Chapter 8
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Part 3: The Continuity of Life
Foundations of Genetics
Review
Gregor
Mendel
studied inheritance by examining seven characteristics, or
, using the
garden
.
In Mendel's
experiments,
the F
1
generation
plants all expressed the
trait.
In the F
2
generation,
3/4 of the offspring were dominant trait and 1/4 were
.
Mendel's theory of
explains these observations.
Characteristics are inherited from parent to offspring as "factors" now
known
as
that can be of different versions called
, one allele inherited from each parent.
If both of the alleles are the same, the individual is
for the trait, otherwise the individual is
and exhibits the
trait.
An individual's alleles are referred to as its
and the expression of those alleles result in observable traits called its
.
A
Punnett
can be used to
predict
the
distribution
of
and
of offspring of a cross.
A
with a homozygous
individual can be used to
determine
the
of a
individual.
Mendel derived two laws from his experiments, including
crosses involving two traits.
Law
of independent
: genes located on different
are inherited independently of each other.
Law
of
: alleles are distributed into
that combine
to produce
offspring.
Alternative forms of a gene (alleles) result
from
.
Review
Many traits exhibit non-Mendelian inheritance.
dominance
results when alternative alleles are not fully dominant or fully recessive; the heterozygote phenotype is
between that of the homozygotes.
occurs
when both alleles are expressed resulting in phenotypic expression of both. The human
ABO
blood group is controlled by
alleles.
Some traits are
and exhibit
variation
which results from the action of multiple genes.
The expression of some genes is also influenced by
factors,
such as photoperiod.
effects result when one gene influences more than one
trait.
occurs when two or more genes interact to produce a
phenotype.
Morgan
showed that traits like eye color in fruit flies are
-
linked;
in this case the eye-color gene resides on the
chromosome.
Human somatic cells have
chromosomes consisting of 22 homologous pairs of
and one pair of
chromosomes.
Homologous pairs or sister
may fail to separate during meiosis, resulting in
, gametes with incorrect number of
chromosomes,
or
.
Nondisjunction abnormalities include
trisomy
21, which causes
syndrome, and sex chromosome
aneuploidies.
Mutations can result in alleles that cause
disorders,
most of which tend to be
: only the
recessive individuals are affected, heterozygotes are
.
can be used to track the
inheritance
of genetic
disorders,
such as
sickle-cell
and
Huntington's
disease, and other traits.
Some genetic disorders can be detected during pregnancy using methods such
as
and
, usually performed in the fourth month of pregnancy.
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Sep 25, 2008
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