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AP Biology 6.3 Transcription and RNA Processing

Practise AP Biology 6.3 questions by connecting transcription, RNA processing, alternative splicing and mRNA stability with gene expression.

Syllabus
Effective Fall 2025
Course
AP Biology

Exam points

  • trace information flow from a DNA template through transcription and RNA processing
  • explain RNA polymerase function, mRNA caps, poly-A tails, intron removal and alternative splicing
  • use mRNA stability and expression data to connect transcript processing with protein production
  • compare prokaryotic and eukaryotic gene expression and follow transcripts between cellular compartments

Covered syllabus points

6.3.A—Describe the mechanisms by which genetic information flows from DNA to RNA to protein

6.3 Transcription and RNA Processing question 1

[Maximum number: 3]

Researchers are studying the use of RNA vaccines to protect individuals against certain diseases. To develop the vaccines, particular cells are first removed from an individual. Then mRNAs coding for specific proteins from a pathogen are introduced into the cells. The altered cells are injected back into the individual, where the cells make the proteins encoded by the introduced mRNAs. The individual then produces an immune response to the proteins that will help to protect the individual from developing a disease if exposed to the pathogen in the future.
When introduced into cells, the mRNAs used for vaccines must be stable so that they are not degraded before the encoded proteins are produced. Researchers developed several modified caps that they hypothesized might make the introduced mRNAs more stable than mRNAs with the normal GTP cap. To test the effect of the modified caps, the researchers produced mRNAs that differed only in their cap structure (no cap, the normal cap, or modified caps I, II, or III). They introduced the same amount of each mRNA to different groups of cells and measured the amount of time required for half of the mRNAs to degrade (mRNA half-life) and the total amount of protein translated from the mRNAs (Table 1).

TABLE 1. EFFECT OF mRNA CAP STRUCTURE ON mRNA HALF-LIFE AND PROTEIN TRANSLATED FROM THE INTRODUCED mRNA

TABLE 1. EFFECT OF mRNA CAP STRUCTURE ON mRNA HALF-LIFE AND PROTEIN TRANSLATED FROM THE INTRODUCED mRNA

Question (a)

(a)

Based on the data, identify which cap structure is most likely to protect the end of the mRNAs from degradation.

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Question (b)

(b)

Based on the data for the mRNAs with modified caps, describe the relationship between the mRNA half-life and the total amount of protein produced.

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Question (c)

(c)

Introduction of mRNAs into cells allows the cells to produce foreign proteins that they might not normally produce. Explain why the production of a foreign protein may be more likely from the introduction of mRNA than DNA into cells.

Write your responses to this question only on the designated pages in the separate Free Response booklet.

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