In Xenopus oocyte, the formation of complexes between neosynthesized cyclin
s and Cdc2 contributes to Cdc2 kinase activation that triggers meiotic divi
sions. It has been proposed that cytoplasmic membranes could be involved in
this process. To investigate this possibility, we have injected in the ooc
yte two undegradable human cyclin A2 mutants anchored to the endoplasmic re
ticulum (ER) membrane. They encode fusion proteins between the truncated cy
clin A2-Delta 152 and a viral or cellular ER-targeting domain. We show that
both mutants are fully functional as mitotic cyclins when expressed in Xen
opus oocytes, bind Cdc2 and activate M-phase promoting factor. (C) 2001 Pub
lished by Elsevier Science B.V. on behalf of the Federation of European Bio
chemical Societies.