Carrick Brian H, Crittenden Sarah L, Linsley MaryGrace, Dos Santos Stephany J Costa, Wickens Marvin, Kimble Judith
Department of Biochemistry, University of Wisconsin-Madison, Madison, WI.
Present address: MRC Laboratory of Molecular Biology, Cambridge, CB2 0QH, UK.
bioRxiv. 2024 Oct 25:2024.10.25.620246. doi: 10.1101/2024.10.25.620246.
Like all canonical PUF proteins, FBF-2 binds to specific RNAs via tripartite recognition motifs (TRMs). Here we report that an FBF-2 mutant protein that cannot bind to RNA, is nonetheless biologically active and maintains stem cells. This unexpected result challenges the conventional wisdom that RBPs must bind to RNAs to achieve biological activity. Also unexpectedly, FBF-2 interactions with partner proteins can compensate for loss of RNA-binding. FBF-2 only loses biological activity when its RNA-binding and partner interactions are both defective. These findings highlight the complementary contributions of RNA-binding and protein partner interactions to activity of an RNA-binding protein.
与所有典型的PUF蛋白一样,FBF-2通过三联体识别基序(TRMs)与特定RNA结合。我们在此报告,一种无法与RNA结合的FBF-2突变蛋白,仍具有生物活性并能维持干细胞。这一意外结果挑战了传统观念,即RNA结合蛋白必须与RNA结合才能实现生物活性。同样出乎意料的是,FBF-2与伴侣蛋白的相互作用可以弥补RNA结合的缺失。只有当FBF-2的RNA结合和与伴侣的相互作用都存在缺陷时,它才会失去生物活性。这些发现突出了RNA结合和蛋白伴侣相互作用对RNA结合蛋白活性的互补作用。