Soyer-Gobillard M O, Ausseil J, Géraud M L
Départment de Biologie Cellulaire, Observatoire Océanologique de Banyuls-sur-mer, CNRS-URA No 2156, Université Paris 6, Laboratoire Arago, Banyuls-sur-mer, France.
Biol Cell. 1996;87(1-2):17-35.
Experiments using monoclonal and polyclonal anti-actin antibodies allowed us to demonstrate the presence of F- or G-actin in original protists, dinoflagellates, either by biochemistry, immunofluorescence and in TEM. SDS-PAGE electrophoresis and immunoblottings made either from total or nuclear protein extracts revealed the presence of a 44-kDa band reacting with monoclonal anti-actin antibody in two species, Prorocentrum micans and Crypthecodinium cohnii, and thus demonstrated the presence of actin in nuclear and cytoplasmic fractions. After squash preparation of P micans cells, actin was identified within the nucleus and in some regions of the cytoplasm by immunofluorescence microscopy. Labelling of both the nucleolus and the centrosome region was evident together with amorphous nucleoplasmic material surrounding the chromosomes. The use of cryosections of intact P micans and C cohnii cells for immunofluorescence along with staining with DAPI to delineate the chromosomes themselves, yielded finer resolution of the intranuclear network labelling pattern and allowed us to complete our observations, in particular on the cytoplasmic labelling. In P micans, in addition to the centrosome region, the cytoplasmic channels passing through the nucleus in dividing cells are labelled. In C cohnii, the cortex, the centrosome region, the cytoplasmic channels, the region surrounding the nucleus, the filaments linking it to the cortex and the cleavage furrow are also labelled. In the nucleus of the two species, there is a prominent "weft' of fine actin filaments in the nucleoplasm forming a matrix of varying density around the persistent chromosomes. This actin matrix, of unknown function, is most conspicuous at the end of the S-phase of the cell cycle. Fluorescent derivatives of phalloidin, used as diagnostic cytochemical probes for polymeric actin (F-actin), gave similar results. Positive TEM immunolabelling of intranuclear actin confirms its presence in the nucleoplasm, in the nucleolus where the preribosomal region is labelled while C cohnii chromosomes are unlabelled and the P micans chromosomes very slightly. In the cytoplasm, lips of the cleavage furrow and kinetosome regions are labelled as well as the centrosome region. The possible functions of this protein located in several compartments of dinoflagellate cells are discussed.
使用单克隆和多克隆抗肌动蛋白抗体进行的实验,使我们能够通过生物化学、免疫荧光和透射电子显微镜(TEM),在原始原生生物、甲藻中证明F - 肌动蛋白或G - 肌动蛋白的存在。从总蛋白提取物或核蛋白提取物进行的SDS - PAGE电泳和免疫印迹显示,在两种甲藻,即海洋原甲藻(Prorocentrum micans)和寇氏隐甲藻(Crypthecodinium cohnii)中,存在一条与单克隆抗肌动蛋白抗体反应的44 kDa条带,从而证明在核和细胞质组分中存在肌动蛋白。对海洋原甲藻细胞进行压片制备后,通过免疫荧光显微镜在细胞核和细胞质的某些区域鉴定出了肌动蛋白。核仁、中心体区域以及围绕染色体的无定形核质物质均有明显标记。使用完整的海洋原甲藻和寇氏隐甲藻细胞的冷冻切片进行免疫荧光,并结合用DAPI染色来描绘染色体本身,对核内网络标记模式有了更精细的分辨率,并使我们能够完成观察,特别是关于细胞质标记的观察。在海洋原甲藻中,除了中心体区域外,分裂细胞中穿过细胞核的细胞质通道也有标记。在寇氏隐甲藻中,皮层、中心体区域、细胞质通道、细胞核周围区域、将其连接到皮层的细丝以及分裂沟也有标记。在这两种甲藻的细胞核中,核质中有一条由细肌动蛋白丝组成的突出“纬线”,在持久染色体周围形成密度不同的基质。这种功能未知的肌动蛋白基质在细胞周期的S期结束时最为明显。作为聚合肌动蛋白(F - 肌动蛋白)诊断性细胞化学探针的鬼笔环肽荧光衍生物给出了类似结果。核内肌动蛋白的阳性TEM免疫标记证实了其在核质、核仁中的存在,在核仁中核糖体前体区域有标记,而寇氏隐甲藻的染色体未标记,海洋原甲藻的染色体仅有非常轻微的标记。在细胞质中,分裂沟边缘、动基体区域以及中心体区域均有标记。本文讨论了这种存在于甲藻细胞多个区室中的蛋白质的可能功能。