Screening for Toxic Amyloid in Yeast Exemplifies the Role of Alternative Pathway Responsible for Cytotoxicity
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Françoise Immel | M. Castroviejo | Julien Couthouis | Christophe Cullin | Karine Berthelot | K. Berthelot | Julien Couthouis | Karine Rébora | Michel Castroviejo | C. Cullin | Karine Rébora | F. Immel
[1] Susan Lindquist,et al. Yeast Genes That Enhance the Toxicity of a Mutant Huntingtin Fragment or α-Synuclein , 2003, Science.
[2] Ronald W. Davis,et al. Functional characterization of the S. cerevisiae genome by gene deletion and parallel analysis. , 1999, Science.
[3] R. D. Gietz,et al. Yeast transformation by the LiAc/SS Carrier DNA/PEG method. , 2006, Methods in molecular biology.
[4] S. Lindquist,et al. Yeast Cells Provide Insight into Alpha-Synuclein Biology and Pathobiology , 2003, Science.
[5] Y. Chernoff,et al. Modulation of Prion Formation, Aggregation, and Toxicity by the Actin Cytoskeleton in Yeast , 2006, Molecular and Cellular Biology.
[6] U. Baxa,et al. Prion generation in vitro: amyloid of Ure2p is infectious , 2005, The EMBO journal.
[7] Brice Kauffmann,et al. Driving amyloid toxicity in a yeast model by structural changes: a molecular approach , 2009, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.
[8] S. Duvezin-Caubet,et al. Amyloid aggregates of the HET-s prion protein are infectious , 2002, Proceedings of the National Academy of Sciences of the United States of America.
[9] C. chou,et al. Is green fluorescent protein toxic to the living cells? , 1999, Biochemical and biophysical research communications.
[10] S. Lindquist,et al. HSP104 required for induced thermotolerance. , 1990, Science.
[11] Y. Chernoff,et al. Abnormal proteins can form aggresome in yeast: aggresome‐targeting signals and components of the machinery , 2009, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.
[12] S. Lindquist,et al. Yeast genes that enhance the toxicity of a mutant huntingtin fragment or alpha-synuclein. , 2003, Science.
[13] C. Dobson,et al. Protein misfolding, functional amyloid, and human disease. , 2006, Annual review of biochemistry.
[14] A. Chacińska,et al. Prion-Dependent Switching between Respiratory Competence and Deficiency in the Yeast nam9-1Mutant , 2000, Molecular and Cellular Biology.
[15] J. Saffitz,et al. Desmin-related cardiomyopathy in transgenic mice: a cardiac amyloidosis. , 2004, Proceedings of the National Academy of Sciences of the United States of America.
[16] J T Finch,et al. Glutamine repeats as polar zippers: their possible role in inherited neurodegenerative diseases. , 1994, Proceedings of the National Academy of Sciences of the United States of America.
[17] S. Lindquist,et al. α-Synuclein Blocks ER-Golgi Traffic and Rab1 Rescues Neuron Loss in Parkinson's Models , 2006, Science.
[18] S. Liebman,et al. "Prion-proof" for [PIN+]: infection with in vitro-made amyloid aggregates of Rnq1p-(132-405) induces [PIN+]. , 2007, Journal of molecular biology.
[19] Flavio Seno,et al. Insight into the Structure of Amyloid Fibrils from the Analysis of Globular Proteins , 2006, PLoS Comput. Biol..
[20] S W Liebman,et al. Role of the chaperone protein Hsp104 in propagation of the yeast prion-like factor [psi+]. , 1995, Science.
[21] V. Coustou,et al. The protein product of the het-s heterokaryon incompatibility gene of the fungus Podospora anserina behaves as a prion analog. , 1997, Proceedings of the National Academy of Sciences of the United States of America.
[22] Thorsten Lührs,et al. Correlation of structural elements and infectivity of the HET-s prion , 2005, Nature.
[23] S. Younkin,et al. The 'Arctic' APP mutation (E693G) causes Alzheimer's disease by enhanced Aβ protofibril formation , 2001, Nature Neuroscience.
[24] S. Lindquist,et al. Hsp104 Catalyzes Formation and Elimination of Self-Replicating Sup35 Prion Conformers , 2004, Science.
[25] P. Westermark,et al. Amyloidogenic potential of foie gras , 2007, Proceedings of the National Academy of Sciences.
[26] R. Diaz-Avalos,et al. Protein-only transmission of three yeast prion strains , 2004, Nature.
[27] Carl W. Cotman,et al. Common Structure of Soluble Amyloid Oligomers Implies Common Mechanism of Pathogenesis , 2003, Science.
[28] R. Wickner,et al. Yeast prions [URE3] and [PSI+] are diseases. , 2005, Proceedings of the National Academy of Sciences of the United States of America.
[29] Silvio C. E. Tosatto,et al. The PASTA server for protein aggregation prediction. , 2007, Protein engineering, design & selection : PEDS.
[30] F. Kametani,et al. Fecal transmission of AA amyloidosis in the cheetah contributes to high incidence of disease , 2008, Proceedings of the National Academy of Sciences.
[31] L. Minvielle-Sebastia,et al. Multipurpose vectors designed for the fast generation of N‐ or C‐terminal epitope‐tagged proteins , 1994, Yeast.
[32] Scott J. Hultgren,et al. Role of Escherichia coli Curli Operons in Directing Amyloid Fiber Formation , 2002, Science.
[33] Y. Chernoff,et al. Huntingtin toxicity in yeast model depends on polyglutamine aggregation mediated by a prion-like protein Rnq1 , 2002, The Journal of cell biology.
[34] Daniel Kaganovich,et al. Misfolded proteins partition between two distinct quality control compartments , 2008, Nature.
[35] A. Matthysse,et al. Characterization of the binding of diarrheagenic strains of E. coli to plant surfaces and the role of curli in the interaction of the bacteria with alfalfa sprouts. , 2005, Molecular plant-microbe interactions : MPMI.
[36] R. Wickner,et al. [URE3] as an altered URE2 protein: evidence for a prion analog in Saccharomyces cerevisiae. , 1994, Science.
[37] M. Perutz,et al. Aggregation of proteins with expanded glutamine and alanine repeats of the glutamine-rich and asparagine-rich domains of Sup35 and of the amyloid β-peptide of amyloid plaques , 2002, Proceedings of the National Academy of Sciences of the United States of America.
[38] J. Weissman,et al. Evidence for the prion hypothesis: induction of the yeast [PSI+] factor by in vitro- converted Sup35 protein. , 2000, Science.
[39] Beat H. Meier,et al. Amyloid Fibrils of the HET-s(218–289) Prion Form a β Solenoid with a Triangular Hydrophobic Core , 2008, Science.
[40] A. Willems,et al. Studies on the transformation of intact yeast cells by the LiAc/SS‐DNA/PEG procedure , 1995, Yeast.
[41] M. Maddelein,et al. A non-Q/N-rich prion domain of a foreign prion, [Het-s], can propagate as a prion in yeast. , 2007, Molecular cell.
[42] Christopher M. Dobson,et al. Prefibrillar Amyloid Aggregates Could Be Generic Toxins in Higher Organisms , 2006, The Journal of Neuroscience.
[43] Dennis Claessen,et al. A novel class of secreted hydrophobic proteins is involved in aerial hyphae formation in Streptomyces coelicolor by forming amyloid-like fibrils. , 2003, Genes & development.
[44] Susan Lindquist,et al. Protein disaggregation mediated by heat-shock protein Hspl04 , 1994, Nature.
[45] Osamu Onodera,et al. Soluble polyglutamine oligomers formed prior to inclusion body formation are cytotoxic. , 2008, Human molecular genetics.
[46] S. Lindquist,et al. Prion Switching in Response to Environmental Stress , 2008, PLoS biology.
[47] Peter T. Lansbury,et al. Accelerated in vitro fibril formation by a mutant α-synuclein linked to early-onset Parkinson disease , 1998, Nature Medicine.
[48] Christiane Ritter,et al. Domain organization and structure–function relationship of the HET‐s prion protein of Podospora anserina , 2003, The EMBO journal.
[49] Taro L. Saito,et al. High-dimensional and large-scale phenotyping of yeast mutants. , 2005, Proceedings of the National Academy of Sciences of the United States of America.
[50] P. Lansbury,et al. A century-old debate on protein aggregation and neurodegeneration enters the clinic , 2006, Nature.