Journal of Cell Science, Vol 113, Issue 16 2897-2907, Copyright © 2000 by Company of Biologists

JOURNAL ARTICLES

Somatic linker histone H1 is present throughout mouse embryogenesis and is not replaced by variant H1 degrees

PG Adenot, E Campion, E Legouy, CD Allis, S Dimitrov, J Renard and EM Thompson
Unite de Biologie du Developpement, Institut National de la Recherche Agronomique, F-78352 Jouy-en-Josas, France. adenot@biotec. jouy.inra.fr

A striking feature of early embryogenesis in a number of organisms is the use of embryonic linker histones or high mobility group proteins in place of somatic histone H1. The transition in chromatin composition towards somatic H1 appears to be correlated with a major increase in transcription at the activation of the zygotic genome. Previous studies have supported the idea that the mouse embryo essentially follows this pattern, with the significant difference that the substitute linker histone might be the differentiation variant H1 degrees, rather than an embryonic variant. We show that histone H1 degrees is not a major linker histone during early mouse development. Instead, somatic H1 was present throughout this period. Though present in mature oocytes, somatic H1 was not found on maternal metaphase II chromatin. Upon formation of pronuclear envelopes, somatic H1 was rapidly incorporated onto maternal and paternal chromatin, and the amount of somatic H1 steadily increased on embryonic chromatin through to the 8-cell stage. Microinjection of somatic H1 into oocytes, and nuclear transfer experiments, demonstrated that factors in the oocyte cytoplasm and the nuclear envelope, played central roles in regulating the loading of H1 onto chromatin. Exchange of H1 from transferred nuclei onto maternal chromatin required breakdown of the nuclear envelope and the extent of exchange was inversely correlated with the developmental advancement of the donor nucleus.
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