Miyagishima Shin-ya, Nozaki Hisayoshi, Nishida Keishin, Nishida Keiji, Matsuzaki Motomichi, Kuroiwa Tsuneyoshi
Department of Life Sciences, College of Science, Rikkyo (St. Paul's) University, 3-34-1 Nishiikebukuro, Toshima-ku, Tokyo 171-8501, Japan,
J Mol Evol. 2004 Mar;58(3):291-303. doi: 10.1007/s00239-003-2551-1.
The ancestors of plastids and mitochondria were once free-living bacteria that became organelles as a result of endosymbiosis. According to this theory, a key bacterial division protein, FtsZ, plays a role in plastid division in algae and plants as well as in mitochondrial division in lower eukaryotes. Recent studies have shown that organelle division is a process that combines features derived from the bacterial division system with features contributed by host eukaryotic cells. Two nonredundant versions of FtsZ, FtsZ1 and FtsZ2, have been identified in green-lineage plastids, whereas most bacteria have a single ftsZ gene. To examine whether there is also more than one type of FtsZ in red-lineage chloroplasts (red algal chloroplasts and chloroplasts that originated from the secondary endosymbiosis of red algae) and in mitochondria, we obtained FtsZ sequences from the complete sequence of the primitive red alga Cyanidioschyzon merolae and the draft sequence of the stramenopile (heterokont) Thalassiosira pseudonana. Phylogenetic analyses that included known FtsZ proteins identified two types of chloroplast FtsZ in red algae (FtsZA and FtsZB) and stramenopiles (FtsZA and FtsZC). These analyses also showed that FtsZB emerged after the red and green lineages diverged, while FtsZC arose by the duplication of an ftsZA gene that in turn descended from a red alga engulfed by the ancestor of stramenopiles. A comparison of the predicted proteins showed that like bacterial FtsZ and green-lineage FtsZ2, FtsZA has a short conserved C-termmal sequence (the C-terminal core domain), whereas FtsZB and FtsZC, like the green-lineage FtsZ1, lack this sequence. In addition, the Cyanidioschyzon and Dictyostelium genomes encode two types of mitochondrial FtsZ proteins, one of which lacks the C-terminal variable domain. These results suggest that the acquisition of an additional FtsZ protein with a modified C terminus was common to the primary and secondary endosymbioses that produced plastids and that this also occurred during the establishment of mitochondria, presumably to regulate the multiplication of these organelles.
质体和线粒体的祖先曾经是自由生活的细菌,通过内共生作用成为了细胞器。根据这一理论,一种关键的细菌分裂蛋白FtsZ在藻类和植物的质体分裂以及低等真核生物的线粒体分裂中发挥作用。最近的研究表明,细胞器分裂是一个将源自细菌分裂系统的特征与宿主真核细胞贡献的特征相结合的过程。在绿色谱系的质体中已鉴定出两种非冗余版本的FtsZ,即FtsZ1和FtsZ2,而大多数细菌只有一个ftsZ基因。为了研究在红色谱系叶绿体(红藻叶绿体以及起源于红藻二次内共生的叶绿体)和线粒体中是否也存在不止一种类型的FtsZ,我们从原始红藻梅氏嗜热栖热菌的完整序列和硅藻(不等鞭毛类)假微型海链藻的草图序列中获得了FtsZ序列。包括已知FtsZ蛋白的系统发育分析确定了红藻(FtsZA和FtsZB)和硅藻(FtsZA和FtsZC)中存在两种类型的叶绿体FtsZ。这些分析还表明,FtsZB在红色和绿色谱系分化后出现,而FtsZC是由一个ftsZA基因的复制产生的,该基因又源自不等鞭毛类祖先吞噬的红藻。对预测蛋白的比较表明,与细菌FtsZ和绿色谱系FtsZ2一样,FtsZA有一个短的保守C末端序列(C末端核心结构域),而FtsZB和FtsZC与绿色谱系FtsZ1一样,缺乏该序列。此外,嗜热栖热菌和盘基网柄菌的基因组编码两种类型的线粒体FtsZ蛋白,其中一种缺乏C末端可变结构域。这些结果表明,获得一种具有修饰C末端的额外FtsZ蛋白是产生质体的初级和次级内共生作用所共有的,并且这在建立线粒体的过程中也发生了,大概是为了调节这些细胞器的增殖。