Department of Biology, Technische Universität Darmstadt, 64287 Darmstadt, Germany.
RNA. 2018 Mar;24(3):324-331. doi: 10.1261/rna.063420.117. Epub 2017 Dec 20.
HnRNP D, better known as AUF1, is an extensively studied protein that controls a variety of cellular pathways. Consequently, its expression has to be tightly regulated to prevent the onset of pathologies. In contrast, the cellular functions and regulation of its ubiquitously expressed paralog hnRNP DL are barely explored. Here, we present an intricate crosstalk between these two proteins. Both hnRNP D and DL are able to control their own expression by alternative splicing of cassette exons in their 3'UTRs. Exon inclusion produces mRNAs degraded by nonsense-mediated decay. Moreover, hnRNP D and DL control the expression of one another by the same mechanism. Thus, we identified two novel ways of how hnRNP D expression is controlled. The tight interconnection of expression control directly links hnRNP DL to hnRNP D-related diseases and emphasizes the importance of a systematic analysis of its cellular functions.
hnRNP D,也被称为 AUF1,是一种广泛研究的蛋白质,它控制着多种细胞途径。因此,它的表达必须受到严格的调控,以防止病理的发生。相比之下,其广泛表达的同源物 hnRNP DL 的细胞功能和调控机制几乎没有被探索过。在这里,我们提出了这两种蛋白质之间复杂的相互作用。hnRNP D 和 DL 都能够通过在其 3'UTR 中剪接盒外显子来控制自身的表达。外显子的包含产生被无意义介导的降解所降解的 mRNA。此外,hnRNP D 和 DL 通过相同的机制来控制彼此的表达。因此,我们确定了 hnRNP D 表达受调控的两种新方式。表达控制的紧密互联直接将 hnRNP DL 与 hnRNP D 相关疾病联系起来,强调了对其细胞功能进行系统分析的重要性。