Review for final exam
Mitosis and meiosis
Stages, pictures, diploid, haploid number, chromosomes, DNA molecules
Differences between mitosis and meiosis
Cell cycle
Know what the following terms mean:
Incomplete dominance
Codominance
Multiple alleles
ABO blood group antigens
Autosomal recessive (what are some examples)
Autosomal dominant (what are some examples)
X-linked inheritance
Polygenic
Gene interactions
Epistasis
Pleiotropy
Sex-limited Phenotypes
Sex-influenced Phenotypes
Penetrance and Expressivity
Imprinting
Phenotype
Genotype
Punnett square
incomplete dominance
homozygous
heterozygous
multiple alleles
blood type antigens
pedigree
karyotype
Crosses for X-linked inheritance and blood type antigens
Know how to do a dihybrid cross and a dihybrid cross with different inheritance patterns
(for example, recessive trait and codominance)
When would you get a 1:2:1 ratio in the offspring?
When would you get a 9:3:3:1 ratio in the offspring?
You do not need to know how to do the trihybrid crosses.
Know how to do the epistasis problems.
Probability problems
How are different diseases, traits inherited?
Color blindness
Tay-Sachs
Huntingtons disease
Fragile-X
Sickle Cell Anemia
Cystic Fibrosis
Diseases due to imprinting: Prader Willi and Angelman Syndrome
Chi square test you will not have to do a problem but you must be able to answer the following question: Inorder to reject the null hypothesis and say that something is statistically significant, what must the p value be?
How does a pedigree from autosomal recessive and autosomal dominant traits differ? How are they different from X-linked? What percentage male and female do you expect to see with the different modes of inheritance?
Trinucleotide repeat diseases, anticipation
There will not be any questions on the model organisms.
Know which diseases results from which chromosomal abnormalities.
No questions on dosage compensation, Barr bodies or X-inactivation.
What is the difference between aneuploidy (monosomy, trisomy, tetrasomy) and euploidy (diploidy, triploidy, tetraploidy)?
Be able to determine the number of chromosomes of each
Changes in the structure and arrangement of chromosomes
How can radioactive labels be used to study DNA, RNA and proteins?
DNA and RNA can be labeled with 32P and proteins can be labeled with 35S
DNA structure
What makes up a nucleotide?
What is at the 1, 2, 3, and 5 positions?
How do nucleotides bind together?
How do the different chains of DNA bind together?
You do not need to know how to draw the different bases but you should know which ones have 1 ring and which have 2 rings.
How do purines bind to the sugar? How do pyrimidines bind to the sugar?
How many hydrogen bonds form between the bases?
What are differences between RNA and DNA?
Comparison between replication, transcription and translation in prokaryotes and eukaryotes.
Mutations
Point mutation
Missense mutation
Nonsense mutation
Silent mutations
Transition
Transversion
Frameshift mutations