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. 1996 Jul;16(7):3720–3729. doi: 10.1128/mcb.16.7.3720

The testis-specific high-mobility-group protein, a phosphorylation-dependent DNA-packaging factor of elongating and condensing spermatids.

N Alami-Ouahabi 1, S Veilleux 1, M L Meistrich 1, G Boissonneault 1
PMCID: PMC231368  PMID: 8668189

Abstract

Mammalian spermiogenesis is characterized by a striking restructuring of the spermatid chromatin caused by the replacement of nucleohistones with transition proteins and their subsequent replacement with nucleoprotamines. The onset of nuclear elongation and chromatin condensation in spermatids is accompanied by a general decrease in the transcriptional activity of the DNA. A recently identified testis-specific high-mobility-group (tsHMG) protein, similar to the human mitochondrial transcription factor I and to the linker-associated protein delta of Tetrahymena thermophila micronuclei, is thought to play a structural role in this process. We confirm by immunoblot analysis of fractionated germ cells that the presence of tsHMG is restricted to transcriptionally quiescent elongating and condensing spermatids. Purified recombinant tsHMG protein displays preferential binding to supercoiled plasmid DNA, which reversibly protects the DNA against the DNA-relaxing activity of eukaryotic topoisomerase I and also impairs the transcriptional activity of this template when assayed in vitro. The tsHMG protein can also introduce negative supercoils into a relaxed plasmid substrate in a topoisomerase I-dependent manner. We also show that the tsHMG protein is the substrate of a Ca2+-phospholipid-dependent protein kinase (protein kinase C) present in testis extracts of adult mice and demonstrate that phosphorylation by protein kinase C is required for both the DNA-binding and the topoisomerase I-dependent supercoiling activities of tsHMG. Our results support the hypothesis that the spermatid tsHMG protein is a topological factor (transition protein) that can modulate the activity of topoisomerase I. This activity could contribute to the important transition in chromatin structure which leads to the decrease in DNA metabolism observed at the early stages of spermatid elongation.

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Selected References

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  1. Alexander-Bridges M., Ercolani L., Kong X. F., Nasrin N. Identification of a core motif that is recognized by three members of the HMG class of transcriptional regulators: IRE-ABP, SRY, and TCF-1 alpha. J Cell Biochem. 1992 Feb;48(2):129–135. doi: 10.1002/jcb.240480204. [DOI] [PubMed] [Google Scholar]
  2. Balasubramanian B., Lowry C. V., Zitomer R. S. The Rox1 repressor of the Saccharomyces cerevisiae hypoxic genes is a specific DNA-binding protein with a high-mobility-group motif. Mol Cell Biol. 1993 Oct;13(10):6071–6078. doi: 10.1128/mcb.13.10.6071. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Barone J. G., De Lara J., Cummings K. B., Ward W. S. DNA organization in human spermatozoa. J Androl. 1994 Mar-Apr;15(2):139–144. [PubMed] [Google Scholar]
  4. Baskaran R., Rao M. R. Mammalian spermatid specific protein, TP2, is a zinc metalloprotein with two finger motifs. Biochem Biophys Res Commun. 1991 Sep 30;179(3):1491–1499. doi: 10.1016/0006-291x(91)91741-t. [DOI] [PubMed] [Google Scholar]
  5. Bhorjee J. S. Differential phosphorylation of nuclear nonhistone high mobility group proteins HMG 14 and HMG 17 during the cell cycle. Proc Natl Acad Sci U S A. 1981 Nov;78(11):6944–6948. doi: 10.1073/pnas.78.11.6944. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Bianchi M. E., Beltrame M., Paonessa G. Specific recognition of cruciform DNA by nuclear protein HMG1. Science. 1989 Feb 24;243(4894 Pt 1):1056–1059. doi: 10.1126/science.2922595. [DOI] [PubMed] [Google Scholar]
  7. Bianchi M. E., Falciola L., Ferrari S., Lilley D. M. The DNA binding site of HMG1 protein is composed of two similar segments (HMG boxes), both of which have counterparts in other eukaryotic regulatory proteins. EMBO J. 1992 Mar;11(3):1055–1063. doi: 10.1002/j.1460-2075.1992.tb05144.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Boissonneault G., Lau Y. F. A testis-specific gene encoding a nuclear high-mobility-group box protein located in elongating spermatids. Mol Cell Biol. 1993 Jul;13(7):4323–4330. doi: 10.1128/mcb.13.7.4323. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Bucci L. R., Brock W. A., Goldknopf I. L., Meistrich M. L. Characterization of high mobility group protein levels during spermatogenesis in the rat. J Biol Chem. 1984 Jul 25;259(14):8840–8846. [PubMed] [Google Scholar]
  10. Bucci L. R., Brock W. A., Meistrich M. L. Heterogeneity of high-mobility-group protein 2. Enrichment of a rapidly migrating form in testis. Biochem J. 1985 Jul 1;229(1):233–240. doi: 10.1042/bj2290233. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Bustin M., Crippa M. P., Pash J. M. Expression of HMG chromosomal proteins during cell cycle and differentiation. Crit Rev Eukaryot Gene Expr. 1992;2(2):137–143. [PubMed] [Google Scholar]
  12. Bustin M., Lehn D. A., Landsman D. Structural features of the HMG chromosomal proteins and their genes. Biochim Biophys Acta. 1990 Jul 30;1049(3):231–243. doi: 10.1016/0167-4781(90)90092-g. [DOI] [PubMed] [Google Scholar]
  13. Clermont Y., Trott M. Duration of the cycle of the seminiferous epithelium in the mouse and hamster determined by means of 3H-thymidine and radioautography. Fertil Steril. 1969 Sep-Oct;20(5):805–817. doi: 10.1016/s0015-0282(16)37153-9. [DOI] [PubMed] [Google Scholar]
  14. Diffley J. F., Stillman B. DNA binding properties of an HMG1-related protein from yeast mitochondria. J Biol Chem. 1992 Feb 15;267(5):3368–3374. [PubMed] [Google Scholar]
  15. Dimov S. I., Alexandrova E. A., Beltchev B. G. Differences between some properties of acetylated and nonacetylated forms of HMG1 protein. Biochem Biophys Res Commun. 1990 Jan 30;166(2):819–826. doi: 10.1016/0006-291x(90)90883-o. [DOI] [PubMed] [Google Scholar]
  16. Fisher R. P., Lisowsky T., Parisi M. A., Clayton D. A. DNA wrapping and bending by a mitochondrial high mobility group-like transcriptional activator protein. J Biol Chem. 1992 Feb 15;267(5):3358–3367. [PubMed] [Google Scholar]
  17. Geremia R., Boitani C., Conti M., Monesi V. RNA synthesis in spermatocytes and spermatids and preservation of meiotic RNA during spermiogenesis in the mouse. Cell Differ. 1977 Mar;5(5-6):343–355. doi: 10.1016/0045-6039(77)90072-0. [DOI] [PubMed] [Google Scholar]
  18. Giese K., Cox J., Grosschedl R. The HMG domain of lymphoid enhancer factor 1 bends DNA and facilitates assembly of functional nucleoprotein structures. Cell. 1992 Apr 3;69(1):185–195. doi: 10.1016/0092-8674(92)90129-z. [DOI] [PubMed] [Google Scholar]
  19. Green G. R., Balhorn R., Poccia D. L., Hecht N. B. Synthesis and processing of mammalian protamines and transition proteins. Mol Reprod Dev. 1994 Mar;37(3):255–263. doi: 10.1002/mrd.1080370303. [DOI] [PubMed] [Google Scholar]
  20. Grimes S. R., Jr, Smart P. G. Changes in the structural organization of chromatin during spermatogenesis in the rat. Biochim Biophys Acta. 1985 Feb 20;824(2):128–139. doi: 10.1016/0167-4781(85)90089-2. [DOI] [PubMed] [Google Scholar]
  21. Grosschedl R., Giese K., Pagel J. HMG domain proteins: architectural elements in the assembly of nucleoprotein structures. Trends Genet. 1994 Mar;10(3):94–100. doi: 10.1016/0168-9525(94)90232-1. [DOI] [PubMed] [Google Scholar]
  22. Hu C. H., McStay B., Jeong S. W., Reeder R. H. xUBF, an RNA polymerase I transcription factor, binds crossover DNA with low sequence specificity. Mol Cell Biol. 1994 May;14(5):2871–2882. doi: 10.1128/mcb.14.5.2871. [DOI] [PMC free article] [PubMed] [Google Scholar]
  23. Kimura K., Kubo S., Sakurada K., Abe K., Katoh N. Protein kinase C phosphorylation of protamine is Ca2+ independent, but the addition of DNA renders it Ca2+ dependent. Biochim Biophys Acta. 1987 Jul 6;929(2):203–207. doi: 10.1016/0167-4889(87)90177-7. [DOI] [PubMed] [Google Scholar]
  24. King C. Y., Weiss M. A. The SRY high-mobility-group box recognizes DNA by partial intercalation in the minor groove: a topological mechanism of sequence specificity. Proc Natl Acad Sci U S A. 1993 Dec 15;90(24):11990–11994. doi: 10.1073/pnas.90.24.11990. [DOI] [PMC free article] [PubMed] [Google Scholar]
  25. Kohlstaedt L. A., Cole R. D. Specific interaction between H1 histone and high mobility protein HMG1. Biochemistry. 1994 Jan 18;33(2):570–575. doi: 10.1021/bi00168a023. [DOI] [PubMed] [Google Scholar]
  26. Lawrence D. L., Engelsberg B. N., Farid R. S., Hughes E. N., Billings P. C. Localization of the binding region of high mobility group protein 2 to cisplatin-damaged DNA. J Biol Chem. 1993 Nov 15;268(32):23940–23945. [PubMed] [Google Scholar]
  27. Lilley D. M. DNA--protein interactions. HMG has DNA wrapped up. Nature. 1992 May 28;357(6376):282–283. doi: 10.1038/357282a0. [DOI] [PubMed] [Google Scholar]
  28. Lima C. D., Wang J. C., Mondragón A. Three-dimensional structure of the 67K N-terminal fragment of E. coli DNA topoisomerase I. Nature. 1994 Jan 13;367(6459):138–146. doi: 10.1038/367138a0. [DOI] [PubMed] [Google Scholar]
  29. Marushige Y., Marushige K. Phosphorylation of sperm histone during spermiogenesis in mammals. Biochim Biophys Acta. 1978 May 23;518(3):440–449. doi: 10.1016/0005-2787(78)90162-4. [DOI] [PubMed] [Google Scholar]
  30. McPherson S. M., Longo F. J. Localization of DNase I-hypersensitive regions during rat spermatogenesis: stage-dependent patterns and unique sensitivity of elongating spermatids. Mol Reprod Dev. 1992 Apr;31(4):268–279. doi: 10.1002/mrd.1080310408. [DOI] [PubMed] [Google Scholar]
  31. McPherson S. M., Longo F. J. Nicking of rat spermatid and spermatozoa DNA: possible involvement of DNA topoisomerase II. Dev Biol. 1993 Jul;158(1):122–130. doi: 10.1006/dbio.1993.1173. [DOI] [PubMed] [Google Scholar]
  32. McPherson S., Longo F. J. Chromatin structure-function alterations during mammalian spermatogenesis: DNA nicking and repair in elongating spermatids. Eur J Histochem. 1993;37(2):109–128. [PubMed] [Google Scholar]
  33. Meistrich M. L., Reid B. O., Barcellona W. J. Changes sperm culei during sperimogensis and epidymal maturation. Exp Cell Res. 1976 Apr;99(1):72–78. doi: 10.1016/0014-4827(76)90681-9. [DOI] [PubMed] [Google Scholar]
  34. Meistrich M. L., Trostle-Weige P. K., Van Beek M. E. Separation of specific stages of spermatids from vitamin A-synchronized rat testes for assessment of nucleoprotein changes during spermiogenesis. Biol Reprod. 1994 Aug;51(2):334–344. doi: 10.1095/biolreprod51.2.334. [DOI] [PubMed] [Google Scholar]
  35. Meistrich M. L., Trostle P. K., Frapart M., Erickson R. P. Biosynthesis and localization of lactate dehydrogenase X in pachytene spermatocytes and spermatids of mouse testes. Dev Biol. 1977 Oct 15;60(2):428–441. doi: 10.1016/0012-1606(77)90140-3. [DOI] [PubMed] [Google Scholar]
  36. 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. 1995 Mar 3;270(9):4355–4360. doi: 10.1074/jbc.270.9.4355. [DOI] [PubMed] [Google Scholar]
  37. Oliva R., Dixon G. H. Vertebrate protamine genes and the histone-to-protamine replacement reaction. Prog Nucleic Acid Res Mol Biol. 1991;40:25–94. doi: 10.1016/s0079-6603(08)60839-9. [DOI] [PubMed] [Google Scholar]
  38. Oosterwegel M., van de Wetering M., Clevers H. HMG box proteins in early T-cell differentiation. Thymus. 1993 Sep;22(2):67–81. [PubMed] [Google Scholar]
  39. Parisi M. A., Clayton D. A. Similarity of human mitochondrial transcription factor 1 to high mobility group proteins. Science. 1991 May 17;252(5008):965–969. doi: 10.1126/science.2035027. [DOI] [PubMed] [Google Scholar]
  40. Pil P. M., Lippard S. J. Specific binding of chromosomal protein HMG1 to DNA damaged by the anticancer drug cisplatin. Science. 1992 Apr 10;256(5054):234–237. doi: 10.1126/science.1566071. [DOI] [PubMed] [Google Scholar]
  41. Pirhonen A., Valtonen P., Linnala-Kankkunen A., Mäenpä P. H. In vitro phosphorylation sites of stallion and bull P1-protamines for cyclic adenosine 3',5'-monophosphate-dependent protein kinase and protein kinase C. Biol Reprod. 1993 Apr;48(4):821–827. doi: 10.1095/biolreprod48.4.821. [DOI] [PubMed] [Google Scholar]
  42. Reeves R., Langan T. A., Nissen M. S. Phosphorylation of the DNA-binding domain of nonhistone high-mobility group I protein by cdc2 kinase: reduction of binding affinity. Proc Natl Acad Sci U S A. 1991 Mar 1;88(5):1671–1675. doi: 10.1073/pnas.88.5.1671. [DOI] [PMC free article] [PubMed] [Google Scholar]
  43. Reeves R., Nissen M. S. Interaction of high mobility group-I (Y) nonhistone proteins with nucleosome core particles. J Biol Chem. 1993 Oct 5;268(28):21137–21146. [PubMed] [Google Scholar]
  44. Roca J., Mezquita C. DNA topoisomerase II activity in nonreplicating, transcriptionally inactive, chicken late spermatids. EMBO J. 1989 Jun;8(6):1855–1860. doi: 10.1002/j.1460-2075.1989.tb03581.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  45. Sheflin L. G., Fucile N. W., Spaulding S. W. The specific interactions of HMG 1 and 2 with negatively supercoiled DNA are modulated by their acidic C-terminal domains and involve cysteine residues in their HMG 1/2 boxes. Biochemistry. 1993 Apr 6;32(13):3238–3248. doi: 10.1021/bi00064a005. [DOI] [PubMed] [Google Scholar]
  46. Sheflin L. G., Spaulding S. W. High mobility group protein 1 preferentially conserves torsion in negatively supercoiled DNA. Biochemistry. 1989 Jun 27;28(13):5658–5664. doi: 10.1021/bi00439a048. [DOI] [PubMed] [Google Scholar]
  47. Studier F. W., Moffatt B. A. Use of bacteriophage T7 RNA polymerase to direct selective high-level expression of cloned genes. J Mol Biol. 1986 May 5;189(1):113–130. doi: 10.1016/0022-2836(86)90385-2. [DOI] [PubMed] [Google Scholar]
  48. Toullec D., Pianetti P., Coste H., Bellevergue P., Grand-Perret T., Ajakane M., Baudet V., Boissin P., Boursier E., Loriolle F. The bisindolylmaleimide GF 109203X is a potent and selective inhibitor of protein kinase C. J Biol Chem. 1991 Aug 25;266(24):15771–15781. [PubMed] [Google Scholar]
  49. Trostle-Weige P. K., Meistrich M. L., Brock W. A., Nishioka K. Isolation and characterization of TH3, a germ cell-specific variant of histone 3 in rat testis. J Biol Chem. 1984 Jul 25;259(14):8769–8776. [PubMed] [Google Scholar]
  50. Unni E., Mayerhofer A., Zhang Y., Bhatnagar Y. M., Russell L. D., Meistrich M. L. Increased accessibility of the N-terminus of testis-specific histone TH2B to antibodies in elongating spermatids. Mol Reprod Dev. 1995 Oct;42(2):210–219. doi: 10.1002/mrd.1080420210. [DOI] [PubMed] [Google Scholar]
  51. Unni E., Meistrich M. L. Purification and characterization of the rat spermatid basic nuclear protein TP4. J Biol Chem. 1992 Dec 15;267(35):25359–25363. [PubMed] [Google Scholar]
  52. Wampler S. L., Tyree C. M., Kadonaga J. T. Fractionation of the general RNA polymerase II transcription factors from Drosophila embryos. J Biol Chem. 1990 Dec 5;265(34):21223–21231. [PubMed] [Google Scholar]
  53. Ward W. S., Coffey D. S. DNA packaging and organization in mammalian spermatozoa: comparison with somatic cells. Biol Reprod. 1991 Apr;44(4):569–574. doi: 10.1095/biolreprod44.4.569. [DOI] [PubMed] [Google Scholar]
  54. Wu M., Allis C. D., Sweet M. T., Cook R. G., Thatcher T. H., Gorovsky M. A. Four distinct and unusual linker proteins in a mitotically dividing nucleus are derived from a 71-kilodalton polyprotein, lack p34cdc2 sites, and contain protein kinase A sites. Mol Cell Biol. 1994 Jan;14(1):10–20. doi: 10.1128/mcb.14.1.10. [DOI] [PMC free article] [PubMed] [Google Scholar]
  55. Zechiedrich E. L., Osheroff N. Eukaryotic topoisomerases recognize nucleic acid topology by preferentially interacting with DNA crossovers. EMBO J. 1990 Dec;9(13):4555–4562. doi: 10.1002/j.1460-2075.1990.tb07908.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  56. van de Wetering M., Clevers H. Sequence-specific interaction of the HMG box proteins TCF-1 and SRY occurs within the minor groove of a Watson-Crick double helix. EMBO J. 1992 Aug;11(8):3039–3044. doi: 10.1002/j.1460-2075.1992.tb05374.x. [DOI] [PMC free article] [PubMed] [Google Scholar]

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