Download PPT

Survey
yes no Was this document useful for you?
   Thank you for your participation!

* Your assessment is very important for improving the work of artificial intelligence, which forms the content of this project

Document related concepts
no text concepts found
Transcript
Applied Biology
Genetics Notes
Genetics Introduction
• Genetics is the study of heredity
• Heredity explains why you look like your
parents or siblings (similar traits)
• Traits (ex. Color, shape) are inherited or
passed down to offspring in genetic
crosses
Essential Vocabulary!
• Gene – parts of DNA that control traits
• Gregor Mendel – “Father of Genetics”, studied inheritable
information & performed plant-cross experiments
Dominant vs Recessive
Dominant gene – trait ALWAYS shows itself
Recessive gene – trait hidden when dominant
gene is present
Allele – forms of a particular gene (we use caps
& lower case letters)
(R = round and r = wrinkled…….but
both code for shape)
Homozygous vs.
Heterozygous
• Homozygous – 2 of same allele for a trait
(RR or rr)
• Heterozygous – 2 different alleles for a
trait (Rr)
Phenotype vs. Genotype
Genotype
• Phenotype –
physical observable
trait (shape, color
ect.)
• Genotype – genetic
make-up,
combination of
alleles (RR, Rr, rr)
Phenotype
(purple)
Solving Genetics Problems
1. Designate letters for traits
(R=Round, r=wrinkled)
2. Determine parent alleles
3. Set up Punnett square
4. Fill – in Squares
5. Determine possible offspring genotypes &
Phenotypes
Practice Problem
Black hair (B) is dominant over brown hair (b). A man
heterozygous for black hair and a woman with
brown hair have children. What are the genotypes
and phenotypes of their offspring?
Step #1
B = black
Step #2 Dad =
Step #3 (punnett square)
Step #4 (fill-in offspring squares)
Step #5 (Genotypes & phenotypes)
b = brown
Mom =
Blood Typing Genetics
(Codominance & Multiple Alleles)
• In simple genetics…there are usually 2 alleles
– 1 dominant (R) & 1 recessive (r)
• In Codominance…neither allele is dominant
over the other!
• Since they are COdominant…they both show up
in the heterozygous phenotype!
Blood Typing Genetics (cont.)
• Usually in simple genetics problems we have:
– 1 Dominant Allele
– 1 Recessive Allele
R
or
r
• In Blood typing, we have:
–2 Dominant Alleles = A & B
–1 Recessive Allele =
o
EXAMPLE: Blood Types!
Blood Typing - Codominance
• In humans, there are 4 possible blood
types: A, B, AB, and O.
• Type O individuals are considered to be the “universal
donors”, whereas type AB individuals are said to be
“universal recipients”!
Blood Type Genotypes
Type A Blood
– AA is homozygous
– Ao is heterozygous
Type B Blood
– BB is homozygous
– Bo is heterozygous
Type AB Blood
– AB (this is the co-dominant blood type!)
Type O Blood
– oo (only 1 way to have Type O blood because o is
recessive!)
Blood Typing – Practice Problem
A man heterozygous for Type A blood and
woman homozygous for Type B blood have
children. What are the possible genotypes and
phenotypes of their offspring?
Practice Problem #2
Two babies are ready to go home from the
hospital…Which baby belongs to which parents?
• Here’s what you know about the babies:
– Baby A bas blood type A
– Baby B has blood type O
Parents #1 - Father (Homozygous Type A) &
Mother (Type O)
Parents #2 - Father & Mother (Heterozygous A)
Sex Linkage – Hemophilia
Some traits are carried on the X
chromosome!! Hemophilia is the most wellknown sex-linked disease!

Males = X Y
Females = X X
Hemophilia
Lacking the ability for blood to clot…can’t
stop bleeding 
Possible Genotypes:
Hemophilic Male Genotype = X Y
Hemophilic Female = X X
Normal Male Genotype = X Y
Normal Female Genotypes = X X
X X (CARRIER)
Practice Sex Linkage (Hemophilia)
Problem
A man with hemophilia and a normal women (but
carrier for hemophilia) have a child. What are the
possible genotypes and phenotypes of their
offspring?
Man = X Y
Woman = X X
Offspring Genotypes:
Offspring Phenotypes:
Human Genetics
Karyotype - the complete
set of chromosomes in a
species. Can show
chromosomal disorders
such as:
1.
Down Syndrome (Trisomy 21)
2.
Turner Syndrome (X missing
pieces)
3.
Klinefelter Syndrome (XXY)
Chromosomal Disorders occur due to NONDISJUNCTION –
error in meiosis where chromosomes don’t separate
correctly during anaphase!
Human Genetics - Pedigrees
Related documents