AQA · A-Level · Biology

    Course version: 7402 · Version from Sept 2016

    There are, for example, non-coding multiple repeats of base sequences…

    Full specification wording

    DNA, genes and chromosomes: There are, for example, non-coding multiple repeats of base sequences between genes.

    Between genes, eukaryotic DNA contains short base sequences repeated many times, known as variable number tandem repeats (VNTRs).

    Checked against the AQA 7402 specification (opens in a new tab) on .

    • Point 9 of 11
    • 4 key terms

    Study notes

    From the checked teaching notes for this specification point.

    The idea

    Between genes, eukaryotic DNA contains short base sequences repeated many times, known as variable number tandem repeats (VNTRs). The repeated sequence, for example AGAT, is common to everyone, but the number of repeats at a given position varies between individuals and is inherited. Because these repeats lie between genes and are non-coding, a change in repeat number often has no effect on a polypeptide, allowing variation to accumulate. This variation is exploited in genetic fingerprinting: DNA is cut with restriction endonucleases at specific recognition sequences, or amplified by PCR. The fragments are then separated by gel electrophoresis according to their length or size, moving towards the positive electrode due to DNA's negative charge.

    What earns the marks

    • The repeated sequences are non-coding and lie between genes, so variation in repeat number often does not alter a polypeptide.
    • The number of repeats varies between individuals while the repeated sequence itself is common to all.
    • Fragments differ in length, size or mass, which allows them to be separated by gel electrophoresis.
    • DNA fragments carry a negative charge, causing them to move towards the positive electrode.
    • Restriction endonucleases cut DNA at specific recognition sequences, not at random positions.

    Common mistakes and how to put them right

    • Giving 'they are short' on its own as the reason fragments separate.

      Put it right: Link separation to differences in length, size or mass.

    • Stating that DNA fragments are positively charged.

      Put it right: DNA is negatively charged and moves to the positive electrode.

    • Claiming the repeats code for a protein.

      Put it right: They are non-coding sequences located between genes.

    • Saying restriction enzymes cut DNA at random positions.

      Put it right: They cut at specific recognition sites.

    Exam tips

    • When explaining separation in gel electrophoresis, clearly distinguish that negative charge causes movement, while differences in length or size cause the actual separation.
    • State early in any fingerprinting answer that the repeats are non-coding.
    • Name restriction endonucleases and recognition sites rather than writing 'cutting enzymes'.

    Try the lesson

    The start of the DNA, genes and chromosomes: There are, for example, non-coding multiple repeats of base sequences between genes. lesson, made from checked teaching notes for this specification point.

    Have a go first

    What is meant by the term non-coding multiple repeats of base sequences between genes?

    Listen

    Between genes, eukaryotic DNA contains short base sequences repeated many times, known as variable number tandem repeats (VNTRs). The repeated sequence, for example AGAT, is common to everyone, but the number of repeats at a given position varies between individuals and is inherited. Because these repeats lie between genes and are non-coding, a change in repeat number often has no effect on a polypeptide, allowing variation to accumulate. This variation is exploited in genetic fingerprinting: DNA is cut with restriction endonucleases at specific recognition sequences, or amplified by PCR. The fragments are then separated by gel electrophoresis according to their length or size, moving towards the positive electrode due to DNA's negative charge. A strong answer earns marks for these points. The repeated sequences are non-coding and lie between genes, so variation in repeat number often does not alter a polypeptide. The number of repeats varies between individuals while the repeated sequence itself is common to all. Fragments differ in length, size or mass, which allows them to be separated by gel electrophoresis. DNA fragments carry a negative charge, causing them to move towards the positive electrode. Exam tip: When explaining separation in gel electrophoresis, clearly distinguish that negative charge causes movement, while differences in length or size cause the actual separation.

    See it

    A flowchart starting with non-coding multiple repeats of base sequences between genes. From this, three branches: the repeated sequence is common to everyone; the number of repeats varies between individuals, and this variation is inherited; and the repeats are non-coding, so a change in repeat number often has no effect on a polypeptide, allowing variation to accumulate. The accumulated variation is exploited in genetic fingerprinting, where DNA is either cut with restriction endonucleases at specific recognition sequences or amplified by PCR. Both routes lead to fragments being separated by gel electrophoresis according to length or size, with fragments moving towards the positive electrode due to DNA's negative charge.
    It shows how non-coding multiple repeats between genes give inherited variation that is exploited in genetic fingerprinting, ending with separation by gel electrophoresis.

    Key words

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    variable number tandem repeats

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    non-coding DNA between genes

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    restriction endonucleases

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    gel electrophoresis

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    See every definition
    variable number tandem repeats
    Short base sequences repeated many times between genes, where the number of repeats at a given position varies between individuals and is inherited.
    non-coding DNA between genes
    Multiple repeats of base sequences that lie between genes, so a change in repeat number often has no effect on a polypeptide.
    restriction endonucleases
    Enzymes that cut DNA at specific recognition sequences, not at random positions.
    gel electrophoresis
    A method that separates fragments according to their length or size, with fragments moving towards the positive electrode due to DNA's negative charge.

    Label the diagram

    Some boxes have lost their names. Pick the right name for each number.

    The diagram again, with 3 boxes numbered instead of named. A flowchart starting with non-coding multiple repeats of base sequences between genes. From this, three branches: the repeated sequence is common to everyone; the number of repeats varies between individuals, and this variation is inherited; and the repeats are non-coding, so a change in repeat number often has no effect on a polypeptide, allowing variation to accumulate. The accumulated variation is exploited in genetic fingerprinting, where DNA is either cut with restriction endonucleases at specific recognition sequences or amplified by PCR. Both routes lead to fragments being separated by gel electrophoresis according to length or size, with fragments moving towards the positive electrode due to DNA's negative charge.
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