Cell cycle dependent expression of Plk1 in synchronized porcine fetal fibroblasts

被引:34
作者
Anger, M
Kues, WA
Klima, J
Mielenz, M
Kubelka, M
Motlik, J
Esner, M
Dvorak, P
Carnwath, JW
Niemann, H
机构
[1] Inst Anim Sci, Dept Biotechnol, D-31535 Neustadt, Germany
[2] Inst Anim Physiol & Genet, Libechov, Czech Republic
[3] Mendel Univ, Mol Embryol Lab, Brno, Czech Republic
关键词
Plk1; serum deprivation; cell cycle; butyrolactonul; aphidicolin;
D O I
10.1002/mrd.10289
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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. PIk1 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 PIk1 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. (C) 2003 Wiley-Liss, Inc.
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页码:245 / 253
页数:9
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