DNA Probes & Screening

01DNA Probes & Screening

DNA probes

This section covers the structure, labelling and specificity of DNA probes used to detect particular alleles.

What is a DNA probe?

A DNA probe is a single strand of DNA made to recognise a chosen allele. The order of its bases is selected so that the probe can pair with a known region of the target allele.

Scientists must therefore know part of the target allele's base sequence before constructing the probe. A gene machine can then synthesise DNA with the required complementary sequence.

For a probe intended to locate a harmful allele, its bases must match the target allele by complementary base pairing without also matching the corresponding region of a normal allele.

Feature Why it is needed
Single-stranded DNA Allows the probe bases to pair with complementary bases in the test DNA.
Known base sequence Enables the probe to be designed for a particular target sequence.
Complementary sequence Gives the probe specificity for the allele or DNA sequence being investigated.
Detectable label Allows the location of a bound probe to be found after hybridisation.

Labelling the probe

A probe can carry a radioactive or fluorescent label. The complementary base sequence determines where the probe can bind, while the label makes the position of a bound probe detectable.

Fluorescent label

The position of a bound fluorescent probe can be detected using suitable light, such as UV.

Radioactive label

The position of a radioactive probe can be revealed using autoradiography.

Exam Tip: Explain probe specificity using complementary base pairing. The label shows where the probe has bound; it does not make the probe specific.

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