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Biology (university) · Part 05

Gene regulation and biotechnology

How cells switch genes on and off, and the lab tools that cut, copy and edit DNA.

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  1. Lac operonA group of bacterial genes switched on together to digest lactose. A repressor protein blocks the genes unless lactose is present. When lactose is there, it binds the repressor, which lets go, and the genes turn on.
  2. Transcription factorA protein that binds DNA near a gene and helps or blocks RNA polymerase. Activators raise transcription. Repressors lower it. Enhancers are DNA sites where activators bind, often far from the gene.
  3. Epigenetic modificationChemical tags on DNA or on the histone proteins it wraps around that change how active a gene is, without changing the DNA letters. DNA methylation usually switches genes off.
  4. Restriction enzymeA bacterial enzyme that cuts DNA at a specific short sequence. Many leave overhanging single-strand ends ('sticky ends') that can pair with matching ends from other DNA.
  5. Recombinant DNADNA made by joining pieces from different sources. A gene is cut out, joined into a plasmid (a small circle of bacterial DNA) with DNA ligase, and put into bacteria, which copy it and make the protein.
  6. Polymerase chain reactionPCR copies a chosen stretch of DNA millions of times. Repeated cycles of heating (to separate strands), cooling (so primers bind) and warming (so heat-stable polymerase copies the DNA) double the amount each time.
  7. Gel electrophoresisA method to sort DNA pieces by size. DNA is negatively charged, so in an electric field it moves through a gel toward the positive end. Small pieces move faster and further.
  8. CRISPR-Cas9A gene-editing tool taken from bacterial defence against viruses. A guide RNA leads the Cas9 enzyme to a matching DNA sequence, where it cuts both strands. The cell's repair then disables or changes the gene.