It is known that a transition in the linker-histone variants takes pla
ce within chromatin during early development of Xenopus laevis; a clea
vage-type H1 is replaced by the somatic type. Based on cytofluorimetri
c analysis of the distribution of the embryo cells in the cell cycle,
we showed that this previously described transition occurs when signif
icant modifications of the proliferative capacities of the cells occur
. Moreover, this analysis allowed us to show that cell proliferation d
ecreases gradually after the gastrula stage of development. This perio
d terminates with the arrest of more than 90% of cells in the G0/G1 ph
ase of the cell cycle at stage 45. We showed that the major accumulati
on of the differentiation-specific H1 subtype, histone H1(0), occurs a
t this time. H1(0), first detected in a restricted set of tissues, is
then widely expressed during the later development at stage 45. Moreov
er, the double staining of nuclei isolated from embryo cells, for H1(0
) and DNA, allowed us to show that this accumulation of H1(0) is not r
estricted to arrested cells. The example of the Xenopus early developm
ent shows that there may be an adaptation of the type of H1 expressed
to the proliferative abilities of cells. This observation may provide
insight into the significance of the expression of different H1 subtyp
es during development, (C) 1995 Academic Press, Inc.