A conserved upstream motif orchestrates autonomous, germline-enriched expression of Caenorhabditis elegans piRNAs

PLoS Genet. 2013;9(3):e1003392. doi: 10.1371/journal.pgen.1003392. Epub 2013 Mar 14.

Abstract

Piwi-interacting RNAs (piRNAs) fulfill a critical, conserved role in defending the genome against foreign genetic elements. In many organisms, piRNAs appear to be derived from processing of a long, polycistronic RNA precursor. Here, we establish that each Caenorhabditis elegans piRNA represents a tiny, autonomous transcriptional unit. Remarkably, the minimal C. elegans piRNA cassette requires only a 21 nucleotide (nt) piRNA sequence and an ∼50 nt upstream motif with limited genomic context for expression. Combining computational analyses with a novel, in vivo transgenic system, we demonstrate that this upstream motif is necessary for independent expression of a germline-enriched, Piwi-dependent piRNA. We further show that a single nucleotide position within this motif directs differential germline enrichment. Accordingly, over 70% of C. elegans piRNAs are selectively expressed in male or female germline, and comparison of the genes they target suggests that these two populations have evolved independently. Together, our results indicate that C. elegans piRNA upstream motifs act as independent promoters to specify which sequences are expressed as piRNAs, how abundantly they are expressed, and in what germline. As the genome encodes well over 15,000 unique piRNA sequences, our study reveals that the number of transcriptional units encoding piRNAs rivals the number of mRNA coding genes in the C. elegans genome.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Animals
  • Caenorhabditis elegans / genetics
  • Female
  • Gene Expression Regulation
  • Genome
  • Germ Cells / metabolism*
  • Male
  • Nucleotide Motifs / genetics*
  • RNA, Small Interfering* / genetics
  • RNA, Small Interfering* / metabolism
  • Regulatory Sequences, Ribonucleic Acid / genetics*

Substances

  • RNA, Small Interfering
  • Regulatory Sequences, Ribonucleic Acid