Abstract

Casein kinase I alpha (CK1α) is a member of serine/threonine protein kinase, generally present in all eukaryotes. In mammals, CK1α regulates the transition from interphase to metaphase in mitosis. However, little is known about its role in meiosis. Here we examined Ck1α mRNA and protein expression, as well as its subcellular localization in mouse oocytes from germinal vesicle to the late 1-cell stage. Our results showed that the expression level of CK1α was increased in metaphase. Immunostaining results showed that CK1α colocalized with condensed chromosomes during oocyte meiotic maturation and early embryo development. We used the loss-of-function approach by employing CK1α specific morpholino injection to block the function of CK1α. This functional blocking leads to failure of polar body 1 (PB1) extrusion, chromosome misalignment and MII plate incrassation. We further found that D4476, a specific and efficient CK1 inhibitor, decreased the rate of PB1 extrusion. Moreover, D4476 resulted in giant polar body extrusion, oocyte pro-MI arrest, chromosome congression failure and impairment of embryo developmental potential. In addition, we employed pyrvinium pamoate (PP), an allosteric activator of CK1α, to enhance CK1α activity in oocytes. Supplementation of PP induced oocyte meiotic maturation failure, severe congression abnormalities and misalignment of chromosomes. Taken together, our study for the first time demonstrates that CK1α is required for chromosome alignment and segregation during oocyte meiotic maturation and early embryo development.

Highlights

  • In mammals, oocyte maturation involves the process of meiosis

  • In order to study the role of CK1a, we examined CK1a expression and subcellular localization during oocyte maturation and early embryo development

  • The third type showed oocytes that had a polar body 1 (PB1) but chromosomes were disordered and spindle assembly failed (Fig. 4D column 5). All these results suggest that pyrvinium pamoate (PP) mediated overactivation of CK1a impairing PB1 extrusion and chromosome congression during oocyte maturation

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Summary

Introduction

Oocyte maturation involves the process of meiosis. Meiosis is characterized by two rounds of chromosome segregation but only one round of DNA replication. This is the foundation of propagation and inheritance in sexual reproduction. Homologous chromosomes separate during anaphase of meiosis I and extrude a tiny non-developmentally competent cell, the first polar body (PB1), which marks the oocyte’s nuclear maturation. Fertilization triggers the second meiosis, in which sister chromatids segregate, resulting in second polar body (PB2) extrusion. Errors in chromosome separation result in aneuploidy, associated with oocyte maturation failure and consequences for aneuploidy or dysplasia in the embryo [1]. The mechanism of regulating chromosome dynamics is highly conservative and precise

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