Itoh R, Takano H, Ohta N, Miyagishima S, Kuroiwa H, Kuroiwa T
Department of Biological Sciences, Graduate School of Science, University of Tokyo, Hongo, Japan.
Plant Mol Biol. 1999 Oct;41(3):321-37. doi: 10.1023/a:1006369104530.
The red algal chloroplast genome encodes an essential prokaryotic cell division gene, ftsH, which has never been found in the mitochondrial genome of any organism. To compare the conserved prokaryote-derived mechanism for mitochondrial division with that of chloroplasts, we cloned chloroplast- and nuclear-encoded ftsH genes from the primitive red alga Cyanidioschyzon merolae. The deduced amino-acid sequence of chloroplast ftsH (ftsHcp) consists of 603 amino acids and shows the highest similarity with algal-chloroplast and cyanobacterial FtsH. On the other hand, the nuclear-encoded ftsH (ftsH2) encodes a protein of 920 amino acids and has the highest similarity with two yeast mitochondrial FtsHs, Rca1p and Afg3p. Furthermore, the amino-terminal extension of FtsH2 appears to be an amphipathic alpha-helix, a characteristic mitochondrial targeting signal, suggesting that FtsH2 is a mitochondrial protein. Southern hybridization revealed that ftsH2 is a single gene located on chromosome III of the 17 C. merolae chromosomes. The level of expression of the 3.0 and 4.0 kb transcripts of this gene decreased in concert during the organelle division phase of a synchronized culture, indicating a cell-cycle-dependent manner of ftsH2 transcription, while northern hybridization did not detect ftsHcp transcripts. Nevertheless, reverse transcription-PCR and immunoblotting demonstrated for the first time that chloroplast-encoded ftsH is transcriptionally and translationally active. Overproduction of FtsHcp and FtsH2 in Escherichia coli disrupted cytokinesis and produced filamentous cells, but had no effect on the replication, segregation, or distribution of their nucleoids, as also occurs in ftsH-deficient E. coli. These observations suggest the possible involvement of both C. merolae FtsHs in organelle division.
红藻叶绿体基因组编码一种必需的原核细胞分裂基因ftsH,该基因在任何生物体的线粒体基因组中都从未被发现。为了比较线粒体分裂与叶绿体分裂中保守的原核生物衍生机制,我们从原始红藻嗜热栖热放线菌中克隆了叶绿体和核编码的ftsH基因。叶绿体ftsH(ftsHcp)推导的氨基酸序列由603个氨基酸组成,与藻类叶绿体和蓝细菌的FtsH具有最高的相似性。另一方面,核编码的ftsH(ftsH2)编码一种920个氨基酸的蛋白质,与两种酵母线粒体FtsH,Rca1p和Afg3p具有最高的相似性。此外,FtsH2的氨基末端延伸似乎是一个两亲性α-螺旋,这是一种典型的线粒体靶向信号,表明FtsH2是一种线粒体蛋白。Southern杂交显示ftsH2是位于嗜热栖热放线菌17条染色体中第三条染色体上的单基因。在同步培养的细胞器分裂阶段,该基因3.0和4.0 kb转录本的表达水平协同下降,表明ftsH2转录具有细胞周期依赖性,而Northern杂交未检测到ftsHcp转录本。然而,逆转录PCR和免疫印迹首次证明叶绿体编码的ftsH具有转录和翻译活性。FtsHcp和FtsH2在大肠杆菌中的过量表达破坏了胞质分裂并产生丝状细胞,但对其类核的复制、分离或分布没有影响,这在ftsH缺陷型大肠杆菌中也会发生。这些观察结果表明嗜热栖热放线菌的两种FtsH可能都参与细胞器分裂。