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Biology: Topic 4, Genetic information, variation and relationships between…
Biology: Topic 4, Genetic information, variation and relationships between organisms
DNA, genes and chromosomes
Both DNA and RNA carry information. DNA holds genetic information whereas RNA then transfers this genetic material from DNA to ribosomes made of rRNA and proteins. Both are polymers of nucleotides.
- The components of DNA nucleotides are deoxyribose, a phosphate group and one of the organic bases adenine, cytosine, guanine or thymine. Adenine and guanine both have double ring structures and are classified as purine bases.
- The components of RNA nucleotides are ribose, a phosphate group and one of the organic bases adenine, cytosine, guanine or uracil. Thymine, uracil and cytosine all have single ring structures and are classified as pyrimidines.
- Nucleotides joined together by phosphodiester bonds formed in condensation reactions.
A DNA molecules is a double helix composed of two polynucleotides joined by hydrogen bonds between complementary bases where as RNA is a relatively short polynucleotide chain.
Genetic code
- Order of bases in DNA is known as the genetic code which consists of triplets of bases, each triplet coding for a particular amino acid known as a codon.
- The amino acids are joined together by peptide bonds to form a polypeptide chain.
- A gene is a sequence of bases on a DNA molecule coding for a sequence of amino acids in a polypeptide chain.
- Not all the genome codes for proteins - Non-coding sections=introns - coding regions = exons.
Triplets
- There are four nucleotide bases which code for 20 different amino acids.
- Each amino acids is coded by one or more combination of triplets.
- There are 64 possible triplets meaning each amino acid is represented by at least one or more triplet.
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Humans
- Humans have 46 chromosomes in each cell arranged in homologous pairs
- Homologous pairs consist of two chromosomes that carry the same gene. They are not identical as they can carry different alleles.
- The 23rd chromosomes determines the sex of the individual.
- An allele is described as an alternative form of the same gene.
- Every individual inherits two allele of every gene from their parents.
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Genetic Mutation
Mutations in chromosomes
- Polyploidy - changes can occur in the whole set of chromosomes so that an individual has three or more sets of chromosomes instead of two.
- Non-disjunction - occurs when chromosomes fail to separate correctly in meiosis. As a result the gametes will have one more or one less chromosome.
Types of mutation
- Substitution - this is when a nucleotide in the DNA sequence is replaced by another. The effect of the change in amino acid depends on the role of the original amino acid. The change may have no effect if the nucleotide codes for the same amino acid.
- Deletion - a deletion is when a nucleotide is lost from the sequence. This can have a significant impact because it leads to a frame shift.
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Species and Taxonomy
Binomial naming system
Every species is given a name with two parts, based on Latin and Greek.
- The generic name is the genus to which the organism belongs. If a species is closely related it will share the same name.
- The specific name is the species the organism belongs too.
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Courtship behaviour
Species recognise one another during mating through courtship behaviour. Members of the same species share similar physical, biochemical and behavioural characteristics. Courtship behaviour takes place before mating and enables individuals to:
- Recognise members of their own species.
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Classification
Classification is the process of naming and organising organisms into groups based on their characteristics.
Organisms can be grouped into one of five kingdoms: animals, plants, fungi, prokaryotes and protocists
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Molecular phylogeny - analysis of molecular differences in the different organisms to determine evolutionary relatedness. The data obtained has been accepted by scientists and this gave rise to new taxonomic groups - three domains: Bacteria, Archea and Eukaryota
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