TY - JOUR
T1 - Ribosome profiling in archaea reveals leaderless translation, novel translational initiation sites, and ribosome pausing at single codon resolution
AU - Gelsinger, Diego Rivera
AU - Dallon, Emma
AU - Reddy, Rahul
AU - Mohammad, Fuad
AU - Buskirk, Allen R.
AU - DiRuggiero, Jocelyne
N1 - Funding Information:
National Aeronautics and Space Administration (NASA) [18-EXO18-0091 to J.D.]; Air Force Office of Scientific Research [FA9950-14-1-0118 to J.D.]; National Institutes of Health [GM110113 to A.B.]. Funding for open access charge: NASA grant. Conflict of interest statement. None declared.
Funding Information:
National Aeronautics and Space Administration (NASA) [18-EXO18-0091 to J.D.]; Air Force Office of Scientific Research [FA9950-14-1-0118 to J.D.]; National Institutes of Health [GM110113 to A.B.]. Funding for open access charge: NASA grant.
Publisher Copyright:
© The Author(s) 2020. Published by Oxford University Press on behalf of Nucleic Acids Research.
PY - 2021
Y1 - 2021
N2 - High-throughput methods, such as ribosome profiling, have revealed the complexity of translation regulation in Bacteria and Eukarya with large-scale effects on cellular functions. In contrast, the translational landscape in Archaea remains mostly unexplored. Here, we developed ribosome profiling in a model archaeon, Haloferax volcanii, elucidating, for the first time, the translational landscape of a representative of the third domain of life. We determined the ribosome footprint of H. volcanii to be comparable in size to that of the Eukarya. We linked footprint lengths to initiating and elongating states of the ribosome on leadered transcripts, operons, and on leaderless transcripts, the latter representing 70% of H. volcanii transcriptome. We manipulated ribosome activity with translation inhibitors to reveal ribosome pausing at specific codons. Lastly, we found that the drug harringtonine arrested ribosomes at initiation sites in this archaeon. This drug treatment allowed us to confirm known translation initiation sites and also reveal putative novel initiation sites in intergenic regions and within genes. Ribosome profiling revealed an uncharacterized complexity of translation in this archaeon with bacteria-like, eukarya-like, and potentially novel translation mechanisms. These mechanisms are likely to be functionally essential and to contribute to an expanded proteome with regulatory roles in gene expression.
AB - High-throughput methods, such as ribosome profiling, have revealed the complexity of translation regulation in Bacteria and Eukarya with large-scale effects on cellular functions. In contrast, the translational landscape in Archaea remains mostly unexplored. Here, we developed ribosome profiling in a model archaeon, Haloferax volcanii, elucidating, for the first time, the translational landscape of a representative of the third domain of life. We determined the ribosome footprint of H. volcanii to be comparable in size to that of the Eukarya. We linked footprint lengths to initiating and elongating states of the ribosome on leadered transcripts, operons, and on leaderless transcripts, the latter representing 70% of H. volcanii transcriptome. We manipulated ribosome activity with translation inhibitors to reveal ribosome pausing at specific codons. Lastly, we found that the drug harringtonine arrested ribosomes at initiation sites in this archaeon. This drug treatment allowed us to confirm known translation initiation sites and also reveal putative novel initiation sites in intergenic regions and within genes. Ribosome profiling revealed an uncharacterized complexity of translation in this archaeon with bacteria-like, eukarya-like, and potentially novel translation mechanisms. These mechanisms are likely to be functionally essential and to contribute to an expanded proteome with regulatory roles in gene expression.
UR - http://www.scopus.com/inward/record.url?scp=85085904525&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85085904525&partnerID=8YFLogxK
U2 - 10.1093/NAR/GKAA304
DO - 10.1093/NAR/GKAA304
M3 - Article
C2 - 32382758
AN - SCOPUS:85085904525
SN - 1362-4962
VL - 48
SP - 5201
EP - 5216
JO - Nucleic Acids Research
JF - Nucleic Acids Research
IS - 10
ER -