-
Články
- Časopisy
- Kurzy
- Témy
- Kongresy
- Videa
- Podcasty
Protein Composition of Infectious Spores Reveals Novel Sexual Development and Germination Factors in
Spores are a critical cell type that allow long-term survival of diverse organisms from bacteria to fungi to plants. Among fungi, spores are often formed when growth conditions are poor; spores can then disperse to more favorable environments and reinitiate growth. Spores of some environmental fungi can cause fatal disease in humans. Here we used the meningitis-causing yeast Cryptococcus neoformans to determine the roles of spore-enriched proteins in spore biology. Using a combined proteomics-genetics approach, we identified eighteen spore-enriched proteins, knocked out the genes encoding each of them, and assessed the resulting strains for phenotypes in a broad array of assays. We predicted that mutant strains would be likely to show defects in spore-specific processes, but instead, we discovered that the majority harbored defects in sexual development, the process by which spores are formed. Only one mutant exhibited a defect in a spore-specific process (germination). Our data reveal that many spore-represented proteins are associated with pre-spore developmental processes, rather than intrinsic spore-specific properties or processes. These findings indicate a previously unknown molecular connection between the developmental process that results in spore biogenesis and the composition of infectious spores.
Vyšlo v časopise: Protein Composition of Infectious Spores Reveals Novel Sexual Development and Germination Factors in. PLoS Genet 11(8): e32767. doi:10.1371/journal.pgen.1005490
Kategorie: Research Article
prolekare.web.journal.doi_sk: https://doi.org/10.1371/journal.pgen.1005490Souhrn
Spores are a critical cell type that allow long-term survival of diverse organisms from bacteria to fungi to plants. Among fungi, spores are often formed when growth conditions are poor; spores can then disperse to more favorable environments and reinitiate growth. Spores of some environmental fungi can cause fatal disease in humans. Here we used the meningitis-causing yeast Cryptococcus neoformans to determine the roles of spore-enriched proteins in spore biology. Using a combined proteomics-genetics approach, we identified eighteen spore-enriched proteins, knocked out the genes encoding each of them, and assessed the resulting strains for phenotypes in a broad array of assays. We predicted that mutant strains would be likely to show defects in spore-specific processes, but instead, we discovered that the majority harbored defects in sexual development, the process by which spores are formed. Only one mutant exhibited a defect in a spore-specific process (germination). Our data reveal that many spore-represented proteins are associated with pre-spore developmental processes, rather than intrinsic spore-specific properties or processes. These findings indicate a previously unknown molecular connection between the developmental process that results in spore biogenesis and the composition of infectious spores.
Zdroje
1. Brown JKM, Hovmøller MS. Aerial dispersal of pathogens on the global and continental scales and its impact on plant disease. Science. 2002; 297 : 537–541. 12142520
2. Wyatt TT, Wösten HAB, Dijksterhuis J. Fungal spores for dispersion in space and time. Adv Appl Microbiol. 2013; 85 : 43–91. doi: 10.1016/B978-0-12-407672-3.00002-2 23942148
3. Neiman AM. Sporulation in the budding yeast Saccharomyces cerevisiae. Genetics. 2011; 189 : 737–765. doi: 10.1534/genetics.111.127126 22084423
4. Freese EB, Chu MI, Freese E. Initiation of yeast sporulation by partial carbon, nitrogen, or phosphate deprivation. J Bacteriol. 1982; 149 : 840–851. 7037742
5. Krijgsheld P, Bleichrodt R, van Veluw GJ, Wang F, Müller WH, Dijksterhuis J, et al. Development in Aspergillus. Stud Mycol. 2013; 74 : 1–29. doi: 10.3114/sim0006 23450714
6. Herman PK, Rine J. Yeast spore germination: a requirement for Ras protein activity during re-entry into the cell cycle. EMBO J. 1997; 16 : 6171–6181. 9321396
7. Dijksterhuis J, van Driel KG, Sanders MG, Molenaar D, Houbraken JA, Samson RA, et al. Trehalose degradation and glucose efflux precede cell ejection during germination of heat-resistant ascospores of Talaromyces macrosporus. Arch Microbiol. 2002; 178 : 1–7. 12070763
8. Dijksterhuis J, Teunissen PGM. Dormant ascospores of Talaromyces macrosporus are activated to germinate after treatment with ultra high pressure. J Appl Microbiol. 2004; 96 : 162–169. 14678170
9. Nemecek JC, Wüthrich M, Klein BS. Global control of dimorphism and virulence in fungi. Science. 2006; 312 : 583–588. 16645097
10. Brown GD, Denning DW, Gow NAR, Levitz SM, Netea MG, White TC. Hidden killers: human fungal infections. Sci Transl Med. 2012; 4 : 165rv13–165rv13. doi: 10.1126/scitranslmed.3004404 23253612
11. Park BJ, Wannemuehler KA, Marston BJ, Govender N, Pappas PG, Chiller TM. Estimation of the current global burden of cryptococcal meningitis among persons living with HIV/AIDS: AIDS. 2009; 23 : 525–530. 19182676
12. Botts MR, Hull CM. Dueling in the lung: how Cryptococcus spores race the host for survival. Curr Opin Microbiol. 2010; 13 : 437–442. doi: 10.1016/j.mib.2010.05.003 20570552
13. Perfect JR, Casadevall A. Cryptococcosis. Infect Dis Clin North Am. 2002; 16 : 837–874, v–vi. 12512184
14. Kwon-Chung KJ. Morphogenesis of Filobasidiella neoformans, the sexual state of Cryptococcus neoformans. Mycologia. 1976; 68 : 821–833. 790172
15. Idnurm A. A tetrad analysis of the basidiomycete fungus Cryptococcus neoformans. Genetics. 2010; 185 : 153–163. doi: 10.1534/genetics.109.113027 20157004
16. Botts MR, Giles SS, Gates MA, Kozel TR, Hull CM. Isolation and characterization of Cryptococcus neoformans spores reveal a critical role for capsule biosynthesis genes in spore biogenesis. Eukaryot Cell. 2009; 8 : 595–605. doi: 10.1128/EC.00352-08 19181873
17. Velagapudi R, Hsueh Y-P, Geunes-Boyer S, Wright JR, Heitman J. Spores as infectious propagules of Cryptococcus neoformans. Infect Immun. 2009; 77 : 4345–4355. doi: 10.1128/IAI.00542-09 19620339
18. Giles SS, Dagenais TRT, Botts MR, Keller NP, Hull CM. Elucidating the pathogenesis of spores from the human fungal pathogen Cryptococcus neoformans. Infect Immun. 2009; 77 : 3491–3500. doi: 10.1128/IAI.00334-09 19451235
19. Gokce E, Franck WL, Oh Y, Dean RA, Muddiman DC. In-depth analysis of the Magnaporthe oryzae conidial proteome. J Proteome Res. 2012; 11 : 5827–5835. doi: 10.1021/pr300604s 23039028
20. Eigenheer RA, Lee YJ, Blumwald E, Phinney BS, Gelli A. Extracellular glycosylphosphatidylinositol-anchored mannoproteins and proteases of Cryptococcus neoformans. FEMS Yeast Res. 2007; 7 : 499–510. 17233760
21. Young M, Macias S, Thomas D, Wormley FL. A proteomic-based approach for the identification of immunodominant Cryptococcus neoformans proteins. PROTEOMICS. 2009; 9 : 2578–2588. doi: 10.1002/pmic.200800713 19343717
22. Santi L, Beys-da-Silva WO, Berger M, Calzolari D, Guimarães JA, Moresco JJ, et al. Proteomic profile of Cryptococcus neoformans biofilm reveals changes in metabolic processes. J Proteome Res. 2014; 13 : 1545–1559. doi: 10.1021/pr401075f 24467693
23. Huang DW, Sherman BT, Lempicki RA. Systematic and integrative analysis of large gene lists using DAVID bioinformatics resources. Nat Protoc. 2009; 4 : 44–57. doi: 10.1038/nprot.2008.211 19131956
24. Huang DW, Sherman BT, Lempicki RA. Bioinformatics enrichment tools: paths toward the comprehensive functional analysis of large gene lists. Nucleic Acids Res. 2009; 37 : 1–13. doi: 10.1093/nar/gkn923 19033363
25. Lundgren DH, Hwang S-I, Wu L, Han DK. Role of spectral counting in quantitative proteomics. Expert Rev Proteomics. 2010; 7 : 39–53. doi: 10.1586/epr.09.69 20121475
26. Chong HS, Campbell L, Padula MP, Hill C, Harry E, Li SS, et al. Time-course proteome analysis reveals the dynamic response of Cryptococcus gattii cells to fluconazole. PLoS ONE. 2012; 7: e42835. doi: 10.1371/journal.pone.0042835 22880118
27. Kurlandzka A, Rytka J, Gromadka R, Murawski M. A new essential gene located on Saccharomyces cerevisiae chromosome IX. Yeast. 1995; 11 : 885–890. 7483852
28. Weidenhammer EM, Singh M, Ruiz-Noriega M, Woolford JL. The PRP31 gene encodes a novel protein required for pre-mRNA splicing in Saccharomyces cerevisiae. Nucleic Acids Res. 1996; 24 : 1164–1170. 8604353
29. Schappert K, Friesen JD. Genetic studies of the PRP11 gene of Saccharomyces cerevisiae. Mol Gen Genet. 1991; 226 : 277–282. 2034220
30. Poeta MD, Toffaletti DL, Rude TH, Dykstra CC, Heitman J, Perfect JR. Topoisomerase I is essential in Cryptococcus neoformans: role in pathobiology and as an antifungal target. Genetics. 1999; 152 : 167–178. 10224251
31. Gerhold D, Thiyagarajan M, Kmiec EB. The topoisomerase I gene from Ustilago maydis: sequence, disruption and mutant phenotype. Nucleic Acids Res. 1994; 22 : 3773–3778. 7937091
32. Thrash C, Bankier AT, Barrell BG, Sternglanz R. Cloning, characterization, and sequence of the yeast DNA topoisomerase I gene. Proc Natl Acad Sci. 1985; 82 : 4374–4378. 2989818
33. Noir S, Colby T, Harzen A, Schmidt J, Panstruga R. A proteomic analysis of powdery mildew (Blumeria graminis f.sp. hordei) conidiospores. Mol Plant Pathol. 2009; 10 : 223–236. doi: 10.1111/j.1364-3703.2008.00524.x 19236571
34. Teutschbein J, Albrecht D, tsch M, Guthke R, Aimanianda V, Clavaud C, et al. Proteome profiling and functional classification of intracellular proteins from conidia of the human-pathogenic mold Aspergillus fumigatus. J Proteome Res. 2010; 9 : 3427–3442. doi: 10.1021/pr9010684 20507060
35. Oh YT, Ahn C-S, Kim JG, Ro H-S, Lee C-W, Kim JW. Proteomic analysis of early phase of conidia germination in Aspergillus nidulans. Fungal Genet Biol. 2010; 47 : 246–253. doi: 10.1016/j.fgb.2009.11.002 19919853
36. Cairns BR, Lorch Y, Li Y, Zhang M, Lacomis L, Erdjument-Bromage H, et al. RSC, an essential, abundant chromatin-remodeling complex. Cell. 1996; 87 : 1249–1260. 8980231
37. Hayles J, Wood V, Jeffery L, Hoe K-L, Kim D-U, Park H-O, et al. A genome-wide resource of cell cycle and cell shape genes of fission yeast. Open Biol. 2013; 3 : 130053–130053. doi: 10.1098/rsob.130053 23697806
38. Damelin M, Simon I, Moy TI, Wilson B, Komili S, Tempst P, et al. The genome-wide cocalization of Rsc9, a component of the RSC chromatin-remodeling complex, changes in response to stress. Mol Cell. 2002; 9 : 563–573. 11931764
39. Marguerat S, Schmidt A, Codlin S, Chen W, Aebersold R, Bähler J. Quantitative analysis of fission yeast transcriptomes and proteomes in proliferating and quiescent cells. Cell. 2012; 151 : 671–683. doi: 10.1016/j.cell.2012.09.019 23101633
40. Ianiri G, Idnurm A. Essential gene discovery in the basidiomycete Cryptococcus neoformans for antifungal drug target prioritization. mBio. 2015; 6: e02334–14. doi: 10.1128/mBio.02334-14 25827419
41. Trautwein M, Schindler C, Gauss R, Dengjel J, Hartmann E, Spang A. Arf1p, Chs5p and the ChAPs are required for export of specialized cargo from the Golgi. EMBO J. 2006; 25 : 943–954. 16498409
42. Steinberg G. Endocytosis and early endosome motility in filamentous fungi. Curr Opin Microbiol. 2014; 20 : 10–18. doi: 10.1016/j.mib.2014.04.001 24835422
43. Jin R, Dobry CJ, McCown PJ, Kumar A. Large-scale analysis of yeast filamentous growth by systematic gene disruption and overexpression. Mol Biol Cell. 2008; 19 : 284–296. 17989363
44. Feretzaki M, Heitman J. Genetic circuits that govern bisexual and unisexual reproduction in Cryptococcus neoformans. PLoS Genet. 2013; 9: e1003688. doi: 10.1371/journal.pgen.1003688 23966871
45. White RE, Dickinson JR, Semple CAM, Powell DJ, Berry C. The retroviral proteinase active site and the N-terminus of Ddi1 are required for repression of protein secretion. FEBS Lett. 2011; 585 : 139–142. doi: 10.1016/j.febslet.2010.11.026 21094643
46. Deutschbauer AM, Williams RM, Chu AM, Davis RW. Parallel phenotypic analysis of sporulation and postgermination growth in Saccharomyces cerevisiae. Proc Natl Acad Sci. 2002; 99 : 15530–15535. 12432101
47. Gómez-Herreros F, de Miguel-Jiménez L, Morillo-Huesca M, Delgado-Ramos L, Muñoz-Centeno MC, Chávez S. TFIIS is required for the balanced expression of the genes encoding ribosomal components under transcriptional stress. Nucleic Acids Res. 2012; 40 : 6508–6519. doi: 10.1093/nar/gks340 22544605
48. Jonikas MC, Collins SR, Denic V, Oh E, Quan EM, Schmid V, et al. Comprehensive characterization of genes required for protein folding in the endoplasmic reticulum. Science. 2009; 323 : 1693–1697. doi: 10.1126/science.1167983 19325107
49. Hauser M, Horn P, Tournu H, Hauser NC, Hoheisel JD, Brown AJP, et al. A transcriptome analysis of isoamyl alcohol-induced filamentation in yeast reveals a novel role for Gre2p as isovaleraldehyde reductase. FEMS Yeast Res. 2007; 7 : 84–92. 16999827
50. Marston AL, Tham W-H, Shah H, Amon A. A genome-wide screen identifies genes required for centromeric cohesion. Science. 2004; 303 : 1367–1370. 14752166
51. Hodges PE, Beggs JD. RNA Splicing: U2 fulfills a commitment. Curr Biol. 1994; 4 : 264–267. 7922333
52. Stevens SW, Abelson J. Purification of the yeast U4/U6•U5 small nuclear ribonucleoprotein particle and identification of its proteins. Proc Natl Acad Sci. 1999; 96 : 7226–7231. 10377396
53. Kelley LA, Sternberg MJE. Protein structure prediction on the Web: a case study using the Phyre server. Nat Protoc. 2009; 4 : 363–371. doi: 10.1038/nprot.2009.2 19247286
54. Strich R, Khakhina S, Mallory MJ. Ume6p is required for germination and early colony development of yeast ascospores. FEMS Yeast Res. 2011; 11 : 104–113. doi: 10.1111/j.1567-1364.2010.00696.x 21059190
55. Kloimwieder A, Winston F. A screen for germination mutants in Saccharomyces cerevisiae. G3. 2011; 1 : 143–149. doi: 10.1534/g3.111.000323 22384326
56. Kwon-Chung KJ, Edman JC, Wickes BL. Genetic association of mating types and virulence in Cryptococcus neoformans. Infect Immun. 1992; 60 : 602–605. 1730495
57. Moore TD, Edman JC. The alpha-mating type locus of Cryptococcus neoformans contains a peptide pheromone gene. Mol Cell Biol. 1993; 13 : 1962–1970. 8441425
58. Sherman F. Getting started with yeast. Methods Enzymol. 2002; 350 : 3–41. 12073320
59. Alspaugh JA, Perfect JR, Heitman J. Signal transduction pathways regulating differentiation and pathogenicity of Cryptococcus neoformans. Fungal Genet Biol. 1998; 25 : 1–14. 9806801
60. Isaacson T, Damasceno CMB, Saravanan RS, He Y, Catalá C, Saladié M, et al. Sample extraction techniques for enhanced proteomic analysis of plant tissues. Nat Protoc. 2006; 1 : 769–774. 17406306
61. Ausubel FM, Brent R, Kingston RE, Moore DD, Seidman JG, Struhl K. Current Protocols in Molecular Biology. John Wiley & Sons; 1988.
62. Wilkins MR, Gasteiger E, Bairoch A, Sanchez JC, Williams KL, Appel RD, et al. Protein identification and analysis tools in the ExPASy server. Methods Mol Biol. 1999; 112 : 531–552. 10027275
63. Sonnhammer EL, von Heijne G, Krogh A. A hidden Markov model for predicting transmembrane helices in protein sequences. Proc Int Conf Intell Syst Mol Biol. 1998; 6 : 175–182. 9783223
64. Horton P, Park K-J, Obayashi T, Fujita N, Harada H, Adams-Collier CJ, et al. WoLF PSORT: protein localization predictor. Nucleic Acids Res. 2007; 35: W585–W587. 17517783
65. Conesa A, Götz S, García-Gómez JM, Terol J, Talón M, Robles M. Blast2GO: a universal tool for annotation, visualization and analysis in functional genomics research. Bioinformatics. 2005; 21 : 3674–3676. 16081474
66. Cox B, Kislinger T, Emili A. Integrating gene and protein expression data: pattern analysis and profile mining. Methods. 2005; 35 : 303–314. 15722226
67. Davidson RC, Blankenship JR, Kraus PR, de J Berrios M, Hull CM, D’Souza C, et al. A PCR-based strategy to generate integrative targeting alleles with large regions of homology. Microbiology. 2002; 148 : 2607–2615. 12177355
68. Toffaletti DL, Rude TH, Johnston SA, Durack DT, Perfect JR. Gene transfer in Cryptococcus neoformans by use of biolistic delivery of DNA. J Bacteriol. 1993; 175 : 1405–1411. 8444802
69. Treco DA, Winston F. Growth and manipulation of yeast. Current Protocols in Molecular Biology. John Wiley & Sons, Inc.; 2001.
Štítky
Genetika Reprodukčná medicína
Článek Loss and Gain of Natural Killer Cell Receptor Function in an African Hunter-Gatherer PopulationČlánek Let-7 Represses Carcinogenesis and a Stem Cell Phenotype in the Intestine via Regulation of Hmga2Článek Binding of Multiple Rap1 Proteins Stimulates Chromosome Breakage Induction during DNA ReplicationČlánek SLIRP Regulates the Rate of Mitochondrial Protein Synthesis and Protects LRPPRC from DegradationČlánek The Formin Diaphanous Regulates Myoblast Fusion through Actin Polymerization and Arp2/3 RegulationČlánek Runx1 Transcription Factor Is Required for Myoblasts Proliferation during Muscle Regeneration
Článok vyšiel v časopisePLOS Genetics
Najčítanejšie tento týždeň
2015 Číslo 8- 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
- Putting the Brakes on Huntington Disease in a Mouse Experimental Model
- Identification of Driving Fusion Genes and Genomic Landscape of Medullary Thyroid Cancer
- Evidence for Retromutagenesis as a Mechanism for Adaptive Mutation in
- TSPO, a Mitochondrial Outer Membrane Protein, Controls Ethanol-Related Behaviors in
- Evidence for Lysosome Depletion and Impaired Autophagic Clearance in Hereditary Spastic Paraplegia Type SPG11
- Loss and Gain of Natural Killer Cell Receptor Function in an African Hunter-Gatherer Population
- Trans-Reactivation: A New Epigenetic Phenomenon Underlying Transcriptional Reactivation of Silenced Genes
- Early Developmental and Evolutionary Origins of Gene Body DNA Methylation Patterns in Mammalian Placentas
- Strong Selective Sweeps on the X Chromosome in the Human-Chimpanzee Ancestor Explain Its Low Divergence
- Dominance of Deleterious Alleles Controls the Response to a Population Bottleneck
- Transient 1a Induction Defines the Wound Epidermis during Zebrafish Fin Regeneration
- Systems Genetics Reveals the Functional Context of PCOS Loci and Identifies Genetic and Molecular Mechanisms of Disease Heterogeneity
- A Genome Scale Screen for Mutants with Delayed Exit from Mitosis: Ire1-Independent Induction of Autophagy Integrates ER Homeostasis into Mitotic Lifespan
- Non-synonymous FGD3 Variant as Positional Candidate for Disproportional Tall Stature Accounting for a Carcass Weight QTL () and Skeletal Dysplasia in Japanese Black Cattle
- The Relationship between Gene Network Structure and Expression Variation among Individuals and Species
- Calmodulin Methyltransferase Is Required for Growth, Muscle Strength, Somatosensory Development and Brain Function
- The Wnt Frizzled Receptor MOM-5 Regulates the UNC-5 Netrin Receptor through Small GTPase-Dependent Signaling to Determine the Polarity of Migrating Cells
- Nbs1 ChIP-Seq Identifies Off-Target DNA Double-Strand Breaks Induced by AID in Activated Splenic B Cells
- CCNYL1, but Not CCNY, Cooperates with CDK16 to Regulate Spermatogenesis in Mouse
- Evidence for a Common Origin of Blacksmiths and Cultivators in the Ethiopian Ari within the Last 4500 Years: Lessons for Clustering-Based Inference
- Of Fighting Flies, Mice, and Men: Are Some of the Molecular and Neuronal Mechanisms of Aggression Universal in the Animal Kingdom?
- Hypoxia and Temperature Regulated Morphogenesis in
- The Homeodomain Iroquois Proteins Control Cell Cycle Progression and Regulate the Size of Developmental Fields
- Evolution and Design Governing Signal Precision and Amplification in a Bacterial Chemosensory Pathway
- Rac1 Regulates Endometrial Secretory Function to Control Placental Development
- Let-7 Represses Carcinogenesis and a Stem Cell Phenotype in the Intestine via Regulation of Hmga2
- Functions as a Positive Regulator of Growth and Metabolism in
- The Nucleosome Acidic Patch Regulates the H2B K123 Monoubiquitylation Cascade and Transcription Elongation in
- Rhoptry Proteins ROP5 and ROP18 Are Major Murine Virulence Factors in Genetically Divergent South American Strains of
- Exon 7 Contributes to the Stable Localization of Xist RNA on the Inactive X-Chromosome
- Regulates Refractive Error and Myopia Development in Mice and Humans
- mTORC1 Prevents Preosteoblast Differentiation through the Notch Signaling Pathway
- Regulation of Gene Expression Patterns in Mosquito Reproduction
- Molecular Basis of Gene-Gene Interaction: Cyclic Cross-Regulation of Gene Expression and Post-GWAS Gene-Gene Interaction Involved in Atrial Fibrillation
- The Spalt Transcription Factors Generate the Transcriptional Landscape of the Wing Pouch Central Region
- Binding of Multiple Rap1 Proteins Stimulates Chromosome Breakage Induction during DNA Replication
- Functional Divergence in the Role of N-Linked Glycosylation in Smoothened Signaling
- YAP1 Exerts Its Transcriptional Control via TEAD-Mediated Activation of Enhancers
- Coordinated Evolution of Influenza A Surface Proteins
- The Evolutionary Potential of Phenotypic Mutations
- Genome-Wide Association and Trans-ethnic Meta-Analysis for Advanced Diabetic Kidney Disease: Family Investigation of Nephropathy and Diabetes (FIND)
- New Routes to Phylogeography: A Bayesian Structured Coalescent Approximation
- SLIRP Regulates the Rate of Mitochondrial Protein Synthesis and Protects LRPPRC from Degradation
- Satellite DNA Modulates Gene Expression in the Beetle after Heat Stress
- SHOEBOX Modulates Root Meristem Size in Rice through Dose-Dependent Effects of Gibberellins on Cell Elongation and Proliferation
- Reduced Crossover Interference and Increased ZMM-Independent Recombination in the Absence of Tel1/ATM
- Suppression of Somatic Expansion Delays the Onset of Pathophysiology in a Mouse Model of Huntington’s Disease
- Protein Composition of Infectious Spores Reveals Novel Sexual Development and Germination Factors in
- The Evolutionarily Conserved LIM Homeodomain Protein LIM-4/LHX6 Specifies the Terminal Identity of a Cholinergic and Peptidergic . Sensory/Inter/Motor Neuron-Type
- SmD1 Modulates the miRNA Pathway Independently of Its Pre-mRNA Splicing Function
- piRNAs Are Associated with Diverse Transgenerational Effects on Gene and Transposon Expression in a Hybrid Dysgenic Syndrome of .
- Retinoic Acid Signaling Regulates Differential Expression of the Tandemly-Duplicated Long Wavelength-Sensitive Cone Opsin Genes in Zebrafish
- The Formin Diaphanous Regulates Myoblast Fusion through Actin Polymerization and Arp2/3 Regulation
- Genome-Wide Analysis of PAPS1-Dependent Polyadenylation Identifies Novel Roles for Functionally Specialized Poly(A) Polymerases in
- Runx1 Transcription Factor Is Required for Myoblasts Proliferation during Muscle Regeneration
- Regulation of Mutagenic DNA Polymerase V Activation in Space and Time
- Variability of Gene Expression Identifies Transcriptional Regulators of Early Human Embryonic Development
- The Drosophila Gene Interacts Genetically with and Shows Female-Specific Effects of Divergence
- Functional Activation of the Flagellar Type III Secretion Export Apparatus
- Retrohoming of a Mobile Group II Intron in Human Cells Suggests How Eukaryotes Limit Group II Intron Proliferation
- PLOS Genetics
- Archív čísel
- Aktuálne číslo
- Informácie o časopise
Najčítanejšie v tomto čísle- Exon 7 Contributes to the Stable Localization of Xist RNA on the Inactive X-Chromosome
- YAP1 Exerts Its Transcriptional Control via TEAD-Mediated Activation of Enhancers
- SmD1 Modulates the miRNA Pathway Independently of Its Pre-mRNA Splicing Function
- Molecular Basis of Gene-Gene Interaction: Cyclic Cross-Regulation of Gene Expression and Post-GWAS Gene-Gene Interaction Involved in Atrial Fibrillation
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