Gunzburg Menachem J, Sivakumaran Andrew, Pendini Nicole R, Yoon Je-Hyun, Gorospe Myriam, Wilce Matthew C J, Wilce Jacqueline A
a Biochemistry and Molecular Biology; Monash University ; Melbourne , VIC Australia.
Cell Cycle. 2015;14(17):2729-33. doi: 10.1080/15384101.2015.1069930. Epub 2015 Jul 15.
Both RNA-binding proteins (RBP) and miRNA play important roles in the regulation of mRNA expression, often acting together to regulate a target mRNA. In some cases the RBP and miRNA have been reported to act competitively, but in other instances they function cooperatively. Here, we investigated HuR function as an enhancer of let-7-mediated translational repression of c-Myc despite the separation of their binding sites. Using an in vitro system, we determined that a let-7 mimic, consisting of single-stranded (ss)DNA complementary to the let-7 binding site, enhanced the affinity of HuR for a 122-nt MYC RNA encompassing both binding sites. This finding supports the biophysical principle of cooperative binding by an RBP and miRNA purely through interactions at distal mRNA binding sites.
RNA结合蛋白(RBP)和微小RNA(miRNA)在mRNA表达调控中均发挥重要作用,它们常常共同作用以调控靶标mRNA。在某些情况下,RBP和miRNA据报道具有竞争性作用,但在其他情况下它们则协同发挥功能。在此,我们研究了HuR作为let-7介导的c-Myc翻译抑制增强子的功能,尽管它们的结合位点相互分离。利用体外系统,我们确定一种由与let-7结合位点互补的单链(ss)DNA组成的let-7模拟物,增强了HuR对包含两个结合位点的122个核苷酸的MYC RNA的亲和力。这一发现支持了RBP和miRNA通过在mRNA远端结合位点的相互作用纯粹进行协同结合的生物物理原理。