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Transcript
Incomplete Dominance, Codominance,
Multiple Alleles, and Sex-Linked Traits




AG
Ag
aG
ag

AG
Ag

Why are there only two possible combinations?





What is the probability of producing an
offspring with the genotype AAGg?
AA -> ½
Gg -> ½
½x½=¼


No, Mendel’s studies with peas applied to
traits controlled by a single gene with two
existing alleles where 1 allele is completely
dominant to the other
This is not the case for MOST genes




Incomplete Dominance
Codominance
Multiple Alleles
Sex-Linked Traits



Heterozygotes show a “blending” or
intermediate form of the homozygous forms
that exist – No true dominant allele
F2 genotypic ratio is 1:2:1 (HH: Hh: hh)
Ex: Snap Dragons, Hypercholesterolemia



Two dominant alleles exist
Heterozygotes express both alleles EQUALLY
Ex: Type AB Blood, Speckled Chickens, Roan
Cattle, Sickle-cell Anemia






More than two alleles exist for a particular
gene, but every organism has only 2 of them
Ex: Blood Types (A B and O alleles)
A and B are codominant
A is dominant to O
B is dominant to O
O is recessive to A and B




Genes located on the sex chromosomes, mainly
X-chromosome
Males XY; Females XX
Males will show recessively inherited
characteristics more often than females.
Ex: Hemophilia, colorblindness, white eyes in
flies
1910 | 1933

Genes are on sex chromosomes



as opposed to autosomal chromosomes
first discovered by T.H. Morgan at Columbia U.
Drosophila breeding
 good genetic subject
 prolific
 2 week generations
 4 pairs of chromosomes
 XX=female, XY=male
autosomal
chromosomes
sex
chromosomes
P
F1
true-breeding
red-eye female
X
true-breeding
white-eye male
100%
red eye offspring
Huh!
Sex matters?!
generation
(hybrids)
F2
generation
100%
red-eye female
50% red-eye male
50% white eye male
x
RR
r
R
Rr
x
rr
Rr
r
Rr
Rr
R
R
r
RR
Rr
Rr
rr
Doesn’t work
that way!
R
Rr
Rr
100% red eyes
r
3 red : 1 white

In humans & other mammals, there are 2 sex
chromosomes: X & Y

2 X chromosomes
 develop as a female: XX
 gene redundancy,
like autosomal chromosomes

an X & Y chromosome
X
Y
X
XX
XY
X
XX
XY
 develop as a male: XY
 no redundancy
50% female : 50% male
x
XR XR
Xr
XR
XR
XR X r
XR X r
x
X rY
XR Xr
Y
XRY
XRY
100% red eyes
XR
BINGO!
Xr
XRY
XR
Y
XR XR
XRY
X R Xr
X rY
100% red females
50% red males; 50% white males

Y chromosome

few genes other than SRY
 sex-determining region
 master regulator for maleness
 turns on genes for production of male hormones

X chromosome

other genes/traits beyond sex determination
 mutations:
 hemophilia
 Duchenne muscular dystrophy
 color-blindness
Ichthyosis, X-linked
Placental steroid sulfatase deficiency
Kallmann syndrome
Chondrodysplasia punctata,
X-linked recessive

Sex-linked


usually means
“X-linked”
more than
60 diseases
traced to genes
on X
chromosome
Duchenne muscular dystrophy
Becker muscular dystrophy
Chronic granulomatous disease
Retinitis pigmentosa-3
Norrie disease
Retinitis pigmentosa-2
Hypophosphatemia
Aicardi syndrome
Hypomagnesemia, X-linked
Ocular albinism
Retinoschisis
Adrenal hypoplasia
Glycerol kinase deficiency
Ornithine transcarbamylase
deficiency
Incontinentia pigmenti
Wiskott-Aldrich syndrome
Menkes syndrome
Androgen insensitivity
Sideroblastic anemia
Aarskog-Scott syndrome
PGK deficiency hemolytic anemia
Anhidrotic ectodermal dysplasia
Agammaglobulinemia
Kennedy disease
Pelizaeus-Merzbacher disease
Alport syndrome
Fabry disease
Immunodeficiency, X-linked,
with hyper IgM
Lymphoproliferative syndrome
Albinism-deafness syndrome
Fragile-X syndrome
Charcot-Marie-Tooth neuropathy
Choroideremia
Cleft palate, X-linked
Spastic paraplegia, X-linked,
uncomplicated
Deafness with stapes fixation
PRPS-related gout
Lowe syndrome
Lesch-Nyhan syndrome
HPRT-related gout
Hunter syndrome
Hemophilia B
Hemophilia A
G6PD deficiency: favism
Drug-sensitive anemia
Chronic hemolytic anemia
Manic-depressive illness, X-linked
Colorblindness, (several forms)
Dyskeratosis congenita
TKCR syndrome
Adrenoleukodystrophy
Adrenomyeloneuropathy
Emery-Dreifuss muscular dystrophy
Diabetes insipidus, renal
Myotubular myopathy, X-linked
< 30 genes on
Y chromosome
Sex-determining Region Y (SRY)
Channel Flipping (FLP)
Catching & Throwing (BLZ-1)
Self confidence (BLZ-2)
Devotion to sports (BUD-E)
Addiction to death &
destruction movies (SAW-2)
note: not linked to ability gene
Air guitar (RIF)
Scratching (ITCH-E)
Spitting (P2E)
Inability to express
affection over phone (ME-2)
linked
Selective hearing loss (HUH)
Total lack of recall for dates (OOPS)