-
Články
- Časopisy
- Kurzy
- Témy
- Kongresy
- Videa
- Podcasty
The [] Prion Exists as a Dynamic Cloud of Variants
[PSI+] is an amyloid-based prion of Sup35p, a subunit of the translation termination factor. Prion “strains” or “variants” are amyloids with different conformations of a single protein sequence, conferring different phenotypes, but each relatively faithfully propagated. Wild Saccharomyces cerevisiae isolates have SUP35 alleles that fall into three groups, called reference, Δ19, and E9, with limited transmissibility of [PSI+] between cells expressing these different polymorphs. Here we show that prion transmission pattern between different Sup35 polymorphs is prion variant-dependent. Passage of one prion variant from one Sup35 polymorph to another need not change the prion variant. Surprisingly, simple mitotic growth of a [PSI+] strain results in a spectrum of variant transmission properties among the progeny clones. Even cells that have grown for >150 generations continue to vary in transmission properties, suggesting that simple variant segregation is insufficient to explain the results. Rather, there appears to be continuous generation of a cloud of prion variants, with one or another becoming stochastically dominant, only to be succeeded by a different mixture. We find that among the rare wild isolates containing [PSI+], all indistinguishably “weak” [PSI+], are several different variants based on their transmission efficiencies to other Sup35 alleles. Most show some limitation of transmission, indicating that the evolved wild Sup35 alleles are effective in limiting the spread of [PSI+]. Notably, a “strong [PSI+]” can have any of several different transmission efficiency patterns, showing that “strong” versus “weak” is insufficient to indicate prion variant uniformity.
Vyšlo v časopise: The [] Prion Exists as a Dynamic Cloud of Variants. PLoS Genet 9(1): e32767. doi:10.1371/journal.pgen.1003257
Kategorie: Research Article
prolekare.web.journal.doi_sk: https://doi.org/10.1371/journal.pgen.1003257Souhrn
[PSI+] is an amyloid-based prion of Sup35p, a subunit of the translation termination factor. Prion “strains” or “variants” are amyloids with different conformations of a single protein sequence, conferring different phenotypes, but each relatively faithfully propagated. Wild Saccharomyces cerevisiae isolates have SUP35 alleles that fall into three groups, called reference, Δ19, and E9, with limited transmissibility of [PSI+] between cells expressing these different polymorphs. Here we show that prion transmission pattern between different Sup35 polymorphs is prion variant-dependent. Passage of one prion variant from one Sup35 polymorph to another need not change the prion variant. Surprisingly, simple mitotic growth of a [PSI+] strain results in a spectrum of variant transmission properties among the progeny clones. Even cells that have grown for >150 generations continue to vary in transmission properties, suggesting that simple variant segregation is insufficient to explain the results. Rather, there appears to be continuous generation of a cloud of prion variants, with one or another becoming stochastically dominant, only to be succeeded by a different mixture. We find that among the rare wild isolates containing [PSI+], all indistinguishably “weak” [PSI+], are several different variants based on their transmission efficiencies to other Sup35 alleles. Most show some limitation of transmission, indicating that the evolved wild Sup35 alleles are effective in limiting the spread of [PSI+]. Notably, a “strong [PSI+]” can have any of several different transmission efficiency patterns, showing that “strong” versus “weak” is insufficient to indicate prion variant uniformity.
Zdroje
1. WicknerRB (1994) [URE3] as an altered URE2 protein: evidence for a prion analog in S. cerevisiae. Science 264 : 566–569.
2. CoxBS (1965) PSI, a cytoplasmic suppressor of super-suppressor in yeast. Heredity 20 : 505–521.
3. FrolovaL, LeGoffX, RasmussenHH, ChepereginS, DrugeonG, et al. (1994) A highly conserved eukaryotic protein family possessing properties of polypeptide chain release factor. Nature 372 : 701–703.
4. StansfieldI, JonesKM, KushnirovVV, DagkesamanskayaAR, PoznyakovskiAI, et al. (1995) The products of the SUP45 (eRF1) and SUP35 genes interact to mediate translation termination in Saccharomyces cerevisiae. EMBO J 14 : 4365–4373.
5. PaushkinSV, KushnirovVV, SmirnovVN, Ter-AvanesyanMD (1997) In vitro propagation of the prion-like state of yeast Sup35 protein. Science 277 : 381–383.
6. KingC-Y, TittmannP, GrossH, GebertR, AebiM, et al. (1997) Prion-inducing domain 2–114 of yeast Sup35 protein transforms in vitro into amyloid-like filaments. Proc Natl Acad Sci USA 94 : 6618–6622.
7. GloverJR, KowalAS, ShirmerEC, PatinoMM, LiuJ-J, et al. (1997) Self-seeded fibers formed by Sup35, the protein determinant of [PSI+], a heritable prion-like factor of S. cerevisiae. Cell 89 : 811–819.
8. KingCY, Diaz-AvalosR (2004) Protein-only transmission of three yeast prion strains. Nature 428 : 319–323.
9. TanakaM, ChienP, NaberN, CookeR, WeissmanJS (2004) Conformational variations in an infectious protein determine prion strain differences. Nature 428 : 323–328.
10. TerAvanesyanA, DagkesamanskayaAR, KushnirovVV, SmirnovVN (1994) The SUP35 omnipotent suppressor gene is involved in the maintenance of the non-Mendelian determinant [psi+] in the yeast Saccharomyces cerevisiae. Genetics 137 : 671–676.
11. HoshinoS, ImaiM, KobayashiT, UchidaN, KatadaT (1999) The eukaryotic polypeptide chain releasing factor (eRF3/GSPT) carrying the translation termination signal to the 3′-poly(A) tail of mRNA. J Biol Chem 274 : 16677–16680.
12. CossonB, CouturierA, ChabelskayaS, KiktevD, Inge-VechtomovS, et al. (2002) Poly(A)-binding protein acts in translation termination via eukaryotic release factor 3 interaction and does not influence [PSI+] propagation. Mol Cell Biol 22 : 3301–3315.
13. HosodaN, KobayashiiT, UchidaN, FunakoshiY, KikuchiY, et al. (2003) Translation termination factor eRF3 mediates mRNA decay through the regulation of deadenylation. J Biol Chem 278 : 38287–38291.
14. KobayashiT, FunakoshiY, HoshinoS, KatadaT (2004) The GTP-binding release factor eRF3 as a key mediator coupling translation termination to mRNA decay. J Biol Chem 279 : 45693–45700.
15. FunakoshiY, DoiY, HosodaN, UchidaN, OsawaM, et al. (2007) Mechanism of mRNA deadenylation: evidence for a molecular interplay between translation termination factor eRF3 and mRNA deadenylases. Genes Dev 21 : 3135–3148.
16. BailleulPA, NewnamGP, SteenbergenJN, ChernoffYO (1999) Genetic study of interactions between the cytoskeletal assembly protein Sla1 and prion - forming domain of the release factor Sup35 (eRF3) in Saccharomyces cerevisiae. Genetics 153 : 81–94.
17. LiuJ-J, SondheimerN, LindquistS (2002) Changes in the middle region of Sup35p profoundly alter the nature of epigenetic inheritance for the yeast prion [PSI+]. Proc Natl Acad Sci U S A 99 : 16446–16453.
18. BradleyME, LiebmanSW (2004) The Sup35 domains required for maintenance of weak, strong or undifferentiated yeast [PSI+] prions. Mol Microbiol 51 : 1649–1659.
19. ChenB, BruceKL, NewnamGP, GyonevaS, RomanyukAV, et al. (2010) Genetic and epigenetic control of the efficiency and fidelity of cross-species prion transmission. Mol Microbiol 76 : 1483–1499.
20. BatemanDA, WicknerRB (2012) [PSI+] prion transmission barriers protect Saccharomyces cerevisiae from infection: intraspecies ‘species barriers’. Genetics 190 : 569–579.
21. ShewmakerF, WicknerRB, TyckoR (2006) Amyloid of the prion domain of Sup35p has an in-register parallel β-sheet structure. Proc Natl Acad Sci USA 103 : 19754–19759.
22. ShewmakerF, KryndushkinD, ChenB, TyckoR, WicknerRB (2009) Two prion variants of Sup35p have in-register β-sheet structures, independent of hydration. Biochemistry 48 : 5074–5082.
23. CuilleJ, ChellePL (1939) Experimental transmission of trembling to the goat. C R Seances Acad Sci 208 : 1058–1060.
24. PrusinerSB, ScottM, FosterD, PanK-M, GrothD, et al. (1990) Transgenic studies implicate interactions between homologous PrP isoforms in scrapie prion replication. Cell 63 : 673–686.
25. ChernoffYO, GalkinAP, LewitinE, ChernovaTA, NewnamGP, et al. (2000) Evolutionary conservation of prion-forming abilities of the yeast Sup35 protein. Molec Microbiol 35 : 865–876.
26. KushnirovVV, Kochneva-PervukhovaNV, CechenovaMB, FrolovaNS, Ter-AvanesyanMD (2000) Prion properties of the Sup35 protein of yeast Pichia methanolica. EMBO J 19 : 324–331.
27. SantosoA, ChienP, OsherovichLZ, WeissmanJS (2000) Molecular basis of a yeast prion species barrier. Cell 100 : 277–288.
28. NakayashikiT, EbiharaK, BannaiH, NakamuraY (2001) Yeast [PSI+] “prions” that are crosstransmissible and susceptible beyond a species barrier through a quasi-prion state. Mol Cell 7 : 1121–1130.
29. ChenB, NewnamGP, ChernoffYO (2007) Prion species barrier between the closely related yeast proteins is detected despite coaggregation. Proc Natl Acad Sci U S A 104 : 2791–2796.
30. VishveshwaraN, LiebmanSW (2009) Heterologous cross-seeding mimics cross-species prion conversion in a yeast model. BMC Biol 7 : 26.
31. EdskesHK, McCannLM, HebertAM, WicknerRB (2009) Prion variants and species barriers among Saccharomyces Ure2 proteins. Genetics 181 : 1159–1167.
32. ResendeCG, OuteiroTF, SandsL, LindquistS, TuiteMF (2003) Prion protein gene polymorphisms in Saccharomyces cerevisiae. Mol Microbiol 49 : 1005–1017.
33. NakayashikiT, KurtzmanCP, EdskesHK, WicknerRB (2005) Yeast prions [URE3] and [PSI+] are diseases. Proc Natl Acad Sci U S A 102 : 10575–10580.
34. McGlincheyR, KryndushkinD, WicknerRB (2011) Suicidal [PSI+] is a lethal yeast prion. Proc Natl Acad Sci USA 108 : 5337–5341.
35. BessenRA, MarshRF (1992) Biochemical and physical properties of the prion protein from two strains of the transmissible mink encephalopathy agent. J Virol 66 : 2096–2101.
36. BessenRA, KociskoDA, RaymondGJ, NandanS, LandsburyPT, et al. (1995) Non-genetic propagation of strain-specific properties of scrapie prion protein. Nature 375 : 698–700.
37. DerkatchIL, ChernoffYO, KushnirovVV, Inge-VechtomovSG, LiebmanSW (1996) Genesis and variability of [PSI] prion factors in Saccharomyces cerevisiae. Genetics 144 : 1375–1386.
38. KushnirovVV, KryndushkinD, BogutaM, SmirnovVN, Ter-AvanesyanMD (2000) Chaperones that cure yeast artificial [PSI+] and their prion-specific effects. Curr Biol 10 : 1443–1446.
39. BradleyME, LiebmanSW (2003) Destabilizing interactions among [PSI+] and [PIN+] yeast prion variants. Genetics 165 : 1675–1685.
40. BorchseniusAS, MullerS, NewnamGP, Inge-VechtomovSG, ChernoffYO (2006) Prion variant maintained only at high levels of the Hsp104 disaggregase. Curr Genet 49 : 21–29.
41. KryndushkinD, ShewmakerF, WicknerRB (2008) Curing of the [URE3] prion by Btn2p, a Batten disease-related protein. EMBO J 27 : 2725–2735.
42. CristCG, KurahashiH, NakayashikiT, NakamuraN (2006) Conformation preserved in a weak-to-strong or strong-to-weak [PSI+] conversion during transmission to Sup35 prion variants. Biochemie 88 : 485–496.
43. MacleanCJ, GreigD (2008) Prezygotic reproductive isolation between Saccharomyces cerevisiae and Saccharomyces paradoxus. BMC Evol Biol 8 doi:10.1186/1471-2148-1188-1181.
44. DelneriD, ColsonI, GrammenoudiS, RobertsIN, LouisEJ, et al. (2003) Engineering evolution to study speciation in yeasts. Nature 422 : 68–72.
45. GreigD, BortsRH, LouisEJ, TravisanoM (2002) Epistasis and hybrid sterility in Saccharomyces. Proc Biol Sci 269 : 1167–1171.
46. KimberlinRH, ColeS, WalkerCA (1987) Temporary and permanent modifications to a single strain of mouse scrapie on transmission to rats and hamsters. J Gen Virol 68 : 1875–1881.
47. LinJY, LiaoTY, LeeHC, KingCY (2011) Inter-allelic prion propagation reveals conformational relationships among a multitude of [PSI] strains. PLoS Genet 7: e1002297 doi:10.1371/journal.pgen.1002297.
48. JungG, MasisonDC (2001) Guanidine hydrochloride inhibits Hsp104 activity in vivo: a possible explanation for its effect in curing yeast prions. Curr Microbiol 43 : 7–10.
49. HalfmannR, JaroszDF, JonesSK, ChangA, LancsterAK, et al. (2012) Prions are a common mechanism for phenotypic inheritance in wild yeasts. Nature 482 : 363–368.
50. BaxaU, WicknerRB, StevenAC, AndersonD, MarekovL, et al. (2007) Characterization of β-sheet structure in Ure2p1-89 yeast prion fibrils by solid state nuclear magnetic resonance. Biochemistry 46 : 13149–13162.
51. WicknerRB, DydaF, TyckoR (2008) Amyloid of Rnq1p, the basis of the [PIN+] prion, has a parallel in-register β-sheet structure. Proc Natl Acad Sci U S A 105 : 2403–2408.
52. ShkundinaIS, KushnirovVV, TuiteMF, Ter-AvanesyanMD (2006) The role of the N-terminal oligopeptide repeats of the yeast Sup35 prion protein in propagation and transmission of prion variants. Genetics 172 : 827–835.
53. RobertsBE, DuennwaldML, WangH, ChungC, LopreiatoNP, et al. (2009) A synergistic small molecule combination directly eradicates diverse prion strain structures. Nat Chem Biol 5 : 936–946.
54. LiJ, MahalSP, DemczykCA, WeissmannC (2011) Mutability of prions. EMBO Rep 12 : 1243–1250.
55. SharmaJ, LiebmanSW (2012) [PSI+] prion variant establishment in yeast. Mol Microbiol epub ahead of print
56. CollingeJ, ClarkeAR (2007) A general model of prion strains and their pathogenicity. Science 318 : 930–936.
57. LiJ, BrowningS, MahalSP, OelschlegelAM, WeissmannC (2010) Darwinian evolution of prions in cell culture. Science 327 : 869–872.
58. Domingo E (2007) Virus Evolution. In: Knipe DM, Howley PM, editors. Field's Virology. Philadelphia, PA: Lippincott, Williams and Wilkins. pp. 389–421.
59. NovickRP, HoppensteadtFC (1978) On plasmid incompatibility. Plasmid 1 : 421–434.
60. CoxBS, NessF, TuiteMF (2003) Analysis of the generation and segregation of propagons: entities that propagate the [PSI+] prion in yeast. Genetics 165 : 23–33.
61. ChangH-Y, LinJ-Y, LeeH-C, WangH-L, KingC-Y (2008) Strain-specific sequences required for yeast prion [PSI+] propagation. Proc Natl Acad Sci U S A 105 : 13345–13350.
62. WilsonPG, CulbertsonMR (1988) SUF12 suppressor protein of yeast: a fusion protein related to the EF-1 family of elongation factors. J Mol Biol 199 : 559–573.
63. KikuchiY, ShimatakeH, KikuchiA (1988) A yeast gene required for the G1 to S transition encodes a protein containing an A kinase target site and GTPase domain. EMBO J 7 : 1175–1182.
64. KushnirovVV, TerAvanesyanMD, TelckovMV, SurguchovAP, SmirnovVN, et al. (1988) Nucleotide sequence of the SUP2(SUP35) gene of Saccharomyces cerevisiae. Gene 66 : 45–54.
65. Sherman F (1991) Getting started with yeast. In: Guthrie C, Fink GR, editors. Guide to yeast genetics and molecular biology. San Diego: Academic Press. pp. 3–21.
66. CondeJ, FinkGR (1976) A mutant of Saccharomyces cerevisiae defective for nuclear fusion. Proc Natl Acad Sci USA 73 : 3651–3655.
67. ChattooBB, ShermanF, AzubalisDA, FjellstedtTA, MehnertD, et al. (1979) Selection of lys2 mutants in the yeast Saccharomyces cerevisiae by the utilization of alpha-aminoadipate. Genetics 93 : 51–65.
Štítky
Genetika Reprodukčná medicína
Článek Comparative Genome Structure, Secondary Metabolite, and Effector Coding Capacity across PathogensČlánek TATES: Efficient Multivariate Genotype-Phenotype Analysis for Genome-Wide Association StudiesČlánek Secondary Metabolism and Development Is Mediated by LlmF Control of VeA Subcellular Localization inČlánek Human Disease-Associated Genetic Variation Impacts Large Intergenic Non-Coding RNA ExpressionČlánek The Roles of Whole-Genome and Small-Scale Duplications in the Functional Specialization of GenesČlánek The Role of Autophagy in Genome Stability through Suppression of Abnormal Mitosis under Starvation
Článok vyšiel v časopisePLOS Genetics
Najčítanejšie tento týždeň
2013 Číslo 1- Gynekologové a odborníci na reprodukční medicínu se sejdou na prvním virtuálním summitu
- Je „freeze-all“ pro všechny? Odborníci na fertilitu diskutovali na virtuálním summitu
-
Všetky články tohto čísla
- A Model of High Sugar Diet-Induced Cardiomyopathy
- Comparative Genome Structure, Secondary Metabolite, and Effector Coding Capacity across Pathogens
- Emerging Function of Fat Mass and Obesity-Associated Protein (Fto)
- Positional Cloning Reveals Strain-Dependent Expression of to Alter Susceptibility to Bleomycin-Induced Pulmonary Fibrosis in Mice
- Genetics of Ribosomal Proteins: “Curiouser and Curiouser”
- Transposable Elements Re-Wire and Fine-Tune the Transcriptome
- Function and Regulation of , a Gene Implicated in Autism and Human Evolution
- MAML1 Enhances the Transcriptional Activity of Runx2 and Plays a Role in Bone Development
- Predicting Mendelian Disease-Causing Non-Synonymous Single Nucleotide Variants in Exome Sequencing Studies
- A Systematic Mapping Approach of 16q12.2/ and BMI in More Than 20,000 African Americans Narrows in on the Underlying Functional Variation: Results from the Population Architecture using Genomics and Epidemiology (PAGE) Study
- Transcription of the Major microRNA–Like Small RNAs Relies on RNA Polymerase III
- Histone H3K56 Acetylation, Rad52, and Non-DNA Repair Factors Control Double-Strand Break Repair Choice with the Sister Chromatid
- Genome-Wide Association Study Identifies a Novel Susceptibility Locus at 12q23.1 for Lung Squamous Cell Carcinoma in Han Chinese
- Genetic Disruption of the Copulatory Plug in Mice Leads to Severely Reduced Fertility
- The [] Prion Exists as a Dynamic Cloud of Variants
- Adult Onset Global Loss of the Gene Alters Body Composition and Metabolism in the Mouse
- Fis Protein Insulates the Gene from Uncontrolled Transcription
- The Meiotic Nuclear Lamina Regulates Chromosome Dynamics and Promotes Efficient Homologous Recombination in the Mouse
- Genome-Wide Haplotype Analysis of Expression Quantitative Trait Loci in Monocytes
- TATES: Efficient Multivariate Genotype-Phenotype Analysis for Genome-Wide Association Studies
- Structural Basis of a Histone H3 Lysine 4 Demethylase Required for Stem Elongation in Rice
- The Ecm11-Gmc2 Complex Promotes Synaptonemal Complex Formation through Assembly of Transverse Filaments in Budding Yeast
- MCM8 Is Required for a Pathway of Meiotic Double-Strand Break Repair Independent of DMC1 in
- Comparative Genomic Analysis of the Endosymbionts of Herbivorous Insects Reveals Eco-Environmental Adaptations: Biotechnology Applications
- Integration of Nodal and BMP Signals in the Heart Requires FoxH1 to Create Left–Right Differences in Cell Migration Rates That Direct Cardiac Asymmetry
- Pharmacodynamics, Population Dynamics, and the Evolution of Persistence in
- A Hybrid Likelihood Model for Sequence-Based Disease Association Studies
- Aberration in DNA Methylation in B-Cell Lymphomas Has a Complex Origin and Increases with Disease Severity
- Multiple Opposing Constraints Govern Chromosome Interactions during Meiosis
- Transcriptional Dynamics Elicited by a Short Pulse of Notch Activation Involves Feed-Forward Regulation by Genes
- Dynamic Large-Scale Chromosomal Rearrangements Fuel Rapid Adaptation in Yeast Populations
- Heterologous Gln/Asn-Rich Proteins Impede the Propagation of Yeast Prions by Altering Chaperone Availability
- Gene Copy-Number Polymorphism Caused by Retrotransposition in Humans
- An Incompatibility between a Mitochondrial tRNA and Its Nuclear-Encoded tRNA Synthetase Compromises Development and Fitness in
- Secondary Metabolism and Development Is Mediated by LlmF Control of VeA Subcellular Localization in
- Single-Stranded Annealing Induced by Re-Initiation of Replication Origins Provides a Novel and Efficient Mechanism for Generating Copy Number Expansion via Non-Allelic Homologous Recombination
- Tbx2 Controls Lung Growth by Direct Repression of the Cell Cycle Inhibitor Genes and
- Suv4-20h Histone Methyltransferases Promote Neuroectodermal Differentiation by Silencing the Pluripotency-Associated Oct-25 Gene
- A Conserved Helicase Processivity Factor Is Needed for Conjugation and Replication of an Integrative and Conjugative Element
- Telomerase-Null Survivor Screening Identifies Novel Telomere Recombination Regulators
- Genome-Wide Analysis Reveals Selection for Important Traits in Domestic Horse Breeds
- Coordinated Degradation of Replisome Components Ensures Genome Stability upon Replication Stress in the Absence of the Replication Fork Protection Complex
- Nkx6.1 Controls a Gene Regulatory Network Required for Establishing and Maintaining Pancreatic Beta Cell Identity
- HIF- and Non-HIF-Regulated Hypoxic Responses Require the Estrogen-Related Receptor in
- Delineating a Conserved Genetic Cassette Promoting Outgrowth of Body Appendages
- The Telomere Capping Complex CST Has an Unusual Stoichiometry, Makes Multipartite Interaction with G-Tails, and Unfolds Higher-Order G-Tail Structures
- Comprehensive Methylome Characterization of and at Single-Base Resolution
- Loci Associated with -Glycosylation of Human Immunoglobulin G Show Pleiotropy with Autoimmune Diseases and Haematological Cancers
- Switchgrass Genomic Diversity, Ploidy, and Evolution: Novel Insights from a Network-Based SNP Discovery Protocol
- Centromere-Like Regions in the Budding Yeast Genome
- Sequencing of Loci from the Elephant Shark Reveals a Family of Genes in Vertebrate Genomes, Forged by Ancient Duplications and Divergences
- Mendelian and Non-Mendelian Regulation of Gene Expression in Maize
- Mutational Spectrum Drives the Rise of Mutator Bacteria
- Human Disease-Associated Genetic Variation Impacts Large Intergenic Non-Coding RNA Expression
- The Roles of Whole-Genome and Small-Scale Duplications in the Functional Specialization of Genes
- Sex-Specific Signaling in the Blood–Brain Barrier Is Required for Male Courtship in
- A Newly Uncovered Group of Distantly Related Lysine Methyltransferases Preferentially Interact with Molecular Chaperones to Regulate Their Activity
- Is Required for Leptin-Mediated Depolarization of POMC Neurons in the Hypothalamic Arcuate Nucleus in Mice
- Unlocking the Bottleneck in Forward Genetics Using Whole-Genome Sequencing and Identity by Descent to Isolate Causative Mutations
- The Role of Autophagy in Genome Stability through Suppression of Abnormal Mitosis under Starvation
- MTERF3 Regulates Mitochondrial Ribosome Biogenesis in Invertebrates and Mammals
- Downregulation and Altered Splicing by in a Mouse Model of Facioscapulohumeral Muscular Dystrophy (FSHD)
- NBR1-Mediated Selective Autophagy Targets Insoluble Ubiquitinated Protein Aggregates in Plant Stress Responses
- Retroactive Maintains Cuticle Integrity by Promoting the Trafficking of Knickkopf into the Procuticle of
- Phenome-Wide Association Study (PheWAS) for Detection of Pleiotropy within the Population Architecture using Genomics and Epidemiology (PAGE) Network
- Genetic and Functional Modularity of Activities in the Specification of Limb-Innervating Motor Neurons
- A Population Genetic Model for the Maintenance of R2 Retrotransposons in rRNA Gene Loci
- A Quartet of PIF bHLH Factors Provides a Transcriptionally Centered Signaling Hub That Regulates Seedling Morphogenesis through Differential Expression-Patterning of Shared Target Genes in
- A Genome-Wide Integrative Genomic Study Localizes Genetic Factors Influencing Antibodies against Epstein-Barr Virus Nuclear Antigen 1 (EBNA-1)
- Mutation of the Diamond-Blackfan Anemia Gene in Mouse Results in Morphological and Neuroanatomical Phenotypes
- Life, the Universe, and Everything: An Interview with David Haussler
- Alternative Oxidase Expression in the Mouse Enables Bypassing Cytochrome Oxidase Blockade and Limits Mitochondrial ROS Overproduction
- An Evolutionarily Conserved Synthetic Lethal Interaction Network Identifies FEN1 as a Broad-Spectrum Target for Anticancer Therapeutic Development
- The Flowering Repressor Underlies a Novel QTL Interacting with the Genetic Background
- Telomerase Is Required for Zebrafish Lifespan
- and Diversified Expression of the Gene Family Bolster the Floral Stem Cell Network
- Susceptibility Loci Associated with Specific and Shared Subtypes of Lymphoid Malignancies
- An Insertion in 5′ Flanking Region of Causes Blue Eggshell in the Chicken
- Increased Maternal Genome Dosage Bypasses the Requirement of the FIS Polycomb Repressive Complex 2 in Arabidopsis Seed Development
- WNK1/HSN2 Mutation in Human Peripheral Neuropathy Deregulates Expression and Posterior Lateral Line Development in Zebrafish ()
- Synergistic Interaction of Rnf8 and p53 in the Protection against Genomic Instability and Tumorigenesis
- Dot1-Dependent Histone H3K79 Methylation Promotes Activation of the Mek1 Meiotic Checkpoint Effector Kinase by Regulating the Hop1 Adaptor
- A Heterogeneous Mixture of F-Series Prostaglandins Promotes Sperm Guidance in the Reproductive Tract
- Starvation, Together with the SOS Response, Mediates High Biofilm-Specific Tolerance to the Fluoroquinolone Ofloxacin
- Directed Evolution of a Model Primordial Enzyme Provides Insights into the Development of the Genetic Code
- Genome-Wide Screens for Tinman Binding Sites Identify Cardiac Enhancers with Diverse Functional Architectures
- PLOS Genetics
- Archív čísel
- Aktuálne číslo
- Informácie o časopise
Najčítanejšie v tomto čísle- Function and Regulation of , a Gene Implicated in Autism and Human Evolution
- An Insertion in 5′ Flanking Region of Causes Blue Eggshell in the Chicken
- Comprehensive Methylome Characterization of and at Single-Base Resolution
- Susceptibility Loci Associated with Specific and Shared Subtypes of Lymphoid Malignancies
Prihlásenie#ADS_BOTTOM_SCRIPTS#Zabudnuté hesloZadajte e-mailovú adresu, s ktorou ste vytvárali účet. Budú Vám na ňu zasielané informácie k nastaveniu nového hesla.
- Časopisy