Ch 7, Part 1: Linkage& Chr mapping in eukaryotes (OCT 3rd)

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What is linkage and how does it affect Mendelian expectations?

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How did "the chromosomal basis of inheritance” start

Friedrich Miescher (1869): discovers DNA in bandage pus


-Contains C, H, O, N and P: Not a protein
-Appears in nucleus of all cells: named nuclein

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How did “meiosis as the basis of inhertance” start

Oscar Hertwig (1876): observes movements of chromosomes in
sea urchin egg mother cells


-later observes that fertilization requires combination of
nuclein from both the egg and sperm cell
-Proposes that nuclein is the material of heredity

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How did “chromosome theory of interitance” start

1902: Walter Sutton and Theodor Boveri independently
recognize correlation between segregation of
chromosomes in meiosis and segregation of Mendelian
factors (alleles)


-Boveri supposes that there are many more factors
than chromosomes; genes that appear on the same
chromosome are said to be in linkage

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Thomas Hunt Morgan Lab…

what does white eyes and miniature wings classify as?

what does F1 generation turn out if recessive female x WT male?

They are both x-linked recessive mutations

<p>They are both x-linked recessive mutations</p>
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In THM lab..

what are the F2 expectations?

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in THM lab..

what actually occured in the F2 generation? what was more present

There was more parental types than recombinant types

<p>There was more parental types than recombinant types</p>
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What are the expectations if: Linkage is complete

what is the noticed trend here and what is it known as?

notice there are no

-MT white eye & WT normal wing

-WT red eye & MT miniature wing

all F2 are either WT for both loci or mutant for both loci. This is known as parental phenotypes

<p>notice there are no </p><p>-MT white eye &amp; WT normal wing</p><p>-WT red eye &amp; MT miniature wing</p><p></p><p>all F2 are either WT for both loci or mutant for both loci. This is known as parental phenotypes</p>
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What are the expectations when: taking into account linkage and crossing over

-Based on recombinance number, you can tell how far apart genes on a chromosome are

-females have 2 x-chromosomes

<p>-Based on recombinance number, you can tell how far apart genes on a chromosome are</p><p>-females have 2 x-chromosomes</p>
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Recombinant frequency and linkage,

what was discovered when genes are further apart?

The further apart two genes are on a chromosome, the higher the probability of recombination

<p><span>The further apart two genes are on a chromosome, the higher the probability of recombination</span></p>
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Recombinant frequency and linkage,

what was discovered when genes are closer together?

-The closer together two genes are on a chromosome, the lower the probability of recombination

-Much more narrow range of equivalent recombinants

<p>-The closer together two genes are on a chromosome, the lower the probability of recombination</p><p>-<span>Much more narrow range of equivalent recombinants</span></p>
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The frequency of recombinants =

the distance between two loci in units called centimorgans (cM).