Abstract
Small interfering RNAs regulate gene expression in diverse biological processes, including heterochromatin formation and DNA elimination, developmental regulation, and cell differentiation. In the single-celled eukaryote Entamoeba histolytica, we have identified a population of small RNAs of 27 nt size that (i) have 5′-polyphosphate termini, (ii) map antisense to genes, and (iii) associate with an E. histolytica Piwi-related protein. Whole genome microarray expression analysis revealed that essentially all genes to which antisense small RNAs map were not expressed under trophozoite conditions, the parasite stage from which the small RNAs were cloned. However, a number of these genes were expressed in other E. histolytica strains with an inverse correlation between small RNA and gene expression level, suggesting that these small RNAs mediate silencing of the cognate gene. Overall, our results demonstrate that E. histolytica has an abundant 27 nt small RNA population, with features similar to secondary siRNAs from C. elegans, and which appear to regulate gene expression. These data indicate that a silencing pathway mediated by 5′-polyphosphate siRNAs extends to single-celled eukaryotic organisms.
Highlights
Small RNAs mediate post-transcriptional gene silencing in a multitude of organisms and in diverse biological processes [1,2,3,4,5]
Regulation of gene expression can occur via multiple conserved pathways. One such mechanism is mediated by RNA molecules of about 21–24 nucleotides, which can affect rates of RNA degradation or protein production
We have made a number of novel observations with respect to small RNA size, structure, and function in Entamoeba histolytica, a single-celled parasite and an important human pathogen
Summary
Small RNAs mediate post-transcriptional gene silencing in a multitude of organisms and in diverse biological processes [1,2,3,4,5]. Multiple classes of small RNAs have recently been described including small interfering RNAs (siRNAs), microRNAs (miRNAs), trans-acting siRNAs (tasiRNAs), tiny noncoding RNAs (tncRNAs), small scan RNA (scRNA), repeat-associated small interfering RNA (rasiRNA), piwi-interacting RNA (piRNA), and secondary siRNAs [6,7,8,9]. Some organisms have multiple populations of small RNAs associated with different mechanisms of gene regulation. SiRNAs, miRNAs, tasiRNAs, tncRNA, and scnRNA are all products of Dicer cleavage. RasiRNA, piRNA, and secondary siRNA appear to be formed independent of Dicer processing [6,7,8,10]
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