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Boveri/Sutton Theory (Chromosome Theory of Inheritance)
explains the underlying mechanism of Mendelian genetics by combining chromosomes with the paired factor postulate by Mendel
homologous chromosomes (one from each parent)
genetic linkage
if alleles are on the same chromosome and close enough together, they will sort together
Bateson, Saunders, and Punnet
used dihybrid crosses looking at flower color and pollen shape
observed phenotypes that were higher than the rest in the F2 generation that were the same as the parental generation
they got a completely different ratio in F2 generation than what Mendel said→ genetic linkage is the cause
Bateson, Saunders, and Punnet hypothesis
there is a connection between the parental alleles for flower color and pollen shape and the results of this connection resulted in deviation from Independent Assortment
sex linkage
genes on a sex chromosome
what gene is a sex factor in fruit flies?
eye color
Linkage
when two (or more) genes are inherited together
-loci on the same chromosome
-loci are located close together and travel as group during meiosis
-DO NOT assort independently
Complete Linakge
loci are very close together on the chromosome and crossover does NOT occur
2 out of the 4 expected phenotypes do NOT show up
crossing over
exchange of genetic information between non-sister chromatids
happens during prophase I
configuration
arrangement of alleles on homologous chromosomes
couple (cis-configuration)
normal (WT) alleles on one chromosomes, mutant alleles on the other
repulsed (trans-configuration)
each chromosome contains one normal (WT) allele and one mutant
what happens when two cis homologous chromosomes are crossed in complete linkage?
you will only see the parents in the F2 generation, not the trans configuration because complete linkage has no crossover
what do you see when trans chromosomes are crossed in complete linkage?
you will only see the recombinants (which are the parents) in the F2 generation, you will not see the cis configurations
what does it mean if you see parental and recombinants in the F2 generation?
you are no longer doing complete linkage because complete linkage gives you one or the other
what can you conclude if there are more parental offspring than recombinant offspring?
the parents are in the cis or coupled configuration
calculating recombination frequency
RF= number of recombinant progent/total number of progeny
recombination
exchange of unique genetic material between non-sister chromatids during meiosis
chisamata
the point of contact, the physical link, between two chromatids belonging to homologous chromosomes
incomplete linkage
recombination occurs between two loci
the amount of (or frequency) of recombination depends on how far apart the two loci are
why are there usually lower numbers of recombinants in offspring?
it takes energy to Recombinate and cells dont want to use that energy
what leads to a decreased RF?
decreased space between the alleles on the chromosome
they wont have a lot of space to recombine
what leads to an increased RF?
more space between the alleles on a chromosome
genetic mapping
methods used to identify the distance between genes
if a gene’s loci had a specific place on a chromosome, then the distance between any two genes was a measurable fixed number
distance of Gene A to Gene C
—-A———B————C—-
(gene A to gene B) + (gene B to gene C)
what does a RF of 50% tell you?
you have independent assortment ( then genes are too far apart from each other to recombinate)
double crossover between two loci
no change
double crossover including two loci
recombination
double crossover between three loci
recombination