-
Články
- Časopisy
- Kurzy
- Témy
- Kongresy
- Videa
- Podcasty
Genome-Scale Mapping of σ Reveals Widespread, Conserved Intragenic Binding
Bacterial RNA polymerases must associate with a σ factor to bind to promoter DNA sequences upstream of genes and initiate transcription. There are two families of σ factor: σ70 and σ54. Members of the σ54 family are distinct from members of the σ70 family in their ability to bind promoter DNA sequences, in association with RNA polymerase, in a transcriptionally inactive state. We have determined positions in the Escherichia coli genome that are bound by σ54, the archetypal member of the σ54 family. Surprisingly, we identified 135 binding sites for σ54, a huge increase over the number of previously described sites. Our data suggest that there are more than 250 σ54 sites in total. Strikingly, most σ54 binding sites are located inside genes, whereas only one intragenic σ54 binding site has previously been described. The location and orientation of intragenic σ54 binding sites is non-random, and many intragenic σ54 binding sites are conserved in other bacterial species. We conclude that many intragenic σ54 binding sites are likely to be functional. Consistent with this notion, we identify three σ54 promoters in E. coli that are located inside genes but drive transcription of unusual mRNAs for the neighboring genes.
Vyšlo v časopise: Genome-Scale Mapping of σ Reveals Widespread, Conserved Intragenic Binding. PLoS Genet 11(10): e32767. doi:10.1371/journal.pgen.1005552
Kategorie: Research Article
prolekare.web.journal.doi_sk: https://doi.org/10.1371/journal.pgen.1005552Souhrn
Bacterial RNA polymerases must associate with a σ factor to bind to promoter DNA sequences upstream of genes and initiate transcription. There are two families of σ factor: σ70 and σ54. Members of the σ54 family are distinct from members of the σ70 family in their ability to bind promoter DNA sequences, in association with RNA polymerase, in a transcriptionally inactive state. We have determined positions in the Escherichia coli genome that are bound by σ54, the archetypal member of the σ54 family. Surprisingly, we identified 135 binding sites for σ54, a huge increase over the number of previously described sites. Our data suggest that there are more than 250 σ54 sites in total. Strikingly, most σ54 binding sites are located inside genes, whereas only one intragenic σ54 binding site has previously been described. The location and orientation of intragenic σ54 binding sites is non-random, and many intragenic σ54 binding sites are conserved in other bacterial species. We conclude that many intragenic σ54 binding sites are likely to be functional. Consistent with this notion, we identify three σ54 promoters in E. coli that are located inside genes but drive transcription of unusual mRNAs for the neighboring genes.
Zdroje
1. Gross CA, Chan C, Dombroski A, Gruber T, Sharp M, et al. (1998) The functional and regulatory roles of sigma factors in transcription. Cold Spring Harb Symp Quant Biol 63 : 141–155. 10384278
2. Wade JT, Struhl K (2004) Association of RNA polymerase with transcribed regions in Escherichia coli. Proc Natl Acad Sci USA 101 : 17777–17782. 15596728
3. Gruber T, Gross CA (2003) Multiple Sigma subunits and the partitioning of bacterial transcription space. Annu Rev Microbiol 57 : 441–466. 14527287
4. Wigneshweraraj S, Bose D, Burrows PC, Joly N, Schumacher J, et al. (2008) Modus operandi of the bacterial RNA polymerase containing the sigma54 promoter-specificity factor. Mol Microbiol 38 : 538–546.
5. Buck M, Cannon W (1992) Specific binding of the transcription factor sigma-54 to promoter DNA. Nature 358 : 422–424. 1641025
6. Shingler V (2011) Signal sensory systems that impact σ54-dependent transcription. FEMS Microbiol Rev 35 : 425–440. doi: 10.1111/j.1574-6976.2010.00255.x 21054445
7. Hunt TP, Magasanik B (1985) Transcription of glnA by purified Escherichia coli components: core RNA polymerase and the products of glnF, glnG, and glnL. Proc Natl Acad Sci USA 82 : 8453–8457. 2867543
8. Tsang J, Hoover TR (2014) Themes and Variations: Regulation of RpoN-Dependent Flagellar Genes across Diverse Bacterial Species. Scientifica 2014 : 681754. doi: 10.1155/2014/681754 24672734
9. Mittenhuber G (2002) An inventory of genes encoding RNA polymerase sigma factors in 31 completely sequenced eubacterial genomes. J Mol Microbiol Biotechnol 4 : 77–91. 11763973
10. Markel E, Butcher BG, Myers CR, Stodghill P, Cartinhour S, et al. (2013) Regulons of three Pseudomonas syringae pv. tomato DC3000 iron starvation sigma factors. Appl Environ Microbiol 79 : 725–727. doi: 10.1128/AEM.02801-12 23124242
11. Markel E, Maciak C, Butcher BG, Myers CR, Stodghill P, et al. (2011) An extracytoplasmic function sigma factor-mediated cell surface signaling system in Pseudomonas syringae pv. tomato DC3000 regulates gene expression in response to heterologous siderophores. J Bacteriol 193 : 5775–5783. doi: 10.1128/JB.05114-11 21840980
12. Myers KS, Yan H, Ong IM, Chung D, Liang K, et al. (2013) Genome-scale analysis of Escherichia coli FNR reveals complex features of transcription factor binding. PLoS Genet 9: e1003565. doi: 10.1371/journal.pgen.1003565 23818864
13. Singh S, Singh N, Bonocora RP, Fitzgerald DM, Wade JT, et al. (2014) Widespread suppression of intragenic transcription initiation by H-NS. Genes Dev 28 : 214–219. doi: 10.1101/gad.234336.113 24449106
14. Samuels DJ, Frye JG, Porwollik S, McClelland M, Mrázek J, et al. (2013) Use of a promiscuous, constitutively-active bacterial enhancer-binding protein to define the σ54 (RpoN) regulon of Salmonella Typhimurium LT2. BMC Genomics 14 : 602. doi: 10.1186/1471-2164-14-602 24007446
15. Wade JT, Roa DC, Grainger DC, Hurd D, Busby SJW, et al. (2006) Extensive functional overlap between Sigma factors in Escherichia coli. Nat Struct Mol Biol 13 : 806–814. 16892065
16. Hartkoorn RC, Sala C, Uplekar S, Busso P, Rougemont J, et al. (2012) Genome-wide definition of the SigF regulon in Mycobacterium tuberculosis. J Bacteriol 194 : 2001–2009. doi: 10.1128/JB.06692-11 22307756
17. Waldminghaus T, Skarstad K (2010) ChIP on Chip: surprising results are often artifacts. BMC Genomics 11 : 414. doi: 10.1186/1471-2164-11-414 20602746
18. Fitzgerald DM, Bonocora RP, Wade JT (2014) Comprehensive mapping of the Escherichia coli flagellar regulatory network. PLoS Genet 10: e1004649. doi: 10.1371/journal.pgen.1004649 25275371
19. Dong TG, Mekalanos JJ (2012) Characterization of the RpoN regulon reveals differential regulation of T6SS and new flagellar operons in Vibrio cholerae O37 strain V52. Nucleic Acids Res 40 : 7766–7775. doi: 10.1093/nar/gks567 22723378
20. Brown DR, Barton G, Pan Z, Buck M, Wigneshweraraj S (2014) Nitrogen stress response and stringent response are coupled in Escherichia coli. Nat Commun 5 : 4115. doi: 10.1038/ncomms5115 24947454
21. Kharchenko PV, Tolstorukov MY, Park PJ (2008) Design and analysis of ChIP-seq experiments for DNA-binding proteins. Nature Biotech 26 : 1351–1359.
22. Bailey TL, Elkan C (1994) Fitting a mixture model by expectation maximization to discover motifs in biopolymers. Proc Int Conf Intell Syst Mol Biol 2 : 28–36. 7584402
23. Teytelman L, Thurtle DM, Rine J, van Oudenaarden A (2013) Highly expressed loci are vulnerable to misleading ChIP localization of multiple unrelated proteins. Proc Natl Acad Sci USA 110 : 18602–18607. doi: 10.1073/pnas.1316064110 24173036
24. Park D, Lee Y, Bhupindersingh G, Iyer VR (2013) Widespread Misinterpretable ChIP-seq Bias in Yeast. PLoS One 8: e83506. doi: 10.1371/journal.pone.0083506 24349523
25. Jain D, Baldi S, Zabel A, Straub T, Becker PB (2015) Active promoters give rise to false positive 'Phantom Peaks' in ChIP-seq experiments. Nucleic Acids Res in press. doi: 10.1093/nar/gkv637 26117547
26. Keseler IM, Collado-Vides J, Gama-Castro S, Ingraham J, Paley S, et al. (2005) EcoCyc: a comprehensive database resource for Escherichia coli. Nucleic Acids Res 33: D334–337. 15608210
27. Zafar MA, Carabetta VJ, Mandel MJ, Silhavy TJ (2014) Transcriptional occlusion caused by overlapping promoters. Proc Natl Acad Sci USA 111 : 1557–1561. doi: 10.1073/pnas.1323413111 24474781
28. Zhao K, Liu K, Burgess RR (2010) Promoter and regulon analysis of nitrogen assimilation factor, σ54, reveal alternative strategy for E. coli MG1655 flagellar biosynthesis. Nucleic Acids Res 38 : 1273–1283. doi: 10.1093/nar/gkp1123 19969540
29. Cho BK, Kim D, Knight EM, Zengler K, Palsson BO (2014) Genome-scale reconstruction of the sigma factor network in Escherichia coli: topology and functional states. BMC Biol 12 : 4. doi: 10.1186/1741-7007-12-4 24461193
30. Berriz GF, King OD, Bryant B, Sander C, Roth FP (2003) Characterizing gene sets with FuncAssociate. Bioinformatics 19 : 2502–2504. 14668247
31. Boucher JC, Schurr MJ, Deretic V (2000) Dual regulation of mucoidy in Pseudomonas aeruginosa and sigma factor antagonism. Mol Microbiol 36 : 341–351. 10792721
32. Shearwin KE, Callen BP, Egan JB (2005) Transcriptional interference—a crash course. Trends Genet 21 : 339–345. 15922833
33. Ninfa AJ, Reitzer LJ, Magasanik B (1987) Initiation of transcription at the bacterial glnAp2 promoter by purified E. coli components is facilitated by enhancers. Cell 50 : 1039–1046. 3304660
34. Jovanovic G, Weiner L, Model P (1996) Identification, nucleotide sequence, and characterization of PspF, the transcriptional activator of the Escherichia coli stress-induced psp operon. J Bacteriol 178 : 1936–1945. 8606168
35. Reichenbach B, Göpel Y, Görke B (2009) Dual control by perfectly overlapping sigma 54 - and sigma 70 - promoters adjusts small RNA GlmY expression to different environmental signals. Mol Microbiol 74 : 1054–1070. doi: 10.1111/j.1365-2958.2009.06918.x 19843219
36. Cho BK, Zengler K, Qiu Y, Park YS, Knight EM, et al. (2009) The transcription unit architecture of the Escherichia coli genome. Nat Biotechnol 27 : 1043–1049. doi: 10.1038/nbt.1582 19881496
37. Zimmer DP, Soupene E, Lee HL, Wendisch VF, Khodursky AB, et al. (2000) Nitrogen regulatory protein C-controlled genes of Escherichia coli: scavenging as a defense against nitrogen limitation. Proc Natl Acad Sci USA 97 : 14674–14679. 11121068
38. Hopper S, Babst M, Schlensog V, Fischer HM, Hennecke H, et al. (1994) Regulated expression in vitro of genes coding for formate hydrogenlyase components of Escherichia coli. J Biol Chem 269 : 19597–19604. 8034728
39. Leonhartsberger S, Huber A, Lottspeich F, Böck A (2001) The hydH/G Genes from Escherichia coli code for a zinc and lead responsive two-component regulatory system. J Mol Biol 307 : 93–105. 11243806
40. Yamamoto T, Gojobori T, Yokota T (1987) Evolutionary origin of pathogenic determinants in enterotoxigenic Escherichia coli and Vibrio cholerae O1. J Bacteriol 169 : 1352–1357. 3546273
41. Blanka A, Schulz S, Eckweiler D, Franke R, Bielecka A, et al. (2014) Identification of the alternative sigma factor SigX regulon and its implications for Pseudomonas aeruginosa pathogenicity. J Bacteriol 196 : 345–356. doi: 10.1128/JB.01034-13 24187091
42. Bibb MJ, Domonkos A, Chandra G, Buttner MJ (2012) Expression of the chaplin and rodlin hydrophobic sheath proteins in Streptomyces venezuelae is controlled by σ(BldN) and a cognate anti-sigma factor, RsbN. Mol Microbiol 84 : 1033–1049. doi: 10.1111/j.1365-2958.2012.08070.x 22582857
43. Ochman H, Wilson AC (1987) Evolution in bacteria: evidence for a universal substitution rate in cellular genomes. J Mol Evol 26 : 74–86. 3125340
44. Haft DH, Self WT (2008) Orphan SelD proteins and selenium-dependent molybdenum hydroxylases. Biol Direct 3 : 4. doi: 10.1186/1745-6150-3-4 18289380
45. Wurtzel O, Sesto N, Mellin JR, Karunker I, Edelheit S, et al. (2012) Comparative transcriptomics of pathogenic and non-pathogenic Listeria species. Mol Syst Biol 8 : 583. doi: 10.1038/msb.2012.11 22617957
46. Georg J, Hess WR (2011) cis-antisense RNA, another level of gene regulation in bacteria. Microbiol Mol Biol Rev 75 : 286–300. doi: 10.1128/MMBR.00032-10 21646430
47. Thomason MK, Storz G (2010) Bacterial antisense RNAs: how many are there, and what are they doing? Annu Rev Genet 44 : 167–188. doi: 10.1146/annurev-genet-102209-163523 20707673
48. Liu N, Niu G, Xie Z, Chen Z, Itzek A, et al. (2015) The Streptococcus mutans irvA gene encodes a trans-acting riboregulatory mRNA. Mol Cell 57 : 179–190. doi: 10.1016/j.molcel.2014.11.003 25574948
49. Schaefer J, Engl C, Zhang N, Lawton E, Buck M (2015) Genome wide interactions of wild-type and activator bypass forms of σ54. Nucleic Acids Res in press. doi: 10.1093/nar/gkv597 26082500
50. Bonocora RP, Fitzgerald DM, Stringer AM, Wade JT (2013) Non-canonical protein-DNA interactions identified by ChIP are not artifacts. BMC Genomics 14 : 254. doi: 10.1186/1471-2164-14-254 23586855
51. Göpel Y, Görke B (2014) Lies and deception in bacterial gene regulation: the roles of nucleic acid decoys. Mol Microbiol 92 : 641–647. doi: 10.1111/mmi.12604 24707963
52. Shimada T, Ishihama A, Busby SJ, Grainger DC (2008) The Escherichia coli RutR transcription factor binds at targets within genes as well as intergenic regions. Nucleic Acids Res 36 : 3950–3955. doi: 10.1093/nar/gkn339 18515344
53. Galagan J, Lyubetskaya A, Gomes A (2013) ChIP-Seq and the Complexity of Bacterial Transcriptional Regulation. Curr Top Microbiol Immunol 363 : 43–68. doi: 10.1007/82_2012_257 22983621
54. Galagan JE, Minch K, Peterson M, Lyubetskaya A, Azizi E, et al. (2013) The Mycobacterium tuberculosis regulatory network and hypoxia. Nature 499 : 178–183. doi: 10.1038/nature12337 23823726
55. Plumbridge J, Bossi L, Oberto J, Wade JT, Figueroa-Bossi N (2014) Interplay of transcriptional and small RNA-dependent control mechanisms regulates chitosugar uptake in Escherichia coli and Salmonella. Mol Microbiol 92 : 648–658. doi: 10.1111/mmi.12573 24593230
56. Qian Z, Dimitriadis EK, Edgar R, Eswaramoorthy P, Adhya S (2012) Galactose repressor mediated intersegmental chromosomal connections in Escherichia coli. Proc Natl Acad Sci U S A 109 : 11336–11341. doi: 10.1073/pnas.1208595109 22733746
57. Blattner FR, Plunkett G III, Bloch CA, Perna NT, Burland V, et al. (1997) The complete genome of Escherichia coli K-12. Science 277 : 1453–1474. 9278503
58. Baba T, Ara T, Hasegawa M, Takai Y, Okumura Y, et al. (2006) Construction of Escherichia coli K-12 in-frame, single-gene knockout mutants: the Keio collection. Mol Syst Biol 2 : 0008. 16738554
59. Stringer AM, Singh N, Yermakova A, Petrone BL, Amarasinghe JJ, et al. (2012) FRUIT, a scar-free system for targeted chromosomal mutagenesis, epitope tagging, and promoter replacement in Escherichia coli and Salmonella enterica. PLoS One 7: e44841. doi: 10.1371/journal.pone.0044841 23028641
60. Datsenko KA, Wanner BL (2000) One-step inactivation of chromosomal genes in Escherichia coli K-12 using PCR products. Proc Natl Acad Sci USA 97 : 6640–6645. 10829079
61. Jarvik T, Smillie C, Groisman EA, Ochman H (2010) Short-term signatures of evolutionary change in the Salmonella enterica serovar Typhimurium 14028 genome. J Bacteriol 192 : 560–567. doi: 10.1128/JB.01233-09 19897643
62. Guzman L-M, Belin D, Carson MJ, Beckwith JR (1995) Tight regulation, modulation, and high-level expression by vectors containing the arabinose PBAD promoter. J Bacteriol 177 : 4121–4130. 7608087
63. Gutnick D, Calvo JM, Klopotowski T, Ames BN (1969) Compounds which serve as the sole source of carbon or nitrogen for Salmonella typhimurium LT-2. J Bacteriol 100 : 215–219. 4898986
64. Stringer AM, Currenti SA, Bonocora RP, Petrone BL, Palumbo MJ, et al. (2014) Genome-Scale Analyses of Escherichia coli and Salmonella enterica AraC Reveal Non-Canonical Targets and an Expanded Core Regulon. J Bacteriol 196 : 660–671. doi: 10.1128/JB.01007-13 24272778
65. McClure R, Balasubramanian D, Sun Y, Bobrovskyy M, Sumby P, et al. (2013) Computational analysis of bacterial RNA-Seq data. Nucleic Acids Res 41: e140. doi: 10.1093/nar/gkt444 23716638
66. Klucar L, Stano M, Hajduk M (2010) phiSITE: Database of Gene Regulation in Bacteriophages. Nucleic Acids Res 38: D366–D370. doi: 10.1093/nar/gkp911 19900969
67. Altschul SF, Gish W, Miller W, Myers EW, Lipman DJ (1990) Basic local alignment search tool. J Mol Biol 215 : 403–410. 2231712
68. Eisen MB, Spellman PT, Brown PO, Botstein D (1998) Cluster analysis and display of genome-wide expression patterns. Proc Natl Acad Sci U S A 95 : 14863–14868. 9843981
69. Machanick P, Bailey TL (2011) MEME-ChIP: motif analysis of large DNA datasets. Bioinformatics 27 : 1696–1697. doi: 10.1093/bioinformatics/btr189 21486936
70. Bailey TL, Machanick P (2012) Inferring direct DNA binding from ChIP-seq. Nucleic Acids Res 40: e128. 22610855
71. Muse WB, Bender RA (1998) The nac (nitrogen assimilation control) gene from Escherichia coli. J Bacteriol 180 : 1166–1173. 9495755
Štítky
Genetika Reprodukčná medicína
Článek Evidence of Selection against Complex Mitotic-Origin Aneuploidy during Preimplantation DevelopmentČlánek A Novel Route Controlling Begomovirus Resistance by the Messenger RNA Surveillance Factor PelotaČlánek A Follicle Rupture Assay Reveals an Essential Role for Follicular Adrenergic Signaling in OvulationČlánek Canonical Poly(A) Polymerase Activity Promotes the Decay of a Wide Variety of Mammalian Nuclear RNAsČlánek FANCI Regulates Recruitment of the FA Core Complex at Sites of DNA Damage Independently of FANCD2Článek Hsp90-Associated Immunophilin Homolog Cpr7 Is Required for the Mitotic Stability of [URE3] Prion inČlánek The Dedicated Chaperone Acl4 Escorts Ribosomal Protein Rpl4 to Its Nuclear Pre-60S Assembly SiteČlánek Chromatin-Remodelling Complex NURF Is Essential for Differentiation of Adult Melanocyte Stem CellsČlánek A Systems Approach Identifies Essential FOXO3 Functions at Key Steps of Terminal ErythropoiesisČlánek Integration of Posttranscriptional Gene Networks into Metabolic Adaptation and Biofilm Maturation inČlánek Lateral and End-On Kinetochore Attachments Are Coordinated to Achieve Bi-orientation in OocytesČlánek MET18 Connects the Cytosolic Iron-Sulfur Cluster Assembly Pathway to Active DNA Demethylation in
Článok vyšiel v časopisePLOS Genetics
Najčítanejšie tento týždeň
2015 Číslo 10- 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
- Gene-Regulatory Logic to Induce and Maintain a Developmental Compartment
- A Decad(e) of Reasons to Contribute to a PLOS Community-Run Journal
- DNA Methylation Landscapes of Human Fetal Development
- Single Strand Annealing Plays a Major Role in RecA-Independent Recombination between Repeated Sequences in the Radioresistant Bacterium
- Evidence of Selection against Complex Mitotic-Origin Aneuploidy during Preimplantation Development
- Transcriptional Derepression Uncovers Cryptic Higher-Order Genetic Interactions
- Silencing of X-Linked MicroRNAs by Meiotic Sex Chromosome Inactivation
- Virus Satellites Drive Viral Evolution and Ecology
- A Novel Route Controlling Begomovirus Resistance by the Messenger RNA Surveillance Factor Pelota
- Sequence to Medical Phenotypes: A Framework for Interpretation of Human Whole Genome DNA Sequence Data
- Your Data to Explore: An Interview with Anne Wojcicki
- Modulation of Ambient Temperature-Dependent Flowering in by Natural Variation of
- The Ciliopathy Protein CC2D2A Associates with NINL and Functions in RAB8-MICAL3-Regulated Vesicle Trafficking
- PPP2R5C Couples Hepatic Glucose and Lipid Homeostasis
- DCA1 Acts as a Transcriptional Co-activator of DST and Contributes to Drought and Salt Tolerance in Rice
- Intermediate Levels of CodY Activity Are Required for Derepression of the Branched-Chain Amino Acid Permease, BraB
- "Missing" G x E Variation Controls Flowering Time in
- The Rise and Fall of an Evolutionary Innovation: Contrasting Strategies of Venom Evolution in Ancient and Young Animals
- Type IV Collagen Controls the Axogenesis of Cerebellar Granule Cells by Regulating Basement Membrane Integrity in Zebrafish
- Loss of a Conserved tRNA Anticodon Modification Perturbs Plant Immunity
- Genome-Wide Association Analysis of Adaptation Using Environmentally Predicted Traits
- Oriented Cell Division in the . Embryo Is Coordinated by G-Protein Signaling Dependent on the Adhesion GPCR LAT-1
- Disproportionate Contributions of Select Genomic Compartments and Cell Types to Genetic Risk for Coronary Artery Disease
- A Follicle Rupture Assay Reveals an Essential Role for Follicular Adrenergic Signaling in Ovulation
- The RNAPII-CTD Maintains Genome Integrity through Inhibition of Retrotransposon Gene Expression and Transposition
- Canonical Poly(A) Polymerase Activity Promotes the Decay of a Wide Variety of Mammalian Nuclear RNAs
- Allelic Variation of Cytochrome P450s Drives Resistance to Bednet Insecticides in a Major Malaria Vector
- SCARN a Novel Class of SCAR Protein That Is Required for Root-Hair Infection during Legume Nodulation
- IBR5 Modulates Temperature-Dependent, R Protein CHS3-Mediated Defense Responses in
- NINL and DZANK1 Co-function in Vesicle Transport and Are Essential for Photoreceptor Development in Zebrafish
- Decay-Initiating Endoribonucleolytic Cleavage by RNase Y Is Kept under Tight Control via Sequence Preference and Sub-cellular Localisation
- Large-Scale Analysis of Kinase Signaling in Yeast Pseudohyphal Development Identifies Regulation of Ribonucleoprotein Granules
- FANCI Regulates Recruitment of the FA Core Complex at Sites of DNA Damage Independently of FANCD2
- LINE-1 Mediated Insertion into (Protein of Centriole 1 A) Causes Growth Insufficiency and Male Infertility in Mice
- Hsp90-Associated Immunophilin Homolog Cpr7 Is Required for the Mitotic Stability of [URE3] Prion in
- Genome-Scale Mapping of σ Reveals Widespread, Conserved Intragenic Binding
- Uncovering Hidden Layers of Cell Cycle Regulation through Integrative Multi-omic Analysis
- Functional Diversification of Motor Neuron-specific Enhancers during Evolution
- The GTP- and Phospholipid-Binding Protein TTD14 Regulates Trafficking of the TRPL Ion Channel in Photoreceptor Cells
- The Gyc76C Receptor Guanylyl Cyclase and the Foraging cGMP-Dependent Kinase Regulate Extracellular Matrix Organization and BMP Signaling in the Developing Wing of
- The Ty1 Retrotransposon Restriction Factor p22 Targets Gag
- Functional Impact and Evolution of a Novel Human Polymorphic Inversion That Disrupts a Gene and Creates a Fusion Transcript
- The Dedicated Chaperone Acl4 Escorts Ribosomal Protein Rpl4 to Its Nuclear Pre-60S Assembly Site
- The Influence of Age and Sex on Genetic Associations with Adult Body Size and Shape: A Large-Scale Genome-Wide Interaction Study
- Parent-of-Origin Effects of the Gene on Adiposity in Young Adults
- Chromatin-Remodelling Complex NURF Is Essential for Differentiation of Adult Melanocyte Stem Cells
- Retinoic Acid Receptors Control Spermatogonia Cell-Fate and Induce Expression of the SALL4A Transcription Factor
- A Systems Approach Identifies Essential FOXO3 Functions at Key Steps of Terminal Erythropoiesis
- Protein O-Glucosyltransferase 1 (POGLUT1) Promotes Mouse Gastrulation through Modification of the Apical Polarity Protein CRUMBS2
- KIF7 Controls the Proliferation of Cells of the Respiratory Airway through Distinct Microtubule Dependent Mechanisms
- Integration of Posttranscriptional Gene Networks into Metabolic Adaptation and Biofilm Maturation in
- Lateral and End-On Kinetochore Attachments Are Coordinated to Achieve Bi-orientation in Oocytes
- Protein Homeostasis Imposes a Barrier on Functional Integration of Horizontally Transferred Genes in Bacteria
- A New Method for Detecting Associations with Rare Copy-Number Variants
- Histone H2AFX Links Meiotic Chromosome Asynapsis to Prophase I Oocyte Loss in Mammals
- The Genomic Aftermath of Hybridization in the Opportunistic Pathogen
- A Role for the Chaperone Complex BAG3-HSPB8 in Actin Dynamics, Spindle Orientation and Proper Chromosome Segregation during Mitosis
- Establishment of a Developmental Compartment Requires Interactions between Three Synergistic -regulatory Modules
- Regulation of Spore Formation by the SpoIIQ and SpoIIIA Proteins
- Association of the Long Non-coding RNA Steroid Receptor RNA Activator (SRA) with TrxG and PRC2 Complexes
- Alkaline Ceramidase 3 Deficiency Results in Purkinje Cell Degeneration and Cerebellar Ataxia Due to Dyshomeostasis of Sphingolipids in the Brain
- ACLY and ACC1 Regulate Hypoxia-Induced Apoptosis by Modulating ETV4 via α-ketoglutarate
- Quantitative Differences in Nuclear β-catenin and TCF Pattern Embryonic Cells in .
- HENMT1 and piRNA Stability Are Required for Adult Male Germ Cell Transposon Repression and to Define the Spermatogenic Program in the Mouse
- Axon Regeneration Is Regulated by Ets–C/EBP Transcription Complexes Generated by Activation of the cAMP/Ca Signaling Pathways
- A Phenomic Scan of the Norfolk Island Genetic Isolate Identifies a Major Pleiotropic Effect Locus Associated with Metabolic and Renal Disorder Markers
- The Roles of CDF2 in Transcriptional and Posttranscriptional Regulation of Primary MicroRNAs
- A Genetic Cascade of Modulates Nucleolar Size and rRNA Pool in
- Inter-population Differences in Retrogene Loss and Expression in Humans
- Cationic Peptides Facilitate Iron-induced Mutagenesis in Bacteria
- EP4 Receptor–Associated Protein in Macrophages Ameliorates Colitis and Colitis-Associated Tumorigenesis
- Fungal Infection Induces Sex-Specific Transcriptional Changes and Alters Sexual Dimorphism in the Dioecious Plant
- FLCN and AMPK Confer Resistance to Hyperosmotic Stress via Remodeling of Glycogen Stores
- MET18 Connects the Cytosolic Iron-Sulfur Cluster Assembly Pathway to Active DNA Demethylation in
- Sex Bias and Maternal Contribution to Gene Expression Divergence in Blastoderm Embryos
- Transcriptional and Linkage Analyses Identify Loci that Mediate the Differential Macrophage Response to Inflammatory Stimuli and Infection
- Mre11 and Blm-Dependent Formation of ALT-Like Telomeres in Ku-Deficient
- Genome Wide Identification of SARS-CoV Susceptibility Loci Using the Collaborative Cross
- Identification of a Single Strand Origin of Replication in the Integrative and Conjugative Element ICE of
- The Type VI Secretion TssEFGK-VgrG Phage-Like Baseplate Is Recruited to the TssJLM Membrane Complex via Multiple Contacts and Serves As Assembly Platform for Tail Tube/Sheath Polymerization
- The Dynamic Genome and Transcriptome of the Human Fungal Pathogen and Close Relative
- Secondary Structure across the Bacterial Transcriptome Reveals Versatile Roles in mRNA Regulation and Function
- ROS-Induced JNK and p38 Signaling Is Required for Unpaired Cytokine Activation during Regeneration
- Pelle Modulates dFoxO-Mediated Cell Death in
- PLOS Genetics
- Archív čísel
- Aktuálne číslo
- Informácie o časopise
Najčítanejšie v tomto čísle- Single Strand Annealing Plays a Major Role in RecA-Independent Recombination between Repeated Sequences in the Radioresistant Bacterium
- The Rise and Fall of an Evolutionary Innovation: Contrasting Strategies of Venom Evolution in Ancient and Young Animals
- Genome Wide Identification of SARS-CoV Susceptibility Loci Using the Collaborative Cross
- DCA1 Acts as a Transcriptional Co-activator of DST and Contributes to Drought and Salt Tolerance in Rice
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