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Transcription is the first stage in gene expression: the copying of the sequence of bases in a gene into a complementary mRNA molecule that can be exported from the nucleus to the ribosomes for translation. This lesson covers the OCR A-Level Biology A specification point 2.1.3 (g) — the process of transcription — including the roles of RNA polymerase, the template strand and mRNA synthesis.
A good understanding of transcription requires you to build on concepts from the previous lessons: base pairing (Lesson 2), DNA vs RNA structure (Lessons 2 and 3), and the genetic code (Lesson 5).
DNA is too precious to let out of the nucleus. It contains the entire genome and must remain intact for the lifetime of the cell. But proteins are made in the cytoplasm (at the ribosomes), so a disposable, single-stranded copy of each gene is made instead: messenger RNA (mRNA). The process of making this RNA copy from a DNA template is called transcription.
Key Definition — Transcription: The process by which a section of DNA (a gene) is used as a template to synthesise a complementary strand of mRNA, catalysed by RNA polymerase.
| Component | Role |
|---|---|
| DNA gene | The portion of the DNA containing the sequence to be transcribed. |
| Template strand (antisense) | The strand of DNA that is read by RNA polymerase. The mRNA is complementary to this strand. |
| Coding strand (sense) | The other strand. Its sequence is (almost) the same as the mRNA, except T is replaced by U. |
| RNA polymerase | The enzyme that unwinds the DNA, pairs free RNA nucleotides with the template strand and joins them via phosphodiester bonds. |
| Free RNA nucleotides | Ribonucleoside triphosphates (rATP, rUTP, rCTP, rGTP) that are incorporated into the growing mRNA strand. |
Exam Tip: The template strand is read 3' to 5'. The mRNA is built 5' to 3'. The mRNA has the same base sequence as the coding strand (except that U replaces T).
graph TD
A[DNA gene - double helix] --> B[RNA polymerase binds to promoter]
B --> C[DNA unwinds; H-bonds break]
C --> D["RNA polymerase reads template strand<br/>in the 3’ to 5’ direction"]
D --> E["Free RNA nucleotides pair with<br/>complementary DNA bases<br/>A–U, T–A, C–G, G–C"]
E --> F["RNA polymerase joins nucleotides<br/>via phosphodiester bonds"]
F --> G[mRNA strand released]
G --> H[DNA re-forms double helix]
H --> I[mRNA leaves nucleus via nuclear pore]
In eukaryotes, the newly made mRNA is then processed (adding a cap and tail and removing non-coding regions called introns), but this is not required by the OCR A-Level Biology A specification and you only need to know the outline above.
Given the following DNA:
| Strand | Direction | Sequence |
|---|---|---|
| Coding (sense) | 5' → 3' | ATG CAT TTC GGA TAA |
| Template (antisense) | 3' → 5' | TAC GTA AAG CCT ATT |
The template strand is read 3' to 5'. The mRNA is built 5' to 3' and is complementary to the template:
| Product | Direction | Sequence |
|---|---|---|
| mRNA | 5' → 3' | AUG CAU UUC GGA UAA |
Notice that:
| Feature | Replication (Lesson 4) | Transcription |
|---|---|---|
| Purpose | To copy the entire genome for cell division | To make an RNA copy of a single gene |
| Product | Two complete double-stranded DNA molecules | One single-stranded mRNA molecule |
| Enzyme | DNA polymerase (+ helicase + others) | RNA polymerase |
| Bases used | A, T, C, G | A, U, C, G |
| Amount of DNA unwound | Entire genome | Just one gene at a time |
| Template | Both strands | Only one strand (the template) |
| Error rate | Very low (proofreading) | Higher (no proofreading) — acceptable because mRNA is disposable |
Exam Tip: Students often confuse the enzymes. DNA polymerase builds new DNA strands; RNA polymerase builds new RNA strands.
Model answer for (2): "5'-AUGCAUUUC-3'."
Spec Mapping: This lesson is mapped to OCR H420 Module 2.1.3 — Nucleotides and nucleic acids, covering the synthesis of mRNA from a DNA template by transcription, including the role of RNA polymerase and the directional reading of the template strand (refer to the official OCR H420 specification document for exact wording).
Transcription is the first step of gene expression and is a recurrent assessment object on Paper 1 and synoptically on Paper 3. The combination of mechanism + comparison with replication is a common 6-mark structure. The clean separation of transcription (nucleus, RNA polymerase) from translation (cytoplasm, ribosome) underlies the eukaryotic cell-architecture content of Module 2.1.1, so this lesson is the bridge between cell structure and molecular biology.
The messenger-RNA hypothesis — that an unstable intermediate ferries genetic information from DNA to ribosome — was proposed in 1961 by François Jacob, Sydney Brenner and Matthew Meselson. Their experiment used phage-infected E. coli labelled with ¹⁵N to show that newly made protein was assembled by old ribosomes reading a new mRNA template — the mRNA, not the ribosome, was the species that turned over rapidly.
Roger Kornberg (son of Arthur Kornberg) won the 2006 Nobel Prize in Chemistry for crystal structures of RNA polymerase II — atomic-resolution images of the enzyme caught in the act of transcribing DNA. The school of thought to take into the exam: transcription is enzymatic copying with template-directed polymerisation, mechanistically parallel to DNA replication but with a single-strand product, ribose sugar and uracil base.
Paraphrase, do not invent quotation: the schools of thought are that "mRNA is an unstable working copy" (Jacob, Brenner, Meselson) and that "RNA polymerase is a molecular machine reading a duplex template" (Kornberg).
This lesson connects forward to:
ocr-alevel-biology-nucleic-acids-enzymes — Translation (Lesson 7): the mRNA produced here is the template for protein synthesis. The 5'→3' directionality you establish here determines the direction of ribosomal scanning.ocr-alevel-biology-genetics-inheritance — Gene expression and regulation: transcription factors, promoters, enhancers and operons (e.g. lac operon in E. coli) all regulate the rate of transcription.ocr-alevel-biology-cell-structure: in eukaryotes, transcription occurs in the nucleus; mRNA processing (capping, splicing, polyadenylation) happens there before export through nuclear pores.ocr-alevel-biology-nucleic-acids-enzymes — DNA replication (Lesson 4): transcription and replication share the principle of template-directed synthesis by complementary base pairing, but differ in product (RNA vs DNA), enzyme (RNA polymerase vs DNA polymerase), extent (one gene vs whole genome), and proofreading (none vs 3'→5' exonuclease).ocr-alevel-biology-photosynthesis-respiration — ATP: ribonucleoside triphosphates (ATP, UTP, GTP, CTP) are the energy-rich precursors for RNA synthesis, paralleling dNTPs in DNA synthesis.Question (6 marks): Describe the process of transcription, and explain how transcription differs from DNA replication.
Mark scheme decomposition (AO breakdown):
| Mark | AO | Awarded for |
|---|---|---|
| 1 | AO1 | RNA polymerase binds to a promoter region of DNA |
| 2 | AO1 | Helix is unwound; hydrogen bonds between the two strands are broken |
| 3 | AO1 | Template strand read 3'→5'; complementary RNA nucleotides align by base pairing (A–U, T–A, G–C, C–G) |
| 4 | AO1 | RNA polymerase joins RNA nucleotides by phosphodiester bonds; mRNA built 5'→3' |
| 5 | AO2 | Difference 1: transcription is single-stranded product / uses ribose / U instead of T |
| 6 | AO2 | Difference 2: transcription copies one gene only; replication copies entire genome; transcription uses RNA polymerase, replication uses DNA polymerase |
Split: AO1 = 4, AO2 = 2.
In transcription, RNA polymerase binds to the promoter on the DNA. The DNA double helix is unwound and the hydrogen bonds between the bases are broken. Only one of the two strands — the template strand — is used to make the mRNA. Free RNA nucleotides line up against the template strand by complementary base pairing. A pairs with U (not T because there is no thymine in RNA), and C pairs with G. RNA polymerase joins the RNA nucleotides together by phosphodiester bonds, building the mRNA in a 5' to 3' direction. The mRNA is single-stranded and is released, then it leaves the nucleus.
Transcription is different from DNA replication because (i) only one strand is used as template, and the product is single-stranded mRNA, not double-stranded DNA; (ii) RNA polymerase is used instead of DNA polymerase, and ribose replaces deoxyribose, with uracil instead of thymine.
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