Incoherent dual regulation by a SAM-II riboswitch controlling translation at a distance
In Sinorhizobium meliloti, the methionine biosynthesis genes metA and metZ are preceded by S-adenosyl-L-methionine (SAM) riboswitches of the SAM-II class. Upon SAM binding, structural changes in the metZ riboswitch were predicted to cause transcriptional termination, generating the sRNA RZ. By contr...
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Taylor & Francis Group
2022-12-01
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Series: | RNA Biology |
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Online Access: | http://dx.doi.org/10.1080/15476286.2022.2110380 |
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author | Robina Scheuer Theresa Dietz Jonas Kretz Lydia Hadjeras Matthew McIntosh Elena Evguenieva-Hackenberg |
author_facet | Robina Scheuer Theresa Dietz Jonas Kretz Lydia Hadjeras Matthew McIntosh Elena Evguenieva-Hackenberg |
author_sort | Robina Scheuer |
collection | DOAJ |
description | In Sinorhizobium meliloti, the methionine biosynthesis genes metA and metZ are preceded by S-adenosyl-L-methionine (SAM) riboswitches of the SAM-II class. Upon SAM binding, structural changes in the metZ riboswitch were predicted to cause transcriptional termination, generating the sRNA RZ. By contrast, the metA riboswitch was predicted to regulate translation from an AUG1 codon. However, downstream of the metA riboswitch, we found a putative Rho-independent terminator and an in-frame AUG2 codon, which may contribute to metA regulation. We validated the terminator between AUG1 and AUG2, which generates the sRNA RA1 that is processed to RA2. Under high SAM conditions, the activities of the metA and metZ promoters and the steady-state levels of the read-through metA and metZ mRNAs were decreased, while the levels of the RZ and RA2 sRNAs were increased. Under these conditions, the sRNAs and the mRNAs were stabilized. Reporter fusion experiments revealed that the Shine–Dalgarno (SD) sequence in the metA riboswitch is required for translation, which, however, starts 74 nucleotides downstream at AUG2, suggesting a novel translation initiation mechanism. Further, the reporter fusion data supported the following model of RNA-based regulation: Upon SAM binding by the riboswitch, the SD sequence is sequestered to downregulate metA translation, while the mRNA is stabilized. Thus, the SAM-II riboswitches fulfil incoherent, dual regulation, which probably serves to ensure basal metA and metZ mRNA levels under high SAM conditions. This probably helps to adapt to changing conditions and maintain SAM homoeostasis. |
first_indexed | 2024-03-09T02:46:31Z |
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issn | 1547-6286 1555-8584 |
language | English |
last_indexed | 2024-03-09T02:46:31Z |
publishDate | 2022-12-01 |
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series | RNA Biology |
spelling | doaj.art-abc6cd134f2842a989e29f3f854a0e2e2023-12-05T16:09:51ZengTaylor & Francis GroupRNA Biology1547-62861555-85842022-12-0119198099510.1080/15476286.2022.21103802110380Incoherent dual regulation by a SAM-II riboswitch controlling translation at a distanceRobina Scheuer0Theresa Dietz1Jonas Kretz2Lydia Hadjeras3Matthew McIntosh4Elena Evguenieva-Hackenberg5University of GiessenUniversity of GiessenUniversity of GiessenInstitute of Molecular Infection Biology (IMIB), University of WürzburgUniversity of GiessenUniversity of GiessenIn Sinorhizobium meliloti, the methionine biosynthesis genes metA and metZ are preceded by S-adenosyl-L-methionine (SAM) riboswitches of the SAM-II class. Upon SAM binding, structural changes in the metZ riboswitch were predicted to cause transcriptional termination, generating the sRNA RZ. By contrast, the metA riboswitch was predicted to regulate translation from an AUG1 codon. However, downstream of the metA riboswitch, we found a putative Rho-independent terminator and an in-frame AUG2 codon, which may contribute to metA regulation. We validated the terminator between AUG1 and AUG2, which generates the sRNA RA1 that is processed to RA2. Under high SAM conditions, the activities of the metA and metZ promoters and the steady-state levels of the read-through metA and metZ mRNAs were decreased, while the levels of the RZ and RA2 sRNAs were increased. Under these conditions, the sRNAs and the mRNAs were stabilized. Reporter fusion experiments revealed that the Shine–Dalgarno (SD) sequence in the metA riboswitch is required for translation, which, however, starts 74 nucleotides downstream at AUG2, suggesting a novel translation initiation mechanism. Further, the reporter fusion data supported the following model of RNA-based regulation: Upon SAM binding by the riboswitch, the SD sequence is sequestered to downregulate metA translation, while the mRNA is stabilized. Thus, the SAM-II riboswitches fulfil incoherent, dual regulation, which probably serves to ensure basal metA and metZ mRNA levels under high SAM conditions. This probably helps to adapt to changing conditions and maintain SAM homoeostasis.http://dx.doi.org/10.1080/15476286.2022.2110380s-adenosyl-methionineriboswitchtranslation initiation regiontranscription terminationribosome standby siterna stabilitysrnametasinorhizobiumalphaproteobacteria |
spellingShingle | Robina Scheuer Theresa Dietz Jonas Kretz Lydia Hadjeras Matthew McIntosh Elena Evguenieva-Hackenberg Incoherent dual regulation by a SAM-II riboswitch controlling translation at a distance RNA Biology s-adenosyl-methionine riboswitch translation initiation region transcription termination ribosome standby site rna stability srna meta sinorhizobium alphaproteobacteria |
title | Incoherent dual regulation by a SAM-II riboswitch controlling translation at a distance |
title_full | Incoherent dual regulation by a SAM-II riboswitch controlling translation at a distance |
title_fullStr | Incoherent dual regulation by a SAM-II riboswitch controlling translation at a distance |
title_full_unstemmed | Incoherent dual regulation by a SAM-II riboswitch controlling translation at a distance |
title_short | Incoherent dual regulation by a SAM-II riboswitch controlling translation at a distance |
title_sort | incoherent dual regulation by a sam ii riboswitch controlling translation at a distance |
topic | s-adenosyl-methionine riboswitch translation initiation region transcription termination ribosome standby site rna stability srna meta sinorhizobium alphaproteobacteria |
url | http://dx.doi.org/10.1080/15476286.2022.2110380 |
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