Topic 4 Flashcards
Compare and contrast DNA in eukaryotic cells with DNA in prokaryotic cells
Similarities
Nucleotide structure is identical - deoxyribose attached to phosphate and a base
• Adjacent nucleotides joined by phosphodiester bonds, complementary bases joined by hydrogen bonds
• DNA in mitochondria / chloroplasts have similar structure to DNA in prokaryotes
• Short, circular, not associated with proteins
Differnces
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 + its associated histone proteins
• In the nucleus of eukaryotic cells
What is a gene
sequence of DNA (nucleotide) bases that codes for:
• The amino acid sequence of a polypeptide
• Or a functional RNA (eg. ribosomal RNA
What is a locus
Fixed position a gene occupies on a particular DNA molecule
Describe the nature of the genetic code
Triplet code A sequence of 3 DNA bases, called a triplet, codes for a specific amino acid
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
What are ‘non-coding base sequences’ and where are they found?
Non-coding base sequence - DNA that does not code for amino acid sequences / polypeptides:
Between genes - eg. non-coding multiple repeats
2. Within genes - introns
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
Define ‘genome’ and ‘proteome’
Genome
The complete set of genes in a cell (including those in mitochondria and /or chloroplasts)
Proteome
The full range of proteins that a cell can produce (coded for by the cell’s DNA / genome)
Compare and contrast the structure of tRNA and mRNA
Comparison (similarities):
• Both single polynucleotide strand
Contrast (differences):
• 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
ERNA has an amino acid binding site, mRNA doesn’t
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 / transports a specific amino acid, in relation to its anticodon
ERNA 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
Catalyses formation of peptide bond between amino acids (held by tRNA molecules)
Moves along (mRNA to the next codon) / translocation
What is a gene mutation?
• A change in the base sequence of DNA (on chromosomes)
• Can arise spontaneously during DNA replication (interphase)
What is a mutagenic agent?
factor that increases rate of gene mutation, eg. 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 / nucleotide (pair) replaced by a different base / nucleotide (pair)
2. This changes one triplet so changes one mRNA codon
So one amino acid in polypeptide changes
• Tertiary structure may change if position of hydrogen / ionic / disulphide bonds change
OR amino acid doesn’t change
• Due to degenerate nature of genetic code (triplet could code for same amino acid) OR if mutation is in an intron so removed during splicing
Explain the possible effects of a deletion mutation
One nucleotide / base (pair) removed from DNA sequence
2. Changes sequence of DNA triplets from point of mutation (frameshift)
Changes sequence of mRNA codons after point of mutation
4. Changes sequence of amino acids in primary structure of polypeptide
5. Changes position of hydrogen / ionic / disulphide bonds in tertiary structure of protein
6. Changes tertiary structure / shape of protein
Describe the difference between diploid and haploid cells
Diploid - has 2 complete sets of chromosomes, represented as 2n
• Haploid - has a single set of unpaired chromosomes, represented as n
Describe features of homologous chromosomes
Same length, same genes at same loci, but may have different alleles
Describe how a cell divides by meiosis
In interphase, DNA replicates → 2 copies of each chromosome (sister chromatids), joined by a centromere
1. Meiosis I (first nuclear division) separates homologous chromosomes
• Chromosomes arrange into homologous pairs
• Crossing over between homologous chromosomes
• Independent segregation of homologous chromosomes
2. Meiosis II (second nuclear division) separates chromatids
Explain why the number of chromosomes is halved during meiosis
Homologous chromosomes are separated during meiosis i
Explain how crossing over creates genetic variation
Homologous pairs of chromosomes associate / form a bivalent
• Chiasmata form (point of contact between (non-sister) chromatids)
• Alleles / (equal) lengths of (non-sister) chromatids exchanged between chromosomes
• Creating new combinations of (maternal & paternal) alleles on chromosomes
Explain how independent segregation creates genetic variation
Homologous pairs randomly align at equator → so random which chromosome from each pair goes into each daughter cell
• Creating different combinations of maternal & paternal chromosomes / alleles in daughter cells
Other than mutation and meiosis, explain how genetic variation within a species is increased
Random fertilisation / fusion of gametes
• Creating new allele combinations / new maternal and paternal chromosome combinations
Explain the different outcomes of mitosis and meiosis
Mitosis produces 2 daughter cells, whereas meiosis produces 4 daughter cells
• As l division in mitosis, whereas 2 divisions in meiosis
2. Mitosis maintains the chromosome number (eg. diploid - diploid or haploid - haploid)
whereas meiosis halves the chromosome number (eg. diploid → haploid)
• As homologous chromosomes separate in meiosis but not mitosis
3. Mitosis produces genetically identical daughter cells, whereas meiosis produces genetically varied daughter cells
• As crossing over and independent segregation happen in meiosis but not mitosis
Explain the importance of meiosis
Two divisions creates haploid gametes (halves number of chromosomes)
• So diploid number is restored at fertilisation → chromosome number maintained between generations
• Independent segregation and crossing over creates genetic variation