Hoshina Ryo, Imamura Nobutaka
Department of Biomedical Science, College of Life Sciences, Ritsumeikan University, Shiga, Japan.
Mol Biol Evol. 2009 Jun;26(6):1309-19. doi: 10.1093/molbev/msp044. Epub 2009 Mar 11.
Group I introns are a distinct RNA group that catalyze their excision from precursor RNA transcripts and ligate the exons. Group I introns have a sporadic and highly biased distribution due to the two intron transfer mechanisms of homing and reverse splicing. These transfer pathways recognize assigned sequences even when introns are transferred beyond the species level. Consequently, introns at homologous gene sites between different host organisms are more related than those at heterologous sites within an organism. We describe the subgroup IE introns of two Chlorella species that are symbiotic green algae (photobionts) of a ciliate, Paramecium bursaria. One strain Chlorella sp. SW1-ZK (Csw.) had two IE introns at S651 and L2449, and the other strain Chlorella sp. OK1-ZK (Cok.) had four IE introns at S943, L1688, L1926, and L2184 (numbering reflects their homologous position in Escherichia coli rRNA gene: S = small subunit rRNA, L = large subunit rRNA). Despite locating on six heterologous sites, the introns formed a monophyletic clade independent of other groups. Phylogenetic and structural analyses of the introns indicated that Csw.L2449 has an archaic state, and the other introns are assumed to be originated from this intron. Some of the introns shared common internal guide sequences, which are necessary for misdirected transfer (i.e., transposition) via reverse splicing. Other introns, however, shared similar sequence fragments further upstream, after the insertions. We propose a hypothetical model to explain how these intron transpositions may have occurred in these photobionts; they transposed by a combination of homing-like event requiring relaxed sequence homology of recognition sequences and reverse splicing. This case study may represent a key to describe how group I intron explores new insertion sites.
I 组内含子是一类独特的RNA,可催化自身从前体RNA转录本中切除,并连接外显子。由于归巢和反向剪接这两种内含子转移机制,I组内含子具有零星且高度偏向的分布。即使内含子转移到物种水平之外,这些转移途径也能识别特定序列。因此,不同宿主生物同源基因位点的内含子比同一生物体内异源位点的内含子更具相关性。我们描述了两种小球藻物种的IE亚组内含子,这两种小球藻是纤毛虫草履虫的共生绿藻(共生体)。一株小球藻SW1-ZK(Csw.)在S651和L2449处有两个IE内含子,另一株小球藻OK1-ZK(Cok.)在S943、L1688、L1926和L2184处有四个IE内含子(编号反映它们在大肠杆菌rRNA基因中的同源位置:S = 小亚基rRNA,L = 大亚基rRNA)。尽管这些内含子位于六个异源位点,但它们形成了一个独立于其他组的单系分支。对这些内含子的系统发育和结构分析表明,Csw.L2449处于古老状态,其他内含子被认为起源于该内含子。一些内含子共享共同的内部引导序列,这是通过反向剪接进行错误定向转移(即转座)所必需的。然而,其他内含子在插入后,在上游更远处共享相似的序列片段。我们提出了一个假设模型来解释这些内含子转座在这些共生体中可能是如何发生的;它们通过需要识别序列具有宽松序列同源性的类归巢事件和反向剪接的组合进行转座。这个案例研究可能是描述I组内含子如何探索新插入位点的关键。