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Genetics
Study of inheritance patterns. Physical and biochemical characteristics can be inheritable
Alleles
Variants of the same gene. Caused by gene mutation
Genotype
Combination of alleles that an individual possesses for a specific gene
Inherited by the parents
Phenotype
The sum of an organism’s observable appearance
Can be influenced by external factors like environment and lifestyle factors
Cannot be inherited by parents
Mutations of Genomic DNA
Creates different alleles of a genotype
Occurs in both the coding and non-coding regions of the DNA
Occurs in both the somatic and/or germ cells
Are spontaneous and can be induced (e.g. UV light)
3 Categories of Genomic DNA Mutations
1) Loss-of-function Mutation: reduces the activity of a gene, either by preventing its production or by decreasing the activity of a product)
2) Gain-of-function Mutation: the normal product of a gene to be expressed inappropriately (high level, wrong time, wrong location), or acquire an abnormal function
3) Silent Mutation: have no effect on the amino acid sequence coded for that gene
3 Types of Genomic DNA Mutations
1) Point Mutations: a single nucleotide base is changed, inserted or deleted
2) Insertion/Deletion Mutations: the addition or removal of a single or group of nucleotides
3) Translocation/Duplication Mutations: a section of a chromosome is added to another or multiple copies of the same segment are produced
Bacteria Genetically Diverse Causes
They are genetically diverse in the absence of sexual reproduction due to
1) Higher mutation rate
2) Rapid reproduction
3) Horizontal DNA transfer
4) Genetic recombination
Bacteria : Conjugation
Direct cell to cell transfer via sex pilus (hair like appendage on the surface of bacteria)
Bacteria : Transformation
Uptake and incorporation of naked DNA from the environment
Bacteria : Transduction
Transfer of DNA via intermediary bacteriophage
Meiosis
Special type of cell division that only occurs in gametes
Process ensures that the fusion of an egg and sperm during sexual reproduction does not lead to an increase chromosome number
Leads to genetic variation via DNA recombination, segregation of homologous chromosomes and independent assortment of non-homologous chromosomes
Consists of Meiosis I and Meiosis II
Unlike Mitosis, produced 4 daughter cells that are genetically different
Meiosis I
Homologous chromosomes are separated
Follows the same steps are mitosis, Prophase I, Prometaphase I, Metaphase I, Anaphase I, Telophase I, Cytokinesis
Meiosis II
Continued from Meiosis II
No DNA replication occurs, therefore the daughter cells have half the number of chromosomes (23 chromosomes)
Follows similar steps except it is occurring twice, Prophase II, Prometaphase II, Metaphase II, Anaphase II, Telophase II and Cytokinesis
DNA Recombination
Occurs during Prophase I when the two homologous chromosomes are in a tetrad
Homologous chromosomes can overlap and swap part of their DNA, forming a unique genetic variation
Segregation of Homologous Chromosomes
Paired homologous chromosomes are separated from each other and migrate to opposite sides of the nucleus
Independent Assortment of Non-Homologous Chromosomes
The random orientation of homologous chromosomes pairs during Metaphase I allow for the production of gametes with many assortments of homologous chromosomes
Aneuploidy
The presence of an abnormal number of chromosomes in the cell
Common example is Down Syndrome where there is an extra Chromosome