DNA Replication and Protein Synthesis Flashcards
(32 cards)
Explain why DNA replication is necessary.
DNA copies itself before cell divisions so that each new cell has the full amount of DNA. This is important for making new cells and for passing genetic information from generation to generation.
Define the term semi-conservative replication.
DNA replication results in one old strand and one new strand present in each daughter DNA molecule
Describe the process of DNA replication in a series of bullet points.
- DNA helicase (enzyme) breaks hydrogen bonds between the two polynucleotide DNA strands. The helix unzips to form two single strands.
- Each original single strand acts as a template for a new strand. Free floating DNA nucleotides join to the exposed bases on each original template strand by complementary base pairing. A-T C-G.
- The nucleotides on the new strand are joined together by DNA polymerase. This forms a sugar-phosphate backbone. H bonds from between the bases on the original and new strand.
- The strands twist to form a double-helix. Each new DNA molecule contains one strand from the original DNA molecule and one new strand.
State the roles of DNA helicase in DNA replication.
DNA helicase breaks the hydrogen bonds between the two polynucleotide DNA strands.
State the roles of DNA polymerase in DNA replication.
DNA polymerase joins the nucleotides on the new strand together.
Describe how, and explain why, DNA replication occurs by continuous replication of one strand and discontinuous replication of the other strand.
- DNA polymerase always moves along the template strand in the same direction.
- It can only binds to the 3’ end so travels in 3’ to 5’ direction (Of original strand).
- This is not a problem for the leading strand of DNA as this travels in the 3’ to 5’ direction- so has continuous replication
- But lagging strand travels in 5’ to 3’ direction, so polymerase can’t attach the nucleotides continuously- discontinuous replication.
- This results in DNA being produced in sections which have to be joined
Explain the importance of DNA replication conserving genetic information with accuracy.
It makes sure genetic information is conserved each time the DNA in a cell is replicated.
Define the term mutation.
A change in the genetic material (a change to the base sequence) which may affect the phenotype of the organism.
Outline how the sequence of bases in DNA can code for the primary structure of a polypeptide chain.
- It’s the order of nucleotide bases in a gene that determines the order of amino acids in a particular protein.
- Each amino acid is coded for by a sequence of three bases (triplet) in a gene.
- Different sequences of bases code for different amino acids.
What is gene
A gene is a section of DNA that contains the complete sequences of bases (codons) to code for a protein.
Define a codon
A three-base sequence of DNA or RNA that codes for an amino acid.
Define triplet code
The genetic code is a sequence of three nucleic acid bases called a codon. Each codon codes for one amino acid.
Define non-overlapping
This means that successive triplets are read in order. Each nucleotide is part of only one triplet codon.
Define degenerate
The genetic code is degenerate because there are many instances in which different codons code for the same amino acid.
Define universal
The same specific base triplets code for the same amino acids in all living things. e.g UAU codes for tyrosine in all organism
Explain why the genetic code is a triplet code, the value of it being non-overlapping and the reason for it being degenerate.
It is a triplet code because it takes a sequence of three bases to code for one amino acid.
It is degenerate because there are 64 possible codons and only 20 different amino acids- so different codons will code for the same amino acid.
Describe what is meant by a start codon
A start codon is the codon that signals the start of a sequence that codes for a protein.
Describe what is meant by a stop codon.
Don’t code for any amino acids and signal the end of a sequence.
Outline how mutations can alter the structure of a protein.
A mutation changes the base sequence of DNA and the base sequence defines the order of amino acids in a protein- the primary structure- this then changes the higher levels of protein structure.
Define the term transcription
The process of copying sections of DNA base sequence to produce smaller molecules of mRNA, which can be transported out of the nucleus via the nuclear pores to the site of protein synthesis.
Define the term translation
The process by which the complementary code carried by mRNA is decoded by tRNA into a sequence of amino acids. Occurs at a ribosome.
State the three types of RNA.
mRNA, tRNA and rRNA.
Describe the structure and function mRNA
- Is a single polynucleotide made in the nucleus during transcription.
- mRNA carries the genetic code from DNA in the nucleus to the cytoplasm where it is used to make a protein during translation.
- 3 groups of three adjacent bases are usually called codons.
Describe the structure and function tRNA
- Transfer RNA- a single polynucleotide strand that’s folded into a clover shape.
- H bonds between specific base pairs hold the molecule in this shape.
- Every tRNA molecule has a specific sequence of 3 bases at one end called an anticodon.
- They also have an amino acid binding site at the other end.
- It is found in the cytoplasm and carries amino acids that are used to make proteins (translation) to the ribosome.