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ECU Genetics Intro

Final, Mendilian Genetics, Meosis, Mitosis, Recombinant DNA

QuestionAnswer
Interphase: chromosomes are extended and uncoiled
Prophase: chromosomes coil up and condense; centrioles divide and move apart
Prometaphase: chromosomes are clearly double structures; centrioles reach the opposite poles; spindle fibers form
Metaphase: centromeres align on metaphase plate
Anaphase: centromeres split and daughter chromosomes migrate to opposite poles
Telophase: daughter chromosomes arrive at the poles; cytokenesis commences
Postulate 1 Unit Factors exist in pairs
Postulate 2 Dominance
Postulate 3 Random Segregation
Codominance: joint expression; black and white parents make gray child
Partial Dominance: pink flowers
Epistasis: a variant at one locus prevents another locus from manifesting it's effect
Where is the bombay effect seen? ABO blood
What type of cross over occurs most frequently? Noncrossover
What type of cross over occurs less frequently than the rest? Double cross over
Linked genes are inherited together
Recombination occurs between two non-sister chromatids of a tetrad during the prophase of meiosis I.
Autosomal Recessive usually skip a generation and also appear equally in sexes
Autosomal dominant almost always appear in each generation, affected individuals all have affected parent, and dominant autosomal traits appear equally in both sexes
hemizygosity males have one y and one x and only have one set of alleles for what you are looking at; usually a shift in phenotypes
Rules for 3 Point Mapping Myst be heterozygous at all loci, must be able to observe gentypes, and must have sufficient progeny
Mitotic prophase have tetraploids
Fathers who carry a dominant X will pass trait to all daughters
If female expresses X linked recessive trait, father also expresses trait
Mothers who are homozygous will always pass these traits to all their sons.
Mitochandrial DNA not chromosomal, related to inheritance of an organelle, only inherited maternally
Edmund Wilson and Nettie Stevens discovered different gamete types (XO, XY)
Euploidy: exact multiples of the haploid set of chromosomes
deletions: loss of DNA sequences
Duplications: Repitition of DNA sequences, usually on the same chromosomes
Inversions: reversal of dna sequences usually on the same chromosome
translocations: movement of sequences from one chromosome to another
reciprocal translocations: sequences from two differenct chromosomes exchange with one another
nonreciprocal translocations: movement only occurs from one chromosome to another
Miescher Family discovered DNA
Griffith tried to find a vaccine for bacterial pneumonia, found transferable material; pnemonia smooth and rough
Oswald Avery interested in Griffiths work; cultivated cells in liquid broth then heat kill... extracted carbs, lipids, and proteins
Irvin Chargaff discovered the four nitrogenous base
Al Hershey and Martha Chase bacteriophage life cycle
James Watson and Francis Crick sugggested the structure of DNA
Rosalind Franklin X-Ray defraction pictures
Genome total genetic information of an organism
transcription: copying one strand of DNA into RNA.
Translation process of copying mRNA into protein
What is the transcription start site called? the 1+ nucleotide
silent mutations don't really do anything
Mutation any change in the DNA; not necessarily detremental
Transcript...think... RNA
Nucleotide substitutions arise because of of triplet code degeneracy
missense mutations: nonsynonymous substitutions
nonsense mutations qchange from an amino acid coding triplet to a translation termination triplet
Inversions can lead to silent, missense of nonsense triplets
Inversions can lead to )))))) if they are large a block of amino acids
If inversions are out of frame, they can lead to polar effects
Transpositions can act like insertions or deletions
Created by: kbm0401
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