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Items: 1 to 20 of 27

1.
Meiotic gene silencing complex MTREC/NURS recruits the nuclear exosome to YTH-RNA-binding protein Mmi1
Yuichi Shichino, Yoko Otsubo, Masayuki Yamamoto, Akira Yamashita
PLoS Genet. 2020 Feb; 16(2): e1008598. Published online 2020 Feb 3. doi: 10.1371/journal.pgen.1008598
PMCID:
PMC7018101
AbstractArticlePDF–2.5M
2.
Meiotic long non-coding meiRNA accumulates as a dot at its genetic locus facilitated by Mmi1 and plays as a decoy to lure Mmi1
Yuichi Shichino, Akira Yamashita, Masayuki Yamamoto
Open Biol. 2014 Jun; 4(6): 140022. Published online 2014 Jun 11. doi: 10.1098/rsob.140022
PMCID:
PMC4077057
AbstractArticlePDF–1.1M
3.
Structural analysis of Red1 as a conserved scaffold of the RNA-targeting MTREC/PAXT complex
Anne-Emmanuelle Foucher, Leila Touat-Todeschini, Ariadna B. Juarez-Martinez, Auriane Rakitch, Hamida Laroussi, Claire Karczewski, Samira Acajjaoui, Montserrat Soler-López, Stephen Cusack, Cameron D. Mackereth, André Verdel, Jan Kadlec
Nat Commun. 2022; 13: 4969. Published online 2022 Aug 24. doi: 10.1038/s41467-022-32542-3
PMCID:
PMC9402713
AbstractArticlePDF–3.9M
4.
YTH-RNA-binding protein prevents deleterious expression of meiotic proteins by tethering their mRNAs to nuclear foci
Yuichi Shichino, Yoko Otsubo, Yoshitaka Kimori, Masayuki Yamamoto, Akira Yamashita
eLife. 2018; 7: e32155. Published online 2018 Feb 9. doi: 10.7554/eLife.32155
PMCID:
PMC5807050
AbstractArticlePDF–4.0M
5.
The fission yeast MTREC and EJC orthologs ensure the maturation of meiotic transcripts during meiosis
Bahjat Fadi Marayati, Victoria Hoskins, Robert W. Boger, James F. Tucker, Emily S. Fishman, Andrew S. Bray, Ke Zhang
RNA. 2016 Sep; 22(9): 1349–1359. doi: 10.1261/rna.055608.115
PMCID:
PMC4986891
AbstractArticlePDF–1003K
6.
Red1 promotes the elimination of meiosis-specific mRNAs in vegetatively growing fission yeast
Tomoyasu Sugiyama, Rie Sugioka-Sugiyama
EMBO J. 2011 Mar 16; 30(6): 1027–1039. Published online 2011 Feb 11. doi: 10.1038/emboj.2011.32
PMCID:
PMC3061036
AbstractArticlePDF–1.1M
7.
Conserved protein Pir2ARS2 mediates gene repression through cryptic introns in lncRNAs
Gobi Thillainadesan, Hua Xiao, Sahana Holla, Jothy Dhakshnamoorthy, Lisa M. Miller Jenkins, David Wheeler, Shiv I. S. Grewal
Nat Commun. 2020; 11: 2412. Published online 2020 May 15. doi: 10.1038/s41467-020-16280-y
PMCID:
PMC7229227
AbstractArticlePDF–1.7M
8.
A novel factor Iss10 regulates Mmi1-mediated selective elimination of meiotic transcripts
Akira Yamashita, Tomomi Takayama, Ryo Iwata, Masayuki Yamamoto
Nucleic Acids Res. 2013 Nov; 41(21): 9680–9687. Published online 2013 Aug 26. doi: 10.1093/nar/gkt763
PMCID:
PMC3834831
AbstractArticlePDF–2.1M
9.
RNAi triggered by specialized machinery silences developmental genes and retrotransposons
Soichiro Yamanaka, Sameet Mehta, Francisca E. Reyes-Turcu, Fanglei Zhuang, Ryan T. Fuchs, Yikang Rong, Gregory B. Robb, Shiv I. S. Grewal
Nature. Author manuscript; available in PMC 2013 Jul 24.
Published in final edited form as: Nature. 2013 Jan 24; 493(7433): 557–560. Published online 2012 Nov 14. doi: 10.1038/nature11716
PMCID:
PMC3554839
AbstractArticlePDF–1.5M
10.
RNA Elimination Machinery Targeting Meiotic mRNAs Promotes Facultative Heterochromatin Formation
Martin Zofall, Soichiro Yamanaka, Francisca E. Reyes-Turcu, Ke Zhang, Chanan Rubin, Shiv I. S. Grewal
Science. Author manuscript; available in PMC 2019 Jan 18.
Published in final edited form as: Science. 2012 Jan 6; 335(6064): 96–100. Published online 2011 Dec 1. doi: 10.1126/science.1211651
PMCID:
PMC6338074
AbstractArticlePDF–1.3M
11.
Ubiquitination-dependent control of sexual differentiation in fission yeast
Fabrizio Simonetti, Tito Candelli, Sebastien Leon, Domenico Libri, Mathieu Rougemaille
eLife. 2017; 6: e28046. Published online 2017 Aug 25. doi: 10.7554/eLife.28046
PMCID:
PMC5614563
AbstractArticlePDF–1.6M
12.
Enhancer of rudimentary cooperates with conserved RNA processing factors to promote meiotic mRNA decay and facultative heterochromatin assembly
Tomoyasu Sugiyama, Gobi Thillainadesan, Venkata R. Chalamcharla, Zhaojing Meng, Vanivilasini Balachandran, Jothy Dhakshnamoorthy, Ming Zhou, Shiv I.S. Grewal
Mol Cell. Author manuscript; available in PMC 2017 Mar 3.
Published in final edited form as: Mol Cell. 2016 Mar 3; 61(5): 747–759. doi: 10.1016/j.molcel.2016.01.029
PMCID:
PMC4791967
AbstractArticlePDF–2.1M
13.
The fission yeast MTREC complex targets CUTs and unspliced pre-mRNAs to the nuclear exosome
Yang Zhou, Jianguo Zhu, Géza Schermann, Corina Ohle, Katja Bendrin, Rie Sugioka-Sugiyama, Tomoyasu Sugiyama, Tamás Fischer
Nat Commun. 2015; 6: 7050. Published online 2015 May 20. doi: 10.1038/ncomms8050
PMCID:
PMC4455066
AbstractArticlePDF–2.2M
14.
Global regulation of heterochromatin spreading by Leo1
Laure Verrier, Francesca Taglini, Ramon R. Barrales, Shaun Webb, Takeshi Urano, Sigurd Braun, Elizabeth H. Bayne
Open Biol. 2015 May; 5(5): 150045. Published online 2015 May 13. doi: 10.1098/rsob.150045
PMCID:
PMC4450266
AbstractArticlePDF–1.2M
15.
Suppressor screening reveals common kleisin–hinge interaction in condensin and cohesin, but different modes of regulation
Xingya Xu, Mitsuhiro Yanagida
Proc Natl Acad Sci U S A. 2019 May 28; 116(22): 10889–10898. Published online 2019 May 9. doi: 10.1073/pnas.1902699116
PMCID:
PMC6561158
AbstractArticlePDF–2.1M
16.
Mtr4-like protein coordinates nuclear RNA processing for heterochromatin assembly and for telomere maintenance
Nathan N. Lee, Venkata R. Chalamcharla, Francisca Reyes-Turcu, Sameet Mehta, Martin Zofall, Vanivilasini Balachandran, Jothy Dhakshnamoorthy, Nitika Taneja, Soichiro Yamanaka, Ming Zhou, Shiv I. S. Grewal
Cell. Author manuscript; available in PMC 2014 Nov 21.
Published in final edited form as: Cell. 2013 Nov 21; 155(5): 1061–1074. Published online 2013 Nov 7. doi: 10.1016/j.cell.2013.10.027
PMCID:
PMC3974623
AbstractArticlePDF–3.7M
17.
Systematic analysis reveals the prevalence and principles of bypassable gene essentiality
Jun Li, Hai-Tao Wang, Wei-Tao Wang, Xiao-Ran Zhang, Fang Suo, Jing-Yi Ren, Ying Bi, Ying-Xi Xue, Wen Hu, Meng-Qiu Dong, Li-Lin Du
Nat Commun. 2019; 10: 1002. Published online 2019 Mar 1. doi: 10.1038/s41467-019-08928-1
PMCID:
PMC6397241
AbstractArticlePDF–1.2M
18.
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
19.
Proteomic profiling and functional characterization of post-translational modifications of the fission yeast RNA exosome
Caroline Telekawa, François-Michel Boisvert, François Bachand
Nucleic Acids Res. 2018 Nov 30; 46(21): 11169–11183. Published online 2018 Oct 13. doi: 10.1093/nar/gky915
PMCID:
PMC6265454
AbstractArticlePDF–6.3M
20.
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

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