Cancer Genetics Program, Beth Israel Deaconess Cancer Center, Department of Medicine, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, Massachusetts 02215, USA.
Nature. 2010 Jun 24;465(7301):1033-8. doi: 10.1038/nature09144.
The canonical role of messenger RNA (mRNA) is to deliver protein-coding information to sites of protein synthesis. However, given that microRNAs bind to RNAs, we hypothesized that RNAs could possess a regulatory role that relies on their ability to compete for microRNA binding, independently of their protein-coding function. As a model for the protein-coding-independent role of RNAs, we describe the functional relationship between the mRNAs produced by the PTEN tumour suppressor gene and its pseudogene PTENP1 and the critical consequences of this interaction. We find that PTENP1 is biologically active as it can regulate cellular levels of PTEN and exert a growth-suppressive role. We also show that the PTENP1 locus is selectively lost in human cancer. We extended our analysis to other cancer-related genes that possess pseudogenes, such as oncogenic KRAS. We also demonstrate that the transcripts of protein-coding genes such as PTEN are biologically active. These findings attribute a novel biological role to expressed pseudogenes, as they can regulate coding gene expression, and reveal a non-coding function for mRNAs.
信使 RNA(mRNA)的规范作用是将蛋白质编码信息传递到蛋白质合成部位。然而,鉴于 microRNA 与 RNA 结合,我们假设 RNA 可以发挥一种调节作用,这种作用依赖于它们结合 microRNA 的能力,而不依赖于它们的蛋白质编码功能。作为 RNA 不依赖于蛋白质编码功能的作用的模型,我们描述了抑癌基因 PTEN 及其假基因 PTENP1 产生的 mRNA 之间的功能关系,以及这种相互作用的关键后果。我们发现 PTENP1 具有生物学活性,因为它可以调节细胞内的 PTEN 水平并发挥生长抑制作用。我们还表明,PTENP1 基因座在人类癌症中是选择性丢失的。我们将我们的分析扩展到其他具有假基因的与癌症相关的基因,如致癌 KRAS。我们还证明了像 PTEN 这样的蛋白质编码基因的转录本具有生物学活性。这些发现赋予表达假基因一种新的生物学作用,因为它们可以调节编码基因的表达,并揭示了 mRNA 的非编码功能。