1. Beyond Mendel’s Laws of Inheritance
Chapter 14.
Beyond Mendel’s Laws of Inheritance

2. Extending Mendelian genetics
Mendel worked with a simple system
peas are genetically simple
most traits are controlled by a single gene
each gene has only 2 alleles, 1 of which is completely dominant to the other
The relationship between genotype & phenotype is rarely that simple

3. Incomplete dominance Heterozygotes show an intermediate phenotype
Lack of a dominant gene - blending
RR = red flowers
rr = white flowers
Rr = pink flowers
make 50% less color

5. Incomplete dominance P F1 100% 1:2:1 F2 X true-breeding red flowers
white flowers P
100% pink flowers F1
generation
(hybrids)
100%
self-pollinate
25%
red
50%
pink
25%
white
1:2:1 F2
generation

6. Incomplete dominance CRCW x CRCW CRCR CR CW CRCW CRCR CRCW CR CW CRCW%
genotype %
phenotype
CRCR
25%
25% CR CW
male / sperm
50%
50%
CRCW
CRCR
CRCW CR CW
female / eggs
CRCW
CWCW
25%
25%
CRCW
CWCW
1:2:1
1:2:1

7. Co- Dominance
Means both alleles are expressed in the heterozygous individual BB- Black WW- White BW- Barred in Plymouth Rocks

8. Co-dominance with multiple alleles
2 alleles affect the phenotype in separate, distinguishable ways
ABO blood groups
3 alleles
IA, IB, i
both IA & IB are dominant to i allele
IA & IB alleles are co-dominant to each other
determines presences of oligosaccharides on the surface of red blood cells

10. Blood type IA IA IA i type A IB IB IB i type B IA IB type AB i i
genotype
phenotype
status
IA IA IA i
type A
type A oligosaccharides on surface of RBC __
IB IB IB i
type B
type B oligosaccharides on surface of RBC
IA IB
type AB
both type A & type B oligosaccharides on surface of RBC
universal recipient
i i
type O
no oligosaccharides on surface of RBC
universal donor

11. Blood compatibility 1901 | 1930 Matching compatible blood groups
critical for blood transfusions
A person produces antibodies against oligosaccharides in foreign blood
wrong blood type
donor’s blood has A or B oligosaccharide that is foreign to recipient
antibodies in recipient’s blood bind to foreign molecules
cause donated blood cells to clump together
can kill the recipient
Karl Landsteiner
( )

12. Blood donation

13. 16.3 Chromosome and Heridity
Mendels work went unnoticed till the 1900’s. He used the term factors.
1902- Sutton and Boveri realized Mendel’s factors were on the chromosomes that separated during meiosis.
From here they formed the chromosome theory.

14. Chromosome Theory 1) Each chromosome contains many different genes
2) Mendels factors or genes are carried on chromosomes. It is the segregation and independent assortment of chromosomes during meiosis that accounts for patterns of inheritence.

15. Chromosome theory cont…..
3) Paired chromosomes segregrate during meiosis, each sex cell has half the chromosomes of somatic cells.
4) These assort independently during meiosis. A gamete recieves 1 pair under no influence of the other pair.

16. Morgan Discovered
1)Sex linkage by working with fruit flies and eye color
2) He also found out that certain genes did not follow the law of independent assortment. He reasoned that these genes must be on the same chromosome; Therefore genes on the same chromosome usually do not segregate.

17. Morgan cont….
Note: This rule does not always apply due to crossing over. The further apart two genes are the more likely they are to cross over and therefore still independently assort.

18. It all started with a fly…
Chromosome theory of inheritance
experimental evidence from improved microscopy & animal breeding led us to a better understanding of chromosomes & genes beyond Mendel
Drosophila studies
A. H. Sturtevant in the Drosophila stockroom at Columbia University

19. Thomas Hunt Morgan 1910 | 1933 embryologist at Columbia University
1st to associate a specific gene with a specific chromosome
Drosophila breeding
prolific
2 week generations
4 pairs of chromosomes
XX=female, XY=male

20. Morgan’s first mutant…
Wild type fly = red eyes
Morgan discovered a mutant white-eyed male
traced the gene for eye color to a specific chromosome

21. Sex- Linked Inheritance
The transmission of traits on the X and Y chromosome are called sex linked inheritance.
Eg. Eye color found in fruit flies on the X chromosome
R- dominant W- recessive

22. Discovery of sex linkage
red eye female
white eye male x
all red eye offspring
75% red eye female
25% white eye male x
How is this possible?
Sex-linked trait!

23. Sex-linked traits
Although differences between women & men are many, the chromosomal basis of sex is rather simple
In humans & other mammals, there are 2 sex chromosomes: X & Y
2 X chromosomes develops as a female: XX
redundancy
an X & Y chromosome develops as a male: XY
no redundancy

24. Sex linked
Sex linked traits always on x-chromosome. Only confirmed y- linked is hairy ear rims.
- Males cannot be heterozygous for a sex linked trait.
- Males always inherit a sex linked trait from their mother.
Ex. Red green color blindness. Recssive on x chromosome (more males then females)

25. autosomal chromosomes
Sex chromosomes
autosomal chromosomes
sex chromosomes

26. Genes on sex chromosomes
Y chromosome
SRY: sex-determining region
master regulator for maleness
turns on genes for production of male hormones
pleiotropy!
X chromosome
other traits beyond sex determination
hemophilia
Duchenne muscular dystrophy
color-blind
Duchenne muscular dystrophy affects one in 3,500 males born in the United States.
Affected individuals rarely live past their early 20s.
This disorder is due to the absence of an X-linked gene for a key muscle protein, called dystrophin.
The disease is characterized by a progressive weakening of the muscles and loss of coordination.

27. Human X chromosome Sex-linked usually X-linked
more than 60 diseases traced to genes on X chromosome

28. Map of Human Y chromosome?
< 30 genes on Y chromosome
SRY

29. Sex-linked traits XHXh XHY Hh x HH XHXh XH Xh XH Y XHXH XHXH XHY XHY
sex-linked recessive
XHXh
XHY
Hh x HH
XHXh XH Xh XH Y
male / sperm
XHXH
XHXH
XHY
XHY XH Xh
female / eggs
XHY Y XH
XHXh
XHXh
XhY
XhY

30. Male pattern baldness Sex influenced trait
autosomal trait influenced by sex hormones
age effect as well: onset after 30 years old
dominant in males & recessive in females
B_ = bald in males; bb = bald in females

31. X-inactivation Female mammals inherit two X chromosomes
one X becomes inactivated during embryonic development
condenses into compact object = Barr body

32. X-inactivation & tortoise shell cat
2 different cell lines in cat

33. Sex-linked traits summary
follow the X chromosomes
males get their X from their mother
trait is never passed from father to son
Y-linked
very few traits
only 26 genes
trait is only passed from father to son
females cannot inherit trait

34. Pedigree
Is a diagram that illustrates the genetic relationship among a group of related individuals
Check out figure 16.17
Male = square
Female= circle
Shading= affected female or male

37. Hemophilia is a sex-linked recessive trait defined by the absence of one or more clotting factors.
These proteins normally slow and then stop bleeding.
Individuals with hemophilia have prolonged bleeding because a firm clot forms slowly.
Bleeding in muscles and joints can be painful and lead to serious damage.
Individuals can be treated with intravenous injections of the missing protein.

38. Pleiotropy Most genes are pleiotropic
one gene affects more than one phenotypic character
wide-ranging effects due to a single gene:
dwarfism (achondroplasia)
gigantism (acromegaly)
The genes that we have covered so far affect only one phenotypic character, but most genes are pleiotropic

39. Acromegaly: André the Giant

40. Pleiotropy
It is not surprising that a gene can affect a number of organism’s characteristics
consider the intricate molecular & cellular interactions responsible for an organism’s development
cystic fibrosis
mucus build up in many organs
sickle cell anemia
sickling of blood cells

41. know that difference wasn’t random chance?
Epistasis
One gene masks another
coat color in mice = 2 genes
pigment (C) or no pigment (c)
more pigment (black=B) or less (brown=b)
cc = albino, no matter B allele
9:3:3:1 becomes 9:3:4
How would you
know that difference wasn’t random chance?
Chi-square test!

42. Epistasis in Labrador retrievers
2 genes: E & B
pigment (E) or no pigment (e)
how dark pigment will be: black (B) to brown (b)

43. Polygenic inheritance
Some phenotypes determined by additive effects of 2 or more genes on a single character
phenotypes on a continuum
human traits
skin color
height
weight
eye color
intelligence
behaviors

44. Johnny & Edgar Winter
Albinism
albino Africans

45. Nature vs. nurture
Phenotype is controlled by both environment & genes
Human skin color is influenced by both genetics & environmental conditions
Coat color in arctic fox influenced by heat sensitive alleles
The relative importance of genes & the environment in influencing human characteristics is a very old & hotly contested debate
a single tree has leaves that vary in size, shape & color, depending on exposure to wind & sun
for humans, nutrition influences height, exercise alters build, sun-tanning darkens the skin, and experience improves performance on intelligence tests
even identical twins — genetic equals — accumulate phenotypic differences as a result of their unique experiences
Color of Hydrangea flowers is influenced by soil pH

46. Mechanisms of inheritance
What causes the differences in alleles of a trait?
yellow vs. green color
smooth vs. wrinkled seeds
dark vs. light skin
Tay sachs disease vs. no disease
Sickle cell anemia vs. no disease

47. Mechanisms of inheritance
What causes dominance vs. recessive?
genes code for polypeptides
polypeptides are processed into proteins
proteins function as…
enzymes
structural proteins
hormones

48. How does dominance work: enzyme
= allele coding for functional enzyme
= allele coding for non-functional enzyme
= 50% functional enzyme • sufficient enzyme present • normal trait is exhibited
• NORMAL trait is DOMINANT Aa
carrier aa
= 100% non-functional enzyme • normal trait is not exhibited
= 100% functional enzyme • normal trait is exhibited AA

49. How does dominance work: structure
= allele coding for functional structural protein
= allele coding for non-functional structural protein
= 50% functional structure • 50% proteins malformed • normal trait is not exhibited • MUTANT trait is DOMINANT Aa AA
= 100% non-functional structure • normal trait is not exhibited
= 100% functional structure • normal trait is exhibited aa

50. Prevalence of dominance
Because an allele is dominant does not mean…
it is better
it is more common
Polydactyly:
dominant allele

51. Polydactyly recessive allele far more common than dominant
individuals are born with extra fingers or toes
dominant to the recessive allele for 5 digits
recessive allele far more common than dominant
 399 individuals out of have only 5 digits
 most people are homozygous recessive (aa)

52. Hound Dog Taylor

53. Any Questions??