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首页> 外文期刊>Nucleic acids research >Nucleotide sequence of a Euglena gracilis chloroplast genome region coding for the elongation factor Tu; evidence for a spliced mRNA
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Nucleotide sequence of a Euglena gracilis chloroplast genome region coding for the elongation factor Tu; evidence for a spliced mRNA

机译:细叶Euglena gracilis叶绿体基因组区域的核苷酸序列,编码延伸因子Tu;剪接的mRNA的证据

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摘要

We characterize a 1.95 kb transcription product of the Euglena gracilis chloroplast DNA fragment Eco-N + Q by SI nuclease analysis and DNA sequencing and show that it is the product of three splicing events. Exon 1 (0.45 kb), exon 2 (0.74 kb) and 175 nucleotides of exon 3 (0.53 kb) code for the chloroplast elongation factor protein (EF-Tu). The remaining part of exon 3 and exon 4 (0.23 kb) have unidentified open reading frames. The chloroplast EF-Tu protein has 408 aminoacids and is to 70percnt; homologous with the E. coli EF-Tu protein. The active site for aminoacyl-tRNA binding is highly conserved, while the active site for GTP/GDP binding lacks the cysteine present in the E. coli EF-Tu protein. The two introns separating exons 1 , 2 and 3 are, respectively, 103 and 110 nucleotides long. The size of the third intron is not yet determined. The splicing rules for eukaryote mRNA are not followed.
机译:我们通过SI核酸酶分析和DNA测序表征了Euglena gracilis叶绿体DNA片段Eco-N + Q的1.95 kb转录产物,并显示它是三个剪接事件的产物。外显子1(0.45 kb),外显子2(0.74 kb)和外显子3的175个核苷酸(0.53 kb)编码叶绿体延伸因子蛋白(EF-Tu)。外显子3和外显子4的其余部分(0.23 kb)具有未识别的开放阅读框。叶绿体EF-Tu蛋白具有408个氨基酸,约为70percnt;与大肠杆菌EF-Tu蛋白同源。氨酰基-tRNA结合的活性位点是高度保守的,而GTP / GDP结合的活性位点缺乏大肠杆菌EF-Tu蛋白中存在的半胱氨酸。分隔外显子1、2和3的两个内含子分别长103和110个核苷酸。第三内含子的大小尚未确定。不遵循真核生物mRNA的剪接规则。

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