Release of nonstop ribosomes is essential
Bacterial ribosomes frequently translate to the 3' end of an mRNA without terminating at a stop codon. Almost all bacteria use the transfer-messenger RNA (tmRNA)-based trans-translation pathway to release these "nonstop" ribosomes and maintain protein synthesis capacity. trans-transla...
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Published in: | mBio Vol. 5; no. 6; p. e01916 |
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American Society of Microbiology
11-11-2014
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Abstract | Bacterial ribosomes frequently translate to the 3' end of an mRNA without terminating at a stop codon. Almost all bacteria use the transfer-messenger RNA (tmRNA)-based trans-translation pathway to release these "nonstop" ribosomes and maintain protein synthesis capacity. trans-translation is essential in some species, but in others, such as Caulobacter crescentus, trans-translation can be inactivated. To determine why trans-translation is dispensable in C. crescentus, a Tn-seq screen was used to identify genes that specifically alter growth in cells lacking ssrA, the gene encoding tmRNA. One of these genes, CC1214, was essential in ΔssrA cells. Purified CC1214 protein could release nonstop ribosomes in vitro. CC1214 is a homolog of the Escherichia coli ArfB protein, and using the CC1214 sequence, ArfB homologs were identified in the majority of bacterial phyla. Most species in which ssrA has been deleted contain an ArfB homolog, suggesting that release of nonstop ribosomes may be essential in most or all bacteria.
Genes that are conserved across large phylogenetic distances are expected to confer a selective advantage. The genes required for trans-translation, ssrA and smpB, have been found in >99% of sequenced bacterial genomes, suggesting that they are broadly important. However, these genes can be deleted in some species without loss of viability. The identification and characterization of C. crescentus ArfB reveals why trans-translation is not essential in C. crescentus and suggests that many other bacteria are likely to use ArfB to survive when trans-translation is compromised. |
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AbstractList | UNLABELLEDBacterial ribosomes frequently translate to the 3' end of an mRNA without terminating at a stop codon. Almost all bacteria use the transfer-messenger RNA (tmRNA)-based trans-translation pathway to release these "nonstop" ribosomes and maintain protein synthesis capacity. trans-translation is essential in some species, but in others, such as Caulobacter crescentus, trans-translation can be inactivated. To determine why trans-translation is dispensable in C. crescentus, a Tn-seq screen was used to identify genes that specifically alter growth in cells lacking ssrA, the gene encoding tmRNA. One of these genes, CC1214, was essential in ΔssrA cells. Purified CC1214 protein could release nonstop ribosomes in vitro. CC1214 is a homolog of the Escherichia coli ArfB protein, and using the CC1214 sequence, ArfB homologs were identified in the majority of bacterial phyla. Most species in which ssrA has been deleted contain an ArfB homolog, suggesting that release of nonstop ribosomes may be essential in most or all bacteria. IMPORTANCEGenes that are conserved across large phylogenetic distances are expected to confer a selective advantage. The genes required for trans-translation, ssrA and smpB, have been found in >99% of sequenced bacterial genomes, suggesting that they are broadly important. However, these genes can be deleted in some species without loss of viability. The identification and characterization of C. crescentus ArfB reveals why trans-translation is not essential in C. crescentus and suggests that many other bacteria are likely to use ArfB to survive when trans-translation is compromised. Bacterial ribosomes frequently translate to the 3′ end of an mRNA without terminating at a stop codon. Almost all bacteria use the transfer-messenger RNA (tmRNA)-based trans -translation pathway to release these “nonstop” ribosomes and maintain protein synthesis capacity. trans -translation is essential in some species, but in others, such as Caulobacter crescentus , trans -translation can be inactivated. To determine why trans -translation is dispensable in C. crescentus , a Tn-seq screen was used to identify genes that specifically alter growth in cells lacking ssrA , the gene encoding tmRNA. One of these genes, CC1214 , was essential in Δ ssrA cells. Purified CC1214 protein could release nonstop ribosomes in vitro . CC1214 is a homolog of the Escherichia coli ArfB protein, and using the CC1214 sequence, ArfB homologs were identified in the majority of bacterial phyla. Most species in which ssrA has been deleted contain an ArfB homolog, suggesting that release of nonstop ribosomes may be essential in most or all bacteria. Genes that are conserved across large phylogenetic distances are expected to confer a selective advantage. The genes required for trans -translation, ssrA and smpB , have been found in >99% of sequenced bacterial genomes, suggesting that they are broadly important. However, these genes can be deleted in some species without loss of viability. The identification and characterization of C. crescentus ArfB reveals why trans -translation is not essential in C. crescentus and suggests that many other bacteria are likely to use ArfB to survive when trans -translation is compromised. ABSTRACT Bacterial ribosomes frequently translate to the 3′ end of an mRNA without terminating at a stop codon. Almost all bacteria use the transfer-messenger RNA (tmRNA)-based trans-translation pathway to release these “nonstop” ribosomes and maintain protein synthesis capacity. trans-translation is essential in some species, but in others, such as Caulobacter crescentus, trans-translation can be inactivated. To determine why trans-translation is dispensable in C. crescentus, a Tn-seq screen was used to identify genes that specifically alter growth in cells lacking ssrA, the gene encoding tmRNA. One of these genes, CC1214, was essential in ΔssrA cells. Purified CC1214 protein could release nonstop ribosomes in vitro. CC1214 is a homolog of the Escherichia coli ArfB protein, and using the CC1214 sequence, ArfB homologs were identified in the majority of bacterial phyla. Most species in which ssrA has been deleted contain an ArfB homolog, suggesting that release of nonstop ribosomes may be essential in most or all bacteria. IMPORTANCE Genes that are conserved across large phylogenetic distances are expected to confer a selective advantage. The genes required for trans-translation, ssrA and smpB, have been found in >99% of sequenced bacterial genomes, suggesting that they are broadly important. However, these genes can be deleted in some species without loss of viability. The identification and characterization of C. crescentus ArfB reveals why trans-translation is not essential in C. crescentus and suggests that many other bacteria are likely to use ArfB to survive when trans-translation is compromised. Bacterial ribosomes frequently translate to the 3′ end of an mRNA without terminating at a stop codon. Almost all bacteria use the transfer-messenger RNA (tmRNA)-based trans -translation pathway to release these “nonstop” ribosomes and maintain protein synthesis capacity. trans -translation is essential in some species, but in others, such as Caulobacter crescentus , trans -translation can be inactivated. To determine why trans -translation is dispensable in C. crescentus , a Tn-seq screen was used to identify genes that specifically alter growth in cells lacking ssrA , the gene encoding tmRNA. One of these genes, CC1214 , was essential in Δ ssrA cells. Purified CC1214 protein could release nonstop ribosomes in vitro . CC1214 is a homolog of the Escherichia coli ArfB protein, and using the CC1214 sequence, ArfB homologs were identified in the majority of bacterial phyla. Most species in which ssrA has been deleted contain an ArfB homolog, suggesting that release of nonstop ribosomes may be essential in most or all bacteria. IMPORTANCE Genes that are conserved across large phylogenetic distances are expected to confer a selective advantage. The genes required for trans -translation, ssrA and smpB , have been found in >99% of sequenced bacterial genomes, suggesting that they are broadly important. However, these genes can be deleted in some species without loss of viability. The identification and characterization of C. crescentus ArfB reveals why trans -translation is not essential in C. crescentus and suggests that many other bacteria are likely to use ArfB to survive when trans -translation is compromised. Genes that are conserved across large phylogenetic distances are expected to confer a selective advantage. The genes required for trans -translation, ssrA and smpB , have been found in >99% of sequenced bacterial genomes, suggesting that they are broadly important. However, these genes can be deleted in some species without loss of viability. The identification and characterization of C. crescentus ArfB reveals why trans -translation is not essential in C. crescentus and suggests that many other bacteria are likely to use ArfB to survive when trans -translation is compromised. Bacterial ribosomes frequently translate to the 3' end of an mRNA without terminating at a stop codon. Almost all bacteria use the transfer-messenger RNA (tmRNA)-based trans-translation pathway to release these "nonstop" ribosomes and maintain protein synthesis capacity. trans-translation is essential in some species, but in others, such as Caulobacter crescentus, trans-translation can be inactivated. To determine why trans-translation is dispensable in C. crescentus, a Tn-seq screen was used to identify genes that specifically alter growth in cells lacking ssrA, the gene encoding tmRNA. One of these genes, CC1214, was essential in ΔssrA cells. Purified CC1214 protein could release nonstop ribosomes in vitro. CC1214 is a homolog of the Escherichia coli ArfB protein, and using the CC1214 sequence, ArfB homologs were identified in the majority of bacterial phyla. Most species in which ssrA has been deleted contain an ArfB homolog, suggesting that release of nonstop ribosomes may be essential in most or all bacteria. Genes that are conserved across large phylogenetic distances are expected to confer a selective advantage. The genes required for trans-translation, ssrA and smpB, have been found in >99% of sequenced bacterial genomes, suggesting that they are broadly important. However, these genes can be deleted in some species without loss of viability. The identification and characterization of C. crescentus ArfB reveals why trans-translation is not essential in C. crescentus and suggests that many other bacteria are likely to use ArfB to survive when trans-translation is compromised. |
Author | Viollier, Patrick H Feaga, Heather A Keiler, Kenneth C |
Author_xml | – sequence: 1 givenname: Heather A surname: Feaga fullname: Feaga, Heather A organization: Department of Biochemistry & Molecular Biology, The Pennsylvania State University, University Park, Pennsylvania, USA – sequence: 2 givenname: Patrick H surname: Viollier fullname: Viollier, Patrick H organization: Department of Microbiology and Molecular Medicine, University of Geneva, Geneva, Switzerland – sequence: 3 givenname: Kenneth C surname: Keiler fullname: Keiler, Kenneth C email: kkeiler@psu.edu organization: Department of Biochemistry & Molecular Biology, The Pennsylvania State University, University Park, Pennsylvania, USA kkeiler@psu.edu |
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Cites_doi | 10.1111/j.1365-2958.2011.07638.x 10.1186/1471-2164-14-450 10.1111/j.1365-2958.2010.07467.x 10.3389/fmicb.2014.00421 10.1371/journal.pone.0057537 10.1146/annurev.micro.62.081307.162948 10.1128/jb.132.1.294-301.1977 10.1016/j.jmb.2012.08.007 10.1111/j.1365-2958.2005.04709.x 10.1093/nar/gkm818 10.1128/MMBR.69.1.101-123.2005 10.1126/science.271.5251.990 10.1128/JB.185.6.1825-1830.2003 10.1128/JB.00269-07 10.1016/j.biochi.2009.11.002 10.1093/nar/gkq1097 10.1128/jb.164.2.918-921.1985 10.1371/journal.pbio.1001749 10.1093/nar/gkh924 10.1128/JB.185.2.573-580.2003 10.1128/JB.01490-14 10.1128/JB.184.8.2155-2166.2002 10.1073/pnas.1302816110 10.1046/j.1365-2958.2003.03301.x 10.1111/j.1365-2958.2011.07607.x 10.1371/journal.pgen.1004463 10.1146/annurev.biochem.75.103004.142733 10.1111/j.1365-2958.2012.08190.x 10.1093/nar/gkt1099 10.1016/S0022-2836(05)80360-2 10.1371/journal.pone.0004459 10.1111/j.1365-2958.2010.07375.x 10.1128/jb.173.20.6373-6382.1991 10.1038/emboj.2010.14 10.1093/genetics/87.3.391 10.1074/jbc.M112.374074 10.1038/nature08403 10.1126/science.1228985 10.1073/pnas.052707199 |
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Snippet | Bacterial ribosomes frequently translate to the 3' end of an mRNA without terminating at a stop codon. Almost all bacteria use the transfer-messenger RNA... Bacterial ribosomes frequently translate to the 3′ end of an mRNA without terminating at a stop codon. Almost all bacteria use the transfer-messenger RNA... UNLABELLEDBacterial ribosomes frequently translate to the 3' end of an mRNA without terminating at a stop codon. Almost all bacteria use the transfer-messenger... ABSTRACT Bacterial ribosomes frequently translate to the 3′ end of an mRNA without terminating at a stop codon. Almost all bacteria use the transfer-messenger... |
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SubjectTerms | Caulobacter crescentus - genetics Caulobacter crescentus - metabolism Gene Deletion Mutagenesis, Insertional Protein Biosynthesis Ribosomes - metabolism RNA, Messenger - metabolism Sequence Analysis, DNA |
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Title | Release of nonstop ribosomes is essential |
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