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Items: 1 to 20 of 44

1.
METTL3 counteracts premature aging via m6A-dependent stabilization of MIS12 mRNA
Zeming Wu, Yue Shi, Mingming Lu, Moshi Song, Zihui Yu, Jilu Wang, Si Wang, Jie Ren, Yun-Gui Yang, Guang-Hui Liu, Weiqi Zhang, Weimin Ci, Jing Qu
Nucleic Acids Res. 2020 Nov 4; 48(19): 11083–11096. Published online 2020 Oct 9. doi: 10.1093/nar/gkaa816
PMCID:
PMC7641765
AbstractArticlePDF–2.7M
2.
Direct binding of Cenp-C to the Mis12 complex joins the inner and outer kinetochore
Emanuela Screpanti, Anna De Antoni, Gregory M. Alushin, Arsen Petrovic, Tiziana Melis, Eva Nogales, Andrea Musacchio
Curr Biol. Author manuscript; available in PMC 2011 Sep 8.
Published in final edited form as: Curr Biol. 2011 Mar 8; 21(5): 391–398. Published online 2011 Feb 25. doi: 10.1016/j.cub.2010.12.039
PMCID:
PMC3074538
AbstractArticlePDF–6.9M
3.
Human centromere chromatin protein hMis12, essential for equal segregation, is independent of CENP-A loading pathway
Gohta Goshima, Tomomi Kiyomitsu, Kinya Yoda, Mitsuhiro Yanagida
J Cell Biol. 2003 Jan 6; 160(1): 25–39. doi: 10.1083/jcb.200210005
PMCID:
PMC2172742
AbstractArticlePDF–11M
4.
Multiple assembly mechanisms anchor the KMN spindle checkpoint platform at human mitotic kinetochores
Soonjoung Kim, Hongtao Yu
J Cell Biol. 2015 Jan 19; 208(2): 181–196. doi: 10.1083/jcb.201407074
PMCID:
PMC4298689
AbstractArticlePDF–4.5M
5.
Molecular basis of outer kinetochore assembly on CENP-T
Pim J Huis in 't Veld, Sadasivam Jeganathan, Arsen Petrovic, Priyanka Singh, Juliane John, Veronica Krenn, Florian Weissmann, Tanja Bange, Andrea Musacchio
eLife. 2016; 5: e21007. Published online 2016 Dec 24. doi: 10.7554/eLife.21007
PMCID:
PMC5241120
AbstractArticlePDF–8.7M
6.
CENP-T provides a structural platform for outer kinetochore assembly
Tatsuya Nishino, Florencia Rago, Tetsuya Hori, Kentaro Tomii, Iain M Cheeseman, Tatsuo Fukagawa
EMBO J. 2013 Feb 6; 32(3): 424–436. Published online 2013 Jan 18. doi: 10.1038/emboj.2012.348
PMCID:
PMC3567495
AbstractArticlePDF–2.4M
7.
Structure of the MIS12 Complex and Molecular Basis of Its Interaction with CENP-C at Human Kinetochores
Arsen Petrovic, Jenny Keller, Yahui Liu, Katharina Overlack, Juliane John, Yoana N. Dimitrova, Simon Jenni, Suzan van Gerwen, Patricia Stege, Sabine Wohlgemuth, Pascaline Rombaut, Franz Herzog, Stephen C. Harrison, Ingrid R. Vetter, Andrea Musacchio
Cell. 2016 Nov 3; 167(4): 1028–1040.e15. doi: 10.1016/j.cell.2016.10.005
PMCID:
PMC5101189
AbstractArticle
8.
Hsp90–Sgt1 and Skp1 target human Mis12 complexes to ensure efficient formation of kinetochore–microtubule binding sites
Alexander E. Davies, Kenneth B. Kaplan
J Cell Biol. 2010 Apr 19; 189(2): 261–274. doi: 10.1083/jcb.200910036
PMCID:
PMC2856898
AbstractArticlePDF–8.4M
9.
The MIS12 complex is a protein interaction hub for outer kinetochore assembly
Arsen Petrovic, Sebastiano Pasqualato, Prakash Dube, Veronica Krenn, Stefano Santaguida, Davide Cittaro, Silvia Monzani, Lucia Massimiliano, Jenny Keller, Aldo Tarricone, Alessio Maiolica, Holger Stark, Andrea Musacchio
J Cell Biol. 2010 Sep 6; 190(5): 835–852. doi: 10.1083/jcb.201002070
PMCID:
PMC2935574
AbstractArticlePDF–5.0M
10.
Lateral to End-on Conversion of Chromosome-Microtubule Attachment Requires Kinesins CENP-E and MCAK
Roshan L. Shrestha, Viji M. Draviam
Curr Biol. 2013 Aug 19; 23(16): 1514–1526. doi: 10.1016/j.cub.2013.06.040
Correction in:
Curr Biol. 2013 Dec 2; 23(23): 2440–2441.
PMCID:
PMC3748344
AbstractArticle
11.
Plk1 Phosphorylates Sgt1 at the Kinetochores To Promote Timely Kinetochore-Microtubule Attachment
X. Shawn Liu, Bing Song, Jiabin Tang, Weiyi Liu, Shihuan Kuang, Xiaoqi Liu
Mol Cell Biol. 2012 Oct; 32(19): 4053–4067. doi: 10.1128/MCB.00516-12
PMCID:
PMC3457539
AbstractArticlePDF–4.9M
12.
Aurora B controls kinetochore–microtubule attachments by inhibiting Ska complex–KMN network interaction
Ying Wai Chan, A. Arockia Jeyaprakash, Erich A. Nigg, Anna Santamaria
J Cell Biol. 2012 Mar 5; 196(5): 563–571. doi: 10.1083/jcb.201109001
PMCID:
PMC3307695
AbstractArticlePDF–2.6M
13.
Protein Interaction Domain Mapping of Human Kinetochore Protein Blinkin Reveals a Consensus Motif for Binding of Spindle Assembly Checkpoint Proteins Bub1 and BubR1
Tomomi Kiyomitsu, Hiroaki Murakami, Mitsuhiro Yanagida
Mol Cell Biol. 2011 Mar; 31(5): 998–1011. Published online 2011 Jan 3. doi: 10.1128/MCB.00815-10
PMCID:
PMC3067818
AbstractArticlePDF–4.5M
14.
The human Mis12 complex is required for kinetochore assembly and proper chromosome segregation
Susan L. Kline, Iain M. Cheeseman, Tetsuya Hori, Tatsuo Fukagawa, Arshad Desai
J Cell Biol. 2006 Apr 10; 173(1): 9–17. doi: 10.1083/jcb.200509158
PMCID:
PMC2063780
AbstractArticlePDF–2.3M
15.
Inner centromere formation requires hMis14, a trident kinetochore protein that specifically recruits HP1 to human chromosomes
Tomomi Kiyomitsu, Osamu Iwasaki, Chikashi Obuse, Mitsuhiro Yanagida
J Cell Biol. 2010 Mar 22; 188(6): 791–807. doi: 10.1083/jcb.200908096
PMCID:
PMC2845078
AbstractArticlePDF–5.0M
16.
Epigenetic displacement of HP1 from heterochromatin by HIV-1 Vpr causes premature sister chromatid separation
Mari Shimura, Yusuke Toyoda, Kenta Iijima, Masanobu Kinomoto, Kenzo Tokunaga, Kinya Yoda, Mitsuhiro Yanagida, Tetsutaro Sata, Yukihito Ishizaka
J Cell Biol. 2011 Sep 5; 194(5): 721–735. doi: 10.1083/jcb.201010118
PMCID:
PMC3171121
AbstractArticlePDF–3.2M
17.
ZW10 links mitotic checkpoint signaling to the structural kinetochore
Geert J.P.L. Kops, Yumi Kim, Beth A.A. Weaver, Yinghui Mao, Ian McLeod, John R. Yates, III, Mitsuo Tagaya, Don W. Cleveland
J Cell Biol. 2005 Apr 11; 169(1): 49–60. doi: 10.1083/jcb.200411118
PMCID:
PMC1351127
AbstractArticlePDF–5.2M
18.
The KMN protein network – chief conductors of the kinetochore orchestra
Dileep Varma, E. D. Salmon
J Cell Sci. 2012 Dec 15; 125(24): 5927–5936. doi: 10.1242/jcs.093724
PMCID:
PMC3585512
AbstractArticle
19.
A conserved protein network controls assembly of the outer kinetochore and its ability to sustain tension
Iain M. Cheeseman, Sherry Niessen, Scott Anderson, Francie Hyndman, John R. Yates, III, Karen Oegema, Arshad Desai
Genes Dev. 2004 Sep 15; 18(18): 2255–2268. doi: 10.1101/gad.1234104
PMCID:
PMC517519
AbstractArticlePDF–426K
20.
AI-guided pipeline for protein-protein interaction drug discovery identifies a SARS-CoV-2 inhibitor
Philipp Trepte, Christopher Secker, Simona Kostova, Sibusiso B. Maseko, Soon Gang Choi, Jeremy Blavier, Igor Minia, Eduardo Silva Ramos, Patricia Cassonnet, Sabrina Golusik, Martina Zenkner, Stephanie Beetz, Mara J. Liebich, Nadine Scharek, Anja Schütz, Marcel Sperling, Michael Lisurek, Yang Wang, Kerstin Spirohn, Tong Hao, Michael A. Calderwood, David E. Hill, Markus Landthaler, Julien Olivet, Jean-Claude Twizere, Marc Vidal, Erich E. Wanker
Version 1. bioRxiv. Preprint. 2023 Jun 14. doi: 10.1101/2023.06.14.544560
Published in:
Mol Syst Biol. 2024 Apr; 20(4): 428–457.
PMCID:
PMC10312674
AbstractArticlePDF–9.6M

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