The Process of Genetic Engineering Flashcards

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What is the first step in the process of genetic engineering?

Identify and isolate the gene for the desired characteristic.

What do restriction enzymes do in genetic engineering?

They cut DNA at specific sequences to remove or open DNA.

Why is the same restriction enzyme used on the gene and the plasmid?

It makes matching sticky ends so the pieces can join.

What are sticky ends?

Short, single-stranded DNA overhangs that help two DNA pieces stick.

What is a vector in genetic engineering?

A carrier that moves the gene into a host cell, such as a plasmid or virus.

What is a plasmid and why is it useful as a vector?

A small circular bacterial DNA that copies easily and is easy to modify.

Which enzyme joins the gene to the vector?

DNA ligase, which seals the DNA to make recombinant DNA.

What does recombinant DNA mean?

DNA made by joining DNA from different sources, like a human gene in a plasmid.

How are host cells given the recombinant DNA?

The vector is inserted into cells (transformation), for example by heat shock or an electric pulse.

How are cells that took up the new gene selected?

Marker genes are used, such as antibiotic resistance or fluorescence, so only modified cells are kept.

What happens after selecting the modified cells?

They are grown to clone the cells so the gene is copied and the new protein is made.

What is a promoter and why may it be added to the gene?

A DNA switch that turns the gene on so it works in the host.