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人类大脑中与年龄相关的基因特异性 A-to-I mRNA 编辑变化。

Age-related gene-specific changes of A-to-I mRNA editing in the human brain.

机构信息

Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, MA 02215, USA.

出版信息

Mech Ageing Dev. 2010 Jun;131(6):445-7. doi: 10.1016/j.mad.2010.06.001. Epub 2010 Jun 9.

Abstract

A-to-I editing is an adenosine-to-inosine modification of mRNA particularly widespread in the human brain, where it affects thousands of genes. A growing body of evidence suggests that A-to-I RNA editing is necessary for normal development and maintenance in mammals and that its deficiencies contribute to a number of pathological states. In this study, we examined whether mRNA editing levels of two mRNA species, CYFIP2 and GABRA3, change with aging. CYFIP2 has been implicated in synaptic maintenance, while GABRA3 is a GABA receptor subunit, a part of the major inhibitory neurotransmitter system in the CNS. The levels of mRNA editing were assessed in cortex samples of 20 subjects 22-102 years old. The data show an age-dependent statistically significant decrease in editing in CYFIP2. GABRA3 editing remained much more stable with age, implying that age-related decline of RNA editing is gene-specific. This is the first report of age-dependent decline in A-to-I editing. Further examination of these and other vulnerable genes may reveal specific RNA editing mechanisms that contribute to the aging phenotype.

摘要

A 到 I 的编辑是 mRNA 的一种腺嘌呤到肌苷的修饰,在人类大脑中特别普遍,它影响着数千个基因。越来越多的证据表明,A 到 I 的 RNA 编辑对于哺乳动物的正常发育和维持是必要的,其缺陷导致许多病理状态。在这项研究中,我们研究了两种 mRNA 物种,CYFIP2 和 GABRA3 的 mRNA 编辑水平是否随年龄而变化。CYFIP2 与突触维持有关,而 GABRA3 是 GABA 受体亚基,是中枢神经系统主要抑制性神经递质系统的一部分。我们评估了 20 名年龄在 22 岁至 102 岁的受试者大脑皮层样本中的 mRNA 编辑水平。数据显示,CYFIP2 的编辑随年龄呈依赖性显著下降。GABRA3 的编辑随年龄的变化相对稳定,这意味着与年龄相关的 RNA 编辑下降是基因特异性的。这是第一个关于 A 到 I 编辑随年龄下降的报告。对这些和其他易受影响的基因的进一步研究可能会揭示导致衰老表型的特定 RNA 编辑机制。

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