these strains showed no growth defects (Supplementary Fig. 1). We then performed fluorescence recovery after photobleaching (FRAP) assays, where the Cnp1-GFP fluorescence intensity at centromeres was measured every 5 min after laser irradiation of the Cnp1-GFP foci. We found that Cnp1-GFP fluorescence intensity gradually recovered after irradiation in G1- or G2-arrested cells (Fig. 1a–d), indicating that bleached Cnp1 was replaced, albeit slowly. In contrast, Cnp1-GFP intensity did not recover after irradiation in metaphase-arrested cells (Fig. 1e, f). These results indicate that Cnp1 is not recruited to centromeres during metaphase, and Mis6 does not play a role in Cnp1 loading in the meantime, whereas Mis6 does contribute to Cnp1 recruitment during interphase by assisting Scm3 localisation to centromeres¹⁶.

**Fig. 1: Deposition of Cnp1 (CENP-A) ceases in metaphase.**

The inner kinetochore subcomplex including Mis6 is required to maintain Cnp1 at centromeres during metaphase

We speculated that Mis6 may play another role at the centromeres during metaphase. We first examined whether the function of Mis6 during metaphase is essential for viability. The mis6-302 mutant was combined with the cut9-665 mutant, which has defects in cell cycle transition from metaphase to anaphase because of the low APC/C (anaphase promoting complex/cyclosome) activity at restrictive temperature³⁹. The resultant mis6-302 cut9-665 double mutant exhibited severe growth defects, even at the semi-restrictive temperature (Fig. 2a). This suggests that the mitotic function of Mis6 is crucial for prolonged metaphase. Likewise, severe growth defects were observed in the cnp1-1 cut9-665 double mutant, suggesting that retention of Cnp1 is required for passage through mitosis (Supplementary Fig. 2). Thus, the mitotic role of Mis6 is possibly maintenance of Cnp1.

**Fig. 2: Mis6 is required for Cnp1 maintenance at the centromere during metaphase.**

To test this hypothesis, we performed assays to monitor Cnp1 maintenance during metaphase. As illustrated in Fig. 2b, WT (mis6⁺) and mis6-302 cells expressing GFP-Cnp1 cells were first arrested in the G1/S phase using hydroxyurea (HU), followed by a temperature shift up to 36 °C in order to inactivate Mis6 before mitotic entry. After hydroxyurea (HU) washout, cells were released into mitosis until telophase (mitotic exit).

In WT cells, the intensity of a single GFP-Cnp1 dot in telophase was approximately half that in the previous G1/S stage. This reduction in GFP-Cnp1 intensity simply reflects the segregation of sister chromatids in the meantime. Therefore, Cnp1 was rarely removed from the centromeres during WT mitosis (Fig. 2c, d). This result is consistent with previous observations in human cells showing that pre-existing CENP-A at centromeres is retained throughout the cell cycle⁶. In the mis6-302 mutant, GFP-Cnp1 intensity during telophase was ~35% of that in G1/S (Fig. 2d), indicating that Cnp1 was dissociated from centromeres when cells passed through mitosis in the absence of Mis6. Thus, Mis6 is required for Cnp1 retention during mitosis.

It could be hypothesised that Scm3 (HJURP), rather than Mis6, is responsible for Cnp1 maintenance, because Scm3 and Mis6 are interdependent for localisation to centromeres¹⁵. This is unlikely, as Scm3 ceases localisation to centromeres in WT cells during mitosis^15,16. To further clarify this point, we isolated a temperature-sensitive scm3 mutant, in which the localisation of Mis6-GFP remained, albeit partially, at the restrictive temperature (Supplementary Fig. 3). The mutant harboured a substitution at position 55 (scm3^S55P), which was close to that in the previous scm3^L56F mutant that also retained Mis6 localisation to centromeres¹⁶. In the scm3^S55P mutant, the reduction in GFP-Cnp1 intensity after mitosis was almost comparable to that in WT cells (~60%, Fig. 2d), indicating that Cnp1 did not dissociate from centromeres during metaphase. Thus, Scm3 was dispensable for the maintenance of mitotic Cnp1.

To further investigate whether Mis6 retains Cnp1 during metaphase, WT and mis6-302 cells expressing GFP-Cnp1 were prepared similarly as in Fig. 2b, but arrested to mitosis (metaphase) for ≥1 h by double inhibition using the microtubule poison carbendazim (CBZ) in combination with the β-tubulin temperature-sensitive mutant alp12-1828³⁸ (Fig. 2e). Metaphase arrest of the cell was confirmed by observing the Plo1 (Polo-like kinase) foci at spindle pole bodies (SPBs; the centrosome equivalent in yeast)^40,41. The GFP-Cnp1 intensity at centromeres decayed more rapidly in mis6-302 cells than in WT cells (Fig. 2f, g and Supplementary Figs. 4 and 5a). Taken together, these results suggest that Mis6, but not Scm3, is responsible for the maintenance of Cnp1 at centromeres during metaphase.

We examined whether the role of Cnp1 maintenance at mitotic centromeres is specifically assigned to Mis6 or shared with other kinetochore components by repeating similar GFP-Cnp1 maintenance assays using the mis15-68, mis12-537, and nuf2-2 mutants. These harbour mutations in Mis15 (belonging to the Mis6-Sim4 subcomplex), Mis12 (to the Mis12/Mtw1 subcomplex), and Nuf2 (to the Ndc80 subcomplex), respectively^42,43,44. Mis15 localises to the inner regions of centromeres as does Mis6, while Mis12 and Nuf2 localise to the outer regions relative to Mis6, and Mis6 localised to centromeres in the mis12 and nuf2 mutants but not in the mis15 mutant (Supplementary Fig. 6)^44,45.

In the mis15-68 mutants, signal intensities of Cnp1 at centromeres during mitotic arrest were decreased like in the mis6-302 mutant, whereas not in the mis12-537 and nuf2-2 mutants (Fig. 2h–j and Supplementary Figs. 5b–d and 7). These assays indicated that involvement in Cnp1 maintenance is not a common feature among kinetochore factors. Rather, it is specifically assigned to the inner kinetochore subcomplex containing Mis6–Mis15.

Enforced dismissal of Mis6 during metaphase reduces Cnp1

To further examine the function of inner kinetochore during mitosis, we sought to introduce experimental conditions in which Mis6 remains functional during interphase but is rapidly inactivated upon entry into mitosis. We developed a strategy for knocksideways experiments using Mis6-GFP and Kis1-GBP (GFP-binding protein⁴⁶), as illustrated in Fig. 3a. Kis1 (Mis19 or Eic1) together with Mis16 and Mis18 forms the Mis18 complex to recruit Cnp1 to centromeres during interphase, whereas the whole complex disperses during metaphase^9,10,11,12 (mis6-GFP kis1⁺, Fig. 3a). Taking advantage of the turnover, the fusion protein Kis1-GBP may dismount Mis6-GFP from centromeres upon mitotic entry (mis6-GFP kis1-GBP, Fig. 3a). As shown in Fig. 3b, Mis6-GFP and Kis1-GBP-mCherry co-localised to centromeres during interphase. In metaphase cells, the Mis6-GFP signal at centromeres substantially decreased, indicating that Mis6-GFP was removed from centromeres specifically during mitosis by the knocksideways system, as expected. Later in anaphase, Mis6-GFP and Kis1-GBP-mCherry re-localised together at centromeres.

**Fig. 3: Metaphase-specific removal of Mis6 causes a decrease of Cnp1.**

We then evaluated whether Cnp1 localisation is reduced in response to the enforced removal of Mis6 during metaphase. In control cells (mis6-GFP kis1⁺, Fig. 3c), mCherry-Cnp1 foci at centromeres were constantly detected along the spindle during prometaphase, and only 10% of control cells failed to retain mCherry-Cnp1 at centromeres (Fig. 3d). In contrast, in mis6-GFP kis1-GBP double-tagged cells, mCherry-Cnp1 signals were clearly detected at centromeres during the initial stage of mitosis (0 min, Fig. 3c and Supplementary Fig. 8a, b), verifying that co-expression of Mis6-GFP and Kis1-GBP did not affect their functions in Cnp1 deposition during interphase. In contrast, immediately after mitosis onset, mCherry-Cnp1 signals dispersed from centromeres in ~30% of the cells (Fig. 3c, d). Moreover, the double-tagged strain displayed growth defects at high temperature, further supporting the importance of Mis6 during mitosis (Fig. 3e and Supplementary Fig. 8c).

Reduction of Cnp1 during metaphase is coupled to transcription at centromeres

A major reason for Cnp1 loss during mitosis may be the transcription of ncRNAs in centromeres. ncRNAs are transcribed in various organisms, including plants, fission yeast and humans²². As our results indicate that the Mis6 subcomplex retains Cnp1 to centromeres, we focused on the relationship between ncRNA transcription at the central core region of centromeres and Cnp1 maintenance. The central core region (cnt) of centromeres is transcriptionally silenced in WT cells, whereas silencing is impaired in the mis6-302 mutant³⁵. This was reproduced in our experiments using the cnt1::ura4⁺ strain, in which the ura4⁺ reporter gene conferring the uracil autotroph was inserted in the central core region of chromosome I (Fig. 4a). Growth of WT cells harbouring the cnt1::ura4⁺ insertion was defective in medium lacking uracil (SD–Ura) and was fine in the counter-selection medium containing 5-fluoroorotic acid (FOA). This indicated that transcription in the central core region is subtle and is mostly silenced. In contrast, the mis6-302 and mis15-68 mutants containing cnt1::ura4⁺ showed the opposite growth pattern, confirming that the central core region in the mis6-302 and mis15-68 mutants was no longer silenced (Fig. 4a and Supplementary Fig. 9a).

**Fig. 4: Loss of Cnp1 in *mis6-302* cells is coupled with centromeric transcription by RNA polymerase II.**

Likewise, mis12-537 and nuf2-2 mutants were used in centromeric silencing assays. In contrast to the inner kinetochore mutants, both mis12-537 and nuf2-2 mutants showed restricted growth in the medium lacking uracil and retained their growth capacity in the presence of 5-fluoroorotic acid (FOA) at semi-restrictive temperatures (Supplementary Fig. 9b). These results demonstrate that kinetochore mutants with the intact inner kinetochore architecture retained the ability to silence transcription at the central core region.

Chromatin IP experiments using an antibody against the C-terminal domain phosphorylated form (pSer5) of RNAPII, a marker for transcription initiation⁴⁷, detected enrichment of the central core sequences in the mis6-302 and mis15-68 mutant compared to WT cells (Fig. 4b and Supplementary Fig. 10a). In contrast, the enrichment was undetectable in both the mis12-537 and nuf2-1 mutants (Supplementary Fig. 10b), wherein the inner kinetochore remained at centromeres. This demonstrates that active RNAPII transcribes ncRNA in the central core region when the inner kinetochore subcomplex including Mis6 is absent.

In general, conventional histone octamers containing H3 are temporarily dismantled by the chromatin remodelling factor Fun30 (Fft3 in fission yeast), allowing RNAPII to proceed with transcription^48,49,50. Analogously, Cnp1-containing octamers must be temporarily dissociated from centromeres upon transcription, which could be a potential reason for Cnp1 loss in mitotic mis6-302 and mis15-68 cells. It is possible that Fft3 also removes Cnp1-containing octamers upon ncRNA transcription at the centromeres. When we followed the temporal kinetics of GFP-Cnp1 intensity during metaphase, the reduction of GFP-Cnp1 intensity seen in mis6-302 and mis15-68 cells was rescued by the additional knockout of Fft3 (mis6-302 fft3∆, Supplementary Fig. 11a–c; mis15-68 fft3∆, Supplementary Fig. 11d–f), confirming that Fft3 removes Cnp1 upon transcription at centromeres.

To find further evidence of transcription-coupled Cnp1 dismantling, we tested whether Cnp1 loss still occurs when transcription is blocked by RNAPII inhibitors such as 1,10-phenanthroline and thiolutin. Experiments were designed as shown in Fig. 2e. In brief, the cells were arrested to metaphase using the microtubule poison carbendazim (CBZ) as well as through alp12-1828 mutation, and GFP-Cnp1 intensity was monitored in the presence or absence of RNAPII inhibitors (Fig. 4c). In WT cells, RNAPII inhibitor 1,10-phenanthroline did not affect the amount of Cnp1 at centromeres (WT, Fig. 4d, e and Supplementary Fig. 12). In mis6-302 cells without RNAPII inhibitor treatment, the GFP-Cnp1 intensity constantly decreased throughout metaphase, as shown in Fig. 2f, g. In contrast, 1,10-phenanthroline treatment resulted in similar GFP-Cnp1 intensity as in WT cells (Fig. 4d, e and Supplementary Fig. 12). Comparable results were obtained in assays using thiolutin as the RNAPII inhibitor (Supplementary Fig. 13). Taken together, the reduction of GFP-Cnp1 during mitosis of the mis6-302 mutant is coupled to the transcription of ncRNAs at the central core region.

These results demonstrated that the inner kinetochore subcomplex including Mis6 prevents unnecessary transcription of ncRNAs at the central core region, thereby maintaining Cnp1 on chromatin during metaphase.

Chromatin remodelling factor Spt6 is required for Cnp1 recycling during mitosis

Transcription of ncRNAs in the central core region occurs at a certain level even in the presence of the functional inner kinetochore containing Mis6. It has been previously shown that phosphorylated RNAPII at the central core region is upregulated during the G2-M transition²³. Thus, some RNAPII passes through the central core region due to the removal of Cnp1 by Fft3 in WT cells, while the Cnp1 fluorescence signal remained during metaphase (Figs. 2 and 3). These results imply that Cnp1 is maintained through additional mechanisms, other than the Mis6-dependent system, during ncRNA transcription. Possible candidates include chromatin remodelling factors, such as FAcilitates Chromatin Transcription (FACT) and Spt6, which recycle nucleosomes after the passage of RNAPII at coding regions in the euchromatin^48,49. Drosophila and human Spt6 have been shown to contribute to CENP-A maintenance during interphase³³. Thus, we tested whether these factors also contribute to Cnp1 recycling when central core ncRNAs are transcribed.

First, we determined the level of GFP-Cnp1 intensity over time during metaphase in the knockout mutant of Spt6 (spt6∆) and the FACT component Pob3 (pob3∆). Cells were arrested to metaphase using the microtubule poison carbendazim (CBZ) as well as through the alp12-1828 mutation (Fig. 5a). GFP-Cnp1 intensity decreased over time in spt6∆ cells but not in pob3∆ cells. The temporal kinetics of GFP-Cnp1 levels in pob3∆ spt6∆ double-knockout cells was similar to that in spt6∆ cells (Fig. 5b and Supplementary Fig. 14a, b). This finding demonstrated that Spt6 recycles Cnp1 in WT cells, as a certain level of RNAPII leaks into the core centromere during mitosis.

**Fig. 5: Recycling of Cnp1 requires the chromatin remodelling factor Spt6.**

During the interphase of Drosophila cells, HJURP deposits de novo CENP-A to centromeres, which is also maintained by Spt6³³. In contrast, de novo CENP-A deposition does not occur during metaphase, suggesting that the role of Spt6 in CENP-A recycling may be particularly crucial in metaphase. Therefore, we investigated whether recycling Cnp1 by Spt6 during metaphase is crucial for chromosome segregation by assessing the segregation pattern of the cen2-GFP signal, with the centromeres of chromosome II visualised using GFP⁵¹. Cells were arrested to metaphase using the cut9-665 mutant, followed by release into anaphase by re-activating Cut9 function. As shown in Fig. 5c, deletion of Spt6 reduced the number of cells showing equal segregation of cen2-GFP among cut9-665 cells.

In the absence of Mis6, a large amount of RNAPII appeared to surge into the central core region. A previous study indicated a direct interaction of Spt6 with RNAPII in human cells⁵². Therefore, we assessed whether there was an upregulation of Spt6 in the mis6-302 mutant. Chromatin IP assays using Spt6-GFP pull-downs demonstrated that DNA fragments corresponding to the central core region were not specifically enriched in the mis6-302 sample compared to the WT (mis6⁺) sample (Fig. 5d). As the amount of the histone recycler Spt6 at the central core region was unaffected despite RNAPII accumulation, Spt6 may not be able to sufficiently cope with the upsurge of ncRNA transcription occurring in the absence of Mis6.

This led us to postulate that two distinct mechanisms contribute to CENP-A maintenance during mitosis, that is, the Mis6–Mis15-mediated system impedes the upsurge of RNAPII into the central core region, whereas Spt6 recycles CENP-A in response to ncRNA transcription.

To investigate this relationship, we compared the level of Cnp1 maintenance during metaphase of mis6-302 and spt6∆ cells. Although both mutants were defective in Cnp1 maintenance during metaphase, mis6-302 cells showed more severe defects than spt6∆ cells (Fig. 5e, f and Supplementary Fig. 14c). Severe reduction of the GFP-Cnp1 signal at centromeres was also detected in the mis6-302 spt6∆ double mutant to a similar degree as in mis6-302 (Fig. 5e, f and Supplementary Fig. 14c). These results indicate that once Cnp1 is lost by an upsurge of ncRNA transcription in the mis6 mutant, the Spt6-mediated recycling system cannot fully operate for Cnp1 maintenance.

Taken together, we conclude that the inner kinetochore subcomplex including Mis6 is the primary factor that maintains Cnp1 during mitosis by blocking the invasion of RNAPII, which minimises the transcription of centromeric ncRNAs. The slight transcription leakage over the blockade causes the removal of Cnp1, which is then reintroduced via Spt6-mediated recycling.

Discussion

This study provides a model for the temporal regulation of CENP-A nucleosomes during the cell cycle. That is, histone octamers containing CENP-A undergo cycles of deposition and turnover at the centromeric DNA. In fission yeast, CENP-A deposition is thought to occur during S phase (upon DNA replication) as well as during the G2 phase^7,53. Our FRAP analysis highlighted the incorporation of CENP-A into centromeres during the G1 phase (Fig. 1). After photobleaching, Cnp1-GFP intensity at interphase centromeres did not recover to its original state. Assuming that the turnover of pre-existing CENP-A or H3 from centromeres may be a prerequisite for the incorporation of new CENP-A, eviction may represent a rate-limiting step for subsequent CENP-A deposition in S. pombe.

We propose that CENP-A can be loaded onto centromeres at any time, except during mitosis (prometaphase). This is in line with the behaviour of the Mis18 complex and Scm3 (HJURP) throughout the cell cycle, both dispersing from kinetochores during early mitosis but returning in late mitosis (anaphase)^11,16. In contrast, the timing of deposition is limited to the early G1 phase in human cells^8,13,14. This discrepancy may be related to differences in the regulation of cyclin-dependent kinase (CDK) activity in each organism.

In human cells, phosphorylation of the Mis18 complex and HJURP by CDK prevents their localisation to centromeres. Since multiple distinct CDKs operate, e.g., Cdk1/2-cyclin A (active from S/G2 phase until metaphase) and Cdk1/cyclin B (prometaphase), CENP-A deposition by the Mis18 complex and HJURP is restricted only to the G1 phase, when they escape CDK phosphorylation⁵⁴.

In fission yeast, a single CDK (Cdc2-Cdc13/cyclin B) may determine its substrates depending on the total level of activity⁵⁵. It is possible that the Mis18 complex and HJURP are phosphorylated only when CDK activity is substantially high, that is, during metaphase. This might explain why fission yeast cells are competent in CENP-A deposition at any time except metaphase. As deposition machinery is compromised during metaphase, cells employ specific mechanisms to not lose CENP-A nucleosomes meanwhile.

The present study elucidates a previously unexplored mechanism through which CENP-A is maintained at the central core region of centromeres. In particular, we demonstrated a role for the Mis6 (CENP-I) subcomplex as a CENP-A maintenance factor. Mis6 has been considered a factor required for CENP-A deposition, since the localisation of Cnp1 and Scm3 is lost in the mis6 mutant^15,17. However, we found that in the absence of functional Mis6, CENP-A at centromeres decreased during metaphase when CENP-A was no longer deposited. Therefore, this reduction directly reflects CENP-A turnover from the centromeres. Similar results were produced by the strain lacking Mis15 (CENP-N), suggesting that the proper organisation of the Mis6 subcomplex of the inner kinetochore is crucial for CENP-A maintenance.

A recent study revealed that HJURP, in cooperation with the MCM complex, is required for CENP-A maintenance during S phase in human cells³². In fission yeast mitosis, however, Scm3 (HJURP) does not contribute to CENP-A maintenance as it delocalises from centromeres. The Mis6 subcomplex deserves to maintain CENP-A, as it persists during mitosis. Although Mis6 possibly plays the role even in interphase, this might be dispensable, because CENP-A is continuously recruited to centromeres in interphase. In practical terms, the observation for chronological changes of Cnp1-GFP signals does not address the issue. Additional techniques including photoactivation would be required in the future to visualise pre-existing Cnp1 at centromeres, but not newly recruited ones.

Transcription of centromeric ncRNA was previously detected throughout the cell cycle in S. pombe²³, with only a certain fraction of RNAPII localising into the central core (cnt) region to transcribe ncRNAs²⁵. As our results demonstrated that RNAPII binding to the cnt region was elevated in the mis6 and mis15 mutants, we propose that the inner kinetochore subcomplex including Mis6 and Mis15 (CENP-I and CENP-N) can act as an insulator for RNAPII invasion into the central core region in other organisms as well. In human cells, unknown factors in addition to HJURP appear to maintain CENP-A³². Moreover, ncRNA transcription at centromeres was detected in higher eukaryotes besides human, including mice and the tammar wallaby²², suggesting that the inner kinetochore subcomplex possibly maintains CENP-A in these species as well. On the other hand, CENP-I-deficient chicken DT40 cells display stable localisation of CENP-A to centromeres^56,57, suggesting that CENP-I might not contribute to CENP-A maintenance. Assuming that CENP-I serves as an insulator, it would be intriguing to investigate whether ncRNAs are actively transcribed at centromeres in DT40 cells. Molecular schemes for CENP-A maintenance may be intimately linked to whether ncRNA transcription occurs in centromeres. The utilisation of Mis6 (CENP-I) represents a suitable solution in organisms which actively transcribe centromeric ncRNAs, as it contributes to both CENP-A deposition and CENP-A maintenance as an RNAPII insulator.

Even though the Mis6 subcomplex impedes the progression of RNAPII into the cnt region of centromeres, transcripts are still detected at a certain level²⁵. This indicates that CENP-A in the cnt region is temporarily removed by the chromatin remodelling factor Fft3 when RNAPII proceeds but is mostly maintained by the histone recycler Spt6. Despite the accumulation of RNAPII within the cnt region of the mis6 mutant, concomitant accumulation of the histone recycler Spt6 was not observed. Unlike in human cells⁵², S. pombe Spt6 might not directly interact with RNAPII. Alternatively, an intense upregulation of RNAPII in the cnt failed to efficiently recruit Spt6. In either case, the capacity of Spt6 at the central core region appears to be limited to recycling CENP-A only at basal levels.

We conclude that two mechanisms operate for CENP-A maintenance. First, the inner kinetochore subcomplex including Mis6–Mis15 serves to insulate against the invasion of RNAPII into the core centromere, thus maintaining CENP-A, particularly during mitosis when de novo CENP-A deposition does not occur. Although Spt6 recycles CENP-A during mitosis in WT cells as the second machinery for CENP-A maintenance, the recycling capacity of Spt6 appears to be limited. Insulation of RNAPII by the inner kinetochore subcomplex is thus employed as the primary machinery, followed by Spt6-mediated CENP-A recycling as a backup, in a stepwise strategy for the epigenetic maintenance of CENP-A until the next cell cycle.

Methods

S. pombe strains and genetics

Strains used in this study are listed in Supplementary Table 1. Standard PCR-based methods for gene targeting were employed for the construction of knockout mutants and strains with fluorescent protein tagging^58,59,60. We used multiple constructs for the visualisation of Cnp1. In Fig. 1, strains expressing the Cnp1-GFP gene under an adh21 promoter at the C locus (adjacent to the SPAC26F1.12c gene of chromosome I) were used (the original strain was a gift from Y. Watanabe)⁶¹. In Fig. 2c, d, GFP-Cnp1 was expressed under the endogenous promoter (a gift from Y. Takayama)⁶². In other figures, the fusion gene of GFP-Cnp1 or mCherry-Cnp1 driven by the nmt1 promoter was inserted at the CO2 locus of chromosome II (adjacent to the SPBPB7E8.01 gene)⁶³ as an extra copy of the endogenous cnp1⁺ gene.

To create these integrant strains, we first created plasmids harboured the nmt1 promoter placed upstream of the cnp1 coding sequence fused with the GFP or mCherry gene via the Golden Gate method⁶³: pFA-Pnmt1-GFP-L-cnp1-kan-CO2-amp (NBRP accession ID: FYP5179) and pFA-Pnmt1-mCh-L-cnp1-hph-CO2-amp (NBRP ID: FYP5180), respectively. The constructed plasmids were digested by the FseI enzyme for linearisation and introduced into strains to induce homologous recombination at the CO2 locus.

For knocksideways experiments, expression of Kis1-GBP and Kis1-GBP-mCherry was induced via pREP1-based plasmids containing the nmt1 promoter: pREP1-kis1-GBP (NBRP ID: FYP5181) and pREP1-kis1(spm1)-GBP-mCherry (NBRP ID: FYP5182), respectively. The GFP-kan gene was inserted to the end of the mis6⁺ coding sequence, so that the strain expresses the fusion protein of Mis6-GFP instead of the endogenous Mis6 protein.

Cells in all figures excepted for Fig. 3 and Supplementary Fig. 8 were cultured in YE5S medium, while those in Fig. 3 and Supplementary Fig. 8 were cultured in Edinburgh minimal medium (EMM).

Mutagenesis of the scm3 gene

We first constructed the scm3-myc-hph strain, in which the scm3⁺ gene was tagged with the c-Myc epitope at the C-terminus marked with the hph selection marker gene, which confers resistance to 100 µg ml⁻¹ hygromycin B. We then induced random point mutations into scm3-myc-hph DNA fragments through an error-prone PCR reaction. The mutated fragments were then introduced into the mis6-GFP-kan strain to induce homologous recombination with the endogenous scm3⁺ gene. Colonies grown on YE5S + hygromycin B at 25 °C were replicated onto YE5S plates containing 2 µg ml⁻¹ phloxine B at 36 °C. Colonies showing temperature sensitivity with the normal localisation of Mis6-GFP were selected for sequencing and further experiments.

Chromatin IP

Cells were cultured at 25 °C in YE5S, followed by a temperature shift up to 36 °C for 4 h or 6 h. The cells were then fixed with 1% formaldehyde for 10 min at 36 °C and left on ice for 50 min. Chromatin IP assays in this study were carried out as previously described¹¹, with minor modifications. In brief, fixed cells were washed four times with Buffer I (50 mM HEPES/NaOH [pH 7.5], 140 mM NaCl, 1 mM EDTA [pH7.5], 1% Triton X-100 and 0.1% sodium deoxycholate) at 4 °C and kept frozen at –80 °C. Cells were then suspended in Buffer I supplemented with Complete Protease Inhibitor cocktail (Roche) and 1 mM phenylmethylsulfonyl fluoride. Cells were destroyed using acid-washed glass beads and a FastPrep-24 bead shocker (4 × 20 s, power = 6.0). The cell lysates were then sonicated using a sonifier VP-050 (PWM 10%). A round of iterative sonication for 10 s comprising ON (0.2 s) and OFF (0.4 s) was repeated 10 or 15 times to shear chromatin DNA into fragments. Lysates were then centrifuged (14,000 rpm for 15 min at 4 °C) to collect supernatants, and the concentration was adjusted to 10 mg ml⁻¹.

For immunoprecipitation, the rabbit anti-RNA polymerase II (phosphoS5) polyclonal antibody (1:100; ab5131) or rabbit anti-GFP polyclonal antibody (1:250; Clontech, 632592) was incubated with 200 µl of the lysate for 1 h at 4 °C. Protein A sepharose (GE) was then added, incubated for 2 h at 4 °C and washed three times with Buffer I, followed by suspension with Buffer I’ (50 mM HEPES/NaOH [pH 7.5], 500 mM NaCl, 1 mM EDTA [pH 7.5], 1% Triton X-100 and 0.1% sodium deoxycholate) twice, Buffer II (10 mM Tris-HCl [pH 8.0], 250 mM LiCl, 0.5% NP-40, 0.5% sodium deoxycholate) twice and TE twice. The amounts of DNA derived from whole-cell extracts and ChIP samples were assessed via quantitative PCR on the StepOne Real-Time PCR system (Applied Biosystems) using SYBR Green (TOYOBO). Oligonucleotide primers for detecting the central core region of centromeres were used based on previous study as follows⁶⁴: 5’-ATCTCATTGCTATTTGGCGAC-3’ and 5’-GCGTTTCCTTCGGCGAAATGC-3’. For the act1⁺ region primers: 5’-TGAGGAGCACCCTTGCTTGT-3’ and 5’-TCTTCTCACGGTTGGATTTGG-3’.

Microscopy

Living cells were transferred to a glass-bottom dish (Matsunami) pre-coated with lectin, and the dish was filled with liquid EMM preheated at 25 or 36 °C. Mounted cells were observed at 25 or 36 °C using a microscope (IX71, Olympus) with the DeltaVision-SoftWoRx system (Applied Precision), as previously described⁶⁵. Cells were imaged in 12 sections at 0.4-µm intervals along the z-axis. The temperature conditions are shown below. In Fig. 1, Cells were observed for 1 h after culturing at 36 °C for 3 h to synchronise them in each cell cycle stage. In Supplementary Fig. 6, overnight cultures were incubated at 36 °C for 4 h, and cells were fixed with 3.2% formaldehyde (Thermo Fisher Scientific) for 20 min. In Fig. 3c and Supplementary Fig. 8, cells were cultured at 25 °C for 20 h in EMM and imaged. As mCherry-Cnp1 was expressed under the nmt1 promoter, cells occasionally exhibited mCherry-Cnp1 localisation as multiple dots. Such cells were excluded from the signal intensity measurement, and cells with a single mCherry-Cnp1 dot were exclusively used for the measurement. The acquired images were processed as follows: images taken along the z-axis were deconvoluted and projected into a single image using the Quick Projection algorithm in the SoftWoRx software (v3.7.0 and v.6.5.1).

The fluorescence intensity of Cnp1 visualised with GFP or mCherry was measured using the Data Inspector command in SoftWoRx. The mean intensity of a single dot signal of Cnp1-GFP or GFP-Cnp1 in 6 × 6 pixels was measured, and the background signal outside of the nucleus was subtracted. GFP-Cnp1 remained exclusively at SPBs during metaphase arrest, which was artificially induced by spindle inhibition. Plo1-2mCherry was then used as a mitotic SPB marker to pinpoint GFP-Cnp1 dots remained at SPBs. Cnp1-GFP or GFP-Cnp1 showed a single dot in the nucleus in most of the experiments. In Supplementary Fig. 8a, cells occasionally showed multiple mCherry-Cnp1 dots in the nucleus. We measured signal intensity of mCherry-Cnp1 that showed a single dot in the nucleus.

For photobleaching of a Cnp1-GFP dot signal, the dot area was successively irradiated four times by the 488 nm laser (50% in power; Seki Technotron) for 0.05 s using the SoftWoRx-QLM system. Procedures for photobleaching and subsequent fluorescent recovery were performed at the restricted temperature. Since Cnp1-GFP co-localised with the kinetochore protein Cnp3-tdTomato or with the SPB protein Plo1-2mCherry, the rectangular region of 6 × 6 pixels were chosen for measurement based on the position of the Cnp3-tdTomato and Plo1-2mCherry signal. In Figs. 1, 2f, 3c–5 and Supplementary Figs. 4, 7, 11, 13, and 14, the resolution of enlarged images was adjusted from 72 to 144 pixels inch⁻¹ using Adobe Photoshop (ver. 2021).

Drug treatment

To inhibit RNAPII, 1,10-phenanthroline (Sigma-Aldrich) diluted to 100 mg ml⁻¹ with ethanol was added to the EMM at a final concentration of 100 µg ml⁻¹. Alternatively, thiolutin (Wako) diluted to 5 mg ml⁻¹ with dimethyl sulfoxide (DMSO) was added to EMM at a final concentration of 20 µg ml⁻¹ as previously described⁶⁶. For mock treatment, the same amount of solvent (ethanol or DMSO) was added to the EMM. Observations began 15 min after the addition of reagents. To arrest cells at metaphase for more than 1 h, the microtubule poison carbendazim (CBZ; Sigma-Aldrich) diluted to 5 mg ml⁻¹ with DMSO was added to EMM at a final concentration of 50 µg ml⁻¹ immediately before observation. To arrest cells during the G1/S phase, hydroxyurea (HU; Sigma-Aldrich) diluted to 1.5 M with DMSO was added to YE5S at a final concentration of 15 mM.

Chromosome segregation assay with cen2-GFP

To evaluate chromosome segregation in cut9-665 and cut9-665 spt6∆ mutants, the cen2-GFP system was employed to visualise the position of chromosome II centromere with GFP⁵¹. For metaphase arrest, cells were first arrested at the G1/S phase using hydroxyurea (HU) for 2 h. In the presence of hydroxyurea (HU), the temperature was then shifted up to 36 °C to inactivate an APC/C (anaphase promoting complex/cyclosome) component Cut9. Cells were then washed with ddH₂O three times and cultured in YE5S for 2 h at 36 °C to release cells from G1/S arrest until metaphase arrest via Cut9-inactivation. The culture was shifted down to 25 °C again to finally release cells from metaphase to anaphase, and the distribution of cen2-GFP dots was observed for 1 h.

Statistics and reproducibility

Statistical analysis was performed by two-tailed Welch’s t-test to calculate p values using Excel (Microsoft). The p values are shown as n.s. if p > 0.05, * if p < 0.05, ** if p < 0.01, *** if p < 0.001, respectively. Sample sizes are specified in the legend of each figure. Reproducibility was confirmed by at least three independent biological experiments.

Reporting summary

Further information on research design is available in the Nature Research Reporting Summary linked to this article.

Data availability

Plasmids created in this study are available in National BioResource Project (NBRP) in Japan. Accession IDs are included in the “Methods” section. The data that support the findings of this study are available from the corresponding author upon reasonable request. The source data of the graphs are provided as a Supplementary Data file.

Code availability

Python (v 3.9.0; https://www.python.org/) was used for creating graphs in this study.

References

Walczak, C. E., Cai, S. & Khodjakov, A. Mechanisms of chromosome behaviour during mitosis. Nat. Rev. Mol. Cell Biol. 11, 91–102 (2010).
Article CAS PubMed PubMed Central Google Scholar
Biggins, S. The composition, functions, and regulation of the budding yeast kinetochore. Genetics 194, 817–846 (2013).
Article CAS PubMed PubMed Central Google Scholar
Pidoux, A. L. & Allshire, R. C. Kinetochore and heterochromatin domains of the fission yeast centromere. Chromosome Res. 12, 521–534 (2004).
Article CAS PubMed Google Scholar
Schueler, M. G. & Sullivan, B. A. Structural and functional dynamics of human centromeric chromatin. Annu. Rev. Genomics Hum. Genet. 7, 301–313 (2006).
Article CAS PubMed Google Scholar
Holland, A. J. & Cleveland, D. W. Boveri revisited: chromosomal instability, aneuploidy and tumorigenesis. Nat. Rev. Mol. Cell Biol. 10, 478–487 (2009).
Article CAS PubMed PubMed Central Google Scholar
Jansen, L. E. T., Black, B. E., Foltz, D. R. & Cleveland, D. W. Propagation of centromeric chromatin requires exit from mitosis. J. Cell Biol. 176, 795–805 (2007).
Article CAS PubMed PubMed Central Google Scholar
Lando, D. et al. Quantitative single-molecule microscopy reveals that CENP-A^Cnp1 deposition occurs during G2 in fission yeast. Open Biol. 2, 120078 (2012).
Article PubMed PubMed Central CAS Google Scholar
Fujita, Y. et al. Priming of centromere for CENP-A recruitment by human hMis18α, hMis18β, and M18BP1. Dev. Cell 12, 17–30 (2007).
Article CAS PubMed Google Scholar
Hayashi, T. et al. Mis16 and Mis18 are required for CENP-A loading and histone deacetylation at centromeres. Cell 118, 715–729 (2004).
Article CAS PubMed Google Scholar
Hayashi, T. et al. Schizosaccharomyces pombe centromere protein Mis19 links Mis16 and Mis18 to recruit CENP-A through interacting with NMD factors and the SWI/SNF complex. Genes Cells 19, 541–554 (2014).
Article CAS PubMed Google Scholar
Hirai, H., Arai, K., Kariyazono, R., Yamamoto, M. & Sato, M. The kinetochore protein Kis1/Eic1/Mis19 ensures the integrity of mitotic spindles through maintenance of kinetochore factors Mis6/CENP-I and CENP-A. PLoS ONE 9, e111905 (2014).
Article PubMed PubMed Central CAS Google Scholar
Subramanian, L., Toda, N. R. T., Rappsilber, J. & Allshire, R. C. Eic1 links Mis18 with the CCAN/Mis6/Ctf19 complex to promote CENP-A assembly. Open Biol. 4, 140043 (2014).
Article PubMed PubMed Central CAS Google Scholar
Foltz, D. R. et al. Centromere-specific assembly of CENP-a nucleosomes is mediated by HJURP. Cell 137, 472–484 (2009).
Article CAS PubMed PubMed Central Google Scholar
Dunleavy, E. M. et al. HJURP is a cell-cycle-dependent maintenance and deposition factor of CENP-A at centromeres. Cell 137, 485–497 (2009).
Article CAS PubMed Google Scholar
Williams, J. S., Hayashi, T., Yanagida, M. & Russell, P. Fission yeast Scm3 mediates stable assembly of Cnp1/CENP-A into centromeric chromatin. Mol. Cell 33, 287–298 (2009).
Article CAS PubMed PubMed Central Google Scholar
Pidoux, A. L. et al. Fission yeast Scm3: A CENP-A receptor required for integrity of subkinetochore chromatin. Mol. Cell 33, 299–311 (2009).
Article CAS PubMed PubMed Central Google Scholar
Takahashi, K., Chen, E. S. & Yanagida, M. Requirement of Mis6 centromere connector for localizing a CENP-A-like protein in fission yeast. Science 288, 2215–2219 (2000).
Article CAS PubMed Google Scholar
Dion, M. F. et al. Dynamics of replication-independent histone turnover in budding yeast. Science 315, 1405–1408 (2007).
Article CAS PubMed Google Scholar
Jin, C. et al. H3.3/H2A.Z double variant-containing nucleosomes mark ‘nucleosome-free regions’ of active promoters and other regulatory regions. Nat. Genet. 41, 941–945 (2009).
Article CAS PubMed PubMed Central Google Scholar
Deal, R. B., Henikoff, J. G. & Henikoff, S. Genome-wide kinetics of nucleosome turnover determined by metabolic labeling of histones. Science 328, 1161–1164 (2010).
Article CAS PubMed PubMed Central Google Scholar
Smoak, E. M., Stein, P., Schultz, R. M., Lampson, M. A. & Black, B. E. Long-term retention of CENP-A nucleosomes in Mammalian oocytes underpins transgenerational inheritance of centromere identity. Curr. Biol. 26, 1110–1116 (2016).
Article CAS PubMed PubMed Central Google Scholar
Talbert, P. B. & Henikoff, S. Transcribing centromeres: noncoding RNAs and kinetochore assembly. Trends Genet. 34, 587–599 (2018).
Article CAS PubMed Google Scholar
Sadeghi, L., Siggens, L., Svensson, J. P. & Ekwall, K. Centromeric histone H2B monoubiquitination promotes noncoding transcription and chromatin integrity. Nat. Struct. Mol. Biol. 21, 236–243 (2014).
Article CAS PubMed Google Scholar
Bergmann, J. H. et al. Epigenetic engineering: histone H3K9 acetylation is compatible with kinetochore structure and function. J. Cell. Sci. 125, 411–421 (2012).
Article CAS PubMed PubMed Central Google Scholar
Carlsten, J. O. et al. Mediator promotes CENP-A incorporation at fission yeast centromeres. Mol. Cell. Biol. 32, 4035–4043 (2012).
Article CAS PubMed PubMed Central Google Scholar
Niikura, Y. et al. CENP-A K124 ubiquitylation is required for CENP-A deposition at the centromere. Dev. Cell 32, 589–603 (2015).
Article CAS PubMed PubMed Central Google Scholar
Carroll, C. W., Silva, M. C. C., Godek, K. M., Jansen, L. E. T. & Straight, A. F. Centromere assembly requires the direct recognition of CENP-A nucleosomes by CENP-N. Nat. Cell Biol. 11, 896–902 (2009).
Article CAS PubMed PubMed Central Google Scholar
Carroll, C. W., Milks, K. J. & Straight, A. F. Dual recognition of CENP-A nucleosomes is required for centromere assembly. J. Cell Biol. 189, 1143–1155 (2010).
Article CAS PubMed PubMed Central Google Scholar
Falk, S. J. et al. CENP-C reshapes and stabilizes CENP-A nucleosomes at the centromere. Science 348, 699–703 (2015).
Article CAS PubMed PubMed Central Google Scholar
Guo, L. Y. et al. Centromeres are maintained by fastening CENP-A to DNA and directing an arginine anchor-dependent nucleosome transition. Nat. Commun. 8, 15775 (2017).
Article PubMed PubMed Central Google Scholar
Cao, S., Zhou, K., Zhang, Z., Luger, K. & Straight, A. F. Constitutive centromere-associated network contacts confer differential stability on CENP-A nucleosomes in vitro and in the cell. Mol. Biol. Cell 29, 751–762 (2018).
Article CAS PubMed PubMed Central Google Scholar
Zasadzińska, E. et al. Inheritance of CENP-A nucleosomes during DNA replication requires HJURP. Dev. Cell 47, 348–362.e7 (2018).
Article PubMed PubMed Central CAS Google Scholar
Bobkov, G. O. M. et al. Spt6 is a maintenance factor for centromeric CENP-A. Nat. Commun. 11, 2919–14 (2020).
Article CAS PubMed PubMed Central Google Scholar
Foltz, D. R. et al. The human CENP-A centromeric nucleosome-associated complex. Nat. Cell Biol. 8, 458–469 (2006).
Article CAS PubMed Google Scholar
Pidoux, A. L., Richardson, W. & Allshire, R. C. Sim4: a novel fission yeast kinetochore protein required for centromeric silencing and chromosome segregation. J. Cell Biol. 161, 295–307 (2003).
Article CAS PubMed PubMed Central Google Scholar
Saitoh, S., Takahashi, K. & Yanagida, M. Mis6, a fission yeast inner centromere protein, acts during G1/S and forms specialized chromatin required for equal segregation. Cell 90, 131–143 (1997).
Article CAS PubMed Google Scholar
Russell, P. & Nurse, P. cdc25⁺ functions as an inducer in the mitotic control of fission yeast. Cell 45, 145–153 (1986).
Article CAS PubMed Google Scholar
Radcliffe, P., Hirata, D., Childs, D., Vardy, L. & Toda, T. Identification of novel temperature-sensitive lethal alleles in essential β-tubulin and nonessential α2-tubulin genes as fission yeast polarity mutants. Mol. Biol. Cell 9, 1757–1771 (1998).
Article CAS PubMed PubMed Central Google Scholar
Samejima, I. & Yanagida, M. Bypassing anaphase by fission yeast cut9 mutation: requirement of cut9⁺ to initiate anaphase. J. Cell Biol. 127, 1655–1670 (1994).
Article CAS PubMed Google Scholar
Bahler, J. et al. Role of polo kinase and Mid1p in determining the site of cell division in fission yeast. J. Cell Biol. 143, 1603–1616 (1998).
Article CAS PubMed PubMed Central Google Scholar
Mulvihill, D. P., Petersen, J., Ohkura, H., Glover, D. M. & Hagan, I. M. Plo1 kinase recruitment to the spindle pole body and its role in cell division in Schizosaccharomyces pombe. Mol. Biol. Cell 10, 2771–2785 (1999).
Article CAS PubMed PubMed Central Google Scholar
Shiroiwa, Y. et al. Mis17 is a regulatory module of the Mis6-Mal2-Sim4 centromere complex that is required for the recruitment of CenH3/CENP-A in fission yeast. PLoS ONE 6, e17761 (2011).
Article CAS PubMed PubMed Central Google Scholar
Takahashi, K., Yamada, H. & Yanagida, M. Fission yeast minichromosome loss mutants mis cause lethal aneuploidy and replication abnormality. Mol. Biol. Cell 5, 1145–1158 (1994).
Article CAS PubMed PubMed Central Google Scholar
Nabetani, A., Koujin, T., Tsutsumi, C., Haraguchi, T. & Hiraoka, Y. A conserved protein, Nuf2, is implicated in connecting the centromere to the spindle during chromosome segregation: a link between the kinetochore function and the spindle checkpoint. Chromosoma 110, 322–334 (2001).
Article CAS PubMed Google Scholar
Goshima, G., Saitoh, S. & Yanagida, M. Proper metaphase spindle length is determined by centromere proteins Mis12 and Mis6 required for faithful chromosome segregation. Genes Dev. 13, 1664–1677 (1999).
Article CAS PubMed PubMed Central Google Scholar
Rothbauer, U. et al. Targeting and tracing antigens in live cells with fluorescent nanobodies. Nat. Methods 3, 887–889 (2006).
Article CAS PubMed Google Scholar
Egloff, S. & Murphy, S. Cracking the RNA polymerase II CTD code. Trends Genet. 24, 280–288 (2008).
Article CAS PubMed Google Scholar
Avvakumov, N., Nourani, A. & Côté, J. Histone chaperones: modulators of chromatin marks. Mol. Cell 41, 502–514 (2011).
Article CAS PubMed Google Scholar
Hammond, C. M., Strømme, C. B., Huang, H., Patel, D. J. & Groth, A. Histone chaperone networks shaping chromatin function. Nat. Rev. Mol. Cell Biol. 18, 141–158 (2017).
Article CAS PubMed PubMed Central Google Scholar
Lee, J. et al. Chromatin remodeller Fun30^Fft3 induces nucleosome disassembly to facilitate RNA polymerase II elongation. Nat. Commun. 8, 14527 (2017).
Article CAS PubMed PubMed Central Google Scholar
Yamamoto, A. & Hiraoka, Y. Monopolar spindle attachment of sister chromatids is ensured by two distinct mechanisms at the first meiotic division in fission yeast. EMBO J. 22, 2284–2296 (2003).
Article CAS PubMed PubMed Central Google Scholar
Yoh, S. M., Cho, H., Pickle, L., Evans, R. M. & Jones, K. A. The Spt6 SH2 domain binds Ser2-P RNAPII to direct Iws1-dependent mRNA splicing and export. Genes Dev. 21, 160–174 (2007).
Article CAS PubMed PubMed Central Google Scholar
Gonzalez, M., He, H., Sun, S., Li, C. & Li, F. Cell cycle-dependent deposition of CENP-A requires the Dos1/2-Cdc20 complex. Proc. Natl Acad. Sci. USA 110, 606–611 (2013).
Article CAS PubMed Google Scholar
Stankovic, A. et al. A dual inhibitory mechanism sufficient to maintain cell-cycle-restricted CENP-A assembly. Mol. Cell 65, 231–246 (2017).
Article CAS PubMed Google Scholar
Swaffer, M. P., Jones, A. W., Flynn, H. R., Snijders, A. P. & Nurse, P. CDK substrate phosphorylation and ordering the cell cycle. Cell 167, 1750–1761.e16 (2016).
Article CAS PubMed PubMed Central Google Scholar
Nishihashi, A. et al. CENP-I is essential for centromere function in vertebrate cells. Dev. Cell 2, 463–476 (2002).
Article CAS PubMed Google Scholar
Okada, M. et al. The CENP-H-I complex is required for the efficient incorporation of newly synthesized CENP-A into centromeres. Nat. Cell Biol. 8, 446–457 (2006).
Article CAS PubMed Google Scholar
Moreno, S., Klar, A. & Nurse, P. Molecular genetic analysis of fission yeast Schizosaccharomyces pombe. Meth. Enzymol. 194, 795–823 (1991).
Article CAS Google Scholar
Bahler, J. et al. Heterologous modules for efficient and versatile PCR-based gene targeting in Schizosaccharomyces pombe. Yeast 14, 943–951 (1998).
Article CAS PubMed Google Scholar
Sato, M., Dhut, S. & Toda, T. New drug-resistant cassettes for gene disruption and epitope tagging in Schizosaccharomyces pombe. Yeast 22, 583–591 (2005).
Article CAS PubMed Google Scholar
Tanaka, K., Chang, H. L., Kagami, A. & Watanabe, Y. CENP-C functions as a scaffold for effectors with essential kinetochore functions in mitosis and meiosis. Dev. Cell 17, 334–343 (2009).
Article PubMed Google Scholar
Takayama, Y. et al. Biphasic incorporation of centromeric histone CENP-A in fission yeast. Mol. Biol. Cell 19, 682–690 (2008).
Article CAS PubMed PubMed Central Google Scholar
Kakui, Y. et al. Module-based construction of plasmids for chromosomal integration of the fission yeast Schizosaccharomyces pombe. Open Biol. 5, 150054 (2015).
Yokobayashi, S., Yamamoto, M. & Watanabe, Y. Cohesins determine the attachment manner of kinetochores to spindle microtubules at meiosis I in fission yeast. Mol. Cell. Biol. 23, 3965–3973 (2003).
Article CAS PubMed PubMed Central Google Scholar
Sato, M., Toya, M. & Toda, T. Visualization of fluorescence-tagged proteins in fission yeast: the analysis of mitotic spindle dynamics using GFP-tubulin under the native promoter. Methods Mol. Biol. 545, 185–203 (2009).
Article CAS PubMed Google Scholar
Takemata, N. et al. Local potentiation of stress-responsive genes by upstream noncoding transcription. Nucleic Acids Res. 44, 5174–5189 (2016).
Article CAS PubMed PubMed Central Google Scholar

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Acknowledgements

We thank Y. Takayama, A. Yamamoto, Y. Hiraoka, T. Sakuno Y. Watanabe, M. Yanagida and the National Bioresource Project (NBRP) of Japan for the yeast strains. We are grateful to K. Ohta for providing part of the experimental space and materials. H.H. was a research fellow of the Japan Society for the Promotion of Science (JSPS; 16J09035). Y.S. was supported by JST SPRING, Grant Number JPMJSP2128. This study was supported by JSPS KAKENHI JP25291041, JP15H01359, JP16H04787, JP16H01317, JP18K19347 and JP21H00261 to M.S. This study was also supported by The Uehara Memorial Foundation, Ohsumi Frontier Science Foundation and Waseda University grants for Special Research Projects 2017B-242, 2017B-243, 2018B-222, 2019C-570, 2020R-038 and 2022C-164 to M.S. This work was also partly supported by the JSPS Core-to-Core Program, A: Advanced Research Networks.

Author information

Authors and Affiliations

Laboratory of Cytoskeletal Logistics, Department of Life Science and Medical Bioscience, Graduate School of Advanced Science and Engineering, Waseda University, TWIns, 2-2 Wakamatsucho, Shinjuku-ku, Tokyo, 162-8480, Japan
Hayato Hirai, Yuki Shogaki & Masamitsu Sato
Department of Life Sciences, Graduate School of Arts and Sciences, The University of Tokyo, Komaba 3-8-1, Tokyo, 153-8902, Japan
Hayato Hirai
Institute for Medical-oriented Structural Biology, Waseda University, TWIns, 2-2 Wakamatsucho, Shinjuku-ku, Tokyo, 162-8480, Japan
Masamitsu Sato
Institute for Advanced Research of Biosystem Dynamics, Waseda Research Institute for Science and Engineering, Graduate School of Advanced Science and Engineering, Waseda University, 3-4-1 Okubo, Shinjuku-ku, Tokyo, 169-8555, Japan
Masamitsu Sato

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Hayato Hirai
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Yuki Shogaki
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Masamitsu Sato
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Contributions

H.H. and M.S. conceived and designed the experiments. H.H. and Y.S. performed the experiments. H.H. wrote the draft of the manuscript. M.S. supervised the project and finalised the manuscript through discussion with H.H. and Y.S.

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Correspondence to Masamitsu Sato.

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Hirai, H., Shogaki, Y. & Sato, M. The Mis6 inner kinetochore subcomplex maintains CENP-A nucleosomes against centromeric non-coding transcription during mitosis. Commun Biol 5, 818 (2022). https://doi.org/10.1038/s42003-022-03786-y

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Received: 28 October 2021
Accepted: 02 August 2022
Published: 15 August 2022
DOI: https://doi.org/10.1038/s42003-022-03786-y