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来自玉兰科线粒体 cox2 基因的两个内含子的缺失暗示了水平基因转移和基因转换是内含子缺失的一种新机制。

Loss of two introns from the Magnolia tripetala mitochondrial cox2 gene implicates horizontal gene transfer and gene conversion as a novel mechanism of intron loss.

机构信息

Center for Plant Science Innovation, University of Nebraska, NE, USA.

出版信息

Mol Biol Evol. 2012 Oct;29(10):3111-20. doi: 10.1093/molbev/mss130. Epub 2012 May 15.

Abstract

Intron loss is often thought to occur through retroprocessing, which is the reverse transcription and genomic integration of a spliced transcript. In plant mitochondria, several unambiguous examples of retroprocessing are supported by the parallel loss of an intron and numerous adjacent RNA edit sites, but in most cases, the evidence for intron loss via retroprocessing is weak or lacking entirely. To evaluate mechanisms of intron loss, we designed a polymerase chain reaction (PCR)-based assay to detect recent intron losses from the mitochondrial cox2 gene within genus Magnolia, which was previously suggested to have variability in cox2 intron content. Our assay showed that all 22 examined species have a cox2 gene with two introns. However, one species, Magnolia tripetala, contains an additional cox2 gene that lacks both introns. Quantitative PCR showed that both M. tripetala cox2 genes are present in the mitochondrial genome. Although the intronless gene has lost several ancestral RNA edit sites, their distribution is inconsistent with retroprocessing models. Instead, phylogenetic and gene conversion analyses indicate that the intronless gene was horizontally acquired from a eudicot and then underwent gene conversion with the native intron-containing gene. The models are presented to summarize the roles of horizontal gene transfer and gene conversion as a novel mechanism of intron loss.

摘要

内含子丢失通常被认为是通过反向剪接发生的,即剪接转录本的反转录和基因组整合。在植物线粒体中,有几个明确的反向剪接的例子,它们伴随着内含子和许多相邻的 RNA 编辑位点的平行丢失,但在大多数情况下,通过反向剪接导致内含子丢失的证据是薄弱的或完全缺乏的。为了评估内含子丢失的机制,我们设计了一种聚合酶链反应(PCR)为基础的检测方法,用于检测木兰属内线粒体 cox2 基因的近期内含子丢失,该属先前被认为 cox2 内含子含量具有可变性。我们的检测表明,所有 22 种被检测的物种都有一个带有两个内含子的 cox2 基因。然而,有一种物种,玉兰,含有一个额外的 cox2 基因,该基因缺失了两个内含子。定量 PCR 显示,玉兰的两个 cox2 基因都存在于线粒体基因组中。尽管无内含子基因丢失了几个祖先 RNA 编辑位点,但它们的分布与反向剪接模型不一致。相反,系统发育和基因转换分析表明,无内含子基因是从一个真双子叶植物中水平获得的,然后与本地内含子基因发生了基因转换。这些模型总结了水平基因转移和基因转换作为一种新的内含子丢失机制的作用。

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