Genetics - the study of Heredity
Foundation of genetics is that traits are produced by genes found on chromosomes
Diploid organisms carry two copies of every gene, one on each of two homologous chromosomes, one that came from their mother and one that came from their father
Homozygous - same alleles
Heterozygous - different alleles
Genes - genotype of an organism
Physical expression of the traits is the phenotype
The allele in heterozygous individuals that directs the phenotype is the dominant allele, and the one that doesn’t show is the recessive allele
Transformation - When a cell (typically when we ) takes in foreign genetic material and incorporates it, resulting in genetic alteration
Transduction - Specific to bacteriophages and how they use bacteria to reproduce
Some viruses have reverse transcriptase
Enzyme that defies the central dogma of biology
Takes mRNA and brings it back to DNA
Whenever the question says “wild type“ it means nonmutant DNA
pglo
Take a gene and insert it to e coli plasmid DNA
Chromosomal DNA (bacteria) - single loop of DNA
Plasmid DNA - can be single stranded or double stranded
Generally smaller than Chromosomal DNA
Gel Electrophoresis
Used to compare the DNA of two individuals
We take two samples (liquids) containing the DNA of the two individuals
Add restriction enzymes to cut up the DNA
put the samples in wells on one side (negative)
The DNA will go to the other side (positive) across the gel because DNA is negatively charged due to the Sugar-Phosphate backbone
Some DNA will be faster than others
Longer sections of DNA are slower, and will lag behind
The DNA will split into different “bands“ across the gel based on how fast they are
The “bands“ can be used to compare if the DNA is the same or different
Simple genetics with dominants and recessives was illuminated by Gregor Mendel
Three laws:
Law of Dominance
Law of Segregation
Each gamete gets only one of two copies
Gametes are haploid
Law of Independent Assortment
How one trait gets split up into gametes has no bearing on how the other trait gets split up
This is because chromosomes segregate independently, homologous chromosomes are split left or right during Meiosis I
Alleles of different genes can mix and match
Use Dihybrid cross punnet square (4×4 looking thing)
Memorize the phenotype ratios ex:
9 tall and green
3 tall and yellow
3 short and green
1 short and yellow
9:3:3:1 only when two heterozygotes for two genes are crossed
6:3:3:2:1:1 when there is incomplete dominance & complete dominance on a dihybrid cross
Monohybrid Cross - when two individuals are crossed and one gene is being studies
Use punnet squares
Humans have 23 pairs of homologous chromosomes for a total of 46
22 pairs are autosomes and 2 pairs are sex chromosomes
Females have XX, males have XY
Because females have two X chromosomes, one is inactivated in each cell and condenses into a Barr body
Most sex-linked traits are on the X-chromosome “X-linked“
Barr bodies - one of the two X linked chromosomes in each female cell is inactivated, creating this
4 blood types:
Type A
Type B
Type AB
Type O
A and B are codominant
O is recessive
Non-Mendelian genetics refers to a situation in which traits do not follow the Mendelian laws
Can be due to being governed by more than one gene
If two genes are on the same chromosome and close together, they are linked
cannot segregate independently, violating the law of independent assortment
Completely linked alleles on the same chromosome are locked together and travel together during gamete formation
Crossing over can separate linked alleles, though unlikely
separation of linked alleles leads to more predictable inheritance patterns with minimal variability
Crossing over can also lead to recombination, allowing for new genetic combinations that seems like it wouldn’t be possible due to linked alleles
Recombination frequency - can be used to measure how far apart two genes are on a chromosome
can be calculated by adding up the recombinants and dividing by the total number of offpsring
Ex: two linked genes A and B recombine with frequency of 9/90 = 10%
Distance on a chromosome is measured in map units/centrimorgans
Ex above: A and B are 10 units apart
Offspring formed form recombination events (crossing over)
Ex of Non Mendelian Genetics:
incomplete dominance
Traits blend together to produce an intermediate phenotype
codominance
heterozygous alleles in a gene pair are simultaneously expressed
neither dominant nor recessive
polygenic inheritance
Traits controlled by many genes
Ex: our height is controlled by over 400 genes
Traits that appear more in one sex than the other are usually sex-linked
Traits that skip generations are usually recessive
AKA gametogenesis
If sperm is produced, it is called spermatogenesis (oogenesis if egg is produced)
4 cells are produced for each diploid cell
Meiosis produced four genetically distinct haploid gametes (sperm or egg cells)
Involved two rounds
Meiosis I - homologous chromosomes separate, and cross over some DNA
Prophase I
Crossing over takes place
Metaphase I
Law of independent assortment takes place
Anaphase I
Law of segregation takes place
Telophase I
Meiosis II - sister chromatids separate
Prophase II
Metaphase II
Anaphase II
Telophase II
Mutations, such as nondisjunction events or whole chromosome translocations, can lead to genetic diseases
Meiotic errors
Nondisjunction - chromosomes failed to separate properly during meiosis, producing the wrong number of chromosomes
Translocation - segment of a chromosome moves to another non homologous chromosome
Occurs when crossing over (recombination) occurs incorrectly
Mitosis
Occurs in somatic (body) cells
Produces identical cells
Diploid cell → diploid cells
1 cell becomes 2 cells
Number of divisions: 1
Meiosis
Occurs in germ (sex) cells
Produced gametes
Diploid cell → haploid cells
1 cell becomes 4 cells
Number of divisions: 2