Shutt Timothy E, Gray Michael W
Program in Evolutionary Biology, Canadian Institute for Advanced Research, and Department of Biochemistry and Molecular Biology, Dalhousie University, Halifax, Nova Scotia, Canada.
J Mol Evol. 2006 May;62(5):588-99. doi: 10.1007/s00239-005-0162-8. Epub 2006 Apr 11.
Recently, the human protein responsible for replicative mtDNA helicase activity was identified and designated Twinkle. Twinkle has been implicated in autosomal dominant progressive external ophthalmoplegia (adPEO), a mitochondrial disorder characterized by mtDNA deletions. The Twinkle protein appears to have evolved from an ancestor shared with the bifunctional primase-helicase found in the T-odd bacteriophages. However, the question has been raised as to whether human Twinkle possesses primase activity, due to amino acid sequence divergence and absence of a zinc-finger motif thought to play an integral role in DNA binding. To date, a primase protein participating in mtDNA replication has not been identified in any eukaryote. Here we investigate the wider phylogenetic distribution of Twinkle by surveying and analyzing data from ongoing EST and genome sequencing projects. We identify Twinkle homologues in representatives from five of six major eukaryotic assemblages ("supergroups") and present the sequence of the complete Twinkle gene from two members of Amoebozoa, a supergroup of amoeboid protists at the base of the opisthokont (fungal/metazoan) radiation. Notably, we identify conserved primase motifs including the zinc finger in all Twinkle sequences outside of Metazoa. Accordingly, we propose that Twinkle likely serves as the primase as well as the helicase for mtDNA replication in most eukaryotes whose genome encodes it, with the exception of Metazoa.
最近,负责复制性线粒体DNA解旋酶活性的人类蛋白质被鉴定出来,并命名为Twinkle。Twinkle与常染色体显性进行性外眼肌麻痹(adPEO)有关,这是一种以线粒体DNA缺失为特征的线粒体疾病。Twinkle蛋白似乎是从与T-odd噬菌体中发现的双功能引发酶-解旋酶共有的祖先进化而来的。然而,由于氨基酸序列的差异以及被认为在DNA结合中起重要作用的锌指基序的缺失,人们对人类Twinkle是否具有引发酶活性提出了疑问。迄今为止,尚未在任何真核生物中鉴定出参与线粒体DNA复制的引发酶蛋白。在这里,我们通过调查和分析正在进行的EST和基因组测序项目的数据,研究Twinkle更广泛的系统发育分布。我们在六个主要真核生物组合(“超群”)中的五个组合的代表中鉴定出Twinkle同源物,并给出了变形虫超组(在opisthokont(真菌/后生动物)辐射基部的变形虫原生生物超组)的两个成员的完整Twinkle基因序列。值得注意的是,我们在后生动物以外的所有Twinkle序列中鉴定出了保守的引发酶基序,包括锌指。因此,我们提出,除后生动物外,Twinkle可能在大多数基因组编码它的真核生物中作为线粒体DNA复制的引发酶和解旋酶。