What are the 4 basic inheritance patterns?

-Autosomal recessive

-Autosomal dominant

- Sex-linked recessive

-Sex-linked dominant

-2 unaffected parents can have affected offspring

-both male and female offspring affected at similar freq.

Autosomal recessive

What are examples of autosomal recessive disorders?

-cystic fibrosis (severe damage to lungs)(causes thickened fluids)

-Sickle cell anemia (affects shape of blood cell)

-Tay-Sachs (toxic build up in brain and spinal cord)

-Affected individuals have at least 1 affected parent

-Affected parent of either sex can pass on to offspring of either sex

-appears in male and female

- not sex linked

Autosomal dominant

-unaffected parents can have affected offspring

-Males affected more frequently than females

-Transmitted from mothers to sons

-50% of child will be affected

Sex-linked recessive

Example of__________

Sex-linked recessive

color blindness is___linked and affects _____more than _______

-x

-male

-female

-affected offspring come from parents

-males pass only to daughters

-females pass to children of either sex

-if dad is affected 100% of daughters are affected

-if mom affected 100% of sons are affected

Sex-linked dominant

What are examples of sex-linked dominant disorders?

-Alport syndrome

-Coffin-Lowry syndrome

-Fragile X syndrome

-Incontinentia pigmenti

-Vitamin D resistant rickets

-only males have it

-pass to all sons, none of daughters

Y-linked trait (dominant)

-Mothers always pass on

-Fathers never pass on

Mitochondrial mutation

What is the chance of their next child being affected?

(a)= affected

(1/2) x (1/2)= (1/4)

-gender x condition

Look at slide 34 in Ch 6. pt 1

DO IT NOW

-non identical twins

-2 zygotic eggs

Dizygotic twins

-identical twins

Monozygotic twins

-the trait shared by the members of a twin pair

-genetically the same

-environment may be similar

-the increased rate is more likely impacted by genetic factors rather than environmental factors

concordant traits

-separate embryotic sacks

dizygotic twinning

-comes from 1 zygote

-early splitting

Dichorionic diamniotic (monozygotic twinning)

-late split

Monochorionic diamniotic (monozygotic twinning)

-very late split

-same sack

Monochorionic monoamniotic (monozygotic twinning)

Overweight biological parents tend to have_______children. There is no ___ _____ between the weight of children and that of their adoptive parents.

-overweight

-consistent association

This is an example of :
A pregnant woman is concerned about exposure to an environmental substance (drug, chemicals, or virus) that cause birth defects.

Environmental impact

Genes on the same chromosomes tend to

get transmitted together

certain combinations of alleles are passed more frequently than others

linkage

Complete linkage leads to;

____% non recombinant gametes and progeny

100

the crossing over between ______ chromosomes can break linkage

homologous

Alleles are passed in different combinations from how they were inherited

Recombination

Recombination leads to:

-recombinant gametes and progeny

________ associated with physical change in chromosomes

recombinant phenotypes

recombinant diagram

When a plant is normal with tall leaves and short with dwarf leaves, they are

nonrecombinant progeny

This is an example of

no crossing over

This is an example of:

which results is;

crossing over

-2 nonrecombinant and 2 recombinant gametes

One chromosome contains both wild-type alleles, one chromosomes contains both mutant alleles

coupling (cis configuration)

wild type allele and mutant alleles are found on the same chromosomes

repulsion (trans configuration)

Usually 2 step process:\

1. determine data are consistent with genes assorting independently (chi-squared test)

2. If the data is not consistent with independent assortment, this suggests genes are linked

- determine how closely linked the genes are

determining genetic distance

How to calculate recombination frequency

recombination freq.=(# of recombinant progeny/ total # of progeny)x100%

No correlation between which alleles are transmitted=50% , recombinant gametes =50cM

independent assortment

Two genes are linked if they are less than____ apart

50cM

If the progeny resulted in:

-66

-77

-28

-33

Which are recombinant, and what would the distance be?

-66 and 77 are the highest number= parental progeny

-28 and 33 lowest numbers= recombinant progeny

(28+33)/(66+77+28+33)=0.303 x100= 30.3 cM

a crossover at one place on the chromosome reduces the likelihood of a second crossover

interference

How to calculate amount of interference:

coefficient of coincidence= observed DCO/expected DCO =

-((2)^3)/(total amount of flies x DCO freq.)

-((2)^3)/12= 0.67

Distances based on crossover/linkage

genetic map

Distances based on actual base-pair differences

physical map

This is an example of

crossovers with three linked loci

recombination distance are ______accurate the larger they get

less

Consider the mutation and cross over

How halotype works

consider how when the top of loci is blue, it shows the blue parents trait

Quantitative trait locus mapping (QTL)

-controls have little to no genes of the condition

-lower freq. of variant

-variant linked to condition

-cases have the condition

Genome-wide association studies (GWAS)

Used to assign a gene to a particular human chromosome

-gene present (given)

-Human chromosomes present ( find most similar to gene presented)

Somatic-cell hybridization

displays the mutant phenotype

displays the wild type

-prepared from cells halted in metaphase(relaxed)

- numbered based on size

-Sex chromosomes

-based on haploid # (23 chromosomes)

Karyotyping

With sex chromosomes, the largest is the ___ chromosome and the short chromosome is the ___ chromosomes

-X

-Y

-moving, gaining, or losing pieces of a chromosome

-2n=6

-duplication

rearrangement

-changes in # of copies of an individual chromosome

-2n+1=7

-trisomy

Aneuploidy

-extra whole set of chromosomes

-3n=9

-autotriploid

polyploidy

Types of rearramgement:

-duplication

-deletion

-translocation

-inversion

Copied region of chromosomes

duplication

deleted region of chromosomes

deletion

inverting (flipping) region of chromosomes

inversion

moving part of chromosome somewhere else

translocation

-bulge during pairing in meiosis 1

Duplication (segment of chromosome is duplicated)

-formation of loop during pairing in prophase 1

Deletion

-turned 180 degrees

inversion

Inversion that doesn't include the centromere

paracentric inversion

inversion includes the centromere

pericentric inversion

If a crossover were to occur in the inverted region,

it would result in a complication

The packaging of tremendous amounts of genetic info. into the small space within a cell has been called

The ultimate storage problem

Is overwound or underwound causing it to twist on itself

Supercoiling DNA

-add two turns

- occurs when DNA is overrotated; the helix twists on itself

Positive supercoil

-removes 2 turns

-occurs when DNA is underwound; the helix twists on itself in the opposite directions

Negative supercoiling

What do these charactericstics describe?

-less condensed

-on chromosome arms

-unique sequences

-many genes

-throughout S phase

- often transcription

- crossing over is common

Euchromatin

What do these characteristics describe?

-more condensed

-At centromeres, telomeres, and other specific places

- repeated sequence

-Late S phase

-infrequent transcription

-crossing over is uncommon

Heterochromatin

Regions of relaxed chromatin where active transcription is taking place

chromosome puffs

Chromosome puffs on giant polytene chromosomes isolated from the __ ____ of larval Drosophila

-salivary glands

Chromosome fragments that lack ______ are lost in mitosis

centromeres

Proposes that mitochondria and chloroplasts in eukaryotic cells arose from bacteria

Endosymbiotic theory

endosymbiotic theory

Organelles in a ______cell segregate randomly into the progeny cells.

heteroplasmic

understand it

What is the importance of mutations?

-provides raw material for evolution

-source of many diseases and disorders

-look at whats wrong when we alter a gene

-Do not get passed on to the offspring

-passed to new cells through mitosis creating a clone of cells having mutant gene

Somatic mutations

-reproductive cell mutations

-passed on

-meiosis and sexual reproduction allow mutation to be passed down to about half the members of next generation

germ-line mutation

One letter is replaced by another

base substitution

A to G & C to T (purines switch with purines) (pyrimidine switches with pyrimidine)

Transition

A or G to C or T (purines switch with pyrimidines) (pyrimidine switch with purines)

Transversion

Frameshift mutations are not_____by 3

divisible

in frame insertions and deletions are divisible by

3

Original sequence:

GGG AGT GTA GAT CGT

What would the sequence look like if a base substitution were to occur on the following nucleotide?

Original sequence:

GGG AGT GCA GAT CGT

What would the sequence look like if a base insertion were to occur on the following nucleotide?

Original sequence:

GGG AGT GTT AGA TCG T

What would the sequence look like if a base deletion were to occur on the following nucleotide?

Repetitive sequence can cause______ of strands during replication

slippage

Dna polymerase adds

more repeats

unequal cross over misaligns

homologous chromosomes

The new codon encodes a different amino acid; there is a change in amino acid sequence

Missense mutation

The new codon is a stop codon; there is a premature termination of translation

Nonsense mutation

The new codon encodes the same amino acid; there is no change in amino acid sequence

Silent mutation

a mutation that hides or suppresses the effect of another mutation

Ex: wild type has red eyes (A+B+), and a mutation causes white eyes (A-B+). This allows for a fly with (A-B-) to have red eyes even if it has two mutant phenotypes.

Suppressor mutation

Second mutation in the same gene "fixes" problem caused by first mutation

intragenic

second mutation in a different gene. "fixes" the problem caused by the first mutation

Intergenic

Purines and pyrimidine bases exist in different forms called

tautomers

____ _____ pairings can occur as a result of the flexibility in DNA structures

EX: T and G binding (wobble)

C and A protonated wobble

Nonstandard base

____ base pairing leads to a replication error

Wobble

____ and ____may result from strand slippage

-insertions

-deletions

____ _____ over produces insertions and deletions

unequal crossing over

loss of purine

Depurination

loss of an amino group

deamination

Used to identify chemical mutagens

Ames test

A___ can result in possible wobble mispairing

bulge

Many incorrectly inserted nucleotides that escape proofreading are

corrected by mismatch repair

Changes nucleotides back into their original structures

Direct repair

A damaged base can be removed by______, and ______ cleaves the deoxyribose sugar.

-DNA glycosylase

-AP endonuclease

DNA _______ adds a new nucleotide and is then sealed by DNA _____ to restore the original sequence.

-polymerase

-ligase

base excision

Removes bulky DNA lesions that distort double helix

Nucleotide-excision

Can cause chromosomal rearrangement

transposons

example of transposons causing rearrangement

How to calculate the frequencies of observed genotypes?

-# of individuals with genotype divided by total # individuals

f(AA)=

f(Aa)=

f(aa)=

-f(AA)= # of AA individuals/#of total individuals

-f(Aa)= # of Aa individuals /# of total individuals

-f(aa)=# of aa individuals /# of total individuals

A population of 868 individuals has 482 AA individuals, 213 Aa individuals, and 173 aa individuals. What are the frequencies of each genotype?

f(AA)= 482/868=0.555

f(Aa)= 213/868=0.245

f(aa)= 173/868=0.199

How to calculate observed allelic frequencies

-# copies of alleles divided by total # alleles

f(A)=

f(a)=

-f(A)=(2 x #AA individuals + #Aa individuals)/(2 x total # of individuals)

-f(a)=(2 x #aa individuals + #Aa individuals)/(2 x total # of individuals)

A population of 868 individuals has 482 AA people, 213 Aa people, and 173 aa people. What are the frequencies of each allele?

-f(A)= (2 x 482 +213)/(2 x 868)=0.678

-f(a)= (2 x 173 + 213)/(2 x 868)=0.322

What does p and q stand for in this equation?

p+q=1

-p: dominant

-q: recessive

equation 1 is used to determine___

p+q=1

equation 2 is used to determine___

p^2+2pq+q^2=1

-frequencies of alleles in population

-frequencies of genotypes in the population

What are the Hardy-Weinberg Equilibrium Assumptions ?

-no selection

-no mutation

-no gene flow

-random mating

-infinite population size

0.000625 Caucasians suffer from cystic fibrosis an autosomal recessive disease.

(1)What is the frequency of the disease-causing allele in the population?

(2) find value of p

(3)What proportion of individuals are carriers?

-(1) q^2 =0.000625, q=√0.000625 =0.025

-(2) p+q=1 -> p=1-0.025= 0.975

-(3) 2pq= 2 x 0.975 x 0.025 = 0.049 , about 5% carry the cystic fibrosis mutation

in cats, all-white is dominant over colors other than all white. In a population of 100 cats, 19 are all white. Assuming that the population is in HArdy-Weinburg equilibrium, what is the frequency of the all-white allele in this population?

How many white cats would be expected to be genotype AA? Aa?

-white =19 out of 100, so 81 of the cats are not white(recessive)

-81/100 = q=0.9

-p=1-0.9 = 0.1 are white and dominant

Can cause severe changes in allelic frequencies and are more severe in smaller populations

Genetic drift

Will alter the genotype frequencies, but not the allele frequencies of a population

nonrandom mating

A tendency of like individuals to mate

-creates more homozygotes then expected

-flies with same eye color mate

Positive assortative mating

A tendency of unlike individuals to mate.

-creates more heterozygotes than expected

-fly with red eyes mates with white eyes

Negative assortative mating

-increases the likelihood of getting two copies of the same allele from the same ancestor

results in more homozygotes

inbreeding

a measure of how likely it is that two alleles are identified by descent

inbreading coefficient (F)

What is this an example of?

Alleles identical by descent

What is this an example of?

alleles identical by state

The more inbreeding the less

heterozygotes

Caused by accumulation of harmful recessive alleles

Inbreeding depression

What equations are needed when calculating with inbreeding factors?

f(AA)= p^2 + Fpq

f(Aa)=2pq-2Fpq

f(aa)= q^2 +Fpq

What will the genotype frequencies be after 1 generation of random mating, followed by 1 generation of inbreeding between siblings?(F=0.25)

p=0.6 q=0.4

Fpq= 0.25 x 0.6 x 0.4=0.06

F(AA)= p^2 =0.6^2=0.36 +0.06= 0.42

F(Aa)= 2pq= 2 x 0.6 x 0.4=0.48 -(2 x 0.06) =0.36

F(aa)=q^2=0.4^2=0.16 + 0.06 = 0.22

-Doesn't change allele frequencies by itself but changes distribution of who has them

-more homozygous

-recessive alleles that are not good will more likely show

non-random mating

Individuals from one population entering another population

migration

The amount of change in allelic frequency due to migration between populations depends on

the difference in allelic frequency and the extent of migration

changes in allele frequency due to different levels of fitness (ability to survive and reproduce)

Natural selection

One allele is always more fit than the other

-the more "fit" allele increases in frequency

Directional selection

The heterozygote is more fit than either homozygotes

-stable equilibrium reached and both alleles remain in population

Overdominance (heterozygote advantage)

Heterozygote is less fit than either homozygotes

-unstable equilibrium reached- one allele will eventually win

Under dominance (heterozygote disadvantage)

What will be the allele frequncies at the time reproduction beings ?

1. divide by the most fit number in this case 180

AA=180/180=1

Aa=162/180= 0.9

aa= 36/180= 0.2

2. A=(180+180+heterozygote)/(2x total number of individuals)

(180 + 180 +162) / (162+180+36) x 2= 0.69

a= (36 +36+ 162) / (756)= 0.31

w11<w12>w22 is an example of what?

-overdominance

w11<w12<w22 is an example of ?

Directional selection against incompletely dominant allele A1

w11>w12>w22 is an example of?

Directional selection against incompletely dominant allele A2

w11=w12<w22 is an example of?

directional selection against dominant allele A1

w11=w12>w22 is an example of

directional selection against recessive allele A2

consider this when looking at distributions