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小麦线粒体 DNA 中的 tRNA(Asp)、tRNA(Pro)、tRNA(Tyr)和两个 tRNA(Ser)基因。

Genes for tRNA(Asp), tRNA (Pro), tRNA (Tyr) and two tRNAs (Ser) in wheat mitochondrial DNA.

机构信息

Department of Biochemistry, Dalhousie University, B3H 4H7, Halifax, Nova Scotia, Canada.

出版信息

Plant Mol Biol. 1988 May;10(3):251-62. doi: 10.1007/BF00027402.

Abstract

We have begun a systematic search for potential tRNA genes in wheat mtDNA, and present here the sequences of regions of the wheat mitochondrial genome that encode genes for tRNA(Asp) (anticodon GUC), tRNA(Pro) (UGG), tRNA(Tyr) (GUA), and two tRNAs(Ser) (UGA and GCU). These genes are all solitary, not immediately adjacent to other tRNA or known protein coding genes. Each of the encoded tRNAs can assume a secondary structure that conforms to the standard cloverleaf model, and that displays none of the structural aberrations peculiar to some of the corresponding mitochondrial tRNAs from other eukaryotes. The wheat mitochondrial tRNA sequences are, on average, substantially more similar to their eubacterial and chloroplast counterparts than to their homologues in fungal and animal mitochondria. However, an analysis of regions ∼ 150 nucleotides upstream and ∼ 100 nucleotides downstream of the tRNA coding regions has revealed no obvious conserved sequences that resemble the promoter and terminator motifs that regulate the expression of eubacterial and some chloroplast tRNA genes. When restriction digests of wheat mtDNA are probed with (32)P-labelled wheat mitochondrial tRNAs, <20 hybridizing bands are detected, whether enzymes with 4 bp or 6 bp recognition sites are used. This suggests that the wheat mitochondrial genome, despite its large size, may carry a relatively small number of tRNA genes.

摘要

我们已经开始在小麦线粒体 DNA 中系统性地寻找潜在的 tRNA 基因,并在此呈现编码 tRNA(Asp)(反密码子 GUC)、tRNA(Pro)(UGG)、tRNA(Tyr)(GUA)和两个 tRNA(Ser)(UGA 和 GCU)的小麦线粒体基因组区域的序列。这些基因都是孤立的,不与其他 tRNA 或已知的蛋白质编码基因相邻。每个编码的 tRNA 都可以采用符合标准三叶草模型的二级结构,并且没有显示出来自其他真核生物的一些对应线粒体 tRNA 的特有结构异常。与真菌和动物线粒体中的同源物相比,小麦线粒体 tRNA 序列与真细菌和叶绿体的对应物平均更为相似。然而,对 tRNA 编码区上下游约 150 个核苷酸的区域进行分析后,并未发现明显的保守序列类似于调节真细菌和一些叶绿体 tRNA 基因表达的启动子和终止子序列。当用 (32)P 标记的小麦线粒体 tRNA 探测小麦 mtDNA 的酶切片段时,无论使用具有 4 个碱基还是 6 个碱基识别位点的酶,都只能检测到<20 个杂交带。这表明,尽管小麦线粒体基因组很大,但可能只携带相对较少的 tRNA 基因。

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