Transcription And Translation Worksheet DNA Template ✓ Solved
Transcription And Translation Worksheetdna Templatedna5 Ctctactataaa
Analyze the provided DNA sequence and perform the following tasks related to transcription and translation processes. This includes finding complementary DNA sequences, identifying key regulatory regions, understanding the initiation and termination of transcription, processing pre-mRNA, and elucidating the steps of protein synthesis. Your responses should demonstrate an understanding of molecular biology principles, including DNA complementarity, the mechanics of transcription, mRNA processing in eukaryotes, codon translation, and polypeptide assembly. Ensure to include diagrams where indicated, label all relevant regions such as 5’ and 3’ ends, start and stop codons, N- and C- termini, and describe the significance of each step within gene expression.
Sample Paper For Above instruction
Introduction
Gene expression involves the transcription of DNA into messenger RNA (mRNA) and the subsequent translation of mRNA into a functional protein. Understanding these processes requires familiarity with DNA structure, sequence complementarity, and the mechanisms that govern initiation, elongation, and termination of transcription and translation. This paper addresses each of these steps based on the provided DNA template sequence and associated questions, elucidating the molecular details of gene expression.
DNA Complementary Sequence
The given DNA template strand is: 5’ -CTCTACTATAAACTCAATAGGTCC- 3’. To find the complementary DNA strand, we need to pair each base with its complement: adenine (A) pairs with thymine (T), and guanine (G) pairs with cytosine (C). Since the template strand is written 5’ to 3’, its complementary strand will be antiparallel and read 3’ to 5’ relative to the template, but for clarity, we will write it 5’ to 3’ as the coding strand.
- Complementary DNA strand: 3’ -GAGATGATATTTGAGTTATCCAGG- 5’
Labeling the 5’ and 3’ ends of the new DNA strand:
- New DNA strand (complement): 5’ - GGACTGATA TTTGAGTTATC CAGG - 3’
Note: the complementary strand provided here is written in the 5’ to 3’ direction, matching the coding strand directionality.
Transcription Mechanics
RNA Polymerase Binding
RNA polymerase binds to a specific sequence called the promoter. It is typically characterized by conserved regions such as the TATA box in eukaryotes. On the DNA template strand provided, the promoter region would be upstream (to the left). The sequence where the RNA polymerase binds is usually located before the start site of transcription.
Assuming the promoter is near the beginning of this sequence, the promoter sequence might be identified as a TATA box or similar element, from the given context, one would draw a box around the sequence suitable for binding, e.g., a TATA box if present. Since no explicit promoter sequence is provided, the general site would be just upstream of the transcription start site.
This sequence is called the promoter.
Transcription Start Site and Direction
The transcription will start at the +1 site, typically indicated by a small arrow placed just downstream of the promoter sequence, on the template strand, and the direction of transcription is downstream, moving rightward in the 5’ to 3’ direction of the newly synthesized RNA.
Which DNA Strand Is Transcribed?
The RNA polymerase transcribes the template strand, which is complementary and antiparallel to the nascent RNA. The coding (sense) strand has the same sequence as the mRNA (except T vs U).
Highlighting or indicating this strand in diagrams helps clarify the process, but physically, RNA synthesis occurs on the template strand.
Polymerase Direction
The arrow indicating the movement of RNA polymerase along the DNA points in the 3’ to 5’ direction of the DNA template, synthesizing RNA in the 5’ to 3’ direction.
RNA Nucleotides and Sequence
RNA nucleotides differ from DNA nucleotides by the presence of uracil (U) instead of thymine (T). Therefore, in RNA, adenine pairs with uracil during transcription, and cytosine pairs with guanine.
The transcribed RNA sequence from the DNA template: 5’ - UGAUCAUGA UCUCGUAAGAUAUC - 3’. This sequence is read in triplets (codons) during translation.
Processing of pre-mRNA
In eukaryotic cells, the initial transcript, pre-mRNA, contains non-coding regions called introns and coding regions called exons. Introns are spliced out during mRNA processing. The exons are joined to form mature mRNA.
Given intron sequences such as GUUCA, UGGC, and CCCA, the processed mRNA will have these removed. The remaining exons will be joined together, resulting in a continuous sequence for translation.
mRNA Processing and Sequence
Post-processing, the mature mRNA might look like: 5’ - ACCCAGUUCAUGCCCGUGGCAUGUCGUGCCCAGU - 3’, with 5’ cap and 3’ poly-A tail added to stabilize the mRNA and facilitate translation.
Start and Stop Signals for Translation
Start Codon
The start codon, typically AUG, signals the beginning of translation and codes for methionine. The box indicating where protein synthesis begins would enclose the AUG codon in the mRNA sequence.
Yes, an amino acid (methionine) gets inserted at this site, initiating translation.
Direction of Ribosomal Movement
The ribosome moves along the mRNA in the 5’ to 3’ direction, reading codons sequentially to assemble the polypeptide chain.
Codon Interpretation
Mark off each codon starting from the start codon, and using the genetic code, identify the corresponding amino acid. For example, if the sequence begins with AUG, the amino acid is methionine.
Stop Codon
The box around the stop codon, such as UAA, UAG, or UGA, signals termination of translation. The polypeptide chain ends at this point.
N-terminus and C-terminus
The N-terminus is the start of the polypeptide, where the first amino acid (methionine) is located, and the C-terminus is at the end, following the last amino acid before termination.
Conclusion
This comprehensive analysis underscores the multi-step nature of gene expression, demonstrating how DNA sequences encode information for proteins, from initial transcription to final polypeptide synthesis. Each stage is tightly regulated, ensuring accurate gene expression essential for cellular function and organismal development.
References
- Alberts, B., Johnson, A., Lewis, J., Morgan, D., Raff, M., Roberts, K., & Walter, P. (2014). Molecular Biology of the Cell. Garland Science.
- Brown, T. A. (2016). Essential Genetics: A Genomics Perspective. Jones & Bartlett Learning.
- Nelson, D. L., & Cox, M. M. (2017). Lehninger Principles of Biochemistry. W. H. Freeman.
- Watson, J. D., Baker, T. A., Bell, S. P., Gann, A., Levine, M., & Losick, R. (2014). Molecular Biology of the Gene. Pearson.
- Strachan, T., & Read, A. P. (2018). Human Molecular Genetics. Garland Science.
- Pierce, B. A. (2017). Genetics: A Conceptual Approach. W. H. Freeman.
- Meselson, M., & Stahl, F. W. (1958). The Replication of DNA in Escherichia coli. Proceedings of the National Academy of Sciences, 44(7), 671-682.
- Molecular Cell Biology. (2018). Edited by Harvey Lodish et al. W. H. Freeman.
- Cummings, M., & Giesey, S. (2020). Regulation of gene expression. Nature Reviews Genetics, 21, 182–197.
- Glick, B., & Conklin, E. (2021). Transcriptional control mechanisms. Cellular and Molecular Life Sciences, 78, 1241–1258.