genetic engineering
single-nucleotide polymorphism
DNA + gene cloning
polymerase chain reaction
recombinant DNA
100

What is genetic engineering?

direct modification of a genome with the intent to modify phenotype


100

What is SNP?

DNA sequence variation that occurs when a single nucleotide differs between members of biological species

100

What are the 2 types of cloning?

replication & reproduction

100

What is the purpose of DNA polymerase?

reads existing DNA strands to create new ones

100

What is recombinant DNA?

DNA formed artificially and contains parts from 2 or more organisms; reproduced when cells divide

200

What is a transgenic?

organism that receives new DNA

200

Why are SNPs important?

essential for medical researchers and making personalized medicine

200

Why do we clone DNA?

- a particular gene can be isolated to determine its nucleotide sequence

- protein, enzyme, and RNA functions can be investigated

- mutations and their related genes can be identified

- organisms can be engineered for specific purposed like insulin production

200

Why are PCRs important?

they allow scientists to make many copies of a piece of DNA

200

What are of restriction enzymes?

enzymes that cut DNA molecules at specific points (scissors)


300

What is the purpose of reverse transcriptase?

copies the sequence of DNA

300

What can a single SNP cause?

Mendelian disease

300

Explain the difference between duplication and replication.

Duplication: amount of DNA inside the nucleus is doubled

Replication: DNA is copied to produce 2 identical strands

300

Why is Taq polymerase used for PCR?

It is resistant to change in heat

300

What is DNA ligase?

enzymes that join cut ends of DNA molecules (glue)


400

What 2 vectors are needed to implant new DNA into the DNA that you want to use?


plasmid and virus

400

How many SNPs are in the human genome?

about 10 million

400

Name the main steps of DNA cloning.

1. Isolate plasmid DNA and DNA containing gene of interest.

2. Insert gene into a plasmid.

3. Insert plasmid into bacterial cell.

4. Cells are cloned with gene of interest.

5. Identify desired clone.

400

What can PCR be used for?

- testing for diseases

- studying isolated genes

400

Name an example of recombinant DNA technology.

- rhInsulin

- recombinant human growth hormone

- recombinant activase (dissolve blockages in blood vessels)

500

Name an example of genetic engineering.

- rainbow papaya

- arctic apple

- enviropig

-web-spinning goats

500

How often do SNPs occur?

1 in every 300 nucleotide base pairs

500

Name the main steps of gene cloning.

1. Obtain gene of interest from a genomic library.

2. Ligate gene into a plasmid vector.

3. Insert plasmid into bacteria to make multiple gene copies.

4. Test for correct insertion of gene into plasmid.

5. Use plasmid to transform plant cells.

6. Regenerate transformed cells into full grown plants.

500

What are the steps of PCR?

1. Heat the DNA so it unzips.

2. Add complementary nitrogenous bases.

3. Allow DNA to cool so strands zip together.

500

What is the difference between recombinant DNA and crossover?

Recombination: combining genes from 2 or more organisms 

Crossing over: exchanging segments of chromosomes between homologous chromosomes