Summary
The pattern of subtypes of the nucleosomal histories and of historic Hl was investigated in human cells from adult and fetal lung and liver, from carcinoma tissues and from carcinoma-derived cell lines, with the object of comparing these patterns, and their relationship to cell growth rate, with those in cells of other species. The subtype pattern of the nucleosomal histories H2A and H3 shows a correlation with replication rate. In adult tissues, subtype H3-3 predominates over H3-2 and H3-1, and the subtype H2A-1 and H2A-2 are approximately equally abundant. In fetal tissues, lung carcinoma and cultured carcinoma-derived cell lines, the subtype H3-1 is predominant and H2A-1 is more abundant than H2A-2. The subtype pattern of H 1 also differs between normal and carcinoma cells, among different tissues, and in different cell lines derived from the same type of carcinoma. In particular, the relative level of H1° differs in several cell lines showing relatively high rates of replication, and in some cases represents more than 25% of the total H1, similar to the level in slowly replicating normal adult liver and lung tissues. The relative level of H1° does not therefore appear to be correlated in a simple manner with cell growth rate in these human cells.
Similar content being viewed by others
Abbreviations
- PhMeS02 :
-
phenylmethylsulfonyl fluoride
- SDS:
-
sodium dodecyl sulphate
References
Isenberg I: Histones. Ann Rev Biochem 48: 159–191, 1979.
Zweidler A: Complexity and variability of the histone complement. Dahlem Konferenzen, Life Sci Rep 4:187–196, 1976.
Zweidler A: Nonallelic histone variants in development and differentiation. Dev Biochem 15:4–36, 1980.
Urban MK, Zweidler A: Changes in nucleosomal core histone variants during chicken development and maturation. Dev Biol 95:421–428, 1983.
Lennox ZW, Cohen LH: The histone H1 complements of dividing and non dividing cells of the mouse. J Biol Chem 258:262–268,1983.
Gjerset R, Gorka C, Hasthorpe S, Lawrence JJ, Eisen H: Developmental and hormonal regulation of protein H1° in rodents. Proc Natl Acad Sci USA 79:2333–2337, 1982.
Strickland M, Strickland WN, Von Holt C: The occurrence of sperm isohistones H2B in single sea urchin. FEBS Lett 135:86–88, 1981.
Ajiro K, Borun TW, Solter D: Quantitative changes in the expression of histone H1 and H2b subtypes and their relationship to the differentiation of mouse embryonal carcinoma cells. Dev Biol 86:206–211, 1981.
Blanckstein LA, Levy SB: Changes in histone f2a2 associated with proliferation of Friend leukaemic cells. Nature (London) 260:638–640, 1976.
Tan KB, Borun TW, Charpentier R, Cristofalo VJ, Croce CM: Normal and neoplastic human cells have different histone H1 composition. J Biol Chem 257:5337–5338, 1982.
Matthis D, Oudet P, Chambon P: Structure of transcribing chromatin. Progr Nucleic Acid Res Mol Biol 24:1–55, 1980.
Gabrielli F, Faber AJ, Hancock R: Characterization of a chromatin fraction bearing pulse-labelled RNA. 2. Quantification of histones and high-mobility-group proteins. Eur J Biochem 120:363–369, 1981.
Kedes LH: Histone genes and histone messengers. Ann Rev Biochem 48:837–870, 1979.
Newrock KM, Alfagame CR, Nardi RV, Cohen LH: Historic changes during chromatin remodeling in embryogenesis. Cold Spring Harbor Symp Quant Biol 42:421–431, 1978.
Gabrielli F, Baglioni C: Maternal messenger RNA and histone synthesis in embryos of the surf clam Spisula solidissima. Dev Biol 43:254–263, 1975.
Homan P, Cole RD: Hormonal effects on amino acid incorporation into lysine-rich histones in the mouse mammary gland. J Mol Biol 8:533–540, 1971.
Albright SC, Nelson PP, Garrard WT: Historic molar ratio among different electrophoretic forms of mono and dinucleosomes. J Biol Chem 254:1065–1073, 1979.
Pehrson JR, Cole RD: Bovine H1° histone subfractions contain an invariant sequence which matches histone H5 rather than H1. Biochemistry 20:2298–2301, 1981.
Varricchio F: Postnatal increase in histone H1a in the rat pancreas. Arch Biochem Biophys 179:715–717, 1977.
Paniym S, Chalkley R: A new histone found only in mammalian tissues with little cell division. Biochem Biophys Res Commun 37:1042–1049, 1969.
Seydin SM, Kistler WS: Isolation and characterization of rat testis Hlt. An H1 histone variant associated with spermatogenesis. J Biol Chem 255:5949–5954, 1980.
Seydin SM, Cole RD, Kistler WS: H1 histone from mammalian testes. The wide-spread occurrence of H1t. Exp Cell Res 136:399–405, 1981.
Brasch K, Adams GHM, Neelin JH: Evidence for erythrocyte-specific histone modification and structural changes in chromatin during goose erythrocyte maturation. J Cell Sci 15:659–677, 1974.
Zlatanova J: Is histone H5 present in mammals? Mol Biol Rep 7:235–239, 1981.
Von Bahr C, Groth G, Jansson H, Lundgen G, Lind M, Glaumann H: Drug metabolism in human liver in vitro: establishment of a human liver bank. Clin Pharmacol Ther 27:711–725, 1980.
Aden DP, Fogel A, Plotkin S, Damjanov I, Knowles BB: Controlled synthesis of HBsAG in a differentiated human liver carcinoma derived cell line. Nature (London) 282: 615–616, 1979.
Wray W, Boulikas T, Wray VP, Hancock R: Silver staining of proteins in polyacrylamide gels. Anal Biochem 118:197–203, 1981.
Zweidler A: Resolution of histones by polyacrylamide gel electrophoresis in presence of non-ionic detergents. Methods Cell Biol 17:223–233, 1978.
Marks DB, Kanefsky T, Keller BJ, Marks AD: The presence of histone Hl° in human tissues. Cancer Res 35:886–889, 1975.
Keppel F, Allet B, Eisen H: Appearance of a chromatin protein during the erythroid differentiation of Friends virustransformed cells. Proc Natl Acad Sci USA 74:635–656, 1977.
Hereford L, Faherner K, Woolford J, Rasbash M, Kaback DB: Isolation of yeast histone genes H2A and H2B. Cell 18:1261–1271, 1979.
Rykowsky MC, Wallis JW, Choe J, Grunstein M: Histone H2B subtypes are despensable during the yeast cell cycle. Cell 25:477–487, 1981.
Kolodrubetz D, Rikowsky MC, Grunstein M: Histone H2A subtypes associate interchangeably in vivo with histone H2B subtypes. Proc Natl Acad Sci USA 79:7814–7818, 1982.
Pieler C, Adolf GR, Swetly P: Accumulation of histone H1° during chemically induced differentiation of murine neuroblastoma cells. Eur J Biochem 115:329–333, 1981.
Zlatanova J, Adolf GR, Swetly P: Expression of histone H1° during differentiation of erythroleukemic mouse cells. In GB Rossi (ed), In Vivo and In Vitro Erythropoiesis: The Friend System. Elsevier/North Holland, Amsterdam, 1980, pp 297–307.
D'Anna JA, Tobey RA, Gurley LR: Concentration-dependent effect of sodium butyrate in chinese hamster cells: cell cycle progression, inner-histone acetylation, histone H l dephosphorylation, and induction of an H1-like protein. Biochemistry 19:2656–2671, 1980.
D'Anna JA, Gurley LR, Becker RR, Barham SS, Tobey RA, Walte RA: Amino acid analysis and cell cycle dependent phosphorylation of an H1-like, butyrate-enhanced protein (BEP;H1°;IP25) from chinese hamster cells. Biochemistry 19:4331–4341, 1980.
Marsh WH, Fitzgerald PJ: Pancreas acinar cell regeneration. XIII. Histone synthesis and modification. Fed Proc 39:2119–2125, 1973.
Pehrson J, Cole RD: Histone H1° accumulates in growth-inhibited cultured cells. Nature (London) 285:43–44, 1980.
Author information
Authors and Affiliations
Rights and permissions
About this article
Cite this article
Gabriellia, F., Aden, D.P., Carrele, S.C. et al. Histone complements of human tissues, carcinomas, and carcinoma-derived cell lines. Mol Cell Biochem 65, 57–66 (1984). https://doi.org/10.1007/BF00226019
Received:
Issue Date:
DOI: https://doi.org/10.1007/BF00226019