TY - JOUR
T1 - The Mis6 inner kinetochore subcomplex maintains CENP-A nucleosomes against centromeric non-coding transcription during mitosis
AU - Hirai, Hayato
AU - Shogaki, Yuki
AU - Sato, Masamitsu
N1 - Funding Information:
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.
Funding Information:
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.
Publisher Copyright:
© 2022, The Author(s).
PY - 2022/12
Y1 - 2022/12
N2 - 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.
AB - 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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UR - http://www.scopus.com/inward/citedby.url?scp=85135904463&partnerID=8YFLogxK
U2 - 10.1038/s42003-022-03786-y
DO - 10.1038/s42003-022-03786-y
M3 - Article
C2 - 35970865
AN - SCOPUS:85135904463
SN - 2399-3642
VL - 5
JO - Communications Biology
JF - Communications Biology
IS - 1
M1 - 818
ER -