Department of Biology and Department of Molecular and Cellular Biochemistry, Indiana University Bloomington, Bloomington, United States; Howard Hughes Medical Institute, Indiana University, Bloomington, United States
Vibhor Mishra
Department of Biology and Department of Molecular and Cellular Biochemistry, Indiana University Bloomington, Bloomington, United States; Howard Hughes Medical Institute, Indiana University, Bloomington, United States
Feng Wang
Department of Biology and Department of Molecular and Cellular Biochemistry, Indiana University Bloomington, Bloomington, United States; Howard Hughes Medical Institute, Indiana University, Bloomington, United States
Department of Biology and Department of Molecular and Cellular Biochemistry, Indiana University Bloomington, Bloomington, United States; Howard Hughes Medical Institute, Indiana University, Bloomington, United States
In plants, selfish genetic elements, including retrotransposons and DNA viruses, are transcriptionally silenced by RNA-directed DNA methylation. Guiding the process are short interfering RNAs (siRNAs) cut by DICER-LIKE 3 (DCL3) from double-stranded precursors of ~30 bp that are synthesized by NUCLEAR RNA POLYMERASE IV (Pol IV) and RNA-DEPENDENT RNA POLYMERASE 2 (RDR2). We show that Pol IV’s choice of initiating nucleotide, RDR2’s initiation 1–2 nt internal to Pol IV transcript ends and RDR2’s terminal transferase activity collectively yield a code that influences which precursor end is diced and whether 24 or 23 nt siRNAs are produced. By diversifying the size, sequence, and strand specificity of siRNAs derived from a given precursor, alternative patterns of DCL3 dicing allow for maximal siRNA coverage at methylated target loci.
