- 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
11. Translation
Translation
Problem 36c
Textbook Question
The flow of genetic information from DNA to protein is mediated by messenger RNA. If you introduce short DNA strands (called antisense oligonucleotides) that are complementary to mRNAs, hydrogen bonding may occur and 'label' the DNA/RNA hybrid for ribonuclease-H degradation of the RNA. One study [Lloyd et al. (2001). Nucl. Acids Res. 29:3664–3673] compared the effect of different-length antisense oligonucleotides upon ribonuclease-H–mediated degradation of tumor necrosis factor (TNFα) mRNA. TNFα exhibits antitumor and pro-inflammatory activities. The following graph indicates the efficacy of various-sized antisense oligonucleotides in causing ribonuclease-H cleavage. Describe how antisense oligonucleotides interrupt the flow of genetic information in a cell.

1
Antisense oligonucleotides are short strands of DNA that are designed to be complementary to specific mRNA sequences.
When introduced into a cell, these antisense oligonucleotides bind to their target mRNA through base pairing, forming a DNA/RNA hybrid.
The formation of this hybrid structure is recognized by ribonuclease-H, an enzyme that specifically degrades the RNA strand of the hybrid.
As a result, the mRNA is cleaved and degraded, preventing it from being translated into protein by the ribosome.
This interruption in the translation process effectively reduces or eliminates the production of the protein encoded by the target mRNA, thereby altering the flow of genetic information from DNA to protein.
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Key Concepts
Here are the essential concepts you must grasp in order to answer the question correctly.
Antisense Oligonucleotides
Antisense oligonucleotides (ASOs) are short, synthetic strands of nucleic acids designed to bind specifically to complementary mRNA sequences. By hybridizing with mRNA, they can block translation or promote degradation of the mRNA, effectively interrupting the flow of genetic information from DNA to protein. This mechanism is crucial in gene regulation and therapeutic applications, particularly in targeting disease-related genes.
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Ribonuclease H
Ribonuclease H (RNase H) is an enzyme that degrades the RNA strand of RNA-DNA hybrids. When antisense oligonucleotides bind to their target mRNA, RNase H recognizes this hybrid and cleaves the RNA, leading to its degradation. This process is a key mechanism by which ASOs exert their effects, as it reduces the levels of specific mRNAs, thereby influencing protein synthesis and cellular function.
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Flow of Genetic Information
The flow of genetic information refers to the process by which genetic instructions are transferred from DNA to RNA and then to proteins, a concept often summarized as the central dogma of molecular biology. This flow is essential for cellular function and involves transcription (DNA to mRNA) and translation (mRNA to protein). Interruptions in this flow, such as those caused by antisense oligonucleotides, can significantly impact gene expression and cellular behavior.
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