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新核基因起源于细胞质细胞器基因组的起源和特征。

The origin and characterization of new nuclear genes originating from a cytoplasmic organellar genome.

机构信息

School of Molecular and Biomedical Science, The University of Adelaide, South Australia 5005 Australia.

出版信息

Mol Biol Evol. 2011 Jul;28(7):2019-28. doi: 10.1093/molbev/msr021. Epub 2011 Jan 20.

Abstract

Endosymbiotic transfer of DNA and functional genes from the cytoplasmic organelles (mitochondria and chloroplasts) to the nucleus has been a major factor driving the origin of new nuclear genes, a process central to eukaryote evolution. Although organelle DNA transfers very frequently to the nucleus, most is quickly deleted, decays, or is alternatively scrapped. However, a very small proportion of it gives rise, immediately or eventually, to functional genes. To simulate the process of functional transfer, we screened for nuclear activation of a chloroplast reporter gene aadA, which had been transferred from the chloroplast to independent nuclear loci in 16 different plant lines. Cryptic nuclear activity of the chloroplast promoter was revealed, which became conspicuous when present in multiple nuclear copies. We screened ∼50 million cells of each line and retrieved three plants in which aadA showed strong nuclear activation. Activation occurred by acquisition of the CaMV 35S nuclear promoter or by nuclear activation of the native chloroplast promoter. Two fortuitous sites within the 3' UTR of aadA mRNA both promoted polyadenylation without any sequence change. Complete characterization of one nuclear sequence before and after gene transfer demonstrated integration by nonhomologous end joining involving simultaneous insertion of multiple chloroplast DNA fragments. The real-time observation of three different means by which a chloroplast gene can become expressed in the nucleus suggests that the process, though rare, may be more readily achieved than previously envisaged.

摘要

内共生体将 DNA 和功能基因从细胞质细胞器(线粒体和叶绿体)转移到细胞核,这是驱动新核基因起源的主要因素,也是真核生物进化的核心过程。尽管细胞器 DNA 经常非常频繁地转移到细胞核,但大多数很快就会被删除、衰减或被替代。然而,只有一小部分会立即或最终产生功能基因。为了模拟功能转移的过程,我们筛选了来自叶绿体的报告基因 aadA 的核激活,该基因已从叶绿体转移到 16 条不同植物品系中的独立核位点。叶绿体启动子的隐匿核活性被揭示出来,当存在多个核拷贝时,这种活性变得明显。我们筛选了每条品系约 5000 万个细胞,并从其中三个植物中回收了 aadA 表现出强烈核激活的植物。激活是通过获得 CaMV 35S 核启动子或通过核激活天然叶绿体启动子来实现的。aadA mRNA 3'UTR 内的两个偶然位点都促进了多聚腺苷酸化,而没有任何序列改变。在基因转移前后对一个核序列的完整特征分析表明,整合是通过非同源末端连接实现的,涉及同时插入多个叶绿体 DNA 片段。对叶绿体基因在核中表达的三种不同方式的实时观察表明,该过程虽然罕见,但可能比之前预期的更容易实现。

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