Genetic information, variation and relationships between organisms Flashcards
Differences between DNA in eukaryotes and DNA in prokaryotes
Eukaryotes- packaged as chromosomes (DNA associated with histones forming chromatin)
DNA is longer, linear
Prokaryotes-free floating in cytoplasm in circular strand not associated with histones so no chromosomes
DNA is shorter, circular
What is a gene?
A base sequence that codes for
-the amino acid sequence of a polypeptide
-a functional RNA (rRNA and tRNA)
What is a locus?
The fixed position that a gene occupies
What are the 3 characteristics of the genetic code and what do they mean?
- Degenerate- each amino acid is coded for by more than 1 triplet (3 DNA bases)
- Non-overlapping- each triplet code is discrete
- Universal- same sequence of bases code for same amino acids in all organisms
Describe the structure of a tRNA molecule
clover-shaped: single stranded held in shape by disulfide bonds
has an amino acid binding site specific to an amino acid
has an anti-codon (3 DNA bases) complementary to codon on mRNA
Describe the process of transcription
The hydrogen bonds between bases break the unwind sections of DNA
Only 1 strand acts as a template (‘antisense’ strand) unlike in DNA replication
Complementary free mRNA nucleotides line up along exposed DNA bases (Uracil not Thymine of mRNA)
RNA polymerase catalyses formation of phosphodiester bonds between mRNA nucleotides forming pre-mRNA
pre-mRNA is spliced removing introns to form mature mRNA that leaves the nucleus via a nuclear pore
Describe the process of translation
The mRNA attaches to a ribosome
2 tRNA molecules and their amino acids associated with the ribosome
The anticodon forms hydrogen bonds with the complementary codon on mRNA
Peptide bonds are formed between amino acids in a condensation reaction using ATP and enzymes
Ribosome moves along mRNA until stop codon is reached
Polypeptide is formed
Define the genome
An organism’s complete set of DNA, including all of its genes
Define the proteome
The full range of different proteins that a cell is able to produce at a given time
Define a gene mutation
A change in the sequence of bases in DNA
-causes change in polypeptide chain
-caused by errors during DNA replication
What causes mutations?
-mutagenic agents (ionising radiation like UV)
-environmental or external factors
-INCREASE MUTATION RATE
-MORE MUTATIONS PER UNIT TIME
What is base substitution?
When a nucleotide in a DNA molecule is replaced by another nucleotide that has a different base
What can base substitutions lead to?
-different codon so different amino acid coded for, change in location of hydrogen, ionic and disulfide bonds causing change in tertiary structure of the protein- change in protein function
-or same amino acid may be coded for as DNA is degenerate
-may code for stop codon- so polypeptide chain would be incomplete
What is a base deletion?
A nucleotide (and therefore base) is removed from a base sequence
-this changes the reading frame, shifting to the left
What can base deletions lead to?
-change in way triplets are read so change in amino acid sequence, change in function of polypeptide
How would a base addition affect the reading frame
Shift to the right
What are chromosome mutations?
Changes in structure or number of whole chromosomes
-caused by errors in cell division
What is non-disjunction and how does this lead to polyploidy and aneuploidy?
Non-disjunction: chromosomes do not separate during meiosis
causing…
-POLYPLOIDY- when organisms have 3 or more sets of chromosomes rather than 2
-ANEUPLOIDY-when organisms have 1 more or 1 fewer chromosomes
Define ‘gene’ mutation and explain how a gene mutation can have no effect on an individual or a positive effect on an individual
-A change in the base/nucleotide
-results in formation of new allele
No effect:
-mutation is in intron
-changes amino acid but not effect on tertiary structure
Positive effect:
-results in change in polypeptide that positively changes the properties
-may result in increased reproductive success
Describe the structure of proteins
-polymer of amino acids
-joined by peptide bonds
-formed by condensation
-primary structure is sequence of amino acids
-secondary structure is folding of polypeptide chain due to hydrogen bonding
-tertiary structure is 3-D folding due to hydrogen, ionic and disulfide bonding
-quaternary structure is 2 or more polypeptide chains
Describe what happens to chromosomes during meiosis
-chromosomes condense
-chromosomes associate in homologous pairs
-homologous pairs line up at equator
-and spindle fibres attach to the centromere
-crossing over occurs
-homologous pairs pulled to opposite poles of the cell in first division
-sister chromatids pulled apart to opposite poles by spindle fibres in second division
Describe and explain the processes that occur during meiosis that increase genetic variation and how is this an advantage for a species
-chromosomes in homologous pairs
-independent segregation
-maternal and paternal chromosomes re-shuffled in any combination
-crossing over where alleles are exchanged between homologous chromosomes
-both result in new combination of alleles
-different adaptations
-pass on alleles
-more likely to survive and reproduce
-less vulnerable to selection pressures
Difference between diploid and haploid cells
Diploid- have the full set of chromosomes (2n)
Haploid- have half the set of chromosomes (n)
Ways genetic variation is achieved through meiosis
independent segregation
crossing over
THEN random fertilisation