Locating genes, genetic screening, and counselling Flashcards

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1
Q

What is a DNA probe

A

Short single stranded length of DNA that has a label to make it identifiable.

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2
Q

2 types of probes

A

Radioactively labelled probes
Fluorescently labelled probes

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3
Q

How are radioactive probes used

A

Nucleotides with isotope 32P. Identified with x ray film

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4
Q

How are fluorescent probes used

A

Emit light under certain conditions.

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5
Q

How are DNA probes used? process

A

DNA probe has base sequence complementary to allele we want to find
DNA is separated into 2 strands
Separate strands mixed with probe which binds to complementary base sequence on one strand - DNA hybridisation
Site where probe binds can be identified by radioactivity or fluorescence

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6
Q

What is DNA hybridisation

A

When a section of DNA or RNA is combined with a single stranded section of DNA which has complementary bases

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7
Q

How is a DNA probe formed

A

Sequence of nucleotides is chosen and then is labelled. PCR is used to make many copies.

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8
Q

What is genetic screening

A

To check if a patient has a mutant allele and their probability of passing it on.

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9
Q

Why is genetic screening beneficial

A

Those at risk can take action to minimise risk earlier, avoid mutagens, make informed decisions about offspring and lifestyle.

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10
Q

What is personalised medicine

A

Where healthcare and advice of a patient is based upon their genotype. Unique to each person.

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11
Q

What is genetic counselling

A

Where advice and information is given that enable people to make personal decisions about themselves and their offspring.
Based off of genetic screening.

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