-
Články
- Časopisy
- Kurzy
- Témy
- Kongresy
- Videa
- Podcasty
HAL-2 Promotes Homologous Pairing during Meiosis by Antagonizing Inhibitory Effects of Synaptonemal Complex Precursors
During meiosis, chromosomes align with their homologous pairing partners and stabilize this alignment through assembly of the synaptonemal complex (SC). Since the SC assembles cooperatively yet is indifferent to homology, pairing and SC assembly must be tightly coordinated. We identify HAL-2 as a key mediator in this coordination, showing that HAL-2 promotes pairing largely by preventing detrimental effects of SC precursors (SYP proteins). hal-2 mutants fail to establish pairing and lack multiple markers of chromosome movement mediated by pairing centers (PCs), chromosome sites that link chromosomes to cytoplasmic microtubules through nuclear envelope-spanning complexes. Moreover, SYP proteins load inappropriately along individual unpaired chromosomes in hal-2 mutants, and markers of PC-dependent movement and function are restored in hal-2; syp double mutants. These and other data indicate that SYP proteins can impede pairing and that HAL-2 promotes pairing predominantly but not exclusively by counteracting this inhibition, thereby enabling activation and regulation of PC function. HAL-2 concentrates in the germ cell nucleoplasm and colocalizes with SYP proteins in nuclear aggregates when SC assembly is prevented. We propose that HAL-2 functions to shepherd SYP proteins prior to licensing of SC assembly, preventing untimely interactions between SC precursors and chromosomes and allowing sufficient accumulation of precursors for rapid cooperative assembly upon homology verification.
Vyšlo v časopise: HAL-2 Promotes Homologous Pairing during Meiosis by Antagonizing Inhibitory Effects of Synaptonemal Complex Precursors. PLoS Genet 8(8): e32767. doi:10.1371/journal.pgen.1002880
Kategorie: Research Article
prolekare.web.journal.doi_sk: https://doi.org/10.1371/journal.pgen.1002880Souhrn
During meiosis, chromosomes align with their homologous pairing partners and stabilize this alignment through assembly of the synaptonemal complex (SC). Since the SC assembles cooperatively yet is indifferent to homology, pairing and SC assembly must be tightly coordinated. We identify HAL-2 as a key mediator in this coordination, showing that HAL-2 promotes pairing largely by preventing detrimental effects of SC precursors (SYP proteins). hal-2 mutants fail to establish pairing and lack multiple markers of chromosome movement mediated by pairing centers (PCs), chromosome sites that link chromosomes to cytoplasmic microtubules through nuclear envelope-spanning complexes. Moreover, SYP proteins load inappropriately along individual unpaired chromosomes in hal-2 mutants, and markers of PC-dependent movement and function are restored in hal-2; syp double mutants. These and other data indicate that SYP proteins can impede pairing and that HAL-2 promotes pairing predominantly but not exclusively by counteracting this inhibition, thereby enabling activation and regulation of PC function. HAL-2 concentrates in the germ cell nucleoplasm and colocalizes with SYP proteins in nuclear aggregates when SC assembly is prevented. We propose that HAL-2 functions to shepherd SYP proteins prior to licensing of SC assembly, preventing untimely interactions between SC precursors and chromosomes and allowing sufficient accumulation of precursors for rapid cooperative assembly upon homology verification.
Zdroje
1. Mlynarczyk-Evans S, Villeneuve AM (2010) Homologous chromosome pairing and synapsis during oogenesis. In: Verlhac M-H, Villeneuve AM, editors. Oogenesis: The Universal Process. Chichester, West Sussex, UK: Wiley-Blackwell. pp. 117–140.
2. de BoerE, HeytingC (2006) The diverse roles of transverse filaments of synaptonemal complexes in meiosis. Chromosoma 115 : 220–234.
3. OllingerR, AlsheimerM, BenaventeR (2005) Mammalian protein SCP1 forms synaptonemal complex-like structures in the absence of meiotic chromosomes. Mol Biol Cell 16 : 212–217.
4. GoldsteinP (1987) Multiple synaptonemal complexes (polycomplexes): origin, structure and function. Cell Biol Int Rep 11 : 759–796.
5. JeffressJK, PageSL, RoyerSK, BeldenED, BlumenstielJP, et al. (2007) The formation of the central element of the synaptonemal complex may occur by multiple mechanisms: the roles of the N - and C-terminal domains of the Drosophila C(3)G protein in mediating synapsis and recombination. Genetics 177 : 2445–2456.
6. SymM, RoederGS (1995) Zip1-induced changes in synaptonemal complex structure and polycomplex assembly. J Cell Biol 128 : 455–466.
7. VilleneuveAM (1994) A cis-acting locus that promotes crossing over between X chromosomes in Caenorhabditis elegans. Genetics 136 : 887–902.
8. MacQueenAJ, PhillipsCM, BhallaN, WeiserP, VilleneuveAM, et al. (2005) Chromosome sites play dual roles to establish homologous synapsis during meiosis in C. elegans. Cell 123 : 1037–1050.
9. McKimKS, PetersK, RoseAM (1993) Two types of sites required for meiotic chromosome pairing in Caenorhabditis elegans. Genetics 134 : 749–768.
10. MacQueenAJ, ColaiacovoMP, McDonaldK, VilleneuveAM (2002) Synapsis-dependent and -independent mechanisms stabilize homolog pairing during meiotic prophase in C. elegans. Genes Dev 16 : 2428–2442.
11. MinnIL, RollsMM, Hanna-RoseW, MaloneCJ (2009) SUN-1 and ZYG-12, mediators of centrosome-nucleus attachment, are a functional SUN/KASH pair in Caenorhabditis elegans. Mol Biol Cell 20 : 4586–4595.
12. PhillipsCM, DernburgAF (2006) A family of zinc-finger proteins is required for chromosome-specific pairing and synapsis during meiosis in C. elegans. Dev Cell 11 : 817–829.
13. PhillipsCM, WongC, BhallaN, CarltonPM, WeiserP, et al. (2005) HIM-8 binds to the X chromosome pairing center and mediates chromosome-specific meiotic synapsis. Cell 123 : 1051–1063.
14. SatoA, IsaacB, PhillipsCM, RilloR, CarltonPM, et al. (2009) Cytoskeletal forces span the nuclear envelope to coordinate meiotic chromosome pairing and synapsis. Cell 139 : 907–919.
15. PenknerAM, FridkinA, GloggnitzerJ, BaudrimontA, MachacekT, et al. (2009) Meiotic chromosome homology search involves modifications of the nuclear envelope protein Matefin/SUN-1. Cell 139 : 920–933.
16. PenknerA, TangL, NovatchkovaM, LadurnerM, FridkinA, et al. (2007) The nuclear envelope protein Matefin/SUN-1 is required for homologous pairing in C. elegans meiosis. Dev Cell 12 : 873–885.
17. MaloneCJ, MisnerL, Le BotN, TsaiMC, CampbellJM, et al. (2003) The C. elegans hook protein, ZYG-12, mediates the essential attachment between the centrosome and nucleus. Cell 115 : 825–836.
18. Martinez-PerezE, VilleneuveAM (2005) HTP-1-dependent constraints coordinate homolog pairing and synapsis and promote chiasma formation during C. elegans meiosis. Genes Dev 19 : 2727–2743.
19. KellyKO, DernburgAF, StanfieldGM, VilleneuveAM (2000) Caenorhabditis elegans msh-5 is required for both normal and radiation-induced meiotic crossing over but not for completion of meiosis. Genetics 156 : 617–630.
20. MacQueenAJ, VilleneuveAM (2001) Nuclear reorganization and homologous chromosome pairing during meiotic prophase require C. elegans chk-2. Genes Dev 15 : 1674–1687.
21. BaudrimontA, PenknerA, WoglarA, MachacekT, WegrostekC, et al. (2010) Leptotene/zygotene chromosome movement via the SUN/KASH protein bridge in Caenorhabditis elegans. PLoS Genet 6: e1001219 doi:10.1371/journal.pgen.1001219.
22. WynneDJ, RogO, CarltonPM, DernburgAF (2012) Dynein-dependent processive chromosome motions promote homologous pairing in C. elegans meiosis. J Cell Biol 196 : 47–64.
23. HodgkinJ, HorvitzHR, BrennerS (1979) Nondisjunction mutants of the nematode CAENORHABDITIS ELEGANS. Genetics 91 : 67–94.
24. LabellaS, WoglarA, JantschV, ZetkaM (2011) Polo kinases establish links between meiotic chromosomes and cytoskeletal forces essential for homolog pairing. Dev Cell 21 : 948–958.
25. HarperNC, RilloR, Jover-GilS, AssafZJ, BhallaN, et al. (2011) Pairing centers recruit a Polo-like kinase to orchestrate meiotic chromosome dynamics in C. elegans. Dev Cell 21 : 934–947.
26. CouteauF, NabeshimaK, VilleneuveA, ZetkaM (2004) A component of C. elegans meiotic chromosome axes at the interface of homolog alignment, synapsis, nuclear reorganization, and recombination. Curr Biol 14 : 585–592.
27. GoodyerW, KaitnaS, CouteauF, WardJD, BoultonSJ, et al. (2008) HTP-3 links DSB formation with homolog pairing and crossing over during C. elegans meiosis. Dev Cell 14 : 263–274.
28. SmolikovS, EizingerA, Schild-PrufertK, HurlburtA, McDonaldK, et al. (2007) SYP-3 restricts synaptonemal complex assembly to bridge paired chromosome axes during meiosis in Caenorhabditis elegans. Genetics 176 : 2015–2025.
29. Schild-PrufertK, SaitoTT, SmolikovS, GuY, HincapieM, et al. (2011) Organization of the synaptonemal complex during meiosis in Caenorhabditis elegans. Genetics 189 : 411–421.
30. GustafssonMG, ShaoL, CarltonPM, WangCJ, GolubovskayaIN, et al. (2008) Three-dimensional resolution doubling in wide-field fluorescence microscopy by structured illumination. Biophys J 94 : 4957–4970.
31. XuH, BeasleyMD, WarrenWD, van der HorstGT, McKayMJ (2005) Absence of mouse REC8 cohesin promotes synapsis of sister chromatids in meiosis. Dev Cell 8 : 949–961.
32. JinH, GuacciV, YuHG (2009) Pds5 is required for homologue pairing and inhibits synapsis of sister chromatids during yeast meiosis. J Cell Biol 186 : 713–725.
33. CouteauF, ZetkaM (2005) HTP-1 coordinates synaptonemal complex assembly with homolog alignment during meiosis in C. elegans. Genes Dev 19 : 2744–2756.
34. ColaiacovoMP, MacQueenAJ, Martinez-PerezE, McDonaldK, AdamoA, et al. (2003) Synaptonemal complex assembly in C. elegans is dispensable for loading strand-exchange proteins but critical for proper completion of recombination. Dev Cell 5 : 463–474.
35. SmolikovS, Schild-PrufertK, ColaiacovoMP (2009) A yeast two-hybrid screen for SYP-3 interactors identifies SYP-4, a component required for synaptonemal complex assembly and chiasma formation in Caenorhabditis elegans meiosis. PLoS Genet 5: e1000669 doi:10.1371/journal.pgen.1000669.
36. NabeshimaK, Mlynarczyk-EvansS, VilleneuveAM (2011) Chromosome painting reveals asynaptic full alignment of homologs and HIM-8-dependent remodeling of X chromosome territories during Caenorhabditis elegans meiosis. PLoS Genet 7: e1002231 doi:10.1371/journal.pgen.1002231.
37. Martinez-PerezE, SchvarzsteinM, BarrosoC, LightfootJ, DernburgAF, et al. (2008) Crossovers trigger a remodeling of meiotic chromosome axis composition that is linked to two-step loss of sister chromatid cohesion. Genes Dev 22 : 2886–2901.
38. NabeshimaK, VilleneuveAM, ColaiacovoMP (2005) Crossing over is coupled to late meiotic prophase bivalent differentiation through asymmetric disassembly of the SC. J Cell Biol 168 : 683–689.
39. McDonnellAV, JiangT, KeatingAE, BergerB (2006) Paircoil2: improved prediction of coiled coils from sequence. Bioinformatics 22 : 356–358.
40. LupasA, Van DykeM, StockJ (1991) Predicting coiled coils from protein sequences. Science 252 : 1162–1164.
41. WangF, YoderJ, AntoshechkinI, HanM (2003) Caenorhabditis elegans EVL-14/PDS-5 and SCC-3 are essential for sister chromatid cohesion in meiosis and mitosis. Mol Cell Biol 23 : 7698–7707.
42. SeversonAF, LingL, van ZuylenV, MeyerBJ (2009) The axial element protein HTP-3 promotes cohesin loading and meiotic axis assembly in C. elegans to implement the meiotic program of chromosome segregation. Genes Dev 23 : 1763–1778.
43. AlpiA, PasierbekP, GartnerA, LoidlJ (2003) Genetic and cytological characterization of the recombination protein RAD-51 in Caenorhabditis elegans. Chromosoma 112 : 6–16.
44. SmolikovS, EizingerA, HurlburtA, RogersE, VilleneuveAM, et al. (2007) Synapsis-defective mutants reveal a correlation between chromosome conformation and the mode of double-strand break repair during Caenorhabditis elegans meiosis. Genetics 176 : 2027–2033.
45. TangL, MachacekT, MamnunYM, PenknerA, GloggnitzerJ, et al. (2010) Mutations in Caenorhabditis elegans him-19 show meiotic defects that worsen with age. Mol Biol Cell 21 : 885–896.
46. BornerGV, BarotA, KlecknerN (2008) Yeast Pch2 promotes domainal axis organization, timely recombination progression, and arrest of defective recombinosomes during meiosis. Proc Natl Acad Sci U S A 105 : 3327–3332.
47. WojtaszL, DanielK, RoigI, Bolcun-FilasE, XuH, et al. (2009) Mouse HORMAD1 and HORMAD2, two conserved meiotic chromosomal proteins, are depleted from synapsed chromosome axes with the help of TRIP13 AAA-ATPase. PLoS Genet 5: e1000702 doi:10.1371/journal.pgen.1000702.
48. MacQueenAJ, RoederGS (2009) Fpr3 and Zip3 ensure that initiation of meiotic recombination precedes chromosome synapsis in budding yeast. Curr Biol 19 : 1519–1526.
49. SmolikovS, Schild-PrufertK, ColaiacovoMP (2008) CRA-1 uncovers a double-strand break-dependent pathway promoting the assembly of central region proteins on chromosome axes during C. elegans meiosis. PLoS Genet 4: e1000088 doi:10.1371/journal.pgen.1000088.
50. PolevodaB, NorbeckJ, TakakuraH, BlombergA, ShermanF (1999) Identification and specificities of N-terminal acetyltransferases from Saccharomyces cerevisiae. EMBO J 18 : 6155–6168.
51. PolevodaB, ShermanF (2003) N-terminal acetyltransferases and sequence requirements for N-terminal acetylation of eukaryotic proteins. J Mol Biol 325 : 595–622.
52. BrennerS (1974) The genetics of Caenorhabditis elegans. Genetics 77 : 71–94.
53. WicksSR, YehRT, GishWR, WaterstonRH, PlasterkRH (2001) Rapid gene mapping in Caenorhabditis elegans using a high density polymorphism map. Nat Genet 28 : 160–164.
54. ChenH, HughesDD, ChanTA, SedatJW, AgardDA (1996) IVE (Image Visualization Environment): a software platform for all three-dimensional microscopy applications. J Struct Biol 116 : 56–60.
55. DernburgAF, McDonaldK, MoulderG, BarsteadR, DresserM, et al. (1998) Meiotic recombination in C. elegans initiates by a conserved mechanism and is dispensable for homologous chromosome synapsis. Cell 94 : 387–398.
Štítky
Genetika Reprodukčná medicína
Článek Mutational Signatures of De-Differentiation in Functional Non-Coding Regions of Melanoma GenomesČlánek Rescuing Alu: Recovery of Inserts Shows LINE-1 Preserves Alu Activity through A-Tail ExpansionČlánek Genetics and Regulatory Impact of Alternative Polyadenylation in Human B-Lymphoblastoid CellsČlánek Retrovolution: HIV–Driven Evolution of Cellular Genes and Improvement of Anticancer Drug ActivationČlánek The Mi-2 Chromatin-Remodeling Factor Regulates Higher-Order Chromatin Structure and Cohesin DynamicsČlánek Identification of Human Proteins That Modify Misfolding and Proteotoxicity of Pathogenic Ataxin-1
Článok vyšiel v časopisePLOS Genetics
Najčítanejšie tento týždeň
2012 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
- Mutational Signatures of De-Differentiation in Functional Non-Coding Regions of Melanoma Genomes
- Rescuing Alu: Recovery of Inserts Shows LINE-1 Preserves Alu Activity through A-Tail Expansion
- Genetics and Regulatory Impact of Alternative Polyadenylation in Human B-Lymphoblastoid Cells
- Chromosome Territories Meet a Condensin
- It's All in the Timing: Too Much E2F Is a Bad Thing
- Fine-Mapping and Initial Characterization of QT Interval Loci in African Americans
- Genome Patterns of Selection and Introgression of Haplotypes in Natural Populations of the House Mouse ()
- A Combinatorial Amino Acid Code for RNA Recognition by Pentatricopeptide Repeat Proteins
- Advances in Quantitative Trait Analysis in Yeast
- Experimental Evolution of a Novel Sexually Antagonistic Allele
- Variation of Contributes to Dog Breed Skull Diversity
- , a Gene Involved in Axonal Pathfinding, Is Mutated in Patients with Kallmann Syndrome
- A Single Origin for Nymphalid Butterfly Eyespots Followed by Widespread Loss of Associated Gene Expression
- Cryptocephal, the ATF4, Is a Specific Coactivator for Ecdysone Receptor Isoform B2
- Retrovolution: HIV–Driven Evolution of Cellular Genes and Improvement of Anticancer Drug Activation
- The PARN Deadenylase Targets a Discrete Set of mRNAs for Decay and Regulates Cell Motility in Mouse Myoblasts
- A Sexual Ornament in Chickens Is Affected by Pleiotropic Alleles at and , Selected during Domestication
- Use of Allele-Specific FAIRE to Determine Functional Regulatory Polymorphism Using Large-Scale Genotyping Arrays
- Novel Loci for Metabolic Networks and Multi-Tissue Expression Studies Reveal Genes for Atherosclerosis
- The Genetic Basis of Pollinator Adaptation in a Sexually Deceptive Orchid
- Uncovering the Genome-Wide Transcriptional Responses of the Filamentous Fungus to Lignocellulose Using RNA Sequencing
- Inheritance Beyond Plain Heritability: Variance-Controlling Genes in
- The Metabochip, a Custom Genotyping Array for Genetic Studies of Metabolic, Cardiovascular, and Anthropometric Traits
- Reprogramming to Pluripotency Can Conceal Somatic Cell Chromosomal Instability
- Condensin II Promotes the Formation of Chromosome Territories by Inducing Axial Compaction of Polyploid Interphase Chromosomes
- PTEN Negatively Regulates MAPK Signaling during Vulval Development
- A Dynamic Response Regulator Protein Modulates G-Protein–Dependent Polarity in the Bacterium
- Population Genomics of the Facultatively Mutualistic Bacteria and
- Components of a Fanconi-Like Pathway Control Pso2-Independent DNA Interstrand Crosslink Repair in Yeast
- Polysome Profiling in Liver Identifies Dynamic Regulation of Endoplasmic Reticulum Translatome by Obesity and Fasting
- Stromal Liver Kinase B1 [STK11] Signaling Loss Induces Oviductal Adenomas and Endometrial Cancer by Activating Mammalian Target of Rapamycin Complex 1
- Reprogramming of H3K27me3 Is Critical for Acquisition of Pluripotency from Cultured Tissues
- Transgene Induced Co-Suppression during Vegetative Growth in
- Hox and Sex-Determination Genes Control Segment Elimination through EGFR and Activity
- A Quantitative Comparison of the Similarity between Genes and Geography in Worldwide Human Populations
- Minibrain/Dyrk1a Regulates Food Intake through the Sir2-FOXO-sNPF/NPY Pathway in and Mammals
- Comparative Analysis of Regulatory Elements between and by Genome-Wide Transcription Start Site Profiling
- Simple Methods for Generating and Detecting Locus-Specific Mutations Induced with TALENs in the Zebrafish Genome
- S Phase–Coupled E2f1 Destruction Ensures Homeostasis in Proliferating Tissues
- Cell-Nonautonomous Signaling of FOXO/DAF-16 to the Stem Cells of
- The Mi-2 Chromatin-Remodeling Factor Regulates Higher-Order Chromatin Structure and Cohesin Dynamics
- Comparative Analysis of the Genomes of Two Field Isolates of the Rice Blast Fungus
- Role of Mex67-Mtr2 in the Nuclear Export of 40S Pre-Ribosomes
- Genetic Modulation of Lipid Profiles following Lifestyle Modification or Metformin Treatment: The Diabetes Prevention Program
- HAL-2 Promotes Homologous Pairing during Meiosis by Antagonizing Inhibitory Effects of Synaptonemal Complex Precursors
- SLX-1 Is Required for Maintaining Genomic Integrity and Promoting Meiotic Noncrossovers in the Germline
- Phylogenetic and Transcriptomic Analysis of Chemosensory Receptors in a Pair of Divergent Ant Species Reveals Sex-Specific Signatures of Odor Coding
- Reduced Prostasin (CAP1/PRSS8) Activity Eliminates HAI-1 and HAI-2 Deficiency–Associated Developmental Defects by Preventing Matriptase Activation
- Dissecting the Gene Network of Dietary Restriction to Identify Evolutionarily Conserved Pathways and New Functional Genes
- Identification of Human Proteins That Modify Misfolding and Proteotoxicity of Pathogenic Ataxin-1
- and Link Transcription of Phospholipid Biosynthetic Genes to ER Stress and the UPR
- CDK9 and H2B Monoubiquitination: A Well-Choreographed Dance
- Rare Copy Number Variations in Adults with Tetralogy of Fallot Implicate Novel Risk Gene Pathways
- Ccdc94 Protects Cells from Ionizing Radiation by Inhibiting the Expression of
- NOL11, Implicated in the Pathogenesis of North American Indian Childhood Cirrhosis, Is Required for Pre-rRNA Transcription and Processing
- Human Developmental Enhancers Conserved between Deuterostomes and Protostomes
- A Luminal Glycoprotein Drives Dose-Dependent Diameter Expansion of the Hindgut Tube
- Melanophore Migration and Survival during Zebrafish Adult Pigment Stripe Development Require the Immunoglobulin Superfamily Adhesion Molecule Igsf11
- Dynamic Distribution of Linker Histone H1.5 in Cellular Differentiation
- Combining Comparative Proteomics and Molecular Genetics Uncovers Regulators of Synaptic and Axonal Stability and Degeneration
- Chemical Genetics Reveals a Specific Requirement for Cdk2 Activity in the DNA Damage Response and Identifies Nbs1 as a Cdk2 Substrate in Human Cells
- Experimental Relocation of the Mitochondrial Gene to the Nucleus Reveals Forces Underlying Mitochondrial Genome Evolution
- Rates of Gyrase Supercoiling and Transcription Elongation Control Supercoil Density in a Bacterial Chromosome
- Mutations in a P-Type ATPase Gene Cause Axonal Degeneration
- A General G1/S-Phase Cell-Cycle Control Module in the Flowering Plant
- Multiple Roles and Interactions of and in Development of the Respiratory System
- UNC-40/DCC, SAX-3/Robo, and VAB-1/Eph Polarize F-Actin during Embryonic Morphogenesis by Regulating the WAVE/SCAR Actin Nucleation Complex
- Epigenetic Remodeling of Meiotic Crossover Frequency in DNA Methyltransferase Mutants
- Modulating the Strength and Threshold of NOTCH Oncogenic Signals by
- Loss of Axonal Mitochondria Promotes Tau-Mediated Neurodegeneration and Alzheimer's Disease–Related Tau Phosphorylation Via PAR-1
- Acetyl-CoA-Carboxylase Sustains a Fatty Acid–Dependent Remote Signal to Waterproof the Respiratory System
- ATXN2-CAG42 Sequesters PABPC1 into Insolubility and Induces FBXW8 in Cerebellum of Old Ataxic Knock-In Mice
- Cohesin Rings Devoid of Scc3 and Pds5 Maintain Their Stable Association with the DNA
- The MicroRNA Inhibits Calcium Signaling by Targeting the TIR-1/Sarm1 Adaptor Protein to Control Stochastic L/R Neuronal Asymmetry in
- Rapid-Throughput Skeletal Phenotyping of 100 Knockout Mice Identifies 9 New Genes That Determine Bone Strength
- The Genes Define Unique Classes of Two-Partner Secretion and Contact Dependent Growth Inhibition Systems
- PLOS Genetics
- Archív čísel
- Aktuálne číslo
- Informácie o časopise
Najčítanejšie v tomto čísle- Dissecting the Gene Network of Dietary Restriction to Identify Evolutionarily Conserved Pathways and New Functional Genes
- It's All in the Timing: Too Much E2F Is a Bad Thing
- Variation of Contributes to Dog Breed Skull Diversity
- The PARN Deadenylase Targets a Discrete Set of mRNAs for Decay and Regulates Cell Motility in Mouse Myoblasts
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