Howard Hughes Medical Institute and Department of Biochemistry and Molecular Pharmacology, University of Massachusetts Medical School, Worcester, MA 01605, USA.
Curr Biol. 2011 Nov 22;21(22):1878-87. doi: 10.1016/j.cub.2011.09.034. Epub 2011 Nov 3.
MicroRNAs (miRNAs) are ~22 nucleotide (nt) small RNAs that control development, physiology, and pathology in animals and plants. Production of miRNAs involves the sequential processing of primary hairpin-containing RNA polymerase II transcripts by the RNase III enzymes Drosha in the nucleus and Dicer in the cytoplasm. miRNA duplexes then assemble into Argonaute proteins to form the RNA-induced silencing complex (RISC). In mature RISC, a single-stranded miRNA directs the Argonaute protein to bind partially complementary sequences, typically in the 3' untranslated regions of messenger RNAs, repressing their expression.
Here, we show that after loading into Argonaute1 (Ago1), more than a quarter of all Drosophila miRNAs undergo 3' end trimming by the 3'-to-5' exoribonuclease Nibbler (CG9247). Depletion of Nibbler by RNA interference (RNAi) reveals that miRNAs are frequently produced by Dicer-1 as intermediates that are longer than ~22 nt. Trimming of miRNA 3' ends occurs after removal of the miRNA* strand from pre-RISC and may be the final step in RISC assembly, ultimately enhancing target messenger RNA repression. In vivo, depletion of Nibbler by RNAi causes developmental defects.
We provide a molecular explanation for the previously reported heterogeneity of miRNA 3' ends and propose a model in which Nibbler converts miRNAs into isoforms that are compatible with the preferred length of Ago1-bound small RNAs.
MicroRNAs (miRNAs) 是约 22 个核苷酸 (nt) 的小 RNA,在动植物中控制着发育、生理和病理。miRNA 的产生涉及到 RNA 聚合酶 II 转录物的初级发夹结构通过核内的 Drosha 和细胞质中的 Dicer 的连续加工。miRNA 双链体然后组装到 Argonaute 蛋白中,形成 RNA 诱导的沉默复合物 (RISC)。在成熟的 RISC 中,单链 miRNA 指导 Argonaute 蛋白与部分互补序列结合,通常在信使 RNA 的 3'非翻译区,抑制其表达。
在这里,我们表明,在加载到 Argonaute1 (Ago1) 后,超过四分之一的果蝇 miRNA 会被 3'-5' 外切核酸酶 Nibbler (CG9247) 进行 3'端修剪。通过 RNA 干扰 (RNAi) 耗尽 Nibbler 表明,miRNA 通常作为比~22 nt 更长的中间产物被 Dicer-1 产生。miRNA 3'端的修剪发生在 pre-RISC 中去除 miRNA*链之后,可能是 RISC 组装的最后一步,最终增强了靶信使 RNA 的抑制。在体内,通过 RNAi 耗尽 Nibbler 会导致发育缺陷。
我们为以前报道的 miRNA 3'端异质性提供了一个分子解释,并提出了一个模型,其中 Nibbler 将 miRNA 转化为与 Ago1 结合的小 RNA 偏好长度兼容的同工型。