Genetic Information and Variation Flashcards
Give 2 similarities between DNA in eukaryotic cells and DNA in prokaryotic cells
- Nucleotide structure is identical - deoxyribose attached to phosphate and a base
- Adjacent nucleotides joined by phosphodiester bonds and complementary bases joined by hydrogen bonds
Give 4 differences between DNA in eukaryotic cells and DNA in prokaryotic cells
- Eukaryotic DNA is longer
- Eukaryotic DNA is linear, prokaryotic DNA is circular
- Eukaryotic DNA is associated with histone proteins, prokaryotic DNA is not
- Eukaryotic DNA contain introns, prokaryotic DNA does not
What is a chromosome?
Long, linear DNA and its associated histone proteins, found in the nucleus of eukaryotic cell
What is a gene?
A sequence of DNA bases that codes for a amino acid sequence of a polypeptide or a functional RNA (e.g. ribosomal RNA or tRNA)
What is a locus?
Fixed position a gene occupies on a particular DNA molecule.
What are the 3 features of the genetic code and explain what they mean.
- Universal: The same base triplets code for the same amino acids in all organisms
- Non-overlapping: Each base is part of only one triplet so each triplet is read as a discrete unit
- Degenerate: An amino acid can be coded for by more than one base triplet
Why is the genetic code described as a triplet code?
Because each amino acid is coded for by 3 DNA bases
What are introns and exons?
Exon: Base sequence of a gene coding for amino acid sequences (in a polypeptide)
Intron: Base sequence of a gene that doesn’t code for amino acids, in eukaryotic cells
What is the genome?
The complete set of genes in a cell
What is the proteome?
The full range of proteins that a cell can produce, coded for by the cell’s DNA
Briefly describe the two stages of protein synthesis
- Transcription: Production of messenger RNA from DNA, happens in the nucleus
- Translation: Production of polypeptides from the sequence of codons carried by mRNA, happens at ribosomes
Give the differences between the structure of tRNA and mRNA
- tRNA is folded into a ‘clover leaf shape’, whereas
mRNA is linear / straight - tRNA has hydrogen bonds between paired bases,
mRNA doesn’t - tRNA is a shorter, fixed length, whereas mRNA is a
longer, variable length (more nucleotides) - tRNA has an anticodon, mRNA has codons
- tRNA has an amino acid binding site, mRNA doesn’t
Describe how mRNA is formed by transcription in eukaryotic cells
- Hydrogen bonds between DNA bases break, catalysed by DNA Helicase
- One DNA strand acts as a template
- Free RNA nucleotides align next to their complementary bases on the template strand. In RNA, uracil is used in place of thymine (pairing with adenine in DNA)
- RNA polymerase joins adjacent RNA nucleotides
- This forms phosphodiester bonds via condensation reactions
- Pre-mRNA is formed and this is spliced to remove introns, forming mRNA
Describe how translation leads to the production of a polypeptide
- mRNA attaches to a ribosome and the ribosome moves to a start codon (AUG)
- tRNA brings a specific amino acid
- tRNA anticodon binds to complementary mRNA codon
- Ribosome moves along to next codon and another tRNA binds so 2 amino acids can be joined by a
condensation reaction forming a peptide bond. Using energy from hydrolysis of ATP - tRNA released after amino acid joined polypeptide
- Ribosome moves along mRNA to form the polypeptide, until a stop codon is reached
Describe the role of ATP, tRNA and ribosomes in translation
- ATP: Hydrolysis of ATP to ADP + Pi releases energy, so amino acids join to tRNAs and peptide bonds form between amino acids
- tRNA: Attaches to and transports specific amino acids in relation to its anticodon. tRNA anticodon complementary base pairs to mRNA codon, forming hydrogen bonds. 2 tRNAs bring amino acids together so peptide bond can form.
- Ribosomes: mRNA binds to ribosome, with space for 2 codons. Allows tRNA with anticodons to bind and catalyses formation of peptide bond between amino acids. It then moves along to the next codon
What is a gene mutation?
A change in the base sequence of DNA, can occur spontaneously during DNA replication in interphase
What is a mutagenic agent?
A factor that increases rate of gene mutation, e.g. ultraviolet (UV) light or alpha particles.
Explain how a mutation can lead to the production of a non-functional protein or enzyme
- Changes sequence of base triplets in DNA (in a gene) so changes sequence of codons on mRNA
- So changes sequence of amino acids in the polypeptide
- So changes position of hydrogen / ionic / disulphide bonds (between amino acids)
- So changes protein tertiary structure (shape) of protein
- Enzymes - active site changes shape so substrate can’t bind, enzyme-substrate complex can’t form
Explain the possible effects of a substitution mutation
- DNA base is replaced by a different base
- This changes one triplet so changes one mRNA codon.
- So one amino acid in the polypeptide chain changes. Tertiary structure may change if position of hydrogen/ionic/disulphide bonds change.
Explain the possible effects of an addition or deletion mutation
- One nucleotide / base removed or added from DNA sequence
- Changes sequence of DNA triplets from point of mutation (frameshift)
- Changes sequence of mRNA codons after point of mutation
- Changes sequence of amino acids in primary structure of polypeptide
- Changes position of hydrogen / ionic / disulphide bonds in tertiary
structure of protein - Changes tertiary structure / shape of protein
Describe the difference between diploid and haploid cells
Diploid cells have 2 complete sets of chromosomes, and Haploid cells have a single set of unpaired chromosomes
Describe how a cell divides by meiosis
- Meiosis I separates homologous chromosomes
* Chromosomes arrange into homologous pairs
* Crossing over between homologous chromosomes
* Independent segregation of homologous chromosomes - Meiosis II separates sister chromatids, resulting in 4 genetically varied haploid daughter cells
Explain why the number of chromosomes is halved during meiosis
Homologous chromosomes are separated during meiosis I
Explain how crossing over creates genetic variation
Alleles are exchanged between chromosomes, creating new combinations of maternal and paternal alleles on chromosomes