Jm. Lemaitre et al., SELECTIVE AND RAPID NUCLEAR TRANSLOCATION OF A C-MYC-CONTAINING COMPLEX AFTER FERTILIZATION OF XENOPUS-LAEVIS EGGS, Molecular and cellular biology, 15(9), 1995, pp. 5054-5062
We report here unusual features of c-Myc specific to early embryonic d
evelopment in Xenopus laevis, a period characterized by generalized tr
anscriptional quiescence and rapid biphasic cell cycles, Two c-Myc pro
tein forms, p61 and p64, are present in large amounts in the oocyte as
well as during early development, In contrast, only p64 c-Myc is pres
ent in Xenopus somatic cells, p61 c-Myc is the direct translation prod
uct from both endogenous c-myc mRNAs and c-myc recombinant DNA, It is
converted to the p64 c-Myc form after introduction into an egg extract
, in the presence of phosphatase inhibitors, p61 and p64 belong to two
distinct complexes localized in the cytoplasm of the oocyte, A 15S co
mplex contains p64 c-Myc, and a 17.4S complex contains p61 c-Myc. Fert
ilization triggers the selective and total entry of only p64 c-Myc int
o the nucleus, This translocation occurs in a nonprogressive manner an
d is completed during the first cell cycles, This phenomenon results i
n an exceptionally high level of c-Myc in the nucleus, which returns t
o a somatic cell-like level only at the end of the blastulation period
. During early development, when the entire embryonic genome is transc
riptionally inactive, c-Myc does not exhibit a DNA binding activity wi
th Max, Moreover, embryonic nuclei not only prevent the formation of c
-Myc/Max complexes but also dissociate such preformed complexes, These
peculiar aspects of c-Myc behavior suggest a function that could be l
inked to the rapid DNA replication cycles occurring during the early c
ell cycles rather than a function involving transcriptional activity.