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The Selenocysteine tRNA Gene in Leishmania major Is Transcribed by both RNA Polymerase II and RNA Polymerase III

机译:大利什曼原虫中的硒代半胱氨酸tRNA基因被RNA聚合酶II和RNA聚合酶III转录。

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摘要

Eukaryotic tRNAs, transcribed by RNA polymerase III (Pol III), contain boxes A and B as internal promoter elements. One exception is the selenocysteine (Sec) tRNA (tRNA-Sec), whose transcription is directed by an internal box B and three extragenic sequences in vertebrates. Here we report on the transcriptional analysis of the tRNA-Sec gene in the protozoan parasite Leishmania major. This organism has unusual mechanisms of gene expression, including Pol II polycistronic transcription and maturation of mRNAs by trans splicing, a process that attaches a 39-nucleotide miniexon to the 5′ end of all the mRNAs. In L. major, tRNA-Sec is encoded by a single gene inserted into a Pol II polycistronic unit, in contrast to most tRNAs, which are clustered at the boundaries of polycistronic units. 5′ rapid amplification of cDNA ends and reverse transcription-PCR experiments showed that some tRNA-Sec transcripts contain the miniexon at the 5′ end and a poly(A) tail at the 3′ end, indicating that the tRNA-Sec gene is polycistronically transcribed by Pol II and processed by trans splicing and polyadenylation, as was recently reported for the tRNA-Sec genes in the related parasite Trypanosoma brucei. However, nuclear run-on assays with RNA polymerase inhibitors and with cells that were previously UV irradiated showed that the tRNA-Sec gene in L. major is also transcribed by Pol III. Thus, our results indicate that RNA polymerase specificity in Leishmania is not absolute in vivo, as has recently been found in other eukaryotes.
机译:由RNA聚合酶III(Pol III)转录的真核tRNA含有框A和框B作为内部启动子元件。一个例外是硒代半胱氨酸(Sec)tRNA(tRNA-Sec),其转录由脊椎动物的内部框B和三个外源序列指导。在这里我们报告在原生动物寄生虫利什曼原虫主要的tRNA-Sec基因的转录分析。这种生物具有异常的基因表达机制,包括Pol II多顺反子转录和通过反式剪接使mRNA成熟,该过程将39个核苷酸的miniexon连接到所有mRNA的5'末端。与大多数聚在多顺反子单元边界处的tRNA相比,在L. major中,tRNA-Sec由插入Pol II多顺反子单元的单个基因编码。 cDNA末端的5'快速扩增和逆转录PCR实验表明,某些tRNA-Sec转录本在5'末端包含miniexon,在3'末端包含poly(A)尾部,表明tRNA-Sec基因是多顺反子最近报道了相关寄生虫布鲁氏锥虫中的tRNA-Sec基因,由Pol II转录并通过反式剪接和聚腺苷酸化处理。但是,用RNA聚合酶抑制剂和先前用紫外线照射过的细胞进行的核试验表明,大麦芽孢杆菌中的tRNA-Sec基因也被Pol III转录。因此,我们的结果表明,在利什曼原虫中,RNA聚合酶的特异性在体内并不是绝对的,正如最近在其他真核生物中发现的那样。

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