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Dairyman Goals with Genetics
- A Pregnancy
- A live calf
- A heifer calf
- (want pregnancy rather than genetics)
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Genomic
measures genes by looking at the individual chromosomes
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Darwins theories
- Organisms Vary
- Variation may or may not be inherited
- Struggle for survived in nature
- The best adapted to survival leave the most descendants
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Basic of Dairy Genetics
- Select most desirable animals
- Produce superior genotypes
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SNP
- Single Nucleotide polymorphisms
- Rung of ladder on DNA sequence
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Number of chromosomes a cow has
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Genotype vs Phenotype
- Phenotype= what the animal looks like
- -Genotype+Environmental
- Genetoype= DNA build up
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3 factors that control genetic gain
- Heritability-the likelihood of a trait to be passed on
- Selection differential-superiority of parents over the mean of the population
- Generation interval-the time between generations
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Cytoplasm
- No genetic material
- Cell Function
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Nucleus
- Genetic Material
- Paired chromosomes
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Somatic Cells
- Body Cells, 2n (cows 60)
- Cytoplasm varies with function
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Gametes
- Reproduction cells 1n (cows 30)
- Male/Female sex cells
- -Spermatogonia
- -Oogonia
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Chromosomes in the cell nucleus contain DNA:
the genetic code
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Homozygous vs. Heterozygous
- Homozygous: identical genes at a locus
- Heterozygous: not identical, different genes at a locus
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Dominant, Recessive, Additive
- Dominant: genes with observable effects in only one member of a chromosomes pair
- Recessive: no effect unless present in both members of a chromo, pair
- Additive: a gene has a given + or - effect
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Cytogenetics
Refers to the study of cell (cyto) genetics
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Chromosomes
- Basis of genetics
- Within the nucleus of all cells
- Made up of DNA
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Centromere vs. Chromatids
- Centromere: attaches to spindle fibers during division
- Chromatids: arms made up of genetic material (chromatin)
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Centromere Position
- Matacentric:in center
- Submatacentric: not in middle
- Acrocentric: close to the end
- Telocentric: at the end or top
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Deoxyribnuclic acid
A molecule that carries genetic material
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Sex chromosomes
- Mammals
- -X and Y
- -XX =female XY=male
- Freemartins
- -XX/XY chimeric
- Birds
- -Z and W
- -ZZ=male ZW=female
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Mutation
- Change in a functional genetic unit
- Could be a single nucleotide
- Biochemical polymorphism
- A genetically determined variant of proteins
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The gene
- A unit of inheritance, which does not subdivide
- A unit of function or expression, a cistron (biochemical term)
- The smallest unit that can undergo change, may be one nucleotide
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Translocations
- A chromosome becomes broken
- Becomes attached to another chromosome
- May be carried through meiosis
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Number of different combinations of chromosomes
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Mitosis
- Each chromosome duplicates itself
- Somatic cell (body cells) division
- Daughter cells have the same number of chromosomes
- (radiation can cause exact replication to sometimes cause genetic abnormalities
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Mitosis Interphase
Mitosis Prophase
- Interphase: Rest phase
- chromatids duplicate near end
- few to 100 hours
- Prophase: chromatids shorten and thicken
- Early-centriol divides and migrates
- Late-Spindle fibers, 30 mins
- (1 pair of tele centric, 1 pair of metracentric)
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Mitosis Metaphase
Mitosis Anaphase
Mitosis Telophase
- Metaphase: chromosomes align along equatorial plane
- 5 mins
- Anaphase: chromosome divides at centromere
- two arms back to one arm, 5 mins
- Telophase: chromosomes cluster around centriol
- Cell divides, ten minutes
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Mitosis Phases
- Interphase: chromatids duplicate
- Prophase: Shorten and thicken
- Metaphase: Chromosomes align
- Anaphase: Centromere divides
- Telophase: Cell divides
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Meiosis
- Cell division in which chromosome number is reduced
- Daughter cells receive one member of the chromosome pair
- Gametes (egg and sperm) are produced
- Have Meiosis I and II
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Meiosis:
Interphase I
Prophase I
Metaphase I
Anaphase I
Telophase I
- Interphase: rest phase, chromatids duplicate near end
- Prophase: chromatids shorten and thicken. Paired chromosomes attach to each other (synapsis)
- Metaphase: Paired chromosomes align along equatorial plane
- Anaphase: Homologus pairs separate (2n to 1n), still have two armed cromatids
- Telophase: chromosomes cluster around centriol, two new haploid daughter cells
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Meiosis
Prophase II
Metaphase II
Anaphase II
Telophase II
- Prophase: shorten and thicken, with 1n
- Metaphase: align along equatorial plane
- Anaphase: centromere divides, 1n remains
- Telophase: chromosomes cluster around centriol, Two new daughter cells
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Diploid vs. Haploid cells
- Diploid-2n cells, somatic cells (body cells)
- Haploid-1n cells, gametes (sex cells)
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Genetic defects
many are simple recessives
- with a single SNP
- Dominant, recessive, etc
- will continue to occur
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Congenital defects
Early embryonic death
- Born with the defect (may or may not be genetic)
- EED: some are repro problems, some are genetic
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Genetic defects may become a problem with:
- Artificial Insemination
- Line breeding (inbreeding)
- If breed numbers are small
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Holstein Association USA genetic codes
BD, BL, TL, MF, PO, PC, PP, RC, B/R, TR
- BD: Bulldog
- BL:Bovine leukocyte adhesion deficiency (BLAD)
- TL: Tested free of BLAD
- MF: Mule-Foot
- PO: Observed Polled
- PC: Tested Heterozygous Polled
- PP: Tested Homozygous Polled
- RC: Red Hair Color
- B/R: Black/Red
- TR: Tested free of Red hair color
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Methods to Identify Defect Carrier Animals
- 1.Progeny Testing (mate a suspect animal)
- 2.Biotechnology (with DNA probes look at strand of DNA that carries)
- 3. Blood Testing
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Possible Measures to Eliminate genetic defects
- 1. Cull sires that have produced genetic defect offspring
- 2. Evaluate pedigrees of future sires
- 3. Remove females that produce genetic defect offspring
- 4. Progeny test prospective herd sires
- 5. Cull other close relatives
- 6. _______
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Progeny Testing
- An animal bred to an affected animal-50% chance of identifying
- An animal bred to a known carrier - 25% chance of identifying
- An animal bred to its own offspring - 12.5% chance of identifying
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One pair of genes, two alleles A and a
three genotypes
Six basic crosses
- AA, Aa, aa
- 1. AA x AA
- 2. AA x as
- 3. aa x aa
- 4. AA x Aa
- 5. Aa x aa
- 6. Aa x Aa
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Black/Red in Holsteins
- Three gene effects at the same allele
- Black dominant over Black/red and over red
- Black/red dominant over red
- 3 alleles= B b bB
- bB=black/red dom. over red
- bb=red
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Codominance
- red x white = roan
- roan x roan = 1/4 red, 1/4 white, 1/2 roan
- F1 mating red bull to white cow (or vise-versa) will produce all roan calves
F2 mating roan to roan 1/4 red, 1/4 white, 1/2 white
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Three gene pairs, additive gene effects
- A = 6,000 lbs. milk
- a = 4,000 lbs. milk
- B = 5,000 lbs. milk
- b = 3,000 lbs. milk
- C = 2,000 lbs. milk
- c = 1,000 lbs. milk
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Additive Genes
- milk
- fat
- protein
- type
- weight gain
- milking speed
- longevity
- mastitis
- overall health
- many others
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Biochemical Polymorhpism
when two or more phenotypes exist in the same population of a species
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Genomic
biotechnology of DNA sequencing of sets of genes of the complete genomes of selected organisms
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Karyotype
the number and visual of the chromosomes in the cell nuclei of an organism or species.
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Nucleotide
a compound consisting of a nucleotide linked to a phosphate group. Nucleotides form the basic structural unit of nucleic acids such as DNA.
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Gene, Genome, Genomics
- Gene: the functional and physical unit of heredity passed from parent to offspring.
- Genome: The DNA comprising the complete genetic complement of an organism
- Genomics: 1986 - a new scientific discipline of mapping, sequencing, and analyzing genomes
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4 organic bases (nucleotides)
G C A T
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QTL
Qualitative Trait Loci: process enzyme taken to cut a piece of DNA to search for a certain gene
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Conclusions about genomics
- Genomic predictions significantly better than parent average for all 26 traits tested
- Gains in reliablity equivalent on average to 15 daughters with records
- -analysis used 3,576 historical bulls
- -Current data includes 5,285 proven bulls
- Larger populations require more SNPs
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Improve what by testing genomics
Improve accuracy
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Haplotype
- something that causes embryonic death
- 23.4% presence in haplotype of Jersey breed
- Holstein presence is 4.5%, 4.6%, and 4.7%
- Stretch of chromosome or DNA that is transmitted as a unit from one generation to the next
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Evidence of Hapolotypes
- these haplotypes are never observed in a homozygous state in any live animals
- Decreased conception rate was observed when a carrier sire was mated to a daughter of a carrier maternal grandsire
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Haplotypes impacting fertility
certain haplotypes never appear in a homozygous condition
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The new normal of hapolotypes
- due to modern genomic technology, undesirable genetic conditions are no longer considered rare
- We expect to find them in some of our best genetic families
- We should use the haplotype information to improve our breeds without causing undue economic hardship to the breeders of these animals
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