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Reverse transcription of the pFOXC mitochondrial retroplasmids of Fusarium oxysporum is protein primed

机译:尖孢镰刀菌pFOXC线粒体逆质粒的逆转录是蛋白质引发的

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Background The pFOXC retroplasmids are small, autonomously replicating DNA molecules found in mitochondria of certain strains of the filamentous fungus Fusarium oxysporum and are among the first linear genetic elements shown to replicate via reverse transcription. The plasmids have a unique clothespin structure that includes a 5'-linked protein and telomere-like terminal repeats, with pFOXC2 and pFOXC3 having iterative copies of a 5 bp sequence. The plasmids contain a single large open reading frame (ORF) encoding an active reverse transcriptase (RT). The pFOXC-RT is associated with the plasmid transcript in a ribonucleoprotein (RNP) complex and can synthesize full-length (-) strand cDNA products. In reactions containing partially purified RT preparations with exogenous RNAs, the pFOXC3-RT has been shown to initiate cDNA synthesis by use of snapped-back RNAs, as well as loosely associated DNA primers. Results The complete sequence of the distantly related pFOXC1 plasmid was determined and found to terminate in 3-5 copies of a 3 bp sequence. Unexpectedly, the majority of (-) strand cDNA molecules produced from endogenous pFOXC1 transcripts were attached to protein. In vitro experiments using partially purified pFOXC3-RT preparations having a single radiolabeled deoxyribonucleotide triphosphate (dNTP) generated a nucleotide-labeled protein that migrated at the size of the pFOXC-RT. The nucleotide preference of deoxynucleotidylation differed between pFOXC3 and pFOXC1 and showed complementarity to the respective 3' terminal repeats. In reactions that include exogenous RNA templates corresponding to the 3' end of pFOXC1, a protein-linked cDNA product was generated following deoxynucleotidylation, suggesting that reverse transcription initiates with a protein primer. Conclusions The finding that reverse transcription is protein primed suggests the pFOXC retroplasmids may have an evolutionary relationship with hepadnaviruses, the only other retroelement family known to initiate reverse transcription via a protein primer. Moreover, the similarity to protein-primed linear DNA elements supports models in which the terminal repeats are generated and maintained by a DNA slideback mechanism. The ability of the pFOXC-RT to utilize RNA, DNA and protein primers is unique among polymerases and suggests that the pFOXC plasmids may be evolutionary precursors of a broad range of retroelements, including hepadnaviruses, non-long terminal repeat (non-LTR) retrotransposons and telomerase.
机译:背景技术pFOXC逆质粒是在丝状真菌尖孢镰刀菌某些菌株的线粒体中发现的小的,可自主复制的DNA分子,是最早通过逆转录复制的线性遗传元件之一。质粒具有独特的晒衣夹结构,包括5'-连接的蛋白质和端粒样末端重复序列,pFOXC2和pFOXC3具有5 bp序列的重复拷贝。质粒包含单个大的开放阅读框(ORF),其编码活性逆转录酶(RT)。 pFOXC-RT与核糖核蛋白(RNP)复合物中的质粒转录物相关,并且可以合成全长(-)链cDNA产物。在包含带有外源RNA的部分纯化RT制剂的反应中,pFOXC3-RT已显示通过使用折回的RNA和松散相关的DNA引物来启动cDNA合成。结果确定了远距离相关的pFOXC1质粒的完整序列,发现其终止于3-5个3 bp序列的拷贝中。出乎意料的是,由内源性pFOXC1转录本产生的大多数(-)链cDNA分子都附着在蛋白质上。使用具有单个放射性标记的三磷酸脱氧核糖核苷酸(dNTP)的部分纯化的pFOXC3-RT制剂进行的体外实验产生了以pFOXC-RT大小迁移的核苷酸标记蛋白。在pFOXC3和pFOXC1之间,脱氧核苷酸的核苷酸偏好不同,并且与各自的3'末端重复序列互补。在包括对应于pFOXC1 3'端的外源RNA模板的反应中,脱氧核苷酸化后生成了一个蛋白质连接的cDNA产物,这表明逆转录始于蛋白质引物。结论反转录是蛋白质引发的发现表明,pFOXC逆质粒可能与肝炎病毒具有进化关系,而肝炎病毒是唯一已知的通过蛋白质引物引发逆转录的其他逆转录因子家族。而且,与蛋白质引发的线性DNA元件的相似性支持了通过DNA滑动机制生成并维持末端重复序列的模型。 pFOXC-RT利用RNA,DNA和蛋白质引物的能力在聚合酶中是独一无二的,这表明pFOXC质粒可能是广泛逆转录因子的进化前体,包括嗜肝DNA病毒,非长末端重复(non-LTR)逆转录转座子和端粒酶。

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