Induction of early transcription in one-cell mouse embryos by microinjection of the nonhistone chromosomal protein HMG-I

Developmental Biology

Volumn 221, Issue 2, 2000, Pages 337-354

  Beaujean, Nathalie ^a   Bouniol Baly, Christine ^a   Monod, Caroline ^b   Kissa, Karima ^a   Jullien, Denis ^b   Aulner, Nathalie ^b   Amirand, Claudine ^c   Debey, Pascale ^a   Käs, Emmanuel ^b  

^a MUSÉUM NATIONAL D'HISTOIRE NATURELLE   (France)

^b Institut d'Exploration Fonctionnelle des Génomes   (France)

^c EUROPEAN SPACE AGENCY   (France)

Author keywords

AT hook; Colocalization software image analysis; Early embryonic transcription; HMG I; Nuclear compartments; Scaffold associated regions

Indexed keywords

CELL DNA; CHROMOSOME PROTEIN; DEOXYRIBONUCLEASE I; PROTEIN HMG 1; UNCLASSIFIED DRUG;

ANIMAL CELL; ANIMAL EXPERIMENT; ANIMAL TISSUE; ARTICLE; BINDING SITE; CHROMATIN STRUCTURE; CONFORMATIONAL TRANSITION; CONTROLLED STUDY; DNA SYNTHESIS; EMBRYO; EMBRYO DEVELOPMENT; HUMAN; HUMAN CELL; MOUSE; NONHUMAN; PRIORITY JOURNAL; PROTEIN DNA BINDING; PROTEIN TRANSPORT; TRANSCRIPTION REGULATION;

EID: 0034657241     PISSN: 00121606     EISSN: None     Source Type: Journal    
DOI: 10.1006/dbio.2000.9668     Document Type: Article

References (53)

1. Amirand C., Viari A., Ballini J.-P., Rezaei H., Beaujean N., Jullien D., Käs E., Debey P. Three distinct sub-nuclear populations of HMG-I protein of different properties revealed by co-localization image analysis. J. Cell Sci. 111:1998;3551-3561.
2. Bellier S., Chastant S., Adenot P., Vincent M., Renard J.-P., Bensaude O. Nuclear translocation and carboxyl-terminal domain phosphorylation of RNA polymerase II delineate the two phases of zygotic gene activation in mammalian embryos. EMBO J. 16:1997;6250-6262.
3. Bouniol C., Nguyen E., Debey P. Endogenous transcription occurs at the 1-cell stage in the mouse embryo. Exp. Cell Res. 218:1995;57-62.
4. Bouniol-Baly C., Nguyen E., Besombes D., Debey P. Dynamic organization of DNA replication in one-cell mouse embryos: Relation to transcription activation. Exp. Cell Res. 236:1997;201-211.
5. Bouvet P., Dimitrov S., Wolffe A. P. Specific regulation of Xenopus chromosomal 5S rRNA gene transcription in vivo by histone H1. Genes Dev. 8:1994;1147-1159.
6. Bustin M., Reeves R. High-mobility-group chromosomal proteins: Architectural components that facilitate chromatin function. Prog. Nucleic Acid Res. Mol. Biol. 54:1996;35-100.
7. Chiappetta G., Avantaggiato V., Visconti R., Fedele M., Battista S., Trapasso F., Merciai B. M., Fidanza V., Giancotti V., Santoro M., Simeone A., Fusco A. High level expression of the HMGI(Y) gene during embryonic development. Oncogene. 13:1996;2439-2446.
8. Christians E., Campion E., Thompson E. M., Renard J.-P. Expression of the HSP 70.1 gene, a landmark of early zygotic activity in the mouse embryo, is restricted to the first burst of transcription. Development. 121:1995;113-122.
9. Cuvier O., Hart C. M., Laemmli U. K. Identification of a class of chromatin boundary elements. Mol. Cell. Biol. 18:1998;7478-7486.
10. Dean W. L., Seufert A. C., Schultz G. A., Prather R. S., Simerly C., Schatten G., Pilch D. R., Marzluff W. F. The small nuclear RNAs for pre-mRNA splicing are coordinately regulated during oocyte maturation and early embryogenesis in the mouse. Development. 106:1989;325-334.
11. Debey P., Szöllösi M. S., Szöllösi D., Vautier D., Girousse A., Besombes D. Competent mouse oocytes isolated from antral follicles exhibit different chromatin organization and follow different maturation dynamics. Mol. Reprod. Dev. 36:1993;59-74.
12. Disney J. E., Johnson K. R., Magnuson N. S., Sylvester S. R., Reeves R. High-mobility-group protein HMG-I localizes to G/Q- and C-bands of human and mouse chromosomes. J. Cell Biol. 109:1989;1975-1982.
13. Elton T. S., Reeves R. Purification and postsynthetic modifications of Friend erythroleukemic cell high mobility group protein HMG-I. Anal. Biochem. 157:1986;53-62.
14. Falvo J. V., Thanos D., Maniatis T. Reversal of intrinsic DNA bends in the IFNβ gene enhancer by transcription factors and the architectural protein HMG I(Y). Cell. 83:1995;1101-1111.
15. Ferreira J., Carmo-Fonseca M. The biogenesis of the coiled body during early mouse development. Development. 121:1995;601-612.
16. French S. W., Schmidt M. C., Glorioso J. C. Involvement of a high-mobility-group protein in the transcriptional activity of herpes simplex virus latency-active promoter 2. Mol. Cell. Biol. 16:1996;5393-5399.
17. Giancotti V., Buratti E., Perissin L., Zorzet S., Balmain A., Portella G., Fusco A., Goodwin G. H. Analysis of the HMGI nuclear proteins in mouse neoplastic cells induced by different procedures. Exp. Cell Res. 184:1989;538-545.
18. Girard F., Bello B., Laemmli U. K., Gehring W. J. In vivo analysis of scaffold-associated regions in Drosophila: A synthetic high-affinity SAR binding protein suppresses position effect variegation. EMBO J. 17:1998;2079-2085.
19. Hart C. M., Zhao K., Laemmli U. K. The scs′ boundary element: Characterization of boundary element-associated factors. Mol. Cell. Biol. 17:1997;999-1009.
20. John S., Robbins C. M., Leonard W. J. An IL-2 response element in the human IL-2 receptor α chain promoter is a composite element that binds Stat5, Elf-1, HMG-I(Y) and a GATA family protein. EMBO J. 15:1995;5627-5635.
21. Johnson K. R., Disney J. E., Wyatt C. R., Reeves R. Expression of mRNAs encoding mammalian chromosomal proteins HMG-I and HMG-Y during cellular proliferation. Exp. Cell Res. 187:1990;69-76.
22. Käs E., Poljak L., Adachi Y., Laemmli U. K. A model for chromatin opening: Stimulation of topoisomerase II and restriction enzyme cleavage of chromatin by distamycin. EMBO J. 12:1993;115-126.
23. Kim J., Reeves R., Rothman P., Boothby M. The non-histone chromosomal protein HMG-I(Y) contributes to repression of the immunoglobulin heavy chain germ-line epsilon RNA promoter. Eur. J. Immunol. 25:1995;798-808.
24. Klein-Hessling S., Schneider G., Heinfling A., Chuvpilo S., Serfling E. HMG-I(Y) interferes with the DNA binding of NF-AT factors and the induction of the interleukin 4 promoter in T cells. Proc. Natl. Acad. Sci. USA. 93:1996;15311-15316.
25. Laemmli U. K., Käs E., Poljak L., Adachi Y. Scaffold-associated regions: cis-acting determinants of chromatin structural loops and functional domains. Curr. Opin. Genet. Dev. 2:1992;275-285.
26. Latham K. E., Solter D., Schultz R. M. Acquisition of a transcriptionally permissive state during the one-cell stage of mouse embryogenesis. Dev. Biol. 149:1992;457-462.
27. Lin P., Clarke H. J. Somatic histone H1 microinjected into fertilized mouse eggs is transported into the pronuclei but does not disrupt subsequent preimplantation development. Mol. Reprod. Dev. 44:1996;185-192.
28. Martinez-Salas E., Linney E., Hassel J., DePamphilis M. L. The need for enhancers in gene expression first appears during mouse development with formation of the zygotic nucleus. Genes Dev. 3:1989;1493-1506.
29. Nissen M. S., Reeves R. Changes in superhelicity are introduced into closed circular DNA by binding of high mobility group protein I/Y. J. Biol. Chem. 270:1995;4355-4360.
30. Oberto J., Drlica K., Rouvière-Yaniv J. Histones, HMG, HU, IHF: Même combat. Biochimie. 76:1994;901-908.
31. Park P. C., De Boni U. Transposition of DNase hypersensitive chromatin to the nuclear periphery coincides temporally with nerve growth factor-induced up-regulation of gene expression in PC12 cells. Proc. Natl. Acad. Sci. USA. 93:1998;11646-11651.
32. Poljak L., Seum C., Mattioni T., Laemmli U. K. SARs stimulate but do not confer position independent gene expression. Nucleic Acids Res. 22:1994;4386-4394.
33. Puck T. T., Barhtoldi M., Krystosek A., Johnson R., Haag M. Confocal microscopy of genome exposure in normal, cancer and reverse-transformed cells. Somatic Cell Mol. Genet. 17:1991;489-503.
34. Reeves R., Nissen M. S. The A/T-DNA-binding domain of mammalian high mobility group I chromosomal proteins. J. Biol. Chem. 265:1990;8573-8582.
35. Reeves R., Wolffe A. P. Substrate structure influences binding of the non-histone protein HMG-I(Y) to free and nucleosomal DNA. Biochemistry. 35:1996;5063-5074.
36. Solomon M. J., Strauss F., Varshavsky A. A mammalian high mobility group protein recognizes any stretch of six A · T base pairs in duplex DNA. Proc. Natl. Acad. Sci. USA. 83:1986;1276-1280.
37. Strauss F., Varshavsky A. A protein binds to a satellite DNA repeat at three specific sites that would be brought into mutual proximity by DNA folding in the nucleosome. Cell. 37:1984;889-901.
38. Strick R., Laemmli U. K. SARs are cis DNA elements of chromosome dynamic: Synthesis of a SAR repressor protein. Cell. 83:1995;1137-1148.
39. Thanos D., Maniatis T. The high mobility group protein HMG I(Y) is required for NF-κB-dependent virus induction of the human IFN-β gene. Cell. 71:1992;777-789.
40. Thanos D., Maniatis T. Virus induction of human IFNβ gene expression requires the assembly of an enhanceosome. Cell. 83:1995;1091-1100.
41. Thompson E. M., Christians E., Stinnakre M. G., Renard J.-P. Scaffold attachment regions stimulate HSP70.1 expression in mouse preimplantation embryos but not in differentiated tissues. Mol. Cell. Biol. 14:1994;4694-4703.
42. Thompson E. M., Legouy E., Christians E., Renard J.-P. Progressive maturation of chromatin structure regulates HSP70.1 gene expression in the preimplantation mouse embryo. Development. 121:1995;3425-3437.
43. Vartiainen E., Palvimo J., Mahonen A., Linnala-Kankkunen A., Maenpaa P. H. Selective decrease in low-Mr HMG proteins HMG I and HMG Y during differentiation of mouse teratocarcinoma cells. FEBS Lett. 228:1988;45-48.
44. Vautier D. Etude de Constituants Nucléaires par Microscopie de Fluorescence: Cas de l'Embryon Précoce de Souris. 1994;Univ. of Paris VI.
45. Vautier D., Besombes D., Chassoux D., Aubry F., Debey P. Redistribution of nuclear antigens linked to cell proliferation and RNA processing in mouse oocytes and early embryos. Mol. Reprod. Dev. 38:1994;119-130.
46. Wiekowski M., Miranda M., DePamphilis M. L. Regulation of gene expression in preimplantation mouse embryos: Effects of the zygotic clock and the first mitosis on promoter and enhancer activities. Dev. Biol. 147:1991;403-414.
47. Wiekowski M., Miranda M., Nothias J.-Y., DePamphilis M. L. Changes in histone synthesis and modification at the beginning of mouse development correlate with the establishment of chromatin mediated repression of transcription. J. Cell Sci. 110:1997;1147-1158.
48. Wolffe A. P. Dominant and specific repression of Xenopus oocyte 5S RNA genes and satellite I DNA by histone H1. EMBO J. 8:1989;527-537.
49. Worrad D. M., Ram P. T., Schultz R. M. Regulation of gene expression in the mouse oocyte and early preimplantation embryo: Developmental changes in Sp1 and TATA box-binding protein, TBP. Development. 120:1994;2347-2357.
50. Worrad D. M., Turner B. M., Schultz R. M. Temporally restricted spatial localization of acetylated isoforms of histone H4 and RNA polymerase II in the 2-cell mouse embryo. Development. 121:1995;2949-2959.
51. Yie J., Liang S., Merika M., Thanos D. Intra- and intermolecular cooperative binding of high-mobility-group protein I(Y) to the beta-interferon promoter. Mol. Cell. Biol. 17:1997;3649-3662.
52. Zhao K., Käs E., Gonzalez E., Laemmli U. K. SAR-dependent mobilization of histone H1 by HMG-I/Y in vitro: HMG-I/Y is enriched in H1-depleted chromatin. EMBO J. 12:1993;3237-3247.
53. Zhou X., Benson K. F., Ashar H. R., Chada K. Mutation responsible for the mouse pygmy phenotype in the developmentally regulated factor HMGI-C. Nature. 376:1995;771-774.