-
organelle genetics
- extra nuclear inheritance
- traits conditioned by genomes OTHER than nuclear one
- these genes are called CYTOPLASMIC genes - they arise in organelles such as mitochondria or plastids
-
Maternal inheritance
- Organelles contributed to zygota via EGG, not sperm:
- 1. chloroplasts or
- 2. mitochondria inherited from MOTHER
-
Maternal inheritance
- Genotype of mother determines phenotype of progeny
- ie snail shells: coiling dominant to maternal - mother's trait present in every offspring
- in a diagram, mother's circle will be shaded in every case
-
X inactivation & Barr bodies
- XX: one female X chromosome in each cell is inactivated
- During development remains inactivated
- In diff development lineages, a different X becomes inactivated
- 1st recog. by Mary Lyon
-
Lyon's hypothesis
- 1. Females have a chromatin body in interphase nucleus, but not in males
- 2. Female cats are mosaic for coat color on gene X (calico cats), human (anhidrotic ectodermal dysplasia, red-green color blindness)
- w/colorblindness, XR Xr, although every cell can't see color, as long as you have some of both you won't be colorblind.
- 3. Female mice w/a translocation b/w X and an autosome w/a coat color gene are MOSAIC
-
quantitative genetics
- continuous traits showing a distribution of phenotypes
- continuous traits are affected by many genes and are also called POLYGENIC or MULTIGENIC traits
-
Quantitative Traits
- 1. Matings b/w extremes in phenotypes will usually result in INTERMEDIATE phenotype (usually occurs when both parents are homozygous for different sets of alleles affecting different characteristics) - ie AA x aa = Aa (tall x short = medium HEIGHT)
- 2. Matings b/w intermediate phenotypes can result in F1 outside the range of parents. (produce progeny from one extreme to the other & in between)
-
Transgression
Phenomenon that progeny can be OUTSIDE the range of the two parents for a particular trait. ie 8ft tall child from 2 tall parents
-
Frequency distribution
- includes Mean and Variance to analyze polygenic traits
- Mean: sum of sample measures / n
- n = # in sample
- Variance: s^2 = (mean - x)^2 / n-1
- x = number ur looking at
- Standard Deviation: Square root of Variance
-
Variance facts
- 1. If variance increases from F1 to F2, Multiple genes are involved.
- 2. Magnitude of increase gives indication of how many genes
- if only a FEW genes, Variance will increase A LOT
- if MORE genes, Variance will increase LESS
- Prob of a few genes getting to extremes is HIGHER than lots of genes getting to extremes
-
Heritable
if offspring resemble parents as result of genetic similarity
-
Heritability
- Has both an environmental VS genetic component
- ie - environmental can be improper nutrition leading to less growth
-
Population Genetics
Study of genes in population of a species w/regards to allele freq and how they change
-
Gene pool
Shared genes in a population
-
Hardy-Weinberg Law
- Test of assumptions about a population
- Allows calculation of genotypic frequencies from allele freq. (and vice versa)
- Need to hold the following true:
- 1. Organisms are diploid
- 2. Reproduction is Sexual
- 3. Large populations
- 4. Random mating
- 5. No evolutionary forces, no mutations, no migration, no natural selection
- p^2 + 2pq + q^2 = 1
-
Nonrandom Mating
- Positive assortment mapping: individuals w/similar phenotypes mate preferentially. (ie humans and height)
- Negative assortment mapping: phenotypically dissimilar individuals mate more often than at random
- Rare male advantage: in fruit flies, an UNUSUAL phenotypic male will be selected by females more often than at random (ie guitar playing band member syndrome)
- Inbreeding: mating among relatives increases homozygosity at expense of heterozygosity. Progeny is small in populations...Makes detrimental mutations homozygous
- Outbreeding: mating b/w non-related individuals. Maintains detrimental mutations heterozygous, but if no mates in small population, no progeny.
-
Fitness
Ability to pass on genes
-
Principles of EVOLUTIONARY genetics
- 1. new genes come from gene duplication
- 2. new alleles come from MUTATION
- 3. Allele freq can change by selection, migration, or in small population, genetic drift
- 4. Genotypic freq can change by in/outbreeding, assortive mating
-
Natural selection
- Can change allele freq thru SEXual selection and environmental factors (migration)
- or can be done through Human selection (ie humans select dogs for pure breeding)
|
|