D3.2 Inheritance Flashcards
describe Gregor Mendel’s experiment and his findings
- placed homozygous dominant male pollen into recessive female ovaries of pea plants
- F1 generation 100% heterozygous
- F2 generation 1:2:1 (homozygous dominant:heterozygous:recessive), 3:1 (dominant:recessive)
when did Mendel conduct his pea experiment, and what did he first call genes?
1865; factors
allele
version of gene; codes same trait but different variations
heterozygote
organism with 1 dominant, 1 recessive allele of a gene
homozygote
organism with either 2 dominant or 2 recessive alleles of a gene
monohybrid cross
cross between two parents focusing on just 1 trait (eg Tt×TT, ff×FF, Gg×Gg, etc)
draw two Punnett grids representing Mendel’s experiment findings
- TT×tt = Tt, Tt, Tt, Tt
- Tt×Tt = TT, Tt, Tt, tt
what is a carrier of a gene?
heterozygous organism having recessive allele that doesn’t affect its phenotype
examples of phenotypical characteristics exclusively due to genetics
ABO blood, Huntington’s, colour blindness, cystic fibrosis
examples of phenotypical characteristics exclusively due to envrionment
learning math and songs, scars, large muscles
examples of phenotypical characteristics due to both genetics and environment
height, cancer
codominant alleles
when heterozygote has two alleles that are dominant and both phenotypes are expressed (eg having both IA and IB alleles results in AB blood type)
incomplete dominance
when heterozygote has two alleles that are dominant and neither phenotype is expressed, only a mix (eg mixing pure-bred white and red four o’clock flowers results in pink flowers)
phenotypic plasticity
ability to express phenotype differently based on environment (adaptation)
phenological events
phenological changes based on changes in environment during cyclical events (like seasonal food availability)
how does freshwater snail physa virgata employ phenoplastic plasticity?
shell normally conical and elongated, different genes expressed to become rounded when predator around so harder to crush
phenylketonuria
autosomal disease from PAH gene mutation, resulting in decreased production of phenylalanine hydroxylase, which converts toxic phenylalanine from proteins to tyrosine
examples of autosomal recessive diseases
albinism, cystic fibrosis, sickle cell disease, Tay Sachs, thalassemia
how do humans taste bitterness?
- if one has TAS2R38 gene that codes for taste receptor 2 member 38, phenylthiocarbamide can attach to receptor, allowing taste bitterness
- single-nucleotide polymorphisms make alleles of TAS2R38 gene, which don’t code for receptor
how many alleles, genotypes, and phenotypes contribute to ABO blood type?
3 alleles, 6 genotypes, 4 phenotypes
what are the two types of chromosomes?
22 autosomes, 1 pair allosomes (sex chromosomes)
differences between X and Y chromosomes
- X codes for oestradiol and progesterone production, Y for testosterone
- Y 70 genes vs X 800, most genes on X no allele on Y to pair with
what determines sex in humans?
XX = female, XY = male; sperm determine gender (50% sperm have Y, 50% X)
sex-linked trait
genetic trait with gene locus on X (rarely Y) chromosome; often affects males more