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Items: 1 to 20 of 28

1.
Translatome and transcriptome analysis of TMA20 (MCT-1) and TMA64 (eIF2D) knockout yeast strains
Desislava S. Makeeva, Andrey S. Lando, Aleksandra Anisimova, Artyom A. Egorov, Maria D. Logacheva, Alexey A. Penin, Dmitry E. Andreev, Pavel G. Sinitcyn, Ilya M. Terenin, Ivan N. Shatsky, Ivan V. Kulakovskiy, Sergey E. Dmitriev
Data Brief. 2019 Apr; 23: 103701. Published online 2019 Feb 2. doi: 10.1016/j.dib.2019.103701
PMCID:
PMC6378902
AbstractArticlePDF–329K
2.
Differential effects of 40S ribosome recycling factors on reinitiation at regulatory uORFs in GCN4 mRNA are not dictated by their roles in bulk 40S recycling
Kristína Jendruchová, Swati Gaikwad, Kristýna Poncová, Stanislava Gunišová, Leoš Shivaya Valášek, Alan G. Hinnebusch
Commun Biol. 2024; 7: 1083. Published online 2024 Sep 4. doi: 10.1038/s42003-024-06761-x
PMCID:
PMC11375166
AbstractArticlePDF–1.3M
3.
Genetic screens in Saccharomyces cerevisiae identify a role for 40S ribosome recycling factors Tma20 and Tma22 in nonsense-mediated decay
Miguel Pacheco, Karole N D’Orazio, Laura N Lessen, Anthony J Veltri, Zachary Neiman, Raphael Loll-Krippleber, Grant W Brown, Rachel Green
G3 (Bethesda) 2024 Mar; 14(3): jkad295. Published online 2024 Jan 10. doi: 10.1093/g3journal/jkad295
PMCID:
PMC10917514
AbstractArticlePDF–2.3M
4.
40S ribosome profiling reveals distinct roles for Tma20/Tma22 (MCT-1/DENR) and Tma64 (eIF2D) in 40S subunit recycling
David J. Young, Sezen Meydan, Nicholas R. Guydosh
Nat Commun. 2021; 12: 2976. Published online 2021 May 20. doi: 10.1038/s41467-021-23223-8
PMCID:
PMC8137927
AbstractArticlePDF–2.0M
5.
Reprogramming of translation in yeast cells impaired for ribosome recycling favors short, efficiently translated mRNAs
Swati Gaikwad, Fardin Ghobakhlou, David J Young, Jyothsna Visweswaraiah, Hongen Zhang, Alan G Hinnebusch
eLife. 2021; 10: e64283. Published online 2021 Mar 25. doi: 10.7554/eLife.64283
PMCID:
PMC7993997
AbstractArticlePDF–3.4M
6.
Elongating RNA polymerase II and RNA:DNA hybrids hinder fork progression and gene expression at sites of head-on replication-transcription collisions
Luca Zardoni, Eleonora Nardini, Alessandra Brambati, Chiara Lucca, Ramveer Choudhary, Federica Loperfido, Simone Sabbioneda, Giordano Liberi
Nucleic Acids Res. 2021 Dec 16; 49(22): 12769–12784. Published online 2021 Dec 8. doi: 10.1093/nar/gkab1146
PMCID:
PMC8682787
AbstractArticlePDF–8.6M
7.
N-Terminal Acetylation by NatC Is Not a General Determinant for Substrate Subcellular Localization in Saccharomyces cerevisiae
Henriette Aksnes, Camilla Osberg, Thomas Arnesen
PLoS One. 2013; 8(4): e61012. Published online 2013 Apr 15. doi: 10.1371/journal.pone.0061012
PMCID:
PMC3626706
AbstractArticlePDF–1.2M
8.
Systematic identification and functional screens of uncharacterized proteins associated with eukaryotic ribosomal complexes
Tracey C. Fleischer, Connie M. Weaver, K. Jill McAfee, Jennifer L. Jennings, Andrew J. Link
Genes Dev. 2006 May 15; 20(10): 1294–1307. doi: 10.1101/gad.1422006
PMCID:
PMC1472904
AbstractArticlePDF–679K
9.
Dosage suppression genetic interaction networks enhance functional wiring diagrams of the cell
Leslie Magtanong, Cheuk Hei Ho, Sarah L Barker, Wei Jiao, Anastasia Baryshnikova, Sondra Bahr, Andrew M Smith, Lawrence E Heisler, John S Choy, Elena Kuzmin, Kerry Andrusiak, Anna Kobylianski, Zhijian Li, Michael Costanzo, Munira A Basrai, Guri Giaever, Corey Nislow, Brenda Andrewa, Charles Boone
Nat Biotechnol. Author manuscript; available in PMC 2020 Jul 28.
Published in final edited form as: Nat Biotechnol. 2011 May 15; 29(6): 505–511. Published online 2011 May 15. doi: 10.1038/nbt.1855
PMCID:
PMC7386433
AbstractArticlePDF–1.0M
10.
The nucleotide sequence of Saccharomyces cerevisiae chromosome V
F. S. Dietrich, J. Mulligan, K. Hennessy, M. A. Yelton, E. Allen, R. Araujo, E. Aviles, A. Berno, T. Brennan, J. Carpenter, E. Chen, J. M. Cherry, E. Chung, M. Duncan, E. Guzman, G. Hartzell, S. Hunicke-Smith, R. W. Hyman, A. Kayser, C. Komp, D. Lashkari, H. Lew, D. Lin, D. Mosedale, K. Nakahara, A. Namath, R. Norgren, P. Oefner, C. Oh, F. X. Petel, D. Roberts, P. Sehl, S. Schramm, T. Shogren, V. Smith, P. Taylor, Y. Wei, D. Botstein, R. W. Davis
Nature. Author manuscript; available in PMC 2011 Mar 15.
Published in final edited form as: Nature. 1997 May 29; 387(6632 Suppl): 78–81.
PMCID:
PMC3057095
AbstractArticlePDF–73K
11.
Identification of karyopherins involved in the nuclear import of RNA exosome subunit Rrp6 in Saccharomyces cerevisiae
Fernando A. Gonzales-Zubiate, Ellen K. Okuda, Julia P. C. Da Cunha, Carla Columbano Oliveira
J Biol Chem. 2017 Jul 21; 292(29): 12267–12284. Published online 2017 May 24. doi: 10.1074/jbc.M116.772376
PMCID:
PMC5519375
AbstractArticlePDF–3.2M
12.
A Genomewide Suppressor and Enhancer Analysis of cdc13-1 Reveals Varied Cellular Processes Influencing Telomere Capping in Saccharomyces cerevisiae
S. G. Addinall, M. Downey, M. Yu, M. K. Zubko, J. Dewar, A. Leake, J. Hallinan, O. Shaw, K. James, D. J. Wilkinson, A. Wipat, D. Durocher, D. Lydall
Genetics. 2008 Dec; 180(4): 2251–2266. doi: 10.1534/genetics.108.092577
PMCID:
PMC2600956
AbstractArticlePDF–1.9M
13.
Functional characterisation of long intergenic non-coding RNAs through genetic interaction profiling in Saccharomyces cerevisiae
Dimitris Kyriakou, Emmanouil Stavrou, Panayiota Demosthenous, Georgia Angelidou, Bryan-Joseph San Luis, Charles Boone, Vasilis J. Promponas, Antonis Kirmizis
BMC Biol. 2016; 14: 106. Published online 2016 Dec 7. doi: 10.1186/s12915-016-0325-7
PMCID:
PMC5142380
AbstractArticlePDF–1.2M
14.
Quantitative Fitness Analysis Shows That NMD Proteins and Many Other Protein Complexes Suppress or Enhance Distinct Telomere Cap Defects
Stephen Gregory Addinall, Eva-Maria Holstein, Conor Lawless, Min Yu, Kaye Chapman, A. Peter Banks, Hien-Ping Ngo, Laura Maringele, Morgan Taschuk, Alexander Young, Adam Ciesiolka, Allyson Lurena Lister, Anil Wipat, Darren James Wilkinson, David Lydall
PLoS Genet. 2011 Apr; 7(4): e1001362. Published online 2011 Apr 7. doi: 10.1371/journal.pgen.1001362
PMCID:
PMC3072368
AbstractArticlePDF–4.0M
15.
Cdc48 and Ufd3, new partners of the ubiquitin protease Ubp3, are required for ribophagy
Batool Ossareh-Nazari, Mélanie Bonizec, Mickael Cohen, Svetlana Dokudovskaya, François Delalande, Christine Schaeffer, Alain Van Dorsselaer, Catherine Dargemont
EMBO Rep. 2010 Jul; 11(7): 548–554. Published online 2010 May 28. doi: 10.1038/embor.2010.74
PMCID:
PMC2897114
AbstractArticlePDF–597K
16.
Dissecting DNA damage response pathways by analyzing protein localization and abundance changes during DNA replication stress
Johnny M. Tkach, Askar Yimit, Anna Y. Lee, Michael Riffle, Michael Costanzo, Daniel Jaschob, Jason A. Hendry, Jiongwen Ou, Jason Moffat, Charles Boone, Trisha N. Davis, Corey Nislow, Grant W. Brown
Nat Cell Biol. Author manuscript; available in PMC 2013 Mar 1.
Published in final edited form as: Nat Cell Biol. 2012 Sep; 14(9): 966–976. Published online 2012 Jul 29. doi: 10.1038/ncb2549
PMCID:
PMC3434236
AbstractArticlePDF–1.5M
17.
Characterization of Cell Cycle Specific Protein Interaction Networks of the Yeast 26S Proteasome Complex by the QTAX Strategy
Robyn M. Kaake, Tijana Milenković, Nataša Pržulj, Peter Kaiser, Lan Huang
J Proteome Res. Author manuscript; available in PMC 2011 Jul 21.
Published in final edited form as: J Proteome Res. 2010 Apr 5; 9(4): 2016–2029. doi: 10.1021/pr1000175
PMCID:
PMC3140958
AbstractArticlePDF–3.2M
18.
An inter‐species protein–protein interaction network across vast evolutionary distance
Quan Zhong, Samuel J Pevzner, Tong Hao, Yang Wang, Roberto Mosca, Jörg Menche, Mikko Taipale, Murat Taşan, Changyu Fan, Xinping Yang, Patrick Haley, Ryan R Murray, Flora Mer, Fana Gebreab, Stanley Tam, Andrew MacWilliams, Amélie Dricot, Patrick Reichert, Balaji Santhanam, Lila Ghamsari, Michael A Calderwood, Thomas Rolland, Benoit Charloteaux, Susan Lindquist, Albert‐László Barabási, David E Hill, Patrick Aloy, Michael E Cusick, Yu Xia, Frederick P Roth, Marc Vidal
Mol Syst Biol. 2016 Apr; 12(4): 865. Published online 2016 Apr 23. doi: 10.15252/msb.20156484
PMCID:
PMC4848758
AbstractArticlePDF–2.1M
19.
Fast-evolving cofactors regulate the role of HEATR5 complexes in intra-Golgi trafficking
Lucas J. Marmorale, Huan Jin, Thomas G. Reidy, Brandon Palomino-Alonso, Christopher J. Zysnarski, Fatima Jordan-Javed, Sagar Lahiri, Mara C. Duncan
J Cell Biol. 2024 Mar 4; 223(3): e202309047. Published online 2024 Jan 19. doi: 10.1083/jcb.202309047
PMCID:
PMC10798858
AbstractArticlePDF–6.4M
20.
Saccharomyces cerevisiae Genetics Predicts Candidate Therapeutic Genetic Interactions at the Mammalian Replication Fork
Derek M. van Pel, Peter C. Stirling, Sean W. Minaker, Payal Sipahimalani, Philip Hieter
G3 (Bethesda) 2013 Feb; 3(2): 273–282. Published online 2013 Feb 1. doi: 10.1534/g3.112.004754
PMCID:
PMC3564987
AbstractArticlePDF–2.3M

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