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341“…RNA aptamers are relatively short nucleic acid sequences that bind targets with high affinity, and when combined with a riboswitch that initiates translation of a fluorescent reporter protein, can be used as a biosensor for chemical detection in various types of media. …”
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343por Schroeder, Griffin M., Kiliushik, Daniil, Jenkins, Jermaine L., Wedekind, Joseph E.“…Riboswitches are small noncoding RNAs found primarily in the 5′ leader regions of bacterial messenger RNAs where they regulate expression of downstream genes in response to binding one or more cellular metabolites. …”
Publicado 2023
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344por Schroeder, Griffin M, Dutta, Debapratim, Cavender, Chapin E, Jenkins, Jermaine L, Pritchett, Elizabeth M, Baker, Cameron D, Ashton, John M, Mathews, David H, Wedekind, Joseph E“…Riboswitches are structured RNA motifs that recognize metabolites to alter the conformations of downstream sequences, leading to gene regulation. …”
Publicado 2020
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345por Ripa, Inés, Ruiz‐Masó, José Ángel, De Simone, Nicola, Russo, Pasquale, Spano, Giuseppe, del Solar, Gloria“…Mutation B2 could decrease the stability of the aptamer’s regulatory P1 helix even in the presence of the effector, thus promoting the antiterminator structure of the riboswitch ON state. Although the B2‐mutant riboswitch showed an impaired regulatory activity, it retained partial functionality being still sensitive to the effector. …”
Publicado 2021
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346por Wencker, Freya D R, Marincola, Gabriella, Schoenfelder, Sonja M K, Maaß, Sandra, Becher, Dörte, Ziebuhr, Wilma“…In Staphylococcus aureus, de novo methionine biosynthesis is regulated by a unique hierarchical pathway involving stringent-response controlled CodY repression in combination with a T-box riboswitch and RNA decay. The T-box riboswitch residing in the 5′ untranslated region (met leader RNA) of the S. aureus metICFE-mdh operon controls downstream gene transcription upon interaction with uncharged methionyl-tRNA. met leader and metICFE-mdh (m)RNAs undergo RNase-mediated degradation in a process whose molecular details are poorly understood. …”
Publicado 2021
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347“…Therefore, it is of interest to glean information on the binding of c-di-GMP ligand to mutated conserved G20 and C92 residues of cyclic diguanosine monophosphate I (c-di-GMP I) riboswitch using molecular dynamics simulation. The result shows that the binding energy of wild/native type riboswitch-ligand complex (3IRW) is lower than the mutant complexes suggesting that the binding affinity for c-di-GMP ligand decreases in case of mutant riboswitches. …”
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348“…To demonstrate the utility of our approach, an adenosylcobalamin (AdoCbl)-responsive riboswitch-based sensor was used in this study to demonstrate that RiboFACSeq can be used to track and sort cells carrying genetic mutations in known AdoCbl transport and biosynthesis genes with desirable sensitivity and specificity. …”
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349“…We compare the broadly used promoter elements P(tac) and P(BAD) to versions that have an additional theophylline-responsive riboswitch (P(tac)-riboswitch and P(BAD)-riboswitch). …”
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350“…ZTP regulates genes involved in purine and folate metabolism through a cognate riboswitch. The linker connecting this riboswitch’s two sub-domains varies in length by over 100 nucleotides. …”
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351por Grieshaber, Nicole A., Chiarelli, Travis J., Appa, Cody R., Neiswanger, Grace, Peretti, Kristina, Grieshaber, Scott S.“…In an effort to address this issue, we developed a translational control system to regulate gene expression in Chlamydia using a synthetic riboswitch. Here we demonstrate that translational control via a riboswitch can be used in combination with a wide range of promoters in C. trachomatis. …”
Publicado 2022
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352“…RESULTS: The results showed that a synthetic glycine-OFF riboswitch (glyOFF6) and an increased-detection-range synthetic glycine-ON riboswitch (glyON14) were successfully screened from a library based on the Bacillus subtilis glycine riboswitch using fluorescence-activated cell sorting (FACS) and tetA-based dual genetic selection. …”
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353“…We developed a synthetic riboswitch that efficiently controls alternative splicing of a cassette exon in response to the small molecule ligand tetracycline. …”
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354por Li, Mengxiao, Deng, Jie, Peng, Xuemei, Wang, Jia, Wilson, Timothy J., Huang, Lin, Lilley, David M.J.“…The key difference between the DUF-3268 and riboswitch k-junctions is the lack of nucleotides inserted between G1b and A2b in the former. …”
Publicado 2023
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355por Pan, Yuchen, Duncombe, Todd A., Kellenberger, Colleen A., Hammond, Ming C., Herr, Amy E.“…The free-standing polyacrylamide gel EMSAs yielded reliable quantification of molecular binding and associated mobility shifts for a riboswitch–ligand interaction, thus demonstrating a screening assay platform suitable for riboswitches and potentially a wide range of RNA and other macromolecular targets.…”
Publicado 2014
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356“…The role of riboswitches in metabolite sensing and gene regulation in bacteria and other lower species was reported almost two decades ago, but riboswitches have not yet been discovered in mammals. …”
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357“…We further demonstrate that this riboswitch can reprogram bacteria to migrate in the presence of atrazine. …”
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358por Aroonsri, Aiyada, Posayapisit, Navaporn, Kongsee, Jindaporn, Siripan, Onsiri, Vitsupakorn, Danoo, Utaida, Sugunya, Uthaipibull, Chairat, Kamchonwongpaisan, Sumalee, Shaw, Philip J.“…The PfDHS protein could be attenuated fivefold in transgenic parasites with an active riboswitch, whereas PfDHS protein expression was unaffected in control transgenic parasites with insertion of the riboswitch-inactive sequence. …”
Publicado 2019
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359por Shin, Jung-Ho, Wakeman, Catherine A., Goodson, Jonathan R., Rodionov, Dmitry A., Freedman, Benjamin G., Senger, Ryan S., Winkler, Wade C.“…We also find gene expression of the new magnesium transporter to be controlled by a magnesium-sensing riboswitch. Importantly, we find additional examples of riboswitch-regulated homologues, suggesting that they are a frequent occurrence in bacteria. …”
Publicado 2014
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360“…A naturally occurring riboswitch can utilize 7-aminomethyl-O(6)-methyl-7-deazaguanine (m(6)preQ(1)) as cofactor for methyl group transfer resulting in cytosine methylation. …”
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