Диссертация (1144700), страница 29
Текст из файла (страница 29)
// Cell. – 2011. - Vol. 146. – P. 448 – 461.108.Huh W.K., Falvo J.V., Gerke L.C., Carroll A.S. et al. Global analysis ofprotein localization in budding yeast. // Nature. – 2003. - Vol. 425. - № 6959. – P.686 - 691.109.Humenik M., Smith A.M., Arndt S., Scheibel T. Ion and seed dependentfibril assembly of a spidroin core domain. // J Struct Biol. – 2015. - pii: S10478477. № 15. P. 30025 - 30033.110.Inge-Vechtomov S.G.
Yeast prions as a model of neurodegenerativeinfectious amyloidoses in humans. // Ontogenez. - 2011. – V. 5. – P. 337-345.111.Inoue H., Nojima H., Okayama H. High Efficiency transformation ofEsherichia coli with plasmids. Gene. – 1990. – Vol. 96. – P. 23–28.112.Iqbal K, Liu F, Gong CX, Alonso Adel C, Grundke-Iqbal I.
Mechanisms oftau-induced neurodegeneration. // Acta Neuropathol. – 2009. – V. 118. - №1. - P.53 - 69.113.Irizarry M.C., Soriano F., McNamara M., Page K.J., Schenk D. et al., Aβdeposition is associated with neuropil changes, but not with overt neuronal loss inthe human amyloid precursor protein V717F (PDAPP) transgenic mouse. // JNeurosci. – 1997. - Vol. 17. - 7053 – 7059.114.Iwatsubo T., Odaka A., Suzuki N., Mizusawa H., Nukina H., Ihara Y.Visualization of Aβ42(43) and Aβ40 in senile plaques with end-specific Aβmonoclonals: Evidence that an initially deposited species is Aβ42(43).
// Neuron.- 1994. – Vol. 13. – P. 45–53.115.Jarosz D.F., Lancaster A.K., Brown J.C., Lindquist S. An evolutionarilyconserved prion-like element converts wild fungi from metabolic specialists togeneralists. // Cell. - 2014. – Vol. 158. -№ 5.
- P. 1072 - 1082.116.Jensen R., Sprague G.F. Jr, Herskowitz I. Regulation of yeast mating-typeinterconversion: feedback control of HO gene expression by the mating-typelocus. // Proc Natl Acad Sci U S A. – 1983. - Vol. 80. - № 10. – P. 3035 - 3039.187117.Joshi P., Benussi L., Furlan R., Ghidoni R., Verderio C. Extracellularvesicles in Alzheimer's disease: friends or foes? Focus on Aβ-vesicle interaction.// Int J Mol Sci. – 2015. – Vol. 16. - № 3. - P. 4800 - 4813.118.Kadnar M.L., Articov G., Derkatch I.L. Distinct type of transmissionbarrier revealed by study of multiple prion determinants of Rnq1. // PLoS Genet.– 2010.
- Vol. 6. - № 1. - e1000824.119.Kaiser C., Michaelis S., Mitchell A. Methods in yeast genetics. N.Y.: ColdSpring Harbor Lab. Press. – 1994. – 234 p.120.Kajava AV1, Baxa U, Steven AC. Beta arcades: recurring motifs innaturally occurring and disease-related amyloid fibrils. // FASEB J. – 2010. - V.5. - P. 1311-1399.121.Kalebina T.S., Plotnikova T.A., Gorkovskii A.A., Selyakh I.O.,Galzitskaya O.V.
et al, Amyloid-like properties of Saccharomyces cerevisiae cellwall glucantransferase Bgl2p: prediction and experimental evidences. // Prion. –2008. - V. 2. - № 2. - P. 91-96.122.Kallmeyer AK, Keeling KM, Bedwell DM. Eukaryotic release factor 1phosphorylation by CK2 protein kinase is dynamic but has little effect on theefficiency of translation termination in Saccharomyces cerevisiae. // EukaryotCell. – 2006. – Vol.
5. - № 8. – P. 1378 - 1387.123.Keeling K.M., Lanier J., Du M., Salas-Marko J., Gao L. et al. Leakytermination at premature stop codons antagonizes nonsense-mediated mRNAdecay in S. cerevisiae. // RNA. – 2006. - Vol. 10. P. 691 - 703.124.Kelly A.C., Wickner R.B. Saccharomyces cerevisiae: a sexy yeast with aprion problem. // Prion.
– 2013. – Vol. 7. - № 3. – P. 215 - 220.125.Kenney J.M., Knight D., Wise M.J., Vollrath F. Amyloidogenic nature ofspider silk. // Eur J Biochem. – 2002. – V. 269. - № 16. - P. 4159-4163.126.Kiktev D, Moskalenko S, Murina O, Baudin-Baillieu A, Rousset JP,Zhouravleva G. The paradox of viable sup45 STOP mutations: a necessaryequilibrium between translational readthrough, activity and stability of theprotein.
// Mol Genet Genomics. – 2009. Vol. 282. № 1. P. 83-96.188127.King C.Y. and Diaz-Avalos R. Protein-only transmission of three yeastprion strains. // Nature. - 2004. - Vol. 428. - P. 319-323.128.Knowles T.P., Vendruscolo M., Dobson C.M. The amyloid state and itsassociation with protein misfolding diseases. // Nat Rev Mol Cell Biol.
– 2014. –Vol. 15. № 6. – P. 384 - 396.129.Kochneva-Pervukhova N.V., Alexander I. Alexandrov, Michael D. Ter-Avanesyan. Amyloid-Mediated Sequestration of Essential Proteins Contributes toMutant Huntingtin Toxicity in Yeast. // PLoS One. – 2012. – Vol. 7. - № 1. e29832.130.Kovacs G.G., Zerbi P., Voigtlander T., Strohschneider M., Trabattoni G. etal. The prion protein in human neurodegenerative disorders.
// Neurosci. Lett. 2002. - V. 329. - № 3. - P. 269-272.131.Kryndushkin D.S., Alexandrov I.M., Ter-Avanesyan M.D., KushnirovV.V. Yeast [PSI+] prion aggregates are formed by small Sup35 polymersfragmented by Hsp104. // J Biol Chem. – 2003. – Vol. 278. - № 49. – P. 49636 49643.132.Kryndushkin D.S., Pripuzova N., Burnett B.G., Shewmaker F. Non-targeted identification of prions and amyloid-forming proteins from yeast andmammalian cells. // J Biol Chem.
– 2013. – Vol. 288. – P. 27100 - 27111.133.Kuchin S., Vyas V.K., Kanter E., Hong S.P., Carlson M. Std1p (Msn3p)positively regulates the Snf1 kinase in Saccharomyces cerevisiae. // Genetics. –2003. – Vol. – 163. - P 507 - 514.134.Kudo W., Petersen R.B., Lee H.G.. Cellular prion protein and Alzheimerdisease: link to oligomeric amyloid-beta and neuronal cell death.
// Prion. – 2013.– Vol. 7. – P. 114 - 116.135.Kushnirov V.V., Ter-Avanesyan M.D., Telcov M.V., Surguchov A.P.,Smirnov V.N., Inge-Vechtomov S.G. Nucleotide sequence of the SUP2 (SUP35)gene of Saccharomyces cerevisiae. // Gene. – 1988. – Vol. 66. – P. 45–54.136.Kushnirov V.V., Ter-Avanesyan M.D. Structure and replication of yeastprions // Cell. – 1998. – Vol. 94. – P. 13–16.189137.Kushnirov V.V., Alexandrov I.M., Mitkevich O.V., Shkundina I.S., Ter-Avanesyan M.D.
Purification and analysis of prion and amyloid aggregates. //Methods. – 2006. - Vol. – 39. P. 50 - 55.138.Kushnirov V.V., Vishnevskaya A.B., Alexandrov I.M., Ter-AvanesyanM.D. Prion and nonprion amyloids: a comparison inspired by the yeast Sup35protein.
// Prion. – 2007. – Vol. 1, № 3. – P. 179 - 184.139.Labbe-Bois R.The ferrochelatase from Saccharomyces cerevisiae.Sequence, disruption, and expression of its structural gene HEM15. // J BiolChem. - 1990. - Vol. 265. – P. 7278-7283.140.Lacroute F. Non-Mendelian mutation allowing ureidosuccinic acid uptakein yeast // J Bacteriol. – 1971. – Vol. 106. – №2. – P. 519–522.141.Laemmli U.K. Cleavage of structural proteins during the assembly of thehead of bacteriophage T4 // Nature. – 1970. – Vol.
227. – P. 680–685.142.Lansbury P.T., Caughey B. The chemistry of scrapie reaction: the “ice 9”metaphore. // Chem. Biol. – 1995. - Vol. 2. - P. 1–5.143.Lansbury P.T. Jr., Costa P.R., Griffiths J.M., Simon E.J., Auger M. et al.Structural model for the beta-amyloid fibril based on interstrand alignment of anantiparallel-sheet comprising a C-terminal peptide. // Nat Struct Biol. – 1995. Vol.
2, №11. – P. 990 - 998.144.Lasagna-Reeves C.A., Castillo-Carranza D.L., Sengupta U, Guerrero-Munoz MJ, Kiritoshi T. et al. Alzheimer brain-derived tau oligomers propagatepathology from endogenous tau. // SciRep. – 2012. - Vol. 2. - e700.145.Laurén J., Gimbel D.A., Nygaard H.B., Gilbert J.W., Strittmatter S.M.Cellular prion protein mediates impairment of synaptic plasticity by amyloid-betaoligomers // Nature. - 2009. - Vol. 457. - P.
1128-1132.146.Lee C.Y., Cantle J.P., Yang X.W. Genetic manipulations of mutanthuntingtin in mice: new insights into Huntington's disease pathogenesis. // FEBSJ. – 2013. Vol. 280, № 18. – P. 4382 - 4394.190147.Li X., Rayman J.B., Kandel E.R., Derkatch I.L. Functional role ofTia1/Pub1 and Sup35 prion domains: directing protein synthesis machinery to thetubulin cytoskeleton. // Mol Cell.
– 2014. – Vol. 55, № 2. – P. 305 - 318.148.Liebman S.W., Sherman F. Extrachromosomal psi+ determinant suppressesnonsense mutations in yeast // J. Bacteriol. - 1979. - Vol. 139. - P. 1068 - 1071.149.Liu J.J., Lindquist S. Oligopeptide-repeat expansions modulate 'protein-only' inheritance in yeast. // Nature. – 1999. Vol. 400, № 6744. – P. 573 - 576.150.Livak KJ, Schmittgen TD. Analysis of relative gene expression data usingreal-time quantitative PCR and the 2(-Delta Delta C(T)) Method. // Methods.
–2001. – V. 25, №4. – P. 402 - 408.151.Lohr D., Venkov P., Zlatanova J. Transcriptional regulation in the yeastGAL gene family: a complex genetic network. // FASEB J. – 1995. – Vol. 9, №9. – P. 777 - 787.152.Luk K. C., Kehm V., Carroll J., et al. Pathological α-synuclein transmissioninitiates Parkinson-like neurodegeneration in nontransgenic mice. // Science. –2012.