-
Články
- Časopisy
- Kurzy
- Témy
- Kongresy
- Videa
- Podcasty
A Genetic Incompatibility Accelerates Adaptation in Yeast
In nature, bacterial populations with high mutation rates can adapt faster to new environments by acquiring beneficial mutations. However, such populations also accumulate harmful mutations that reduce their fitness. We show that the model eukaryote baker’s yeast can use a similar mutator strategy to adapt to new environments. The mutator state that we observed resulted from an incompatibility involving two genes, MLH1 and PMS1, that work together to remove DNA replication errors through a spellchecking mismatch repair mechanism. This incompatibility can occur through mating between baker’s yeast from different genetic backgrounds, yielding mutator offspring containing an MLH1-PMS1 combination not present in either parent. Interestingly, these offspring adapted more rapidly to stress, compared to the parental strains, and did so without an overall loss in fitness. DNA sequencing analyses of baker’s yeast strains from across the globe support the presence of incompatible hybrid yeast strains in nature. These observations provide a powerful model to understand how the segregation of defects in DNA mismatch repair can serve as an effective strategy to enable eukaryotes to adapt to changing environments.
Vyšlo v časopise: A Genetic Incompatibility Accelerates Adaptation in Yeast. PLoS Genet 11(7): e32767. doi:10.1371/journal.pgen.1005407
Kategorie: Research Article
prolekare.web.journal.doi_sk: https://doi.org/10.1371/journal.pgen.1005407Souhrn
In nature, bacterial populations with high mutation rates can adapt faster to new environments by acquiring beneficial mutations. However, such populations also accumulate harmful mutations that reduce their fitness. We show that the model eukaryote baker’s yeast can use a similar mutator strategy to adapt to new environments. The mutator state that we observed resulted from an incompatibility involving two genes, MLH1 and PMS1, that work together to remove DNA replication errors through a spellchecking mismatch repair mechanism. This incompatibility can occur through mating between baker’s yeast from different genetic backgrounds, yielding mutator offspring containing an MLH1-PMS1 combination not present in either parent. Interestingly, these offspring adapted more rapidly to stress, compared to the parental strains, and did so without an overall loss in fitness. DNA sequencing analyses of baker’s yeast strains from across the globe support the presence of incompatible hybrid yeast strains in nature. These observations provide a powerful model to understand how the segregation of defects in DNA mismatch repair can serve as an effective strategy to enable eukaryotes to adapt to changing environments.
Zdroje
1. Kunkel TA. Erie DA (2005) DNA mismatch repair. Annu Rev Biochem 74 : 681–710. 15952900
2. Nishant KT, Wei W, Mancera E, Argueso JL, Schlattl A, et al. (2010) The baker's yeast diploid genome is remarkably stable in vegetative growth and meiosis. PLoS Genet 6: e1001109. doi: 10.1371/journal.pgen.1001109 20838597
3. Zanders S, Ma X, Roychoudhury A, Hernandez RD, Demogines A, Barker B et al. (2010) Detection of heterozygous mutations in the genome of mismatch repair defective diploid yeast using a Bayesian approach. Genetics 186 : 493–503. doi: 10.1534/genetics.110.120105 20660644
4. Hombauer H, Campbell CS, Smith CE, Desai A, Kolodner RD (2011) Visualization of eukaryotic DNA mismatch repair reveals distinct recognition and repair intermediates. Cell 147 : 1040–1053. doi: 10.1016/j.cell.2011.10.025 22118461
5. Jiricny J (2013) Postreplicative mismatch repair. Cold Spring Harb Perspect Biol 5: a012633. doi: 10.1101/cshperspect.a012633 23545421
6. Ma X, Rogacheva MV, Nishant KT, Zanders S, Bustamante CD, Alani E. (2012) Mutation hot spots in yeast caused by long-range clustering of homopolymeric sequences. Cell Rep 1 : 36–42. doi: 10.1016/j.celrep.2011.10.003 22832106
7. Lynch M. (2010) Evolution of the mutation rate. Trends in Genetics 26 : 345–352. doi: 10.1016/j.tig.2010.05.003 20594608
8. Drake JW (1991) A constant rate of spontaneous mutation in DNA-based microbes. Proc Natl Acad Sci USA 88 : 7160–7164. 1831267
9. Drake JW, Charlesworth B, Charlesworth D, Crow JF (1998) Rates of Spontaneous Mutation. Genetics 148 : 1667–1686. 9560386
10. Zeyl C, DeVisser JA (2001) Estimates of the rate and distribution of fitness effects of spontaneous mutation in Saccharomyces cerevisiae. Genetics 157 : 53–61. 11139491
11. LeClerc JE, Li B, Payne WL, Cebula TA (1996) High mutation frequencies among Escherichia coli and Salmonella pathogens. Science 274 : 1208–1211. 8895473
12. Matic I, Radman M, Taddei F, Picard B, Doit C, et al. (1997) Highly variable mutation rates in commensal and pathogenic Escherichia coli. Science 277 : 1833–1834. 9324769
13. Boe L, Danielsen M, Knudsen S, Petersen JB, Maymann J, et al. (2000) The frequency of mutators in populations of Escherichia coli. Mutat Res 448 : 47–55. 10751622
14. Denamur E., Lecointre G, Darlu P, Tenaillon O, Acquaviva C et al. (2000) Evolutionary implications of the frequent horizontal transfer of mismatch repair genes. Cell 103 : 711–721. 11114328
15. Sniegowski PD, Dombrowski PG, Fingerman E (2002) Saccharomyces cerevisiae and Saccharomyces paradoxus coexist in a natural woodland site in North America and display different levels of reproductive isolation from European conspecifics. FEMS Yeast Res 1 : 299–306. 12702333
16. Taddei F, Radman M, Maynard-Smith J, Toupance B, Gouyon PH, et al. (1997) Role of mutator alleles in adaptive evolution. Nature 387 : 700–702. 9192893
17. Tanaka MM, Bergstrom CT, Levin BR (2003) The evolution of mutator genes in bacterial populations: the roles of environmental change and timing. Genetics 164 : 843–854. 12871898
18. Townsend JP, Nielsen KM, Fisher DS, Hartl DL (2003) Horizontal acquisition of divergent chromosomal DNA in bacteria: effects of mutator phenotypes. Genetics 164 : 13–21. 12750317
19. Giraud A, Matic I, Tenaillon O, Clara A, Radman M, et al. (2001) Costs and benefits of high mutation rates: adaptive evolution of bacteria in the mouse gut. Science 291 : 2606–2608. 11283373
20. Chao L, Cox EC (1983) Competition between high and low mutating strains of Escherichia coli. Evolution 37 : 125–134.
21. Thompson DA, Desai MM, Murray AW. (2006) Ploidy controls the success of mutators and nature of mutations during budding yeast evolution. Curr Biol 16 : 1581–1590. 16920619
22. Heck JA, Argueso JL, Gemici Z, Reeves RG, Bernard A, et al. (2006) Negative epistasis between natural variants of the Saccharomyces cerevisiae MLH1 and PMS1 genes results in a defect in mismatch repair. Proc Natl Acad Sci USA 103 : 3256–3261. 16492773
23. Muller HJ, Pontecorvo G (1940) Recombinants between Drosophila Species the F1 Hybrids of which are sterile. Nature 146 : 199–200.
24. Muller HJ (1939) Reversibility in evolution considered from the standpoint of genetics. Biol Rev Camb Philos Soc 14 : 261–280.
25. Orr HA (1995) The population genetics of speciation: the evolution of hybrid incompatibilities. Genetics 139 : 1805–1813. 7789779
26. Dobzhansky T (1936) Studies on Hybrid Sterility. II. Localization of Sterility Factors in Drosophila Pseudoobscura Hybrids. Genetics 21 : 113–135. 17246786
27. Demogines A, Wong A, Aquadro C, Alani E (2008) Incompatibilities involving yeast mismatch repair genes: a role for genetic modifiers and implications for disease penetrance and variation in genomic mutation rates. PLoS Genetics 4: e1000103. doi: 10.1371/journal.pgen.1000103 18566663
28. Wu CI, Ting CT (2004) Genes and speciation. Nat Rev Genet 5 : 114–122. 14735122
29. Coyne JA, Orr HA (2004) Speciation, Sinauer Associates, Sunderland, MA.
30. Ting CT, Tsaur SC, Wu ML, Wu CI (1998) A rapidly evolving homeobox at the site of a hybrid sterility gene. Science 282 : 1501–1504. 9822383
31. Barbash DA, Siino DF, Tarone AM, Roote J (2003) A rapidly evolving MYB-related protein causes species isolation in Drosophila. Proc Natl Acad Sci USA 100 : 5302–5307. 12695567
32. Wittbrodt J, Adam D, Malitschek B, Maueler W, Raulf F et al. (1989) Novel putative receptor tyrosine kinase encoded by the melanoma-inducing Tu locus in Xiphophorus. Nature 341 : 415–421. 2797166
33. Rawson RD, Burton RS (2002) Functional coadaptation between cytochrome c and cytochrome c oxidase within allopatric populations of a marine copepod. Proc Natl Acad Sci USA 99 : 12955–12958. 12271133
34. Hartl D, Clark A (2007) Principles of Population Genetics. 4rth Edition. Sinauer Associates.
35. Dykhuizen D, Hartl DL (1980) Selective neutrality of 6GPD allozymes in E. coli and the effects of genetic background. Genetics 96 : 801–817. 7021316
36. McDonald JH (2014) Handbook of Biological Statistics (3rd ed) p 145–156. Sparky House Publishing, Baltimore, Maryland.
37. Raynes Y, Gazzara MR, Sniegowski PD (2012) Contrasting dynamics of a mutator allele in asexual populations of differing size. Evolution 66 : 2329–2334. doi: 10.1111/j.1558-5646.2011.01577.x 22759305
38. Antebi A, and Fink GR (1992) The yeast Ca2+-ATPase homologue, PMR1, is required for normal Golgi function and localizes in a novel Golgi-like distribution. Mol Biol Cell 3 : 633–654. 1379856
39. Park SY, Seo SB, Lee SJ, Na JG, Kim YJ (2001). Mutation in PMR1, a Ca(2+)-ATPase in Golgi, confers salt tolerance in Saccharomyces cerevisiae by inducing expression of PMR2, an Na(+)-ATPase in plasma membrane. J Biol Chem 276 : 28694–28699. 11387321
40. Zhao J, Lin W, Ma X, Lu Q, Ma X, Bian G, Jiang L (2010) The protein kinase Hal5p is the high-copy suppressor of lithium-sensitive mutations of genes involved in the sporulation and meiosis as well as the ergosterol biosynthesis in Saccharomyces cerevisiae. Genomics 95 : 290–298. doi: 10.1016/j.ygeno.2010.02.010 20206679
41. Cunningham KW, Fink GR (1996) Calcineurin inhibits VCX1-dependent H+/Ca2+ exchange and induces Ca2+ ATPases in Saccharomyces cerevisiae. Mol Cell Biol 16 : 2226–2237. 8628289
42. Anderson JB, Funt J, Thompson DA, Prabhu S, Socha A et al. (2010) Determinants of divergent adaptation and Dobzhansky-Muller interaction in experimental yeast populations. Curr Biol 20 : 1383–1388. doi: 10.1016/j.cub.2010.06.022 20637622
43. Lenassi M, Gostinčar C, Jackman S, Turk M, Sadowski I, Nislow C, et al. (2013) Whole genome duplication and enrichment of metal cation transporters revealed by de novo genome sequencing of extremely halotolerant black yeast Hortaea werneckii. PLoS One 8: e71328. doi: 10.1371/journal.pone.0071328 23977017
44. Zhou M, Schekman R (1999) The engagement of Sec61p in the ER dislocation process. Mol Cell 4 : 925–934. 10635318
45. Cyert MS and Thorner J (1992) Regulatory subunit (CNB1 gene product) of yeast Ca2+/calmodulin-dependent phosphoprotein phosphatases is required for adaptation to pheromone. Mol Cell Biol 12 : 3460–3469. 1321337
46. Kohn LM, Anderson JB (2014) The underlying structure of adaptation under strong selection in 12 experimental yeast populations. Eukaryot Cell 13 : 1200–1206. doi: 10.1128/EC.00122-14 25016004
47. Hinnebusch AG and Natarajan K (2002) Gcn4p, a master regulator of gene expression, is controlled at multiple levels by diverse signals of starvation and stress. Eukaryot Cell 1 : 22–32. 12455968
48. Kakinuma Y, Maruyama T, Nozaki T, Wada Y, Ohsumi Y, Igarashi K (1995) Cloning of the gene encoding a putative serine threonine protein kinase which enhances spermine uptake in Saccharomyces cerevisiae. Biochem Biophys Res Commun 216 : 985–992. 7488221
49. Sniegowski PD, Gerrish PJ, Lenski RE (1997) Evolution of high mutation rates in experimental populations of E. coli. Nature 387 : 703–705. 9192894
50. Funchain P, Yeung A, Stewart JL, Lin R, Slupska MM, Miller JH (2000) The consequences of growth of a mutator strain of Escherichia coli as measured by loss of function among multiple gene targets and loss of fitness. Genetics 154 : 959–970. 10757746
51. Woods RJ, Barrick JE, Cooper TF, Shrestha U, Kauth MR, Lenski RE. (2011) Second-order selection for evolvability in a large Escherichia coli population. Science 331 : 1433–1436. doi: 10.1126/science.1198914 21415350
52. Elena SF, Lenski RE (2003) Evolution experiments with microorganisms: the dynamics and genetic bases of adaptation. Nat Rev Genet 4 : 457–469. 12776215
53. Sprouffske K, Merlo LM, Gerrish PJ, Maley CC, Sniegowski PD (2012) Cancer in light of experimental evolution. Curr Biol 22: R762–771. doi: 10.1016/j.cub.2012.06.065 22975007
54. Liti G, Louis EJ (2005) Yeast evolution and comparative genomics. Annu Rev Microbiol 59 : 135–153. 15877535
55. Tsai IJ, Bensasson D, Burt A, Koufopanou V (2008) Population genomics of the wild yeast Saccharomyces paradoxus: Quantifying the life cycle. Proc Natl Acad Sci USA 105 : 4957–4962. doi: 10.1073/pnas.0707314105 18344325
56. Magwene PM, Kayıkçı Ö, Granek JA, Reininga JM, Scholl Z, Murray D (2011) Outcrossing, mitotic recombination, and life-history trade-offs shape genome evolution in Saccharomyces cerevisiae. Proc Natl Acad Sci USA 108 : 1987–1992. doi: 10.1073/pnas.1012544108 21245305
57. Ruderfer DM, Pratt SC, Seidel HS, Kruglyak L (2006) Population genomic analysis of outcrossing and recombination in yeast. Nat Genet 38 : 1077–1081. 16892060
58. Murphy HA, Zeyl CW (2010) Yeast Sex: Surprisingly high rates of outcrossing between asci. PLoS One 5: e10461. doi: 10.1371/journal.pone.0010461 20463964
59. Reuter M, Bell G, Greig D (2007) Increased outbreeding in yeast in response to dispersal by an insect vector. Curr Biol 17: R81–83. 17276903
60. Lang GI, Botstein D, Desai MM (2011) Genetic variation and the fate of beneficial mutations in asexual populations. Genetics 188 : 647–661. doi: 10.1534/genetics.111.128942 21546542
61. Corbett-Detig RB, Zhou J, Clark AG, Hartl DL, Ayroles JF (2013) Genetic incompatibilities are widespread within species. Nature 504 : 135–137. doi: 10.1038/nature12678 24196712
62. Brem RB, Storey JD, Whittle J, Kruglyak L (2005) Genetic interactions between polymorphisms that affect gene expression in yeast. Nature 436 : 701–703. 16079846
63. Hunter N, Chambers SR, Louis EJ, Borts RH (1996) The mismatch repair system contributes to meiotic sterility in an interspecific yeast hybrid. EMBO J 15 : 1726–1733. 8612597
64. Naumov GI, Naumova ES, Lantto RA, Louis EJ, Korhola M (1992) Genetic homology between Saccharomyces cerevisiae and its sibling species S. paradoxus and S. bayanus: electrophoretic karyotypes. Yeast 8 : 599–612. 1441740
65. Winston F, Dollard C, Ricupero-Hovasse SL (1995) Construction of a set of convenient Saccharomyces cerevisiae strains that are isogenic to S288C. Yeast 11 : 53–55. 7762301
66. Rose MD, Winston F, Hieter P (1990) Methods in yeast genetics: A Laboratory Course Manual. Cold Spring Harbor Laboratory Press, Cold Spring Harbor, NY.
67. Gietz RD, Schiestl RH (2007) Large-scale high-efficiency yeast transformation using the LiAc/SS carrier DNA/PEG method. Nat Protoc 2 : 38–41. 17401336
68. Holm C, Meeks-Wagner DW, Fangman WL, Botstein D (1986) A rapid, efficient method for isolating DNA from yeast. Gene 42 : 169–173. 3015730
69. Rosner B, Glynn RJ, Lee M-LT (2006) The Wilcoxon signed rank test for paired comparisons of clustered data. Biometrics 62 : 185–192. 16542245
70. Goldstein AL, McCusker JH (1999) Three new dominant drug resistance cassettes for gene disruption in Saccharomyces cerevisiae. Yeast 15 : 1541–1553. 10514571
71. Baganz F, Hayes A, Marren D, Gardner DC, Oliver SG (1997) Suitability of replacement markers for functional analysis studies in Saccharomyces cerevisiae. Yeast 13 : 1563–1573. 9509575
72. Tran HT, Keen JD, Kricker M, Resnick MA, Gordenin DA (1997) Hypermutability of homonucleotide runs in mismatch repair and DNA polymerase proofreading yeast mutants. Mol Cell Biol 17 : 2859–2865. 9111358
73. Dixon WJ, Massey FJ (1969) Introduction to Statistical Analysis. New York: McGraw-Hill.
74. McKenna A, Hanna M, Banks E, Sivachenko A, Cibulskis K, et al. (2010) The Genome Analysis Toolkit: a MapReduce framework for analyzing next-generation DNA sequencing data. Genome Res 20 : 1297–1303. doi: 10.1101/gr.107524.110 20644199
75. Wanat JJ, Singh N, Alani E (2007) The effect of genetic background on the function of Saccharomyces cerevisiae mlh1 alleles that correspond to HNPCC missense mutations. Hum Mol Genet 16 : 445–452. 17210669
Štítky
Genetika Reprodukčná medicína
Článek Discovery and Fine-Mapping of Glycaemic and Obesity-Related Trait Loci Using High-Density ImputationČlánek AAA-ATPase FIDGETIN-LIKE 1 and Helicase FANCM Antagonize Meiotic Crossovers by Distinct MechanismsČlánek A Conserved Pattern of Primer-Dependent Transcription Initiation in and Revealed by 5′ RNA-seqČlánek TopBP1 Governs Hematopoietic Stem/Progenitor Cells Survival in Zebrafish Definitive HematopoiesisČlánek Redundant Roles of Rpn10 and Rpn13 in Recognition of Ubiquitinated Proteins and Cellular Homeostasis
Článok vyšiel v časopisePLOS Genetics
Najčítanejšie tento týždeň
2015 Číslo 7- 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
- LINE-1 Retroelements Get ZAPped!
- /p23: A Small Protein Heating Up Lifespan Regulation
- Hairless Streaks in Cattle Implicate TSR2 in Early Hair Follicle Formation
- Ribosomal Protein Mutations Result in Constitutive p53 Protein Degradation through Impairment of the AKT Pathway
- Molecular Clock of Neutral Mutations in a Fitness-Increasing Evolutionary Process
- Modeling Implicates in Nephropathy: Evidence for Dominant Negative Effects and Epistasis under Anemic Stress
- The Alternative Sigma Factor SigX Controls Bacteriocin Synthesis and Competence, the Two Quorum Sensing Regulated Traits in
- BMP Inhibition in Seminomas Initiates Acquisition of Pluripotency via NODAL Signaling Resulting in Reprogramming to an Embryonal Carcinoma
- Comparative Study of Regulatory Circuits in Two Sea Urchin Species Reveals Tight Control of Timing and High Conservation of Expression Dynamics
- EIN3 and ORE1 Accelerate Degreening during Ethylene-Mediated Leaf Senescence by Directly Activating Chlorophyll Catabolic Genes in
- Genome Wide Binding Site Analysis Reveals Transcriptional Coactivation of Cytokinin-Responsive Genes by DELLA Proteins
- Sensory Neurons Arouse . Locomotion via Both Glutamate and Neuropeptide Release
- A Year of Infection in the Intensive Care Unit: Prospective Whole Genome Sequencing of Bacterial Clinical Isolates Reveals Cryptic Transmissions and Novel Microbiota
- Inference of Low and High-Grade Glioma Gene Regulatory Networks Delineates the Role of Rnd3 in Establishing Multiple Hallmarks of Cancer
- Novel Role for p110β PI 3-Kinase in Male Fertility through Regulation of Androgen Receptor Activity in Sertoli Cells
- A Novel Locus Harbouring a Functional Nonsense Mutation Identified in a Large Danish Family with Nonsyndromic Hearing Impairment
- Checkpoint Activation of an Unconventional DNA Replication Program in
- A Genetic Incompatibility Accelerates Adaptation in Yeast
- The SMC Loader Scc2 Promotes ncRNA Biogenesis and Translational Fidelity
- Blimp1/Prdm1 Functions in Opposition to Irf1 to Maintain Neonatal Tolerance during Postnatal Intestinal Maturation
- Discovery and Fine-Mapping of Glycaemic and Obesity-Related Trait Loci Using High-Density Imputation
- JAK/STAT and Hox Dynamic Interactions in an Organogenetic Gene Cascade
- Emergence, Retention and Selection: A Trilogy of Origination for Functional Proteins from Ancestral LncRNAs in Primates
- MoSET1 (Histone H3K4 Methyltransferase in ) Regulates Global Gene Expression during Infection-Related Morphogenesis
- Arabidopsis PCH2 Mediates Meiotic Chromosome Remodeling and Maturation of Crossovers
- AAA-ATPase FIDGETIN-LIKE 1 and Helicase FANCM Antagonize Meiotic Crossovers by Distinct Mechanisms
- A Conserved Pattern of Primer-Dependent Transcription Initiation in and Revealed by 5′ RNA-seq
- Tempo and Mode of Transposable Element Activity in Drosophila
- The Shelterin TIN2 Subunit Mediates Recruitment of Telomerase to Telomeres
- SAMHD1 Inhibits LINE-1 Retrotransposition by Promoting Stress Granule Formation
- A Genome Scan for Genes Underlying Microgeographic-Scale Local Adaptation in a Wild Species
- TopBP1 Governs Hematopoietic Stem/Progenitor Cells Survival in Zebrafish Definitive Hematopoiesis
- Analysis of the Relationships between DNA Double-Strand Breaks, Synaptonemal Complex and Crossovers Using the Mutant
- Assessing Mitochondrial DNA Variation and Copy Number in Lymphocytes of ~2,000 Sardinians Using Tailored Sequencing Analysis Tools
- Allelic Spectra of Risk SNPs Are Different for Environment/Lifestyle Dependent versus Independent Diseases
- CSB-PGBD3 Mutations Cause Premature Ovarian Failure
- Irrepressible: An Interview with Mark Ptashne
- Genetic Evidence for Function of the bHLH-PAS Protein Gce/Met As a Juvenile Hormone Receptor
- Inactivation of Retinoblastoma Protein (Rb1) in the Oocyte: Evidence That Dysregulated Follicle Growth Drives Ovarian Teratoma Formation in Mice
- Redundant Roles of Rpn10 and Rpn13 in Recognition of Ubiquitinated Proteins and Cellular Homeostasis
- Pyrimidine Pool Disequilibrium Induced by a Cytidine Deaminase Deficiency Inhibits PARP-1 Activity, Leading to the Under Replication of DNA
- Molecular Framework of a Regulatory Circuit Initiating Two-Dimensional Spatial Patterning of Stomatal Lineage
- RFX2 Is a Major Transcriptional Regulator of Spermiogenesis
- A Role for Macro-ER-Phagy in ER Quality Control
- Corp Regulates P53 in via a Negative Feedback Loop
- Common Cell Shape Evolution of Two Nasopharyngeal Pathogens
- Contact- and Protein Transfer-Dependent Stimulation of Assembly of the Gliding Motility Machinery in
- Endothelial Snail Regulates Capillary Branching Morphogenesis via Vascular Endothelial Growth Factor Receptor 3 Expression
- Functional Constraint Profiling of a Viral Protein Reveals Discordance of Evolutionary Conservation and Functionality
- Temporal Coordination of Carbohydrate Metabolism during Mosquito Reproduction
- mTOR Directs Breast Morphogenesis through the PKC-alpha-Rac1 Signaling Axis
- Reversible Oxidation of a Conserved Methionine in the Nuclear Export Sequence Determines Subcellular Distribution and Activity of the Fungal Nitrate Regulator NirA
- Nutritional Control of DNA Replication Initiation through the Proteolysis and Regulated Translation of DnaA
- Cooperation between Paxillin-like Protein Pxl1 and Glucan Synthase Bgs1 Is Essential for Actomyosin Ring Stability and Septum Formation in Fission Yeast
- Encodes a Highly Conserved Protein Important to Neurological Function in Mice and Flies
- Identification of a Novel Regulatory Mechanism of Nutrient Transport Controlled by TORC1-Npr1-Amu1/Par32
- Aurora-A-Dependent Control of TACC3 Influences the Rate of Mitotic Spindle Assembly
- Large-Scale Phenomics Identifies Primary and Fine-Tuning Roles for CRKs in Responses Related to Oxidative Stress
- TFIIS-Dependent Non-coding Transcription Regulates Developmental Genome Rearrangements
- Genome-Wide Reprogramming of Transcript Architecture by Temperature Specifies the Developmental States of the Human Pathogen
- Identification of Chemical Inhibitors of β-Catenin-Driven Liver Tumorigenesis in Zebrafish
- The Catalytic and Non-catalytic Functions of the Chromatin-Remodeling Protein Collaborate to Fine-Tune Circadian Transcription in
- PLOS Genetics
- Archív čísel
- Aktuálne číslo
- Informácie o časopise
Najčítanejšie v tomto čísle- Functional Constraint Profiling of a Viral Protein Reveals Discordance of Evolutionary Conservation and Functionality
- Reversible Oxidation of a Conserved Methionine in the Nuclear Export Sequence Determines Subcellular Distribution and Activity of the Fungal Nitrate Regulator NirA
- Modeling Implicates in Nephropathy: Evidence for Dominant Negative Effects and Epistasis under Anemic Stress
- Nutritional Control of DNA Replication Initiation through the Proteolysis and Regulated Translation of DnaA
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