Pedigree and Karyotype Power point
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Transcript Pedigree and Karyotype Power point
Genetics ~ Part III
Karyotypes and Pedigrees
Karyotype- a chart of
chromosomes pairs
Male
Karyotype
Any individual with at least one
Y chromosome is male and
without one Y is female.
XX- Female
XY –Male
Down Syndrome (trisomy-21)
Autosomal nondisjunction
affected individuals survive to
adulthood
It occurs in about 1 and 700 live
births
- There is a third chromosome on the
21st pair.
- They have varying degrees of mental
disability.
- The incidence is higher among older
mothers, especially those over 40.
Characteristics: short, slanted eyes,
thick tongue
SEX CHROMOSOME
NONDISJUNCTION –
Unusual numbers of sex
chromosomes
Turner’s Syndrome
XO
One X chromosome is missing
• FEMALES ONLY!
• Monosomy X – gets only
ONE X chromosome
•Sterile female
•Low intelligence
•No breasts (no secondary sex
characteristics)
Klinefelter syndrome
XXY
-Extra X chromosome
-MALES ONLY!
- causes a male to be
sterile
-No beard, no deep voice, no
masculine muscle tone (no
secondary sex characteristics)
Most of these individuals lead
normal lives, but they can not have
children and some may have some
degree of mental retardation.
Superman Syndrome
XYY
Male
Has an extra Y chromosome
On average 3” taller than your average male
Clinical phenotype of this syndrome is
normal
RECESSIVE AUTOSOMAL
DISORDERS-Deals with
chromosome pairs #1-22
Cystic Fibrosis
Excess mucus in lungs
Mostly found in Caucasian
population
Chromosome #7
Phenylketonuria (PKU)
Lack of normal skin
pigmentation
Mental retardation
Can prevent with special diet
Chromosome #12
Absence of certain enzyme
Damage to Central Nervous
System
Tay-Sachs Disease
Lipids (fats) in brain cells
Affects Central Nervous System
Mental deficiency
Fatal, usually causes death by
age 2
Mostly in Jewish population
Chromosome #15
DOMINANT AUTOSOMAL
DISORDERS - Deals with
chromosome pairs #1-22
Huntington’s Disease
Chromosome #4
Memory loss
Uncontrolled movements
Onset occurs between the ages of
30-50 (middle age)
Forgets things, stumbles
Cause: abnormal repeating of
certain bases
CODOMINANT AUTOSOMAL
DISORDERS
Sickle Cell Anemia
Sickle-shaped red blood cells
Difficulty breathing
Nitrogen base is changed, affects
HEMOGLOBIN that carries oxygen
Mostly in African Americans
Cells clot
Capillaries are cut causing
bleeding internally.
Chromosome #11
Pedigree-
a graphic
representation of genetic
inheritance from generation to
generation
Pedigree Symbols
Normal female
Affected female
Carrier/heterozygous female
Normal male
Affected male
Carrier/heterozygous male
Death
Married
Parent and Offspring
A
carrier is represented by a
half shaded circle or square.
They are heterozygous- they
have a recessive gene but it
does not show.
DNA
FINGERPRINTING
aka
GEL ELECTROPHORESIS
Why ?? To determine whether
suspects have been at a crime
scene/location
Who?? Law enforcement
How
does it work???
Small DNA samples can be obtained
from blood, hair, skin, and copied
millions of times.
The DNA is cut into fragments of
different lengths
DNA fragments can then be separated
by electrophoresis, and compared with
those obtained from a crime scene
The
genes follow standard
patterns from person to person
BUT the non-coding segments
produce distinct combinations
of patterns that are unique to
each individual
SO unique fingerprints can be
used to identify a single person.
No
two people have the
same DNA (except identical
twins)