One allele for a trait will mask the alternate allele
Law of segregation
Each individual has two alleles for a trait, alleles segregate separately when making gametes, each gamete has one allele for a trait, fertilization gives each new individual two alleles for a trait
Genes
Sections of chromosomes coded by a sequence of nucleotides which are the instructions to build an organism, genes code for traits
Locus
Position where the gene is found on the chromosome
Phenotype
Physical characteristic expressed by the gene, e.g. eye colour, hair colour, enzyme active or inactive
Alleles
Alternative forms of a gene that control the phenotype
Genotype
Shorthand way of describing a gene and its alleles, indicated by two letters
Dominant trait
Overpowering, hides the second trait, represented by a capital letter
Recessive trait
Hidden allele, represented by a lowercase letter
Homozygous
Both alleles are identical (can be dominant or recessive)
Heterozygous
Both alleles are different (1 dominant, 1 recessive)
At the end of Meiosis
gametes have only 1 allele for a trait
Fertilization
Gives offspring 2 alleles for a trait
Punnett Square
Determines the genotype and phenotypes of the offspring
The dominant color masks the recessive color and all offspring are carriers of the recessive gene
Carriers have the gene but don't show it in the phenotype
linked or sex-linked disorders
only males have the disorder, rare for females to have it
Autosomal chromosomes are 1-22, X or Y are sex chromosomes
The sex of the baby is determined by the X or Y chromosome
linked disorders like hemophilia, muscular dystrophy, and color blindness are recessive</b>
Law of independent assortment
Each pair of traits segregate independently of other pairs, 2) All possible allele combinations occur in the gametes
Widow's peak, detached earlobes
Possible genotypes and phenotypes
The classic Mendelian 9:3:3:1 dihybrid ratio
DNA
Controls the production of proteins via the genetic code, found in the nucleus
Transcription
DNA code is transcribed into mRNA in the nucleus
mRNA
Messenger RNA, carries the DNA code to the cytoplasm for protein synthesis
Translation
Genetic code language (nucleotide alphabet) is translated into the language of protein (amino acid alphabet)
Ribosome
Translates the mRNA to make a polypeptide
tRNA
Transfer RNA brings amino acids to the mRNA-ribosome complex
Protein synthesis
Initiation: Ribosome binds to mRNA, 2) Elongation: Ribosome moves along mRNA adding amino acids, 3) Termination: Ribosome reaches stop codon and releases polypeptide
Polypeptide
Linear chain of amino acids, needs to be folded into 3D shape to be functional
Gene mutation
Change in the nucleotide sequence of a gene
Types of gene mutations
Frameshift
Point mutation
Expansion mutation
Frameshift mutation
Deletion or insertion of a base, results in a non-functioning protein
Point mutation
One base within a codon is changed to another, can be silent, missense, or nonsense
Expansion mutation
Repeating sequence of nucleotides, up to 100 times
DNA
Controls the production of proteins via the genetic code
Genetic code
Series of nucleotide bases that code for the genes