Abstract

In several species, including Xenopus, mouse and human, two members of cyclin A family were identified. Cyclin A2, which is ubiquitously expressed in dividing cells and plays role in DNA replication, entry into mitosis and spindle assembly, and cyclin A1, whose function is less clear and which is expressed in spermatocytes, leukemia cells and in postmitotic multiciliated cells. Deletion of the gene showed that cyclin A1 is essential for male meiosis, but nonessential for female meiosis. Our results revealed, that the cyclin A1 is not only dispensable in oocytes, we show here that its expression is in fact undesirable in these cells. Our data demonstrate that the APC/C and proteasome in oocytes are unable to target sufficiently cyclin A1 before anaphase, which leads into anaphase arrest and direct inhibition of separase. The cyclin A1-induced cell cycle arrest is oocyte-specific and the presence of cyclin A1 in early embryos has no effect on cell cycle progression or chromosome division. Cyclin A1 is therefore not only an important cell cycle regulator with biased expression in germline, being essential for male and damaging for female meiosis, its persistent expression during anaphase in oocytes shows fundamental differences between APC/C function in oocytes and in early embryos.

Highlights

  • Cyclins are proteins which, together with cyclin dependent kinases (Cdks), control cell cycle progression[1,2]

  • In order to assess its effect on meiotic division, Germinal vesicle (GV) oocytes were microinjected with cRNAs encoding tagged histone and tubulin and untagged cyclin A1, and the first meiotic division was monitored using confocal time lapse imaging (Fig. 1A)

  • Our results showed that whereas 92% of uninjected cells and 85% of cells injected with cyclin A2 underwent polar body extrusion (PBE), 100% of cells injected with cyclin A1 were arrested in meiosis I

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Summary

Introduction

Together with cyclin dependent kinases (Cdks), control cell cycle progression[1,2]. We analyzed the phenotype after expression of cyclin A1 in fully-grown mouse GV oocytes These cells are at similar stage of meiosis as spermatocytes arrested by cyclin A1 deletion. Our experiments revealed that the APC/C and proteasome are in oocytes unable to remove completely cyclin A1 before anaphase, which leads into failure to extrude the polar body and to direct inhibition of separase. To our knowledge this is the first example of an important cell cycle regulator exhibiting such strong bias between male and female meiosis. Our results showed that cyclin A1 has deleterious effect on female meiosis

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