Dickey Thayne H, Pyle Anna M
Department of Molecular, Cellular and Developmental Biology, Yale University, New Haven, CT 06511, USA.
Howard Hughes Medical Institute, Chevy Chase, MD 20815, USA.
Nucleic Acids Res. 2017 Nov 16;45(20):11980-11988. doi: 10.1093/nar/gkx846.
Several members of the SMAD family of transcription factors have been reported to bind RNA in addition to their canonical double-stranded DNA (dsDNA) ligand. RNA binding by SMAD has the potential to affect numerous cellular functions that involve RNA. However, the affinity and specificity of this RNA binding activity has not been well characterized, which limits the ability to validate and extrapolate functional implications of this activity. Here we perform quantitative binding experiments in vitro to determine the ligand requirements for RNA binding by SMAD3. We find that SMAD3 binds poorly to single- and double-stranded RNA, regardless of sequence. However, SMAD3 binds RNA with large internal loops or bulges with high apparent affinity. This apparent affinity matches that for its canonical dsDNA ligand, suggesting a biological role for RNA binding by SMAD3.
据报道,SMAD转录因子家族的几个成员除了能结合其典型的双链DNA(dsDNA)配体外,还能结合RNA。SMAD与RNA的结合有可能影响众多涉及RNA的细胞功能。然而,这种RNA结合活性的亲和力和特异性尚未得到很好的表征,这限制了验证和推断该活性功能意义的能力。在这里,我们进行了体外定量结合实验,以确定SMAD3结合RNA的配体需求。我们发现,无论序列如何,SMAD3与单链和双链RNA的结合都很差。然而,SMAD3能以较高的表观亲和力结合具有大内部环或凸起的RNA。这种表观亲和力与其典型的dsDNA配体相匹配,表明SMAD3与RNA的结合具有生物学作用。