Anger Martin, Kues Wilfried A, Klima Jiri, Mielenz Manfred, Kubelka Michal, Motlik Jan, Esner Milan, Dvorak Petr, Carnwath Joseph W, Niemann Heiner
Institute of Animal Physiology and Genetics, Libechov, Czech Republic.
Mol Reprod Dev. 2003 Jul;65(3):245-53. doi: 10.1002/mrd.10289.
Enzymes of the Polo-like kinase (Plk) family are active in the pathways controlling mitosis in several species. We have cloned cDNA fragments of the porcine homologues of Plk1, Plk2, and Plk3 employing fetal fibroblasts as source. All three partial cDNAs showed high sequence homology with their mouse and human counterparts and contained the Polo box, a domain characteristic for all Polo kinases. The expression levels of Plk1 mRNA at various points of the cell cycle in synchronized porcine fetal fibroblasts were analyzed by both RT-PCR and the ribonuclease protection assay. Plk1 mRNA was barely detectable in G0 and G1, increased during S phase and peaked after the G2/M transition. A monoclonal antibody was generated against an in vitro expressed porcine Plk1-protein fragment and used to detect changes in Plk1 expression at the protein level. Plk1 protein was first detected by immunoblotting at the beginning of S phase and was highest after the G2/M transition. In summary, the Plk1 expression pattern in the pig is similar to that reported for other species. The absence of Plk1 mRNA and protein appears to be a good marker for G0/G1 and thus for the selection of donor cells for nuclear transfer based somatic cloning.
Polo样激酶(Plk)家族的酶在控制多个物种有丝分裂的途径中具有活性。我们以胎儿成纤维细胞为来源,克隆了猪Plk1、Plk2和Plk3同源物的cDNA片段。所有这三个部分cDNA与其小鼠和人类对应物显示出高度的序列同源性,并包含Polo框,这是所有Polo激酶的特征性结构域。通过RT-PCR和核糖核酸酶保护试验分析了同步化猪胎儿成纤维细胞在细胞周期不同点的Plk1 mRNA表达水平。Plk1 mRNA在G0和G1期几乎检测不到,在S期增加,并在G2/M期转换后达到峰值。针对体外表达的猪Plk1蛋白片段产生了一种单克隆抗体,并用于检测Plk1在蛋白质水平上的表达变化。通过免疫印迹在S期开始时首次检测到Plk1蛋白,在G2/M期转换后最高。总之,猪中Plk1的表达模式与其他物种报道的相似。Plk1 mRNA和蛋白质的缺失似乎是G0/G1期的良好标志物,因此也是基于体细胞克隆的核移植供体细胞选择的良好标志物。