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Epigenetics, Genomic Imprinting and Mitochondrial Inheritance Quiz

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What is the defining feature of epigenetic regulation compared with mutation?

  1. A It controls gene use independently of DNA-binding transcription factors
  2. B It transmits acquired marks unchanged from body cells to offspring
  3. C It changes how genes are used without changing the order of DNA bases
  4. D It permanently rewrites the order of DNA bases at the regulated locus
  5. E It regulates gene use only in cells that form eggs or sperm
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Answer: C. It changes how genes are used without changing the order of DNA bases

See Section. Option C is correct: epigenetic regulation changes gene use without changing DNA base sequence. Chemical marks on DNA and on histones, the proteins around which DNA is wrapped, can make a gene more or less accessible. DNA methylation adds small methyl groups to DNA, while histone modifications alter the surrounding packaging. These changes help cells with much the same genome use different sets of genes, so a neurone behaves differently from a liver cell. Some regulatory states persist when cells divide, helping daughter cells retain their specialised identity. A useful distinction is that mutation changes the written instructions, whereas epigenetic regulation changes how those instructions are read.

A change in the order of DNA bases (D) alters the instructions themselves and is a mutation. B confuses inheritance between daughter cells with inheritance between generations: much of the epigenome is reset during reproduction. Transcription factors, proteins that bind regulatory DNA and influence transcription, still matter (A); epigenetic marks affect whether they can reach and use their target sequences. E wrongly limits the process to the germ line, the cells that form eggs or sperm, even though epigenetic regulation also maintains the identities of ordinary body cells.

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More questions from this set. Start the quiz to answer them and see each explanation.

  1. 1

    Prader-Willi syndrome results from which functional loss at 15q11-q13?

  2. 2

    Testing finds uniparental disomy for a chromosome segment that contains no relevant imprinted genes and no unmasked recessive disease alleles. Why may this finding be clinically silent?

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