Matsuoka Yoh, Kobayashi Tohru, Kihara Kazunori, Nagahama Yoshitaka
Laboratory of Reproductive Biology, Department of Developmental Biology, National Institute for Basic Biology, Okazaki, Aichi, Japan.
Mol Reprod Dev. 2008 Jun;75(6):989-1001. doi: 10.1002/mrd.20843.
Polo-like kinase 1 (Plk1) and NIMA-related kinase 2 (Nek2) are serine/threonine kinases that are involved in the G2/M phase transition of the cell cycle in vertebrates. Although they also play critical roles in the regulation of spermatogenesis and oogenesis, their characterization in meiosis has not been elucidated fully, particularly in teleost fish. To investigate the evolutionary significance of serine/threonine kinases in the reproductive system of fish, we cloned the cDNAs of Plk1 and Nek2 from a Nile tilapia (Oreochromis niloticus) testicular cDNA library. Tilapia Plk1 encodes a protein of 582 amino acids that shares 75% homology with human Plk1, while tilapia Nek2 encodes a putative protein of 446 amino acids that shares 70% homology with human Nek2. Analyses of tissue distribution by RT-PCR and Southern blotting revealed that Plk1 and Nek2 are strongly expressed in the ovary and testis. Northern blot analysis revealed two Nek2 transcripts in the ovary and testis with different expression patterns, which indicates the presence of two structural variants for tilapia Nek2. Moreover, the localization of Plk1 and Nek2 mRNAs in tilapia gonads was determined by in situ hybridization analysis. In the ovary, Plk1 and Nek2 were expressed predominantly in oocytes. In the testis, on the other hand, Plk1 was expressed in primary spermatocytes, while Nek2 was generally expressed in primary and secondary spermatocytes. These results suggest that Plk1 and Nek2 are key factors in the progression of meiosis in fish.
Polo样激酶1(Plk1)和NIMA相关激酶2(Nek2)是丝氨酸/苏氨酸激酶,参与脊椎动物细胞周期的G2/M期转换。尽管它们在精子发生和卵子发生的调控中也发挥着关键作用,但它们在减数分裂中的特征尚未完全阐明,尤其是在硬骨鱼类中。为了研究丝氨酸/苏氨酸激酶在鱼类生殖系统中的进化意义,我们从尼罗罗非鱼(Oreochromis niloticus)睾丸cDNA文库中克隆了Plk1和Nek2的cDNA。罗非鱼Plk1编码一个由582个氨基酸组成的蛋白质,与人Plk1具有75%的同源性,而罗非鱼Nek2编码一个推定的由446个氨基酸组成的蛋白质,与人Nek2具有70%的同源性。通过RT-PCR和Southern印迹分析组织分布,结果显示Plk1和Nek2在卵巢和睾丸中强烈表达。Northern印迹分析显示卵巢和睾丸中有两种具有不同表达模式的Nek2转录本,这表明罗非鱼Nek2存在两种结构变体。此外,通过原位杂交分析确定了Plk1和Nek2 mRNA在罗非鱼性腺中的定位。在卵巢中,Plk1和Nek2主要在卵母细胞中表达。另一方面,在睾丸中,Plk1在初级精母细胞中表达,而Nek2通常在初级和次级精母细胞中表达。这些结果表明Plk1和Nek2是鱼类减数分裂进程中的关键因子。