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来自小麦1号染色体的乙醇脱氢酶(Adh)基因的分子分析。

Molecular analysis of an alcohol dehydrogenase (Adh) gene from chromosome 1 of wheat.

作者信息

Mitchell L E, Dennis E S, Peacock W J

机构信息

Commonwealth Scientific and Industrial Research Organization, Division of Plant Industry, Canberra, Australia.

出版信息

Genome. 1989 Jun;32(3):349-58. doi: 10.1139/g89-454.

Abstract

We have cloned and determined the nucleotide sequence of a gene encoding alcohol dehydrogenase (Adh) from Triticum aestivum cv. Millewa. Southern analysis using cv. Chinese Spring nullisomic-tetrasomic and ditelosomic lines established that the cloned gene mapped to the long arm of chromosome 1A and does not correspond to any previously identified wheat Adh locus. Southern analysis also provided evidence for triplicate copies of this Adh gene on the homoeologous group 1 chromosomes, while Northern blots indicated that the homoeologous group 1 Adh genes, like several other plant Adh genes, are transcribed under anaerobic conditions. Sequence analysis indicates that the cloned gene has a structure similar to both monocot and dicot Adh genes with an open reading frame encoding a polypeptide of 379 amino acids. Sequences important for eucaryotic gene expression such as the TATA box, polyadenylation signal, and intron splice sites were found in the expected positions. The open reading frame is interrupted by 8 introns which are in identical positions with 8 of the 9 introns in maize and pea Adh genes, suggesting that during evolution there are processes occurring that result in the loss of introns. Sequence analysis also revealed that the cloned wheat Adh gene shared extensive homology with the barley Adh3 gene not only in the coding region but also in the noncoding regions. However, this homology is discontinuous as a result of a 1.8-kbp insertion (TLM), which is present in the cloned wheat Adh gene and absent in the barley Adh3 gene. Sequence analysis of this insertion reveals features characteristic of the short terminal inverted repeat class of eucaryotic transposable elements. We have no evidence for the transposition of the TLM element. However, Southern blots reveal multiple copies of sequences related to TLM in the wheat genome and in other closely related species, suggesting that transposition may once have played an important role in the evolution of the Gramineae family.

摘要

我们已经克隆并测定了来自普通小麦品种Millewa的一个编码乙醇脱氢酶(Adh)的基因的核苷酸序列。利用中国春缺体-四体和双端体品系进行的Southern分析表明,克隆的基因定位于1A染色体的长臂上,且与任何先前鉴定的小麦Adh基因座均不对应。Southern分析还为该Adh基因在同源群1染色体上的三个重复拷贝提供了证据,而Northern杂交表明,同源群1的Adh基因与其他几种植物Adh基因一样,在厌氧条件下转录。序列分析表明,克隆的基因具有与单子叶和双子叶Adh基因相似的结构,其开放阅读框编码一个由379个氨基酸组成的多肽。在预期位置发现了对真核基因表达重要的序列,如TATA框、多聚腺苷酸化信号和内含子剪接位点。开放阅读框被8个内含子打断,这些内含子与玉米和豌豆Adh基因9个内含子中的8个处于相同位置,这表明在进化过程中发生了导致内含子丢失的过程。序列分析还显示,克隆的小麦Adh基因不仅在编码区,而且在非编码区与大麦Adh3基因具有广泛的同源性。然而,由于一个1.8kbp的插入片段(TLM),这种同源性是不连续的,该插入片段存在于克隆的小麦Adh基因中,而在大麦Adh3基因中不存在。对该插入片段的序列分析揭示了真核转座元件短末端反向重复类别的特征。我们没有证据表明TLM元件发生了转座。然而,Southern杂交揭示了小麦基因组和其他密切相关物种中与TLM相关的序列的多个拷贝,这表明转座可能曾经在禾本科家族的进化中发挥了重要作用。

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