Expression of murine H1 histone genes during postnatal development

Biochimica et Biophysica Acta - Gene Structure and Expression

Volumn 1398, Issue 3, 1998, Pages 232-242

  Franke, K ^a   Drabent, B ^a   Doenecke, D ^a  

^a UNIVERSITY OF GÖTTINGEN   (Germany)

Author keywords

H1 subtype; Histone gene expression; Histone H1; Histone H1 ; RNase protection; Tissue specific gene expression

Indexed keywords

HISTONE;

ARTICLE; CHROMATIN STRUCTURE; GENE EXPRESSION; GENE ISOLATION; GENE SEQUENCE; NONHUMAN; POSTNATAL DEVELOPMENT; PRIORITY JOURNAL; PROTEIN EXPRESSION; TISSUE DISTRIBUTION; TISSUE SPECIFICITY;

3T3 CELLS; AGING; ANIMALS; CELL LINE; GENE EXPRESSION; HISTONES; MICE; RIBONUCLEASES; RNA, MESSENGER;

ANIMALIA; MAMMALIA; MURINAE;

EID: 0032500076     PISSN: 01674781     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0167-4781(98)00062-1     Document Type: Article

References (49)

1. A.P. Wolffe, Chromatin: Structure and Function, Academic Press, London, 1995.
2. J. Allan, P.G. Hartman, C. Crane-Robinson, F.X. Aviles, The structure of histone H1 and its location in chromatin, Nature 288 (1980) 675-679.
3. R.T. Simpson, Structure of the chromatosome, a chromatin particle containing 160 base pairs of DNA and all the histones, Biochemistry 17 (1978) 5524-5531.
4. D. Pruss, B. Bartholomew, J. Persinger, J. Hayes, G. Arents, E.N. Moudrianakis, A.P. Wolffe, An asymmetric model for the nucleosome: a binding site for linker histones inside the DNA gyres, Science 274 (1996) 614-617.
5. F. Thoma, T. Koller, A. Klug, Involvement of histone H1 in the organization of the nucleosome and of the salt-dependent superstructures of chromatin, J. Cell Biol. 83 (1979) 403-427.
6. S.M. Paranjape, R.T. Kamakaka, J.T. Kadonaga, Role of chromatin structure in the regulation of transcription by RNA polymerase II, Annu. Rev. Biochem. 63 (1994) 265-297.
7. P. Bouvet, A. Dimitrov, A.P. Wolffe, Specific regulation of Xenopus chromosomal 5S rRNA gene transcription in vivo by histone H1 Genes Dev. 8 (1994) 1147-1159.
8. O.C. Steinbach, A.P. Wolffe, R.A.W. Rupp, Somatic linker histones cause loss of mesodermal competence in Xenopus, Nature 389 (1997) 395-399.
9. X. Shen, M.A. Gorovsky, Linker histone H1 regulates specific gene expression but not global transcription in vivo, Cell 86 (1996) 475-483.
10. W. Albig, D. Doenecke, The human histone gene cluster at the D6S105 locus, Hum. Genet. 106 (1997) 247-251.
11. B. Drabent, K. Franke, C. Bode, U. Kosciessa, H. Bouterfa, H. Hameister, D. Doenecke, Isolation of two murine H1 histone genes and chromosomal mapping of the H1 gene complement, Mamm. Genome 6 (1995) 505-511.
12. Z.F. Wang, A.M. Sirotkin, G.M. Buchhold, A.I. Skoultchi, W.F. Marzluff, The mouse histone H1 genes: gene organization and differential regulation, J. Mol. Biol. 271 (1997) 124-138.
13. R.W. Lennox, L.H. Cohen, The histone H1 complements of dividing and nondividing cells of the mouse, J. Biol. Chem. 258 (1983) 262-268.
14. D. Doenecke, A. Alonso, Organization and expression of the developmentally regulated H1° histone gene in vertebrates, Int. J. Dev. Biol. 40 (1996) 395-401.
15. J. Zlatanova, D. Doenecke, Histone H1°: a major player in cell differentiation?, FASEB J. 8 (1994) 1260-1268.
16. B. Drabent, B. Bramlage, C. Bode, D. Doenecke, Expression of the mouse testicular histone gene Hit during spermato-genesis, Histochem. Cell Biol. 106 (1996) 247-251.
17. J. Chirgwin, A. Przybyla, R. MacDonald, W. Rutter, Isolation of biologically active ribonucleic acid from sources enriched in ribonuclease, Biochemistry 18 (1979) 5291-5299.
18. J.P. Mather, Establishment and characterization of two distinct mouse testicular epithelial cell lines, Biol. Reprod. 23 (1980) 243-252.
19. M.W. McBurney, B.J. Rogers, Isolation of male embryonal carcinoma cells and their chromosome replication patterns, Dev. Biol. 89 (1982) 503-508.
20. J.L. Jainchill, S.A. Aronson, G.J. Todaro, Murine sarcoma and leukemia viruses: assay using cloned lines of contact-inhibited mouse cells, J. Virol. 4 (1969) 503-508.
21. T. Friedberg, M.A. Grassow, F. Oesch, Selective detection of mRNA forms encoding the major phenobarbital inducible cytochrome P450IIB family by the RNase A protection assay, Arch. Biochem. Biophys. 279 (1990) 167-173.
22. K. Franke, B. Drabent, D. 〉 Doenecke, Testicular expression of the mouse histone H1.1 gene, Histochem. Cell Biol. 109 (1998) 383-390.
23. A. Alonso, B. Breuer, H. Bouterfa, D. Doenecke, Early increase in histone H1° mRNA during differentiation of F9 cells to parietal endoderm, EMBO J. 7 (1988) 3003-3008.
24. M.L. Birnstiel, M. Busslinger, K. Strub, Transcription termination and 3′ processing: the end is in site!, Cell 41 (1985) 349-359.
25. D. Doenecke, W. Albig, H. Bouterfa, B. Drabent, Organization and expression of H1 histone and H1 replacement histone genes, J. Cell. Biochem. 54 (1994) 423-431.
26. M.E. Harris, R. Böhni, M.H. Schneiderman, L. Ramamurthy, D. Schümperli, W.F. Marzluff, Regulation of histone mRNA in the unperturbed cell cycle: evidence suggesting control at two posttranscriptional steps, Mol. Cell. Biol. 11 (1991) 2416-2424.
27. R.W. Lennox, L.H. Cohen, The alterations in H1 histone complement during mouse spermatogenesis and their significance for H1 subtype function, Dev. Biol. 103 (1984) 80-84.
28. H. Lindner, M. Wurm, A. Dirschlmayer, B. Sarg, W. Helliger, Application of high-performance capillary electrophoresis to the analysis of H1 histones, Electrophoresis 14 (1993) 480-485.
29. T. Meergans, W. Albig, D. Doenecke, Varied expression patterns of human H1 histone genes in different cell lines, DNA Cell Biol. 16 (1997) 1041-1049.
30. S. Panyim, R.G. Chalkley, A new histone found only in mammalian tissue with little cell division, Biochem. Biophys. Res. Commun. 37 (1969) 1042-1049.
31. S. Khochbin, C. Gorka, J.J. Lawrence, Multiple control level governing H1° mRNA and protein accumulation, FEBS Lett. 283 (1991) 65-67.
32. D. Rousseau, S. Khochbin, C. Gorka, J.J. Lawrence, Regulation of histone H1° accumulation during induced differentiation of murine erythroleukemia cells, J. Mol. Biol. 217 (1991) 85-92.
33. R.R. Tönjes, D. Paul, D. Doenecke, Transgenic mice transcribing the human H1° histone gene exhibit a normal phenotype, Eur. J. Biochem. 245 (1997) 97-102.
34. M.J. Garcia-Iglesias, A. Ramirez, M. Monzo, B. Steuer, J.M. Martinez, J.L. Jorcano, A. Alonso, Specific expression in adult mice and post-implantation embryos of a transgene carrying the histone H1° regulatory region, Differentiation 55 (1993) 27-35.
35. J.R. Pehrson, R.D. Cole, Histone H1 subfractions and H1° turnover in nondividing cells, Biochemistry 21 (1982) 456-460.
36. I.M. Chiu, W.F. Marzluff, Uncoordinate synthesis of histone H1 in cells arrested in the G1 phase, Biochim. Biophys. Acta 699 (1982) 173-182.
37. G. Cheng, A. Nandi, S. Clerk, A.I. Skoultchi, Different 3′-end processing produces two independently regulated mRNAs from a single H1 histone gene, Proc. Natl. Acad. Sci. USA 86 (1989) 7002-7006.
38. U. Dong, A.M. Sirotkin, Y.-S. Yang, D.T. Brown, D.B. Sittman, A.I. Skoultchi, Isolation and characterization of two replication-dependent mouse H1 histone genes, Nucleic Acids Res. 22 (1994) 1421-1428.
39. Z.F. Wang, R. Tisoree, R.W. Debry, M.R. Frey, A.G. Matera, W.F. Marzluff, Characterization of the mouse histone gene cluster on chromosome 13: 45 histone genes in three patches spread over one megabase, Genome Res. 6 (1996) 688-701.
40. W. Albig, B. Drabent, J. Kunz, M. Kalff-Suske, K.H. Grzeschik, D. Doenecke, All known human H1 histone genes except the H1° gene are clustered on chromosome 6, Genomics 16 (1993) 649-654.
41. C.I. Brannan, D.J. Gilbert, J.D. Ceci, Y. Matsuda, V.M. Chapman, J.A. Mercer, H. Eisen, L.A. Johnston, N.G. Copeland, N.A. Jenkins, An interspecific linkage map of mouse chromosome 15 positioned with respect to the centromere, Genomics 13 (1992) 1075-1081.
42. S. Mader, K. Thiele, B. Breuer, A. Alonso, The promoter of the H1° histone gene contains a DNA element bound by retinoic receptors, J. Mol. Biol. 242 (1994) 37-44.
43. H.L. Bouterfa, F.J. Piedrafita, D. Doenecke, M. Pfahl, Regulation of H1° gene expression by nuclear receptors through an unusual response element: implications for regulation of cell proliferation, DNA Cell Biol. 14 (1995) 909-919.
44. S. Khochbin, A.P. Wolffe, Developmentally regulated expression of linker-histone variants in vertebrates, Eur. J. Biochem. 225 (1994) 501-510.
45. L. Yu, M.A. Gorovsky, Constitutive expression, not a particular primary sequence, is the important feature of the H3 replacement variant hv2 in Tetrahymena thermophila, Mol. Cell. Biol. 17 (1997) 6303-6310.
46. J.R. Khadake, M.R.S. Rao, DNA- and chromatin-condensing properties of rat testes H1a and H1t compared to those of rat liver H1bdec: Hit is a poor condenser of chromatin, Biochemistry 34 (1995) 15792-15801.
47. S. Nagaraja, G.P. Delcuve, J.R. Davie, Differential compaction of transcriptionally competent and repressed chromatin reconstituted with histone H1 subtypes, Biochim. Biophys. Acta 1260 (1995) 207-214.
48. D.T. Brown, B.T. Alexander, D.B. Sittman, Differential effect of H1 variant overexpression on cell cycle progression and gene expression, Nucleic Acids Res. 24 (1996) 486-493.
49. D.T. Brown, A. Gunjan, B.T. Alexander, D.B. Sittman, Differential effect of H1 variant overproduction on gene expression is due to differences in the central globular domain, Nucleic Acids Res. 25 (1997) 5003-5009.