Both attenuation of the trp operon in E. coli and riboswitches in B. subtilis rely on changes in the secondary structure of the leader regions of mRNA to regulate gene expression. Compare and contrast the specific mechanisms in these two types of regulation with those involving short noncoding RNAs (sRNAs).
Table of contents
- 1. Introduction to Genetics51m
- 2. Mendel's Laws of Inheritance3h 37m
- 3. Extensions to Mendelian Inheritance2h 41m
- 4. Genetic Mapping and Linkage2h 28m
- 5. Genetics of Bacteria and Viruses1h 21m
- 6. Chromosomal Variation1h 48m
- 7. DNA and Chromosome Structure56m
- 8. DNA Replication1h 10m
- 9. Mitosis and Meiosis1h 34m
- 10. Transcription1h 0m
- 11. Translation58m
- 12. Gene Regulation in Prokaryotes1h 19m
- 13. Gene Regulation in Eukaryotes44m
- 14. Genetic Control of Development44m
- 15. Genomes and Genomics1h 50m
- 16. Transposable Elements47m
- 17. Mutation, Repair, and Recombination1h 6m
- 18. Molecular Genetic Tools19m
- 19. Cancer Genetics29m
- 20. Quantitative Genetics1h 26m
- 21. Population Genetics50m
- 22. Evolutionary Genetics29m
12. Gene Regulation in Prokaryotes
Riboswitches
Problem 23
Textbook Question
What is a riboswitch? Describe the riboswitch mechanism that regulates transcription of the thi operon in B. subtilus. What parallels can you see between this mechanism and the regulation of transcription of the trp operon in E. coli?

1
A riboswitch is a regulatory segment of an mRNA molecule that can bind a small molecule ligand directly, causing a conformational change in the mRNA structure. This change influences gene expression by affecting transcription or translation.
To regulate transcription of the thi operon in *Bacillus subtilis*, the riboswitch mechanism involves the binding of thiamine pyrophosphate (TPP), a derivative of vitamin B1, to the riboswitch located in the leader sequence of the mRNA. When TPP levels are high, it binds to the riboswitch, stabilizing a structure that forms a transcription termination signal, halting transcription of the thi operon.
When TPP levels are low, the riboswitch does not bind TPP, allowing the mRNA to adopt a structure that permits transcription of the thi operon, leading to the production of enzymes involved in thiamine biosynthesis.
The regulation of the thi operon in *B. subtilis* parallels the regulation of the trp operon in *E. coli* in that both systems use feedback mechanisms to control transcription based on the availability of a metabolite. In the trp operon, high levels of tryptophan activate a repressor protein that binds to the operator region, preventing transcription. Similarly, high levels of TPP bind to the riboswitch, halting transcription of the thi operon.
Both mechanisms exemplify how cells conserve energy and resources by regulating gene expression in response to metabolite concentrations, ensuring that biosynthetic pathways are active only when their products are needed.

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Key Concepts
Here are the essential concepts you must grasp in order to answer the question correctly.
Riboswitches
Riboswitches are regulatory segments of RNA that can bind small molecules, leading to changes in gene expression. They typically exist in the untranslated regions of mRNA and can influence transcription or translation by altering the RNA structure in response to the presence of specific metabolites.
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Thi Operon Regulation in B. subtilis
The thi operon in Bacillus subtilis is regulated by a riboswitch that responds to thiamine (vitamin B1) levels. When thiamine is abundant, it binds to the riboswitch, causing a conformational change that promotes the formation of a transcription terminator, halting transcription. Conversely, low thiamine levels lead to the formation of an anti-terminator structure, allowing transcription to proceed.
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Trp Operon Regulation in E. coli
The trp operon in Escherichia coli is also regulated by a riboswitch mechanism, but it primarily responds to tryptophan levels. High tryptophan concentrations lead to the formation of a transcription terminator, while low levels allow for the anti-terminator structure to form, enabling transcription. This mechanism highlights a common theme in bacterial gene regulation, where nutrient availability directly influences gene expression.
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