Genetics Flashcards
1
Q
what is the genetic code?
A
when a sequence of bases codes for an amino acid
2
Q
what is an non-overlapping code?
A
when an amino acid is only coded for by one triplet
3
Q
what is a degenerate code?
A
when an amino acid is coded for by more than one triplet
4
Q
State the difference between the structure of mRNA and tRNA
A
- mRNA carries the genetic code from the DNA in a nucleus to the cytoplasm
- mRNA has three adjacent bases
- tRNA carries amino acids that are used to make proteins to the ribosomes
- has amino acid binding site and a squeuence of three bases ( anti-codon)
5
Q
explain transcription
A
- RNA polymerase attatches to the double helix
- Hydrogen bonds breaks causing the strand to uncoil
- One strand acts as a template ( antisense strand) for mRNA
- RNA polymerase lines up free RNA nucleotides by the antisense strand
- complementary base pairing occurs which forms a complementary mRNA
- RNA nucleotides pairs up with bases on the antisense strand
- RNA polymerase moves along the strand to form the mRNA strand
- Hydorgen bonds reform after RNA polymerase has passed by
- When RNA polymerase reaches the stop codon, mRNA detatches and leaves the nucleus through a nuclear pore and into the cytoplasm
6
Q
explain transcription
A
- mRNA binds to a ribosome in the cytoplasm
- tRNA with anticodons attatches to mRNA by cimplemntary base paring.
- second tRNA molculcule attatches to the next codon on mRNA
- amino acids on the tRNA are joined by a peptide bond
- First tRNA moves away
- Third tRNA molcule binds to the next codon and the amino acid bonds forms another peptide bond
- second tRNA moves away
- process continues until a stop codon is reached
- polypeptide chain moves away
7
Q
how does a gene give rise to more than one protein?
A
- through post transcription changes
- occurs in the nucleus before translation
- mRNA is modified
- genes contain introns (do not code for amno acids) and exons (codes for amino acids)
- introns and exons are included in transcription
- introns are removed by splicing and exons are joined together randonmly
- different mRNA strands are formed
- more than one amino acid sequence therefore different proteins from one gene
8
Q
what is the process of DNA profiling?
A
- DNA sample obtained e.g. blood and saliva
- PCR used to amplify DNA
- fluorescent tag added ( used to allow DNA to be seen under u.v light)
- gel electrophoresis is used to sperate DNA
- gel viewed under U.V light
9
Q
explain the polymerase chain reaction
A
- Reaction mixture containing DNA sample, free nucleotides, primers and DNA polymerase
- DNA mixture heated to 95 degrees to break hydrogen bonds
- mixure is then cooled to 50-65 degrees to allow primers to bind to strands
- reaction heated to 72 degrees to allow the DNA polymerase to function
- DNA polymerase lines up free DNA nucleotide alongside the template strands where complementary base pairing occurs
- two new copies of DNA is formed per cycle
- each cycle doubles the amount of DNA present
10
Q
Explain how gel electrophoresis works?
A
- sample of DNA is exposed to restriction enzymes
- small tank filled with agarose gel and a potential difference is applied
- DNA fragments is placed on the gel
- as DNA carries a small negative charge , they move towards the positive terminal
- the larger they are , the slower they move
11
Q
how is DNA profiling used to identify people?
A
- DNA profiles are used.
- The more DNA bands match the sample DNA, after gel electrophoresis, the closer related