Riparbelli Maria G, Gottardo Marco, Glover David M, Callaini Giuliano
Department of Life Sciences; University of Siena; Siena, Italy.
Department of Genetics; University of Cambridge; Cambridge, UK.
Cell Cycle. 2014;13(13):2064-72. doi: 10.4161/cc.29083. Epub 2014 May 6.
Pharmacological inhibition of Drosophila Polo kinase with BI2536 has allowed us to re-examine the requirements for Polo during Drosophila male gametogenesis. BI2536-treated spermatocytes persisted in a pro-metaphase state without dividing and had condensed chromosomes that did not separate. Centrosomes failed to recruit γ-tubulin and centrosomin (Cnn) and were not associated with microtubule arrays that were abnormal and did not form proper bipolar spindles. Centrioles, which usually separate during the anaphase of the first meiosis, remained held together in a V-shaped configuration suggesting that Polo kinase regulates the proteolysis that breaks centriole linkage to ensure their disengagement. Despite these defects spermatid differentiation proceeds, leading to axoneme formation.
用BI2536对果蝇Polo激酶进行药理学抑制,使我们能够重新审视Polo在果蝇雄性配子发生过程中的需求。经BI2536处理的精母细胞停滞在前期状态而不分裂,并且染色体浓缩但不分离。中心体无法募集γ-微管蛋白和中心体蛋白(Cnn),并且与异常的微管阵列不相关,也无法形成正常的双极纺锤体。通常在第一次减数分裂后期分离的中心粒,仍以V形结构聚集在一起,这表明Polo激酶调节蛋白水解作用,以破坏中心粒连接,确保它们分离。尽管存在这些缺陷,精子细胞仍能分化,导致轴丝形成。