Académique Documents
Professionnel Documents
Culture Documents
Chromosomes replicate
Meiosis I
Alleles segregate
Meiosis II
Gametes
R
y y R Replicated chromosomes
r prior to meiosis
r
Y
Y
R R Meiosis I r r R R Meiosis I r r
Y Y y y y y Y Y
Meiosis II Meiosis II
r r
Gametes
R r R R r
R
y y y Y Y
Y Y y
Principle of independent assortment: The genes for seed shape and seed color
assort independently, because they are located on different chromosomes.
Types of crosses
Monohybrids-tracing inheritance of 1
trait at a time
Dihybrids-tracing inheritance of 2
traits together at a time
Testcross-crossing individual
expressing dominant gene with an
individual expressing the recessive to
determine the dominants genotype
Figure 13-4
A cross between two homozygotes
Homozygous
mother
Meiosis
Female gametes
Male gametes
Homozygous
father
Meiosis
Female gametes
Heterozygous
Male gametes
father
Male gametes
Male parent
F2 female parent
Alleles at R gene and Y gene
go to gametes independently
of each other
F2 male
parent
Male gametes
Parental
generation
F1 generation
Self-fertilization
F2 generation
Wheat kernel color is a quantitative trait. Hypothesis to explain inheritance of kernel color
Parental aa bb cc AA BB CC
generation (pure-line white) (pure-line red)
F1 Aa Bb Cc
generation (medium red)
Self-fertilization
F2 20
generation
15 15
6 6
1 1
Other Genetic Patterns
X-Inactivation-In females only, one X chromosome is
inactivated (Barr Body) in each cell.
Different cells may inactivate a different X
ex: calico cats (Black, orange), lymph node patterns
in women
Linkage-Recall that genes found on the same
chromosome are linked
These dont segregate via meiosis
The only way to get recombinations is via crossing
over, therefore the further apart these are, the more
chance of a crossover between them
% recombinants is proportional to the distance linked
traits have between them-see AP Lab 3 Sordaria
Does Genotype determine
Phenotype?
The short answer is no!
Environmental influences also affect
gene expression, giving us a norm of
reaction for a phenotype (range of
possible phenotypes)
Pedigree Analysis
Pedigrees are family trees that use
specific notations that geneticists use
to predict the inheritance pattern of a
trait
Figure 13-21
Carriers
(heterozygotes)
are indicated
with half-filled
symbols
II
Affected
III male
Affected
IV female
Figure 13-23
Female carrier of
hemophilia allele
II
Affected
male
III
IV
Commonly Inherited Disorders
Recessives
Tay-Sachs, Sickle Cell, Cystic Fibrosis,
albinism
Dominants
Marfan syndrome, Huntingtons disease,
Dwarfism
Sex-linked, X-chromosome
Color-blindness, several forms of
muscular dystrophy, pattern baldness,
hemophilia
Beyond the Chromosome Theory of
Inheritance
Genomic Imprinting
Occurs in about 2-3 dozen autosomally inherited
traits
Which parent passed the gene matters in the
inheritance pattern
Ex: Insulin-like growth factor 2 in mice-only
paternally inherited forms are active
Extranuclear Genes
Recall that organelles, like mitochondria and
chloroplasts have circular pieces of DNA
These are capable of replicating and being
passed to daughter organelles during Mitosis
These are matrolineal