biology
Autosomal dominant:
all affected individuals have at least one affected parent
once the trait disappears, it cannot reappear in later generations
affects both males and females, and can be transmitted via any sex (male/female)
Autosomal recessive:
both males and females can be affected
two unaffected parents can have an affected child
all children of two affected parents must also show the condition
the trait can disappear & reappear through generations
genotype | genetic makeup of a trait for an individualm (e.g. eye colour - BB, Bb, bb) |
phenotype | observable expression of a trait on an individual (e.g. brown [BB, Bb] or blue [bb] eyes) |
traits | feature of an organism passed from parent to offspring |
heredity | passing down of traits from parents |
diploid | a cell containing the full set of chromosomes, half from each parent (body cell) |
haploid | a cell containing half the amount of chromosomes in a diploid (sex cell) |
A DNA molecule is in a double helix shape — two strands, bonded in the middle, twisted into a spiral
Nucleotide:
basic building block of RNA and DNA
consists of phosphate group, pentose sugar, nitrogenous base
DNA is made into RNA by ribosomes
nitrogenous bases are connected by hydrogen bonds
bases (adenine & thymine, cytosine & guanine)
chromosome - compacted DNA, a human has 46 in each body cell
G1 — Growth occurs as organelles double (cell repair, growth, reproduction preparation)
S — DNA replication occurs as chromosomes duplicate
G2 — Growth occurs as cell prepares to divide
M — Mitosis & cytokinesis occurs
Prophase:
Think — chromosomes physically condenses
chromatin (DNA + protein) shortens and thicken to form chromosomes (can be observed through microscope)
chromosome is made up of two identical threads called sister chromatids
sister chromatids are joined at the centromere
Metaphase:
Think — middle is where the chromosomes line up
microtubules pull chromosomes to align at the equator of the cell
centrosomes at the opposite poles of the cell extend spindle fibres, connect to centromeres and align chromosomes in a row (equator)
metaphase ends when the centromere starts to divide
Anaphase:
Think — chromatids comes apart
the centromere divides into two, the sister chromatids seperate
spindle fibres shorten & contract
chromatids are pulled to the opposite poles of the cell
Telophase:
Think — two new nuclei form
the chromatids at the opposite ends are now called daughter chromosomes
chromosomes are formed
spindle fibres disappear
new nucleus membranes are formed
Cytokinesis (both mitosis & meiosis):
the very last step of cell division
the physical process of cell division
cytoplasm of parental cell divides into two daughter cells
Variation
genetic variation:
variation between each of the genomes’ variation in the DNA sequence
genome 1 - genome 46
makes everyone unique
evolution ensures more individuals in a population to likely have variations
increases chance of more of the population surviving when conditions change
be careful when saying
“the organism’s genetic variation is caused by the environment”
rather say
“organisms with these genetic variations were more successful in surviving & reproducing in this environment”
meiosis:
creates gametes (sex cells)
two ‘cycles’ of the mitosis phases
one parental cell separates into two, then four daughter cells
23 chromosomes in each daughter cell
daughter cells are gametes, or haploids
chromosomes cross over when first aligned together in the middle of the cell
in the process of crossing over, parts of the mother and father’s chromosomes containing different forms of the same gene is switched
crossing over increases variety in genes, aiding more population within a species pass natural selection
Traits & Alleles
Dominant traits
represented by capital letter (e.g. T)
a single copy of the allele is enough to observe the phenotype
Recessive traits
represented by lower case letter (e.g. t)
two copies of the allele is necessary to observe the phenotype
Homozygous dominant = two dominant alleles
Homozygous recessive = two recessive alleles
Heterozygous = one dominant, one recessive allele
The dominant allele is always written before the recessive allele.
Each individual has a karyotype - their complete set of chromosomes
The chromosomes for sex determination are chromosomes X & Y
→ Male XY
→ Female XX