Fujino T, Navaratnam N, Jarmuz A, von Haeseler A, Scott J
Tohoku University Gene Research Centre, 1-1 Tsutsumidori-Amamiya, Aoba, Sendai 981-0914, Japan,
Nucleic Acids Res. 1999 Jul 1;27(13):2662-71. doi: 10.1093/nar/27.13.2662.
The C->U editing of RNA is widely found in plant and animal species. In mammals it is a discrete process confined to the editing of apolipoprotein B (apoB) mRNA in eutherians and the editing of the mitochondrial tRNA for glycine in marsupials. Here we have identified and characterised apoB mRNA editing in the American opossum Monodelphus domestica. The apoB mRNA editing site is highly conserved in the opossum and undergoes complete editing in the small intestine, but not in the liver or other tissues. Opossum APOBEC-1 cDNA was cloned, sequenced and expressed. The encoded protein is similar to APOBEC-1 of eutherians. Motifs previously identified as involved in zinc binding, RNA binding and catalysis, nuclear localisation and a C-terminal leucine-rich domain are all conserved. Opossum APOBEC-1 contains a seven amino acid C-terminal extension also found in humans and rabbits, but not present in rodents. The opossum APOBEC-1 gene has the same intron/exon organisation in the coding sequence as the eutherian gene. Northern blot and RT-PCR analyses and an editing assay indicate that no APOBEC-1 was expressed in the liver. Thus the far upstream promoter responsible for hepatic expression in rodents does not operate in the opossum. An APOBEC-1-like enzyme such as might be involved in C->U RNA editing of tRNA in marsupial mitochondria was not demonstrated. The activity of opossum APOBEC-1 in the presence of both chicken and rodent auxiliary editing proteins was comparable to that of other mammals. These studies extend the origins of APOBEC-1 back 170 000 000 years to marsupials and help bridge the gap in the origins of this RNA editing process between birds and eutherian mammals.
RNA的C到U编辑在植物和动物物种中广泛存在。在哺乳动物中,它是一个离散的过程,仅限于真兽类动物载脂蛋白B(apoB)mRNA的编辑以及有袋类动物线粒体甘氨酸tRNA的编辑。在这里,我们鉴定并表征了美洲负鼠(Monodelphus domestica)中的apoB mRNA编辑。apoB mRNA编辑位点在负鼠中高度保守,在小肠中发生完全编辑,但在肝脏或其他组织中不发生。克隆、测序并表达了负鼠APOBEC-1 cDNA。编码的蛋白质与真兽类动物的APOBEC-1相似。先前确定参与锌结合、RNA结合和催化、核定位以及C末端富含亮氨酸结构域的基序均保守。负鼠APOBEC-1含有一个七氨基酸的C末端延伸,在人类和兔子中也有发现,但在啮齿动物中不存在。负鼠APOBEC-1基因在编码序列中的内含子/外显子组织与真兽类动物基因相同。Northern印迹和RT-PCR分析以及编辑试验表明,肝脏中未表达APOBEC-1。因此,负责啮齿动物肝脏表达的远上游启动子在负鼠中不起作用。未证明存在可能参与有袋类动物线粒体tRNA的C到U RNA编辑的类似APOBEC-但在啮齿动物中不存在。负鼠APOBEC-1基因在编码序列中的内含子/外显子组织与真兽类动物基因相同。Northern印迹和RT-PCR分析以及编辑试验表明,肝脏中未表达APOBEC-1。因此,负责啮齿动物肝脏表达的远上游启动子在负鼠中不起作用。未证明存在可能参与有袋类动物线粒体tRNA的C到U RNA编辑的类似APOBEC-1的酶。在存在鸡和啮齿动物辅助编辑蛋白的情况下,负鼠APOBEC-1的活性与其他哺乳动物相当。这些研究将APOBEC-1的起源追溯到1.7亿年前的有袋类动物,并有助于弥合鸟类和真兽类哺乳动物之间这种RNA编辑过程起源的差距。 1的酶。在存在鸡和啮齿动物辅助编辑蛋白的情况下,负鼠APOBEC-1的活性与其他哺乳动物相当。这些研究将APOBEC-1的起源追溯到1.7亿年前的有袋类动物,并有助于弥合鸟类和真兽类哺乳动物之间这种RNA编辑过程起源的差距。