Warning: mkdir(): Permission denied in /home/virtual/lib/view_data.php on line 81

Warning: fopen(upload/ip_log/ip_log_2024-12.txt): failed to open stream: No such file or directory in /home/virtual/lib/view_data.php on line 83

Warning: fwrite() expects parameter 1 to be resource, boolean given in /home/virtual/lib/view_data.php on line 84
Study on the chromosomal proteins of Fasciola hepatica
| Home | E-Submission | Sitemap | Contact us |  
top_img
Korean J Parasito Search

CLOSE

Korean J Parasito > Volume 16(1):1978 > Article

Original Article
Korean J Parasitol. 1978 Jun;16(1):26-40. English.
Published online Mar 20, 1994.  http://dx.doi.org/10.3347/kjp.1978.16.1.26
Copyright © 1978 by The Korean Society for Parasitology
Study on the chromosomal proteins of Fasciola hepatica
Soon-Hyung Lee,Chul-Yong Song,Keun-Bae Lee and Hi-Sung Lee
Department of Parasitology, College of Medicine, Chung-Ang University, Korea.
Department of Biochemistry, College of Medicine, Chung-Ang University, Korea.
Abstract

In attempt to investigate histone fractions and non-histones of parasites, nuclei were isolated from Fasciola hepatica by the procedure of Pogo et al. (1966). Histone fractions H1, H2a, H2b, H3 and H4 were prepared from isolated nuclei by the procedure of Johns (1964 and l967). The five histone fractions found in most tissues were also present in the Fasciola hepatica histones. These histone fractions were characterized by amino acid analysis and by polyacrylamide disc gel electrophoresis. Non-histone proteins were extracted from isolated Fasciola hepatica nuclei and separated by SDS-polyacrylamide gel electrophoresis.

The results of the experiment were summarized as follows:

1. The yield of whole histone recovered was 2.47 mg per 1 g of Fasciola hepatica.

2. The yield of DNA was 1.02 mg per gm of tissues. Consequently the DNA to histone ratio was 1:2.44.

3. The relative amounts of five fractions, i.e., Hl, H2a, H2b, H3 and H4 were 19.96%, 26.48%, 29.60%, 12.56% and 14.37%, respectively.

4. Amino acid analysis of the individual histone fractions showed that the over-all compositions were similar but not identical to those of corresponding fraction from calf thymus.

5. It was found that histone H2b fraction of Fasciola hepatica contained detectable amounts of ε-N-monomethyllysine. No evidence for the presence of methylated lysine or other side-chain derivatives was reported on this histone fraction.

6. In SDS-polyacrylamide disc gel, it showed that 17 protein bands of nuclear acidic protein can be identified visually.

Figures


Fig. 1
Chromatographic separation of the amino acids of Fasciola hepatica histone fraction H1 under the standard conditions described under "Materials and Methods". Ninhydrin color intensity is plotted against the time of elution.


Fig. 2
Elution profile of a standard amino acid mixture containing the methylated derivatives of lysine and histidine. This standard amino-acid mixture was separated on the amine analyzer column under the conditions described under "Materials and Methods". Nin-hydrin color intensity is plotted against the time of elution. DML: N-dimethyllysine; MML: N-monomethyllysine; 3-MH: 3-methy-1histidine.


Fig. 3
Chromatography of the amino acids of Fasciola hepatica histone fraction H2b under the conditions described in Fig. 2. Ninhydrin color intensity is plotted against the time of elution, beginning with the appearance of the lysine peak.


Fig. 4
Non-histone proteins which were isolated from Fasciola hepatica were soluble in 0.01 M sodium phosphate buffer(pH 7.2) containing 0.1% sodium dodecy1 sulphate and 0.14M 2-mercaptoethanol. Samples containing 200µg of proteins were analyzed by 10% polyacry-lamide-gel electrophoresis at room temperature, at a constant voltage of 6V/cm. The gels were stained with Amido Black 1OB.


Fig. 5
Non-histone proteins were obtained from Fasciola hepatica nuclei. These proteins were fractionated by polyacrylamide gel electrophoresis. The gels were stained with Amido Black 10B and scanned at 570 nm as described in the "Materials and Methods".

Tables


Table I
Contents of DNA and total histone from Fasciola hepatica


Table II
Yields of histone from Fasciola hepatica


Table III
Relative yields of histone fractions from various sourses. Values are expressed as per cent of total histone


Table IV
Amino acid compostition of histone fractions from Fasciola hepatica. Results are given as moles/100 moles of all amino acids recovered


Table V-1
Amino acid compositions of histones from Fasciola hepatica in comparison with those of calf thymus


Tables V-2
Amino acid compositions of histones from Fasciola hepatica comparison with those of calf thymus


Table VI
Contents of methylated amino acid residues in histone fractions of Fasciola hepatica. Values are expressed as moles/100 moles of all amino acids recovered.


Table VII
Distribution of protein in extracts of Fasciola hepatica nuclei

References
1. Gershey EL, Vidali G, Allfrey VG. Chemical studies of histone acetylation. The occurrence of epsilon-N-acetyllysine in the f2a1 histone. J Biol Chem 1968;243(19):5018–5022.
 
2. Ambler RP, Rees MW. Epsilon-N-Methyl-lysine in bacterial flagellar protein. Nature 1959;184:56–57.
  
3. Asatoor AM, Armstrong MD. 3-methylhistidine, a component of actin. Biochem Biophys Res Commun 1967;26(2):168–174.
  
4. Bellair JT, et al. Biochem Biophys Acta 1967;133:263–271.
 
5. Benjamin W, Gellhorn A. Acidic proteins of mammalian nuclei: isolation and characterization. Proc Natl Acad Sci U S A 1968;59(1):262–268.
  
6. Blankstein LA, Stollar BD, Franklin SG, Zweidler A, Levy SB. Biochemical and immunological characterization of two distinct variants of histone H2A in Friend leukemia. Biochemistry 1977;16(21):4557–4562.
  
7. Bonner J, Dahmus ME, Fambrough D, Huang RC, Marushige K, Tuan DY. The Biology of Isolated Chromatin: Chromosomes, biologically active in the test tube, provide a powerful tool for the study of gene action. Science 1968;159(3810):47–56.
  
8. Borun TW, Pearson D, Paik WK. Studies of histone methylation during the HeLa S-3 cell cycle. J Biol Chem 1972;247(13):4288–4298.
 
9. Burton K. A study of the conditions and mechanism of the diphenylamine reaction for the colorimetric estimation of deoxyribonucleic acid. Biochem J 1956;62(2):315–323.
 
10. Crampton CF, Stein WH, Moore S. Comparative studies on chromatographically purified histones. J Biol Chem 1957;225(1):363–386.
 
11. Daskal Y, Ballal NR, Busch H. Scanning electron microscopy and biochemical studies on reconstituted and native chromatin fractions of Novikoff hepatoma ascites cells. Exp Cell Res 1977;108(2):301–309.
  
12. DeLange RJ, et al. Proc Natl Acad Sci USA 1968;61:1145–1146.
13. DeLange RJ, Fambrough DM, Smith EL, Bonner J. Calf and pea histone IV. 3. Complete amino acid sequence of pea seedling histone IV; comparison with the homologous calf thymus histone. J Biol Chem 1969;244(20):5669–5679.
 
14. DeLange RJ, et al. Ann Rev Biochem 1971;40:279–287.
  
15. Dick C, Johns EW. The biosynthesis of the five main histone fractions of rat thymus. Biochim Biophys Acta 1969;174(1):380–386.
 
16. Duerre JA, Chakrabarty S. Methylated basic amino acid composition of histones from the various organs from the rat. J Biol Chem 1975;250(21):8457–8461.
 
17. Ewars PA, Sooter KV. Ultracentrifuge tudies of histone fractions from calf thymus deoxyribonucleoprotein. Biochem J 1969;114(2):227–235.
 
18. Elgin SC, Bonner J. Limited heterogeneity of the major nonhistone chromosomal proteins. Biochemistry 1970;9(22):4440–4447.
  
19. Farmbrough DM, Fujimura F, Bonner J. Quantitative distribution of histone components in the pea plant. Biochemistry 1968;7(2):575–585.
  
20. Gershey EL, Haslett GW, Vidali G, Allfrey VG. Chemical studies of histone methylation. Evidence for the occurrence of 3-methylhistidine in avian erythrocyte histone fractions. J Biol Chem 1969;244(18):4871–4877.
 
21. Gurley LR, Walters RA, Tobey RA. Cell cycle-specific changes in histone phosphorylation associated with cell proliferation and chromosome condensation. J Cell Biol 1974;60(2):356–364.
  
22. Gurley LR, Walters RA, Tobey RA. Sequential phsophorylation of histone subfractions in the Chinese hamster cell cycle. J Biol Chem 1975;250(10):3936–3944.
 
23. Honda BM, Dixon GH, Candido EP. Sites of in vivo histone methylation in developing trout testis. J Biol Chem 1975;250(22):8681–8685.
 
24. Iwai K, Ishikawa K, Hayashi H. Amino-acid sequence of slightly lysine-rich histone. Nature 1970;226(5250):1056–1058.
  
25. Jackson V, Shires A, Chalkley R, Granner DK. Studies on highly metabolically active acetylation and phosphorylation of histones. J Biol Chem 1975;250(13):4856–4863.
 
26. Johns EW. A method for the selective extraction of histone fractions f2(a)1 and f2(a)2 from calf thymus deoxyribonucleoprotein at pH7. Biochem J 1967;105(2):611–614.
 
27. Johnson P, Harris CI, Perry SV. 3-methylhistidine in actin and other muscle proteins. Biochem J 1967;105(1):361–370.
 
28. Jungmann RA, Schweppe JS, Lestina FA. Studies on adrenal histones. Characterization, biosynthesis, enzymatic phosphorylation, and acetylation of histones from a human adrenal carcinoma. J Biol Chem 1970;245(17):4321–4326.
 
29. Kamiyama M, Wang TY. Activated transcription from rat liver chromatin by non-histone proteins. Biochim Biophys Acta 1971;228(2):563–576.
 
30. Kaplowitz PB, Platz RD, Kleinsmith LJ. Nuclear phosphoproteins 3 Increase in phosphory- lation during histone-phosphoprotein interaction. Biochim Biophys Acta 1971;229(3):739–748.
 
31. Kinkade JM Jr. Qualitative species differences and quantitative tissue differences in the distribution of lysine-rich histones. J Biol Chem 1969;244(12):3375–3386.
 
32. Kleinsmith LJ. Specific binding of phosphorylated non-histone chromatin proteins to deoxyribonucleic acid. J Biol Chem 1973;248(16):5648–5653.
 
33. Kornberg RD. Ann Rev Biochem 1977;46:931–954.
  
34. Lee KS. Korean Biochem J 1971;4:77–99.
35. Lowry OH, Rosebrough NJ, Farr AL, Randall RJ. Protein measurement with the Folin phenol reagent. J Biol Chem 1951;193(1):265–275.
 
36. MacGillivray AJ, Cameron A, Krauze RJ, Rickwood D, Paul J. The non-histone proteins of chromatin, their isolation and composition in a number of tissues. Biochim Biophys Acta 1972;277(2):384–402.
 
37. Marzluff WF Jr, McCarty KS. Two classes of histone acetylation in developing mouse mammary gland. J Biol Chem 1970;245(21):5635–5642.
 
38. Murray K. The Occurrence of Epsilon-N-methyl Lysine in Histones. Biochemistry 1964;3:10–15.
  
39. Okita K, Zardi L. Immunofluorescent study of chromatin proteins in cultured fibroblasts. Exp Cell Res 1974;86(1):59–62.
  
40. Olins AL, Olins DE. Spheroid chromatin units (v bodies). Science 1974;183(4122):330–332.
  
41. Ord MG, Stocken LA. Metabolic properties of histones from rat liver and thymus gland. Biochem J 1966;98(3):888–897.
 
42. Ord MG, Stocken LA. Variations in the phosphate content and thiol/disulphide ratio of histones during the cell cycle. Studies with regenerating rat liver and sea urchins. Biochem J 1968;107(3):403–410.
 
43. Paik WK, et al. Biochem Biophys Res Commun 1967;27:479–483.
 
44. Paik WK, Lee HW, Morris HP. Protein methylases in hepatomas. Cancer Res 1972;32(1):37–40.
 
45. Panyim S, Bilek D, Chalkley R. An electrophoretic comparison of vertebrate histones. J Biol Chem 1971;246(13):4206–4215.
 
46. Patthy L, Smith EL. Histone 3. V. The amino acid sequence of pea embryo histone 3. J Biol Chem 1973;248(19):6834–6840.
 
47. Phelan JJ, Colom J, Cozcolluela C, Subirana JA, Cole RD. A lysine-rich protein from spermatozoa of the mollusc Mytilus edulis. J Biol Chem 1974;249(4):1099–1102.
 
48. Phillips DM, Johns EW. A Fractionation of the Histones of Group F2a From Calf Thymus. Biochem J 1965;94:127–130.
 
49. Pogo AO, Allfrey VG, Mirsky AE. Evidence for increased DNA template activity in regenerating liver nuclei. Proc Natl Acad Sci U S A 1966;56(2):550–557.
  
50. Rall SC, Cole RD. Amino acid sequence and sequence variability of the amino-terminal regions of lysine-rich histones. J Biol Chem 1971;246(23):7175–7190.
 
51. Reisfeld RA, et al. Nature 1962;21:281–283.
 
52. Sherod D, Johnson G, Chalkley R. Studies on the hetrogeneity of lysine-rich histones in dividing cells. J Biol Chem 1974;249(12):3923–3931.
 
53. Shires A, Carpenter MP, Chalkley R. A cysteine-containing H2B-like histone found in mature mammalian testis. J Biol Chem 1976;251(13):4155–4158.
 
54. Spelsberg TC, Steggles AW, Chytil F, O'Malley BW. Progesterone-binding components of chick oviduct. V. Exchange of progesterone-binding capacity from target to nontarget tissue chromatins. J Biol Chem 1972;247(5):1368–1374.
 
55. Spackman DH, et al. Anal Chem 1958;30:1190–1206.
 
56. Spiker S, Isenberg I. Cross-complexing pattern of plant histones. Biochemistry 1977;16(9):1819–1826.
  
57. Stedman E. Cell specificity of histones. Nature 1950;166(4227):780–781.
  
58. Stein G, Farber J. Role of nonhistone chromosomal proteins in the restriction of mitotic chromatin template activity. Proc Natl Acad Sci U S A 1972;69(10):2918–2921.
  
59. Stein GS, Hunter G, Lavie L. Non-histone chromosomal proteins. Evidence for their role in mediating the binding of histones to deoxyribonucleic acid during the cell cycle. Biochem J 1974;139(1):71–76.
 
60. Stocker BAD, et al. Nature 1961;189:556–558.
 
61. Wagner TE, Hartford JB, Serra M, Vandegrift V, Sung MT. Phosphorylation and dephosphorylation of histone (V (H5): controlled condensation of avian erythrocyte chromatin. Appendix: Phosphorylation and dephosphorylation of histone H5. II. Circular dichroic studies. Biochemistry 1977;16(2):286–290.
  
62. Sung MT, Harford J, Bundman M, Vidalakas G. Metabolism of histones in avian erythroid cells. Biochemistry 1977;16(2):279–285.
  
63. Suria D, Liew CC. Isolation of nuclear acidic proteins from rat tissues. Characterization of acetylated liver nuclear acidic proteins. Biochem J 1974;137(2):355–362.
 
64. Teng CS, Teng CT, Allfrey VG. Studies of nuclear acidic proteins. Evidence for their phosphorylation, tissue specificity, selective binding to deoxyribonucleic acid, and stimulation effects on transcription. J Biol Chem 1971;246(11):3597–3609.
 
65. Thomas JO, Kornberg RD. An octamer of histones in chromatin and free in solution. Proc Natl Acad Sci U S A 1975;72(7):2626–2630.
  
66. Vidali G, Boffa LC, Allfrey VG. Properties of an acidic histone-binding protein fraction from cell nuclei. Selective precipitation and deacetylation of histones F2A1 and F3. J Biol Chem 1972;247(22):7365–7373.
 
67. Weber K, Osborn M. The reliability of molecular weight determinations by dodecyl sulfate-polyacrylamide gel electrophoresis. J Biol Chem 1969;244(16):4406–4412.
 
Editorial Office
Department of Molecular Parasitology, Samsung Medical Center, School of Medicine, Sungkyunkwan University,
2066 Seobu-ro, Jangan-gu, Suwon 16419, Gyeonggi-do, Korea.
Tel: +82-31-299-6251   FAX: +82-1-299-6269   E-mail: kjp.editor@gmail.com
About |  Browse Articles |  Current Issue |  For Authors and Reviewers
Copyright © 2024 by The Korean Society for Parasitology and Tropical Medicine.     Developed in M2PI