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Histone Gene Expression in the Human Testis

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Book cover The Fate of the Male Germ Cell

Part of the book series: Advances in Experimental Medicine and Biology ((AEMB,volume 424))

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Abstract

The function of histones has been classically assigned to the formation of DNA-protein-complexes, called nucleosomes. A nucleosomal core consists of a stretch of DNA wrapped around an octamer of core histones (H2A, H2B, H3 and H4). A further condensation into higher order chromatin is achieved by the linker histone H1, which is associated with the nucleosome. Additionally, recent evidence suggest an active participation of histones in the transcription and regulation of genes (Wolfe, 1995). Several histone subtypes have been isolated which can be divided into replication-dependent, replication-independent (replacement) and tissue-specific isoforms. The expression of these subtypes varies with respect to the cell line and tissue investigated (Meergans et al., 1996). During spermatogenesis, the histone fraction of spermatogenic cells is largely replaced by testis specific isoforms in rat and mice (Doenecke and Drabent, 1995).

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References

  • Albig W, Ebentheuer J, Klobeck G, Kunz J, and Doenecke D 1996 Human Genetics 97: 486–491

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  • Doenecke D & Drabent B 1995 in Advances in spermatozoa’ Phylogeny and Taxonomy (Jamieson, B. G. M., Au- sio, J., and Justine, J.-L., Ed.). Vol. 166: 525–535. Mémoires du Muséum National d’Histoire Naturale, Paris.

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  • Meergans T. Albig W, and Doenecke D 1997 submitted for publication.

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  • Wolffe A 1995 Chromatin Structure and Function ( London: Academic Press).

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© 1997 Springer Science+Business Media New York

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Witt, O., Gavénis, K., Doenecke, D. (1997). Histone Gene Expression in the Human Testis. In: Ivell, R., Holstein, AF. (eds) The Fate of the Male Germ Cell. Advances in Experimental Medicine and Biology, vol 424. Springer, Boston, MA. https://doi.org/10.1007/978-1-4615-5913-9_5

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  • DOI: https://doi.org/10.1007/978-1-4615-5913-9_5

  • Publisher Name: Springer, Boston, MA

  • Print ISBN: 978-1-4613-7711-5

  • Online ISBN: 978-1-4615-5913-9

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