Reconstituting plant miRNA biogenesis

The genomes of higher eukaryotes encode not only proteins but also diverse noncoding RNAs, particularly small (20- to 30-nt) regulatory RNAs (1–3). The small RNAs include microRNAs (miRNAs), siRNAs, and piwi-interacting RNAs (piRNAs) (4, 5). These small RNAs repress gene expression at the transcriptional or posttranscriptional levels and have critical functions in genome defense, growth, development, diseases, and stress responses (1, 3, 6–8). Small RNAs are classified largely on the basis of their biogenesis requirements. miRNAs arise from single-stranded primary miRNA transcripts (pri-miRNAs) that can form imperfect stem–loop structures (6) (Fig. 1). In animals, pri-miRNAs are processed in the nucleus into shorter hairpin RNAs of ≈65 nt (premiRNAs) by the microprocessor complex containing the RNaseIII enzyme Drosha and its cofactor DGCR8/Pasha, a dsRNA-binding protein (5, 9). The premiRNA is then exported to the cytoplasm, where it is further processed by another RNaseIII enzyme, Dicer, to release an ≈22-nt miRNA/miRNA* duplex (5, 9). Dicer function also requires a dsRNA-binding protein, TRBP, as a cofactor. The miRNA is loaded into the effector complex, known as RISC, to direct complementary or partially complementary mRNAs for cleavage or translational repression (5, 6). In plants, the two-step processing of pri-miRNAs into mature miRNAs occurs entirely in the nucleus and is carried out by a single RNaseIII enzyme, DCL1 (Dicer-like 1) (6). In addition to DCL1, genetic analysis revealed that HYL1, a dsRNA-binding protein, and SE, a C2H2-type zinc finger, are also required for processing pri-miRNAs and for accumulation of mature miRNAs (10–12) (Fig. 1). However, whether DCL1 alone is active in processing pri-miRNAs into miRNAs and how HYL1 and SE may function in the processing steps are not known. In this issue of PNAS, Dong et al. (13) reconstituted the processing of pri-miRNAs in vitro by using recombinant proteins and thereby provided much-needed biochemical data to explain the genetic roles of DCL1, HYL1, and SE in miRNA biogenesis in plants.

[1]  N. Fedoroff,et al.  Arabidopsis primary microRNA processing proteins HYL1 and DCL1 define a nuclear body distinct from the Cajal body , 2007, Proceedings of the National Academy of Sciences.

[2]  C. Mello,et al.  Revealing the world of RNA interference , 2004, Nature.

[3]  D. Baulcombe RNA silencing in plants , 2004, Nature.

[4]  N. Fedoroff,et al.  The Arabidopsis double-stranded RNA-binding protein HYL1 plays a role in microRNA-mediated gene regulation. , 2004, Proceedings of the National Academy of Sciences of the United States of America.

[5]  R. Lister,et al.  A link between RNA metabolism and silencing affecting Arabidopsis development. , 2008, Developmental cell.

[6]  Xuemei Chen,et al.  Methylation as a Crucial Step in Plant microRNA Biogenesis , 2005, Science.

[7]  D. Bartel,et al.  MicroRNAS and their regulatory roles in plants. , 2006, Annual review of plant biology.

[8]  V. Ambros,et al.  Role of MicroRNAs in Plant and Animal Development , 2003, Science.

[9]  P. Zamore,et al.  Small silencing RNAs , 2007, Current Biology.

[10]  Hai Huang,et al.  SERRATE is a novel nuclear regulator in primary microRNA processing in Arabidopsis. , 2006, The Plant journal : for cell and molecular biology.

[11]  Byoung-Tak Zhang,et al.  Molecular Basis for the Recognition of Primary microRNAs by the Drosha-DGCR8 Complex , 2006, Cell.

[12]  H. Vaucheret,et al.  The Nuclear dsRNA Binding Protein HYL1 Is Required for MicroRNA Accumulation and Plant Development, but Not Posttranscriptional Transgene Silencing , 2004, Current Biology.

[13]  Y. Ohba,et al.  Location of a possible miRNA processing site in SmD3/SmB nuclear bodies in Arabidopsis. , 2007, Plant & cell physiology.

[14]  O. Borsani,et al.  Endogenous siRNAs Derived from a Pair of Natural cis-Antisense Transcripts Regulate Salt Tolerance in Arabidopsis , 2005, Cell.

[15]  J. Messing,et al.  CARPEL FACTORY, a Dicer Homolog, and HEN1, a Novel Protein, Act in microRNA Metabolism in Arabidopsis thaliana , 2002, Current Biology.

[16]  Yuda Fang,et al.  Identification of Nuclear Dicing Bodies Containing Proteins for MicroRNA Biogenesis in Living Arabidopsis Plants , 2007, Current Biology.

[17]  James C. Carrington,et al.  Specialization and evolution of endogenous small RNA pathways , 2007, Nature Reviews Genetics.

[18]  N. Fedoroff,et al.  The RNA-binding proteins HYL1 and SE promote accurate in vitro processing of pri-miRNA by DCL1 , 2008, Proceedings of the National Academy of Sciences.

[19]  Ramanjulu Sunkar,et al.  Small RNAs as big players in plant abiotic stress responses and nutrient deprivation. , 2007, Trends in plant science.