Warrander Fiona, Faas Laura, Kovalevskiy Oleg, Peters Daniel, Coles Mark, Antson Alfred A, Genever Paul, Isaacs Harry V
Department of Biology, University of York, York, YO10 5DD, UK.
York Structural Biology Laboratory, Department of Chemistry, University of York, Heslington York, YO10 5DD, UK.
Dev Dyn. 2016 Jan;245(1):34-46. doi: 10.1002/dvdy.24358. Epub 2015 Nov 14.
Lin28 proteins are post-transcriptional regulators of gene expression with multiple roles in development and the regulation of pluripotency in stem cells. Much attention has focussed on Lin28 proteins as negative regulators of let-7 miRNA biogenesis; a function that is conserved in several animal groups and in multiple processes. However, there is increasing evidence that Lin28 proteins have additional roles, distinct from regulation of let-7 abundance. We have previously demonstrated that lin28 proteins have functions associated with the regulation of early cell lineage specification in Xenopus embryos, independent of a lin28/let-7 regulatory axis. However, the nature of lin28 targets in Xenopus development remains obscure.
Here, we show that mir-17∼92 and mir-106∼363 cluster miRNAs are down-regulated in response to lin28 knockdown, and RNAs from these clusters are co-expressed with lin28 genes during germ layer specification. Mature miRNAs derived from pre-mir-363 are most sensitive to lin28 inhibition. We demonstrate that lin28a binds to the terminal loop of pre-mir-363 with an affinity similar to that of let-7, and that this high affinity interaction requires to conserved a GGAG motif.
Our data suggest a novel function for amphibian lin28 proteins as positive regulators of mir-17∼92 family miRNAs.
Lin28蛋白是基因表达的转录后调节因子,在发育和干细胞多能性调控中具有多种作用。Lin28蛋白作为let-7 miRNA生物合成的负调节因子备受关注;这一功能在多个动物群体和多个过程中保守。然而,越来越多的证据表明,Lin28蛋白具有不同于调节let-7丰度的其他作用。我们之前已经证明,lin28蛋白具有与非洲爪蟾胚胎早期细胞谱系特化调控相关的功能,独立于lin28/let-7调控轴。然而,非洲爪蟾发育过程中lin28靶点的性质仍不清楚。
在这里,我们表明mir-17∼92和mir-106∼363簇miRNA在响应lin28敲低时下调,并且这些簇中的RNA在胚层特化过程中与lin28基因共表达。源自pre-mir-363的成熟miRNA对lin28抑制最敏感。我们证明lin28a以与let-7相似的亲和力结合pre-mir-363的末端环,并且这种高亲和力相互作用需要保守的GGAG基序。
我们的数据表明两栖动物lin28蛋白具有作为mir-17∼92家族miRNA正调节因子的新功能。