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Items: 1 to 20 of 23

1.
Structure of the replication regulator Sap1 reveals functionally important interfaces
Maria M. Jørgensen, Babatunde Ekundayo, Mikel Zaratiegui, Karen Skriver, Geneviève Thon, Thomas Schalch
Sci Rep. 2018; 8: 10930. Published online 2018 Jul 19. doi: 10.1038/s41598-018-29198-9
PMCID:
PMC6053445
AbstractArticlePDF–1.5M
2.
Molecular signature of the imprintosome complex at the mating-type locus in fission yeast
Célia Raimondi, Bernd Jagla, Caroline Proux, Hervé Waxin, Serge Gangloff, Benoit Arcangioli
Microb Cell. 2018 Apr 2; 5(4): 169–183. Published online 2018 Jan 16. doi: 10.15698/mic2018.04.623
PMCID:
PMC5878685
AbstractArticlePDF–2.1M
3.
A non-transcriptional role for the glucocorticoid receptor in mediating the cell stress response
Marina Ptushkina, Toryn Poolman, Mudassar Iqbal, Mark Ashe, Janni Petersen, Joanna Woodburn, Magnus Rattray, Anthony Whetton, David Ray
Sci Rep. 2017; 7: 12101. Published online 2017 Sep 21. doi: 10.1038/s41598-017-09722-z
PMCID:
PMC5608759
AbstractArticlePDF–1.8M
4.
Shelterin components mediate genome reorganization in response to replication stress
Takeshi Mizuguchi, Nitika Taneja, Emiko Matsuda, Jon-Matthew Belton, Peter FitzGerald, Job Dekker, Shiv I. S. Grewal
Proc Natl Acad Sci U S A. 2017 May 23; 114(21): 5479–5484. Published online 2017 May 10. doi: 10.1073/pnas.1705527114
PMCID:
PMC5448194
AbstractArticlePDF–1.2M
5.
Sap1 is a replication-initiation factor essential for the assembly of pre-replicative complex in the fission yeast Schizosaccharomyces pombe
Ling Guan, Peng He, Fang Yang, Yuan Zhang, Yunfei Hu, Jienv Ding, Yu Hua, Yi Zhang, Qiong Ye, Jiazhi Hu, Tao Wang, Changwen Jin, Daochun Kong
J Biol Chem. 2017 Apr 14; 292(15): 6056–6075. Published online 2017 Feb 21. doi: 10.1074/jbc.M116.767806
PMCID:
PMC5391739
AbstractArticlePDF–4.3M
6.
Chromatin remodeller Fun30Fft3 induces nucleosome disassembly to facilitate RNA polymerase II elongation
Junwoo Lee, Eun Shik Choi, Hogyu David Seo, Keunsoo Kang, Joshua M. Gilmore, Laurence Florens, Michael P. Washburn, Joonho Choe, Jerry L. Workman, Daeyoup Lee
Nat Commun. 2017; 8: 14527. Published online 2017 Feb 20. doi: 10.1038/ncomms14527
PMCID:
PMC5321744
AbstractArticlePDF–1.4M
7.
Arrested replication forks guide retrotransposon integration
Jake Z. Jacobs, Jesus D. Rosado-Lugo, Susanne Cranz-Mileva, Keith M. Ciccaglione, Vincent Tournier, Mikel Zaratiegui
Science. Author manuscript; available in PMC 2016 Apr 15.
Published in final edited form as: Science. 2015 Sep 25; 349(6255): 1549–1553. doi: 10.1126/science.aaa3810
PMCID:
PMC4832573
AbstractArticlePDF–746K
8.
A proteome-wide fission yeast interactome reveals network evolution principles from yeasts to human
Tommy V. Vo, Jishnu Das, Michael J. Meyer, Nicolas A. Cordero, Nurten Akturk, Xiaomu Wei, Benjamin J. Fair, Andrew G. Degatano, Robert Fragoza, Lisa G. Liu, Akihisa Matsuyama, Michelle Trickey, Sachi Horibata, Andrew Grimson, Hiroyuki Yamano, Minoru Yoshida, Frederick P. Roth, Jeffrey A. Pleiss, Yu Xia, Haiyuan Yu
Cell. Author manuscript; available in PMC 2017 Jan 14.
Published in final edited form as: Cell. 2016 Jan 14; 164(0): 310–323. doi: 10.1016/j.cell.2015.11.037
PMCID:
PMC4715267
AbstractArticlePDF–1.4M
9.
Post-transcriptional regulation of meiotic genes by a nuclear RNA silencing complex
Emily D. Egan, Craig R. Braun, Steven P. Gygi, Danesh Moazed
RNA. 2014 Jun; 20(6): 867–881. doi: 10.1261/rna.044479.114
PMCID:
PMC4024641
AbstractArticlePDF–1.8M
10.
The proteasome factor Bag101 binds to Rad22 and suppresses homologous recombination
Yuichiro Saito, Jun Takeda, Masahiro Okada, Junya Kobayashi, Akihiro Kato, Kouji Hirota, Masato Taoka, Tomohiro Matsumoto, Kenshi Komatsu, Toshiaki Isobe
Sci Rep. 2013; 3: 2022. Published online 2013 Jun 19. doi: 10.1038/srep02022
PMCID:
PMC3685826
AbstractArticlePDF–1.1M
11.
Comprehensive Proteomics Analysis Reveals New Substrates and Regulators of the Fission Yeast Clp1/Cdc14 Phosphatase
Jun-Song Chen, Matthew R. Broadus, Janel R. McLean, Anna Feoktistova, Liping Ren, Kathleen L. Gould
Mol Cell Proteomics. 2013 May; 12(5): 1074–1086. Published online 2013 Jan 7. doi: 10.1074/mcp.M112.025924
PMCID:
PMC3650322
AbstractArticlePDF–914K
12.
Predicting the Fission Yeast Protein Interaction Network
Vera Pancaldi, Ömer S. Saraç, Charalampos Rallis, Janel R. McLean, Martin Převorovský, Kathleen Gould, Andreas Beyer, Jürg Bähler
G3 (Bethesda) 2012 Apr; 2(4): 453–467. Published online 2012 Apr 1. doi: 10.1534/g3.111.001560
PMCID:
PMC3337474
AbstractArticlePDF–2.4M
13.
CENP-B preserves genome integrity at replication forks paused by Retrotransposon LTR
Mikel Zaratiegui, Matthew W. Vaughn, Danielle V. Irvine, Derek Goto, Stephen Watt, Jürg Bähler, Benoit Arcangioli, Robert A. Martienssen
Nature. Author manuscript; available in PMC 2011 Jul 6.
Published in final edited form as: Nature. 2011 Jan 6; 469(7328): 112–115. Published online 2010 Dec 12. doi: 10.1038/nature09608
PMCID:
PMC3057531
AbstractArticlePDF–877K
14.
Sap1 Promotes the Association of the Replication Fork Protection Complex With Chromatin and Is Involved in the Replication Checkpoint in Schizosaccharomyces pombe
Chiaki Noguchi, Eishi Noguchi
Genetics. 2007 Feb; 175(2): 553–566. doi: 10.1534/genetics.106.065334
PMCID:
PMC1800610
AbstractArticlePDF–1.4M
15.
Molecular Architecture of a Eukaryotic DNA Replication Terminus-Terminator Protein Complex
Gregor Krings, Deepak Bastia
Mol Cell Biol. 2006 Nov; 26(21): 8061–8074. Published online 2006 Aug 28. doi: 10.1128/MCB.01102-06
PMCID:
PMC1636744
AbstractArticlePDF–988K
16.
Transcription and RNA-processing in fission yeast mitochondria
BERND SCHÄFER, MONIKA HANSEN, B. FRANZ LANG
RNA. 2005 May; 11(5): 785–795. doi: 10.1261/rna.7252205
PMCID:
PMC1370763
AbstractArticlePDF–474K
17.
The Mating Type Switch-Activating Protein Sap1 Is Required for Replication Fork Arrest at the rRNA Genes of Fission Yeast
Eva Mejía-Ramírez, Alicia Sánchez-Gorostiaga, Dora B. Krimer, Jorge B. Schvartzman, Pablo Hernández
Mol Cell Biol. 2005 Oct; 25(19): 8755–8761. doi: 10.1128/MCB.25.19.8755-8761.2005
PMCID:
PMC1265749
AbstractArticlePDF–274K
18.
The mitochondrial genome of the fission yeast Schizosaccharomyces pombe: highly homologous introns are inserted at the same position of the otherwise less conserved cox1 genes in Schizosaccharomyces pombe and Aspergillus nidulans.
B F Lang
EMBO J. 1984 Sep; 3(9): 2129–2136. doi: 10.1002/j.1460-2075.1984.tb02102.x
PMCID:
PMC557654
SummaryPage BrowsePDF–1.3M
19.
A novel switch-activating site (SAS1) and its cognate binding factor (SAP1) required for efficient mat1 switching in Schizosaccharomyces pombe.
B Arcangioli, A J Klar
EMBO J. 1991 Oct; 10(10): 3025–3032. doi: 10.1002/j.1460-2075.1991.tb07853.x
PMCID:
PMC453017
SummaryPage BrowsePDF–1.7M
20.
Sap1, a protein that binds to sequences required for mating-type switching, is essential for viability in Schizosaccharomyces pombe.
B Arcangioli, T D Copeland, A J Klar
Mol Cell Biol. 1994 Mar; 14(3): 2058–2065. doi: 10.1128/mcb.14.3.2058
PMCID:
PMC358566
SummaryPage BrowsePDF–1.8M

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