MSA CHAPTER 12 TEST Flashcards
Explain what recombinant DNA is
Recombinant DNA is formed when scientists combine nucleotide sequences for two different sources.
Explain gene cloning.
- plasmid is isolated
- cell’s DNA is isolated
- plasmid is cut with restriction enzyme
- cell’s DNA is cut with the same restriction enzyme
- targeted fragment/plasmid DNA is mixed
- DNA ligase joins the fragments of genetic material together
- Recombinant plasmid is taken up by bacterium in transformation
- Bacteria reproduces
- Harvested proteins may be used indirectly
What is a vector?
A vector is a gene carrier
Explain what DNA ligase is.
an enzyme that glues genetic fragments together, forms a covalent bond
Explain transformation.
Transformation is the uptaking of foreign DNA from the surrounding environment
What do restriction enzymes do? and where do they come from?
Restriction enzymes are used to cut DNA into smaller fragments. They come from bacteria
What are “sticky ends”?
Sticky ends are the ends of a DNA double helix at which unpaired nucleotides of one strand extends beyond the other.
Why are “sticky ends” important? What makes them sticky?
Sticky ends are important because they ensure that the DNA fragment is inserted in the plasmid in the right direction.
sticky ends are named “sticky” because they are able to form base pairs with any DNA molecule with the complementary sticky end
Explain the shotgun approach to gene cloning.
The shotgun approach to gene cloning is a method for determining the DNA sequence of an entire genome. After the genome is cut into small fragments, each fragment is sequenced and placed in the proper order.
What is a genomic library?
-A genomic library is the whole collection of all the cloned DNA fragments from a genome.
What are the ways to construct a genomic library?
plasmid library, bacteriophages, bacterial artificial chromosome
Explain what reverse transcriptase does? What is unique about the product formed?
everse transcriptase is an enzyme that reverses transcription. Instead of turning DNA into RNA, RNA it turned to DNA. This process happens after RNA splicing where all the introns are removed leaving behind only exons to be joined.
What is unique about this is forming cDNA or complementary DNA. cDNA is like a regular DNA molecule except that it contains no introns and only contains exons making it easier to work with than a regular DNA molecule.
What is cDNA? Not just the name, how is it formed? What is it composed of?
cDNA is a DNA molecule made from using mRNA as a template and the enzyme reverse transcriptase. It is composed like a regular DNA molecule except with no introns
What is a nucleic acid probe? Give two examples of how scientists can detect them.
A nucleic acid probe is molecule used to find a specific gene or nucleotide sequence. 1 way to find them is to putting a radioactive probes on DNA. 2nd way is to put DNA in a probe solution.
What does a vaccine do?
What is it composed of?
Vaccines stimulate the immune system to mount a lasting defense against a pathogen.
A vaccine is composed of a harmless variant or a derivative of a pathogen, such as a bacterium or a virus.
What is Golden Rice
What makes it gold
Golden rice is a transgenic variety of rice that produces yellow grains containing beta-carterone, used by our bodies to make vitamin A
The rice is gold because it was created with daffodil genes
What is a transgenic organism?
A transgenic organism is an organism that contains genes from another organism
What is necessary for gene therapy to be permanent for the individual person? What about for further generations?
In order for gene therapy to be permanent, the normal gene must be transferred to somatic cells that can continuously multiply. It can be permanent in further generations if gene therapy is used on sex cells that undergo fertilization.
What is DNA profiling?
DNA profiling is a procedure that analyzes DNA samples to determine if they come for the same individual.
What is PCR and what does it do?
What does amplifying DNA mean?
How does Amplifying DNA work?
PCR is a technique by which a specific segment of a DNA molecule can be targeted and quickly amplified.
Copying it many times.
To amplify DNA, the DNA must go through a process called PCR or polymerase chain reaction. -
How does gel electrophoresis separate DNA fragments?
The DNA is negative and the electric pull of the positive end of the gel electrophoresis bring the smaller fragments towards it to separate it.
Explain STR analysis.
Short Tandem Repeat analysis is the most useful method in molecular biology. The STR is a microsatellite, consisting of a unit of two to thirteen nucleotides repeated hundreds of times in a row on a DNA strand.
Approximately what percentage of human DNA is noncoding?
Approximately 98% of human DNA is noncoding.
What are transposable elements?
Transposable elements are sequences that can move about in the genome (jumping genes). Often times they are the cause of mutations.