D1.2.13 (HL)—Initiation of transcription at promoter
Promoters are upstream non-coding DNA regions that position RNA polymerase and help initiate regulated transcription of a gene in cells.
- Syllabus
- First assessment 2025
- Objective
- D1.2.13
- Level
- HL
Promoters are upstream non-coding DNA regions that position RNA polymerase and help initiate regulated transcription of a gene in cells.

Coverage 2024–2024 · Updated 16 Jul 2026
A promoter is a DNA region where transcription machinery binds to position RNA polymerase and define where transcription begins.
Promoter sequence and associated factors determine strand choice, start site and transcription level. Opening and early RNA synthesis proceed from that positioned complex.
Name: promoter; binding factor; start site; direction of RNA synthesis.
A promoter mutation can reduce mRNA production without changing the protein-coding sequence. RNA polymerase begins at the promoter and then moves along the template, so promoter position fixes which downstream sequence is copied.
A promoter is regulatory DNA, not the entire gene or translated region.
This objective is assessed through structured response, commonly using Explain.
Explain
Build the answer around this relationship: Promoters are non-coding DNA sequences linked to transcription start sites.
Representative question
Explain the function of a promoter in DNA.
| a | is a non-coding/non-transcribed section of DNA/bases; |
| b | transcription starts/is initiated at the promoter; |
| c | region for binding (to DNA) of RNA polymerase OR region for RNA polymerase to separate the DNA strands; |
| d | located upstream of the gene/coding sequence; |
| e | helps to control/regulate gene expression; |
RNA polymerase reads template DNA 3' to 5' and synthesizes RNA 5' to 3'; ribosomes translate mRNA codons in the 5' to 3' direction. Promoters mark transcription start regions and orientation; transcription factors help RNA polymerase bind and initiate in eukaryotes. Non-coding DNA does not code for polypeptide amino acid sequences and includes introns, regulatory sequences, telomeres, rRNA genes, and tRNA genes. Eukaryotic pre-mRNA is modified before export and translation by adding a 5' cap and poly-A tail and removing introns by splicing. Alternative splicing joins different exon combinations from one pre-mRNA, so one gene can produce multiple protein variants in different cells or stages. Translation initiation assembles ribosomal subunits at the start codon AUG; initiator tRNA enters the P site and A, P, and E sites organize tRNA movement. Newly made polypeptides may be folded, cleaved, or chemically modified; preproinsulin processing to active insulin is a key example. Proteasomes degrade tagged, damaged, or unneeded proteins; amino acid recycling supports new protein synthesis and proteome quality control.