Uploaded by KEREEN KATE RODA

Non-Mendelian Genetics

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GOOD
MORNING
TEACHER KEREEN KATE RODA
I
X
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Pi
MEETING
REMINDERS
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LET'S
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NON-MENDELIAN
GENETICS
OBJECTIVES
distinguish Mendelian
from non-Mendelian describe some
cases of nonmodes of
Mendelian genetic
inheritance
traits
explain sexrelated
inheritance
distinguish sexlinked traits from
other sex-related
trait
NON-MENDELIAN GENETICS
Non-Mendelian inheritance is any pattern of inheritance in
which traits do not segregate in accordance with Mendel's laws.
MENDELIAN VS. NON-MENDELIAN
GENETICS
GENETICS
the way in which genes and their
corresponding traits are passed
from parents to their offspring
by means of dominant and
recessive alleles
involve only two alleles
two alleles are either dominant
or recessive
phenotypic proportions can be
pre determined theoretically
phenotypic traits of pea plants
the patterns of inheritance
which do not follow the Mendelian
inheritance
involve multiple alleles or polygenes
two alleles are neither dominant or
recessive
phenotypic proportions differ from
theoretic proportions
examples include many human traits
NON-MENDELIAN GENETICS
THE SECOND CONCEPT
THE FIRST CONCEPT
Incomplete Dominance
and Codominance
Multiple Alleles
THE THIRD CONCEPT
Sex Linkage
INCOMPLETE
DOMINANCE
A case in which one allele is
not completely dominant over
another
Homozygous red flowers (RR)
when crossed with
homozygous white flowers
(rr), will produce a
heterozygote (Rr)pink
flowered plants.
White
rr
Red
RR
Pink
Rr
Snapdragon
plants
CODOMINANCE
When both alleles contribute
to the phenotype
Colors are not blended; they
appear separately.
Heterozygote simultaneously
expresses the phenotypes of
both homozygotes
A
B
AB
O
MULTIPLE ALLELES
When there are more than
two types of alleles for a
given locus or trait, this
will result in more than
two kinds of phenotypes
that may be expressed for
that trait.
AGOUTI:
AGOUTI:
dominance hierarchy:
C> cch>ch> c
AGOUTI:
i. CC – Agouti
ii. Ccch – Agouti
iii. Cch – Agouti
iv. Cc – Agouti
v. cchcch – Chinchilla
vi. cchch – Chinchilla
vii. cchc – Chinchilla
viii.chch – Himalayan
ix. chc – Himalayan
x. cc – Albino
Inheritance of
the ABO blood
types in humans
involves multiple
alleles.
Inheritance of
the ABO blood
types in humans
involves multiple
alleles.
SEX LINKAGE
is the phenotypic expression
of an allele that is dependent
on the gender of the
individual and is directly tied
to the sex chromosomes.
SEX CHROMOSOMES
are responsible for the sex or
gender of the carrier while
autosomes carry all other genes of
an organism. In humans, you have
learned that females contain two X
chromosomes (XX) while males
have one X and one Y chromosomes
(XY).
The sex of humans is determined by the presence or
absence of a Y chromosome
The inheritance of genes located in the sex chromosomes is referred to
as SEX-LINKED INHERITANCE
Anne Boleyn
Henry VIII
SEX-LINKED TRAITS
is the phenotype produced by a recessive
gene that is located on the sex chromosome
X-LINKED TRAIT
Y-LINKED TRAIT
A sex-linked trait is where the
gene or allele for the trait is
found on the X chromosome
A sex-linked trait where the
gene or allele for the trait is
found on the Y chromosome.
X-LINKED TRAIT
Color blindness
An X-linked recessive trait
where an affected individual
could not distinguish red from
green color (red green color
blindness). The color blindness
gene is located on the X
chromosome, so men are more
likely to be color blind than
women.
TRIVIA
Ishihara test
is a common color perception test to
determine color blindness in a person. The
test consists of pseudo-isochromatic
plates that contain dots that appear in
random sizes and colors. It was first
developed by Dr. Shinobu Ishihara in 1917 at
the University of Tokyo. Persons with
normal vision will often see a number at
the middle of PIP whereas those with color
blindness will not recognize any number or
will see a different number.
X-LINKED TRAIT
Hemophilia
An X-linked recessive trait
where an affected individual
suffers from delayed blood
clotting during injuries because
of the absence of certain
blood clotting factors
Y-LINKED TRAIT
Hypertrichosis pinnae auris
a phenotypic trait observed
mainly on the human ears. It
has been described as the
presence of hairs on the lower
part of the distal half of the
helix of the ears.
SEX INFLUENCED
TRAIT
Any trait in a diploid organism whose
expression is affected by an
individual’s biological sex; a trait that
occurs at a higher frequency in one
sex over the other.
Sex-influenced traits follow the
Mendelian pattern of dominance and
recessiveness. However the effect in
one sex is dominant whereas it is
recessive in another sex.
male-pattern hair loss
female-pattern hair loss
SEX LIMITED TRAIT
Any trait in a diploid organism
whose expression is limited to just
one biological sex
Functional mammary glands as an
example of a sexlimited trait. Only
females can express functional
mammary glands that produce milk
immediately after giving birth.
SEX-LINKED TRAITS
caused by genes in X or Y chromosomes
SEX-INFLUENCED TRAITS
Autosomal trait expressed more
frequently in one sex than
another.
-trait modified by the sex of
the individual
-male pattern baldness is more
frequent in males due to sex
hormones differences.
SEX-LIMITED TRAIT
Autosomal trait expressed ONLY
in one sex.
-due to anatomical but not
genetical differences
-uterine defects or sperm
motility problems
A local hospital has sent word to a family of a
possible mix up of some of the children with other
families when they were born. To rule out any
possible mix up, the hospital obtained the blood
types of every individual in the family, including
the surviving maternal grandfather and paternal
grandmother. The results were as follows:
Father: Type O
Mother: Type A
1st child: Type O
2nd child: Type A
3rd child: Type B
Maternal
grandfather:
Type AB
Paternal
grandmother:
Type B
The police have rounded up the usual suspects in
the latest rash of bookstore robberies. The thief
got a nasty paper cut at the scene of the crime.
The suspects are of blood type A, B, AB, and O.
The blood at the crime scene contained i alleles.
Which suspect therefore cannot have been
involved? Explain.
The last Emperor of Russia, Nicolas II, was
married to Empress Alexandra, and they had five
children, Olga, Tatiana, Maria, Anastasia, and
Alexis. Alexis was the only one who was afflicted
with hemophilia or the royal bleeding disease; all
other members were normal.
• If only Prince Alexis was afflicted with
the disease, determine his genotype.
• What could be the genotypes of the
Emperor and Empress?
• Is it possible that each daughter could
have been a carrier? Explain
THANK YOU
DO YOU HAVE ANY QUESTIONS?
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