Kabeya Yukihiro, Sato Naoki
Department of Life Sciences, Graduate School of Arts and Sciences, University of Tokyo, Meguro-ku, Tokyo 153-8902, Japan.
Plant Physiol. 2005 May;138(1):369-82. doi: 10.1104/pp.105.059501. Epub 2005 Apr 15.
The nuclear genome of the moss Physcomitrella patens contains two genes encoding phage-type RNA polymerases (PpRPOT1 and PpRPOT2). Each of the PpRPOT1 and PpRPOT2 transcripts possesses two in-frame AUG codons at the 5' terminus that could act as a translational initiation site. Observation of transient and stable Physcomitrella transformants expressing the 5' terminus of each PpRPOT cDNA fused with the green fluorescent protein gene suggested that both PpRPOT1 and PpRPOT2 are not translated from the first (upstream) AUG codon in the natural context but translated from the second (downstream) one, and that these enzymes are targeted only to mitochondria, although they are potentially targeted to plastids when translation is forced to start from the first AUG codon. The influence of the 5'-upstream sequence on the translation efficiency of the two AUG codons in PpRPOT1 and PpRPOT2 was quantitatively assessed using a beta-glucuronidase reporter. The results further supported that the second AUG codon is the sole translation initiation site in Physcomitrella cells. An Arabidopsis (Arabidopsis thaliana) RPOT homolog AtRpoT;2 that possesses two initiation AUG codons in its transcripts, as do the RPOTs of P. patens, has been regarded as a dually targeted protein. When the localization of AtRpoT;2 was tested using green fluorescent protein in a similar way, AtRpoT;2 was also observed only in mitochondria in many Arabidopsis tissues. These results suggest that, despite the presence of two in-frame AUGs at the 5' termini of RPOTs in Physcomitrella and Arabidopsis, the second AUG is specifically recognized as the initiation site in these organisms, resulting in expression of a protein that is targeted to mitochondria. This finding may change the current framework of thinking about the transcription machinery of plastids in land plants.
小立碗藓的核基因组包含两个编码噬菌体类型RNA聚合酶的基因(PpRPOT1和PpRPOT2)。PpRPOT1和PpRPOT2转录本在5'末端均具有两个符合读框的AUG密码子,可作为翻译起始位点。对表达与绿色荧光蛋白基因融合的每个PpRPOT cDNA 5'末端的小立碗藓瞬时和稳定转化体的观察表明,在自然情况下,PpRPOT1和PpRPOT2均不是从第一个(上游)AUG密码子开始翻译,而是从第二个(下游)AUG密码子开始翻译,并且这些酶仅靶向线粒体,尽管当翻译被迫从第一个AUG密码子开始时它们可能靶向质体。使用β - 葡萄糖醛酸酶报告基因定量评估了5'上游序列对PpRPOT1和PpRPOT2中两个AUG密码子翻译效率的影响。结果进一步支持第二个AUG密码子是小立碗藓细胞中唯一的翻译起始位点。拟南芥的RPOT同源物AtRpoT;2在其转录本中具有两个起始AUG密码子,就像小立碗藓的RPOT一样,被认为是一种双靶向蛋白。当以类似方式使用绿色荧光蛋白测试AtRpoT;2的定位时,在许多拟南芥组织中也仅在线粒体中观察到AtRpoT;2。这些结果表明,尽管小立碗藓和拟南芥的RPOTs在5'末端存在两个符合读框的AUG,但第二个AUG在这些生物体中被特异性识别为起始位点,从而导致靶向线粒体的蛋白质表达。这一发现可能会改变目前关于陆地植物质体转录机制的思维框架。