Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 2014;11(5):484-93.
doi: 10.4161/rna.28452. Epub 2014 Mar 31.

Small regulatory RNAs in Archaea

Affiliations
Review

Small regulatory RNAs in Archaea

Julia Babski et al. RNA Biol. 2014.

Abstract

Small regulatory RNAs (sRNAs) are universally distributed in all three domains of life, Archaea, Bacteria, and Eukaryotes. In bacteria, sRNAs typically function by binding near the translation start site of their target mRNAs and thereby inhibit or activate translation. In eukaryotes, miRNAs and siRNAs typically bind to the 3'-untranslated region (3'-UTR) of their target mRNAs and influence translation efficiency and/or mRNA stability. In archaea, sRNAs have been identified in all species investigated using bioinformatic approaches, RNomics, and RNA-Seq. Their size can vary significantly between less than 50 to more than 500 nucleotides. Differential expression of sRNA genes has been studied using northern blot analysis, microarrays, and RNA-Seq. In addition, biological functions have been unraveled by genetic approaches, i.e., by characterization of designed mutants. As in bacteria, it was revealed that archaeal sRNAs are involved in many biological processes, including metabolic regulation, adaptation to extreme conditions, stress responses, and even in regulation of morphology and cellular behavior. Recently, the first target mRNAs were identified in archaea, including one sRNA that binds to the 5'-region of two mRNAs in Methanosarcina mazei Gö1 and a few sRNAs that bind to 3'-UTRs in Sulfolobus solfataricus, three Pyrobaculum species, and Haloferax volcanii, indicating that archaeal sRNAs appear to be able to target both the 5'-UTR or the 3'-UTRs of their respective target mRNAs. In addition, archaea contain tRNA-derived fragments (tRFs), and one tRF has been identified as a major ribosome-binding sRNA in H. volcanii, which downregulates translation in response to stress. Besides regulatory sRNAs, archaea contain further classes of sRNAs, e.g., CRISPR RNAs (crRNAs) and snoRNAs.

Keywords: Haloferax volcanii; Methanosarcina mazei; Nanoarchaeum equitans; Sulfolobus solfataricus; archaea; small regulatory RNAs; tRNA-derived fragments; translation.

PubMed Disclaimer

Figures

None
Figure 1. Modes of interactions between archaeal sRNAs and target mRNAs characterized until now. (A) A novel mode of interaction of a sRNA that acts as a cis-encoded antisense sRNA as well as a trans-encoded sRNA, in both cases interacting with the 5′-region of the target mRNA. (B) sRNAs that interact with the 3′-UTRs of target mRNAs in several species of archaea, both of leadered and of leaderless transcripts.

References

    1. Woese CR, Fox GE. Phylogenetic structure of the prokaryotic domain: the primary kingdoms. Proc Natl Acad Sci U S A. 1977;74:5088–90. doi: 10.1073/pnas.74.11.5088. - DOI - PMC - PubMed
    1. Mardanov AV, Ravin NV. The impact of genomics on research in diversity and evolution of archaea. Biochemistry (Mosc) 2012;77:799–812. doi: 10.1134/S0006297912080019. - DOI - PubMed
    1. Brochier-Armanet C, Forterre P, Gribaldo S. Phylogeny and evolution of the Archaea: one hundred genomes later. Curr Opin Microbiol. 2011;14:274–81. doi: 10.1016/j.mib.2011.04.015. - DOI - PubMed
    1. Klenk HP, Göker M. En route to a genome-based classification of Archaea and Bacteria? Syst Appl Microbiol. 2010;33:175–82. doi: 10.1016/j.syapm.2010.03.003. - DOI - PubMed
    1. Mizuno T, Chou MY, Inouye M. A unique mechanism regulating gene expression: translational inhibition by a complementary RNA transcript (micRNA) Proc Natl Acad Sci U S A. 1984;81:1966–70. doi: 10.1073/pnas.81.7.1966. - DOI - PMC - PubMed

Publication types

MeSH terms

LinkOut - more resources