#PAGE_PARAMS# #ADS_HEAD_SCRIPTS# #MICRODATA#

Temporal Coordination of Gene Networks by Zelda in the Early Embryo


In past years, much attention has focused on the gene networks that regulate early developmental processes, but less attention has been paid to how multiple networks and processes are temporally coordinated. Recently the discovery of the transcriptional activator Zelda (Zld), which binds to CAGGTAG and related sequences present in the enhancers of many early-activated genes in Drosophila, hinted at a mechanism for how batteries of genes could be simultaneously activated. Here we use genome-wide binding and expression assays to identify Zld target genes in the early embryo with the goal of unraveling the gene circuitry regulated by Zld. We found that Zld binds to genes involved in early developmental processes such as cellularization, sex determination, neurogenesis, and pattern formation. In the absence of Zld, many target genes failed to be activated, while others, particularly the patterning genes, exhibited delayed transcriptional activation, some of which also showed weak and/or sporadic expression. These effects disrupted the normal sequence of patterning-gene interactions and resulted in highly altered spatial expression patterns, demonstrating the significance of a timing mechanism in early development. In addition, we observed prevalent overlap between Zld-bound regions and genomic “hotspot” regions, which are bound by many developmental transcription factors, especially the patterning factors. This, along with the finding that the most over-represented motif in hotspots, CAGGTA, is the Zld binding site, implicates Zld in promoting hotspot formation. We propose that Zld promotes timely and robust transcriptional activation of early-gene networks so that developmental events are coordinated and cell fates are established properly in the cellular blastoderm embryo.


Vyšlo v časopise: Temporal Coordination of Gene Networks by Zelda in the Early Embryo. PLoS Genet 7(10): e32767. doi:10.1371/journal.pgen.1002339
Kategorie: Research Article
prolekare.web.journal.doi_sk: https://doi.org/10.1371/journal.pgen.1002339

Souhrn

In past years, much attention has focused on the gene networks that regulate early developmental processes, but less attention has been paid to how multiple networks and processes are temporally coordinated. Recently the discovery of the transcriptional activator Zelda (Zld), which binds to CAGGTAG and related sequences present in the enhancers of many early-activated genes in Drosophila, hinted at a mechanism for how batteries of genes could be simultaneously activated. Here we use genome-wide binding and expression assays to identify Zld target genes in the early embryo with the goal of unraveling the gene circuitry regulated by Zld. We found that Zld binds to genes involved in early developmental processes such as cellularization, sex determination, neurogenesis, and pattern formation. In the absence of Zld, many target genes failed to be activated, while others, particularly the patterning genes, exhibited delayed transcriptional activation, some of which also showed weak and/or sporadic expression. These effects disrupted the normal sequence of patterning-gene interactions and resulted in highly altered spatial expression patterns, demonstrating the significance of a timing mechanism in early development. In addition, we observed prevalent overlap between Zld-bound regions and genomic “hotspot” regions, which are bound by many developmental transcription factors, especially the patterning factors. This, along with the finding that the most over-represented motif in hotspots, CAGGTA, is the Zld binding site, implicates Zld in promoting hotspot formation. We propose that Zld promotes timely and robust transcriptional activation of early-gene networks so that developmental events are coordinated and cell fates are established properly in the cellular blastoderm embryo.


Zdroje

1. LecuitTWieschausE 2000 Polarized insertion of new membrane from a cytoplasmic reservoir during cleavage of the Drosophila embryo. J Cell Biol 150 849 860

2. ten BoschJRBenavidesJAClineTW 2006 The TAGteam DNA motif controls the timing of Drosophila pre-blastoderm transcription. Development 133 1967 1977

3. LiangHLNienCYLiuHYMetzsteinMMKirovN 2008 The zinc-finger protein Zelda is a key activator of the early zygotic genome in Drosophila. Nature 456 400 403

4. De RenzisSDElementoOTavazoieSWieschausEF 2007 Unmasking activation of the zygotic genome using chromosomal deletions in the Drosophila embryo. PLoS Biol 5 e117 doi:10.1371/journal.pbio.0050117

5. RoySErnstJKharchenkoPVKheradpourPNegreN 2010 Identification of functional elements and regulatory circuits by Drosophila modENCODE. Science 330 1787 1797

6. EdgarBASchubigerG 1986 Parameters controlling transcriptional activation during early Drosophila development. Cell 44 871 877

7. AndersonKVLengyelJA 1979 Rates of synthesis of major classes of RNA in Drosophila embryos. Dev Biol 70 217 231

8. GregorTWieschausEFMcGregorAPBialekWTankDW 2007 Stability and nuclear dynamics of the Bicoid morphogen gradient. Cell 130 141 152

9. RushlowCAHanKManleyJLLevineM 1989 The graded distribution of the dorsal morphogen is initiated by selective nuclear transport in Drosophila. Cell 59 1165 1177

10. LibermanLMReevesGTStathopoulosA 2009 Quantitative imaging of the Dorsal nuclear gradient reveals limitations to threshold-dependent patterning in Drosophila. Proc Natl Acad Sci U S A 106 22317 22322

11. KanodiaJSRikhyRKimYLundVKDeLottoR 2009 Dynamics of the Dorsal morphogen gradient. Proc Natl Acad Sci U S A 106 21707 21712

12. HarrisonMMBotchanMRClineTW 2010 Grainyhead and Zelda compete for binding to the promoters of the earliest-expressed Drosophila genes. Dev Biol 345 248 255

13. LiXYMacArthurSBourgonRNixDPollardDA 2008 Transcription factors bind thousands of active and inactive regions in the Drosophila blastoderm. PLoS Biol 6 e27 doi:10.1371/journal.pbio.0060027

14. MacArthurSLiXYLiJBrownJBChuHCZengL 2009 Developmental roles of 21 Drosophila transcription factors are determined by quantitative differences in binding to an overlapping set of thousands of genomic regions. Genome Biol 10 R80

15. BadisGBergerMFPhilippakisAATalukderSGehrkeAR 2009 Diversity and complexity in DNA recognition by transcription factors. Science 324 1720 1723

16. GalloSMLiLHuZHalfonMS 2006 REDfly: A regulatory element database for Drosophila. Bioinformatics 22 381 383

17. PerryMWBoettigerANBothmaJPLevineM 2010 Shadow enhancers foster robustness of Drosophila gastrulation. Curr Biol 20 1562 1567

18. BiemarFNixDAPielJPetersonBRonshaugenM 2006 Comprehensive identification of Drosophila dorsal-ventral patterning genes using a whole-genome tiling array. Proc Natl Acad Sci U S A 103 12763 12768

19. WrischnikLATimmerJRMegnaLAClineTW 2003 Recruitment of the proneural gene scute to the Drosophila sex-determination pathway. Genetics 165 2007 2027

20. RoseLSWieschausE 1992 The Drosophila cellularization gene nullo produces a blastoderm-specific transcript whose levels respond to the nucleocytoplasmic ratio. Genes Dev 6 1255 1268

21. PostnerMAWieschausEF 1994 The nullo protein is a component of the actin-myosin network that mediates cellularization in Drosophila melanogaster embryos. J Cell Sci 107 1863 1873

22. SchweisguthFLepesantJAVincentA 1990 The serendipity alpha gene encodes a membrane-associated protein required for the cellularization of the Drosophila embryo. Genes Dev 4 922 931

23. LecuitTSamantaRWieschausE 2002 slam encodes a developmental regulator of polarized membrane growth during cleavage of the Drosophila embryo. Dev Cell 2 425 436

24. SteinJABroihierHTMooreLALehmannR 2002 Slow as molasses is required for polarized membrane growth and germ cell migration in Drosophila. Development 129 3925 3934

25. GrosshansJMüllerHAWieschausE 2003 Control of cleavage cycles in Drosophila embryos by frühstart. Dev Cell 5 285 294

26. AsheHLMannervikMLevineM 2000 Dpp signaling thresholds in the dorsal ectoderm of the Drosophila embryo. Development 127 3305 3312

27. StathopoulosALevineM 2005 Genomic regulatory networks and animal development. Dev Cell 9 449 462

28. PritchardDKSchubigerG 1996 Activation of transcription in Drosophila embryos is a gradual process mediated by the nucleocytoplasmic ratio. Genes Dev 10 1131 1142

29. StanojevicDSmallSLevineM 1991 Regulation of a segmentation stripe by overlapping activators and repressors in the Drosophila embryo. Science 254 1385 1387

30. YuDSmallS 2008 Precise registration of gene expression boundaries by a repressive morphogen in Drosophila. Curr Biol 18 868 876

31. PisarevAPoustelnikovaESamsonovaMReinitzJ 2009 FlyEx, the quantitative atlas on segmentation gene expression at cellular resolution. Nucleic Acids Res 37 D560 D566

32. KrautRLevineM 1991 Mutually repressive interactions between the gap genes giant and Krüppel define middle body regions of the Drosophila embryo. Development 111 611 621

33. WuXVakaniRSmallS 1998 Two distinct mechanisms for differential positioning of gene expression borders involving the Drosophila gap protein giant. Development 125 3765 3774

34. MoranEJimenezG 2006 The tailless nuclear receptor acts as a dedicated repressor in the early Drosophila embryo. Mol Cell Biol 26 3446 3454

35. ZeitlingerJZinzenRPStarkAKellisMZhangH 2007 Whole-genome ChIP-chip analysis of Dorsal, Twist, and Snail suggests integration of diverse patterning processes in the Drosophila embryo. Genes Dev 21 385 390

36. HiroseFYamaguchiMHandaHInomataYMatsukageA 1993 Novel 8-base pair sequence (Drosophila DNA replication-related element) and specific binding factor involved in the expression of Drosophila genes for DNA polymerase alpha and proliferating cell nuclear antigen. J Biol Chem 268 2092 2099

37. BryneJCValenETangMHMarstrandTWintherO 2008 JASPAR, the open access database of transcription factor-binding profiles: new content and tools in the 2008 update. Nucleic Acids Res 36 D102 106

38. LibermanLMStathopoulosA 2009 Design flexibility in cis-regulatory control of gene expression: synthetic and comparative evidence. Dev Biol 327 578 589

39. IpYTParkREKosmanDBierELevineM 1992 The Dorsal gradient morphogen regulates stripes of rhomboid expression in the presumptive neuroectoderm of the Drosophila embryo. Genes Dev 6 1728 1739

40. GaudetJMangoSE 2002 Regulation of organogenesis by the Caenorhabditis elegans FoxA protein PHA-4. Science 295 821 5

41. GaudetJMuttumuSHornerMMangoSE 2004 Whole genome analysis of temporal gene expression during foregut development. PLoS Biol 2 e352 doi:10.1371/journal.pbio.0020352

42. Shen-OrrSSMiloRManganSAlonU 2002 Network motifs in the transcriptional regulation network of Escherichia coli. Nat Genet 31 64 68

43. ManganSAlonU 2003 Structure and function of the feed-forward loop network motif. Proc Natl Acad Sci U S A 100 11980 11985

44. BradleyRKLiXYTrapnellCDavidsonSPachterL 2010 Binding site turnover produces pervasive quantitative changes in transcription factor binding between closely related Drosophila species. PLoS Biol 8 e1000343 doi:10.1371/journal.pbio.1000343

45. LevineM 2011 Paused RNA Polymerase II as a developmental checkpoint. Cell 145 502 11

46. ZeitlingerJStarkAKellisMHongJWNechaevS 2007 RNA polymerase stalling at developmental control genes in the Drosophila melanogaster embryo. Nat Genet 39 1512 1516

47. StaudtNFellertSChungHRJäckleHVorbrüggenG 2006 Mutations of the Drosophila zinc finger-encoding gene vielfältig impair mitotic cell divisions and cause improper chromosome segregation. Mol Biol Cell 17 2356 2365

48. HarlowELaneD 1999 Using antibodies: A laboratory manual Cold Spring Harbor Laboratory Press, CSH, NY

49. YangYHDudoitSLuuPLinDMPengV 2002 Normalization for cDNA microarray data: a robust composite method addressing single and multiple slide systematic variation. Nucleic Acids Res 30 e15

50. StrimmerK 2008 fdrtool: a versatile R package for estimating local and tail area-based false discovery rates. Bioinformatics 24 1461 1462

51. ManakJRDikeSSementchenkoVKapranovPBiemarF 2006 Biological function of unannotated transcription during the early development of Drosophila melanogaster. Nat Genet 38 1151 1158

52. TadrosWGoldmanALBabakTMenziesFVardyL 2007 SMAUG is a major regulator of maternal mRNA destabilization in Drosophila and its translation is activated by the PAN GU kinase. Dev Cell 12 143 155

53. ThomsenSAndersSJangaSCHuberWAlonsoCR 2010 Genome-wide analysis of mRNA decay patterns during early Drosophila development. Genome Biology 11 R93

54. ToedlingJSkylarOKruegerTFischerJJSperlingS 2007 Ringo–an R/Bioconductor package for analyzing ChIP-chip readouts. Bioinformatics 8 221 224

55. NicolJWHeltGABlanchardSGRajaALoraineAE 2009 The Integrated Genome Browser: free software for distribution and exploration of genome-scale datasets. Bioinformatics 25 2730 2731

56. PagesHAboyounPGentlemanRDebRoyS 2009 String objects representing biological sequences, and matching algorithms. R package version 2.18.2

57. BembomOKelesSvan der LaanMJ 2007 Supervised detection of conserved motifs in DNA sequences with cosmo. Stat Appl Genet Mol Biol 6 Article8

58. BaileyTLElkanC 1994 Fitting a mixture model by expectation maximization to discover motifs in biopolymers. Proc Int Conf Intell Syst Mol Biol 2 28 36

59. DennisGShermanBTHosackDAYangJGaoW 2003 DAVID: Database for annotation, visualization, and integrated discovery. Genome Biol 4 P3

60. HuangDWShermanBTLempickiRA 2009 Systematic and integrative analysis of large gene lists using DAVID Bioinformatics Resources. Nature Protoc 4 44 57

61. FoeVEAlbertsBM 1983 Studies of nuclear and cytoplasmic behaviour during the five mitotic cycles that precede gastrulation in Drosophila embryogenesis. J Cell Sci 61 31 70

62. SiepelABejeranoGPedersenJSHinrichsASHouM 2005 Evolutionarily conserved elements in vertebrate, insect, worm, and yeast genomes. Genome Res 15 1034 1050

63. EstesPAKeyesLNSchedlP 1995 Multiple response elements in the Sex-lethal early promoter ensure its female-specific expression pattern. Mol Cell Biol 15 904 917

64. KuroiwaAKloterUBaumgartnerPGehringWJ 1985 Cloning of the homeotic Sex combs reduced gene in Drosophila and in situ localization of its transcripts. EMBO J 4 3757 3764

Štítky
Genetika Reprodukčná medicína

Článok vyšiel v časopise

PLOS Genetics


2011 Číslo 10
Najčítanejšie tento týždeň
Najčítanejšie v tomto čísle
Kurzy

Zvýšte si kvalifikáciu online z pohodlia domova

Aktuální možnosti diagnostiky a léčby litiáz
nový kurz
Autori: MUDr. Tomáš Ürge, PhD.

Všetky kurzy
Prihlásenie
Zabudnuté heslo

Zadajte e-mailovú adresu, s ktorou ste vytvárali účet. Budú Vám na ňu zasielané informácie k nastaveniu nového hesla.

Prihlásenie

Nemáte účet?  Registrujte sa

#ADS_BOTTOM_SCRIPTS#