Colantonio Jessica R, Bekker Janine M, Kim Sarah J, Morrissey Kari M, Crosbie Rachelle H, Hill Kent L
Department of Microbiology, Immunology and Molecular Genetics, University of California, Los Angeles, CA 90095, USA.
Traffic. 2006 May;7(5):538-48. doi: 10.1111/j.1600-0854.2006.00411.x.
The mammalian GAS11 gene is a candidate tumor suppressor of unknown function that was previously identified as one of several genes upregulated upon growth arrest. Interestingly, although GAS11 homologs in Trypanosoma brucei (trypanin) and Chlamydomonas reinhardtii (PF2) are integral components of the flagellar axoneme and are necessary for regulating flagellar beat, the GAS11 gene was discovered based on its expression in cells that do not assemble a motile cilium. This suggests that GAS11 function might not be restricted to the cilium. To investigate this possibility, we generated GAS11-specific antibodies and demonstrate here that GAS11 is expressed in a variety of mammalian cells that lack a motile cilium. In COS7 cells, GAS11 is associated with the detergent-insoluble cytoskeleton and exhibits a juxtanuclear localization that overlaps with the pericentrosomal Golgi apparatus. This localization is dependent upon intact microtubules and is cell-cycle regulated, such that GAS11 is dispersed throughout the cytoplasm as cells progress through mitosis. GAS11 remains associated with Golgi fragments following depolymerization of cytoplasmic microtubules but is dispersed upon disruption of the Golgi with brefeldin A. These data suggest that GAS11 is associated with the Golgi apparatus. In support of this, recombinant GAS11 binds Golgi membranes in vitro. In growth-arrested mIMCD3 cells, GAS11 co-localizes with gamma-tubulin at the base of the primary cilium. The pericentrosomal Golgi apparatus and base of the cilium both represent convergence points for microtubule minus ends and correspond to sites where dynein regulation is required. The algal GAS11 homolog functions as part of a dynein regulatory complex (DRC) in the axoneme (Rupp and Porter. J Cell Biol 2003;162:47-57) and our findings suggest that components of this axonemal dynein regulatory system have been adapted in mammalian cells to participate in non-axonemal functions.
哺乳动物的GAS11基因是一个功能未知的候选肿瘤抑制基因,之前被鉴定为生长停滞时上调的几个基因之一。有趣的是,尽管布氏锥虫(trypanin)和莱茵衣藻(PF2)中的GAS11同源物是鞭毛轴丝的组成成分,且对调节鞭毛摆动是必需的,但GAS11基因是基于其在不组装运动纤毛的细胞中的表达而被发现的。这表明GAS11的功能可能不限于纤毛。为了研究这种可能性,我们制备了GAS11特异性抗体,并在此证明GAS11在多种缺乏运动纤毛的哺乳动物细胞中表达。在COS7细胞中,GAS11与去污剂不溶性细胞骨架相关,并呈现出与中心体周围高尔基体重叠的近核定位。这种定位依赖于完整的微管,并且受细胞周期调节,以至于随着细胞进入有丝分裂,GAS11会分散到整个细胞质中。细胞质微管解聚后,GAS11仍与高尔基体片段相关,但用布雷菲德菌素A破坏高尔基体后,GAS11会分散。这些数据表明GAS11与高尔基体相关。支持这一点的是,重组GAS11在体外能结合高尔基体膜。在生长停滞的mIMCD3细胞中,GAS11与γ-微管蛋白在初级纤毛的基部共定位。中心体周围的高尔基体和纤毛基部都是微管负端的汇聚点,并且对应于需要动力蛋白调节的位点。藻类的GAS11同源物在轴丝中作为动力蛋白调节复合体(DRC)的一部分发挥作用(Rupp和Porter。《细胞生物学杂志》2003年;162:47 - 57),我们的研究结果表明,这种轴丝动力蛋白调节系统的成分在哺乳动物细胞中已被改造以参与非轴丝功能。