BIOL1003 Lecture Notes - Lecture 3: Hbb, Haemophilia, Chromosome

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Mendel genetics, Dominant disorders, blood groups
Mendel's observations were used as the first process to actually numerically analyse
inheritance
Not everyone will have the same trait but everybody will have teh same genes This is
showed in alleles as you may have defend traits on the gene thus having differences. One
will be dominant and one will be recessive. Everybody has a little finger but the aren't
always the same.
If 2 alternative forms of the gene are present, one is fully expressed (dominant) and the
other completely hidden (recessive).... This must BE DIPLOID! Not eh same for wheat. There
are two genes for teh one trait in humans as we are 2n
Pedigree trees...
If one ancestor has a recessive trait, they have 2 copy's of the bad allele.... ... If it skips a
generation it is thought that one person from the parents would have homozygous
dominant genes. Because the other parent had a recessive allele, all teh kids will be
heterozygous (you cant dodge it).... If the next generation then has kids, and teh kids are
effected teh genotype must be heterozygous... To be affected you have to have both of teh
bad traits and since neither parents were showing the bad gene... They must of had a good
and bad copy. To be effected you have to get both of teh bad genes this teh children have a
25% chance of being effected. (Mendels 3:1 ration) you can get 2 good, 1 bad 1 good, 1
good 1 bad and then 2 bad, so thus 25% chance of expressing teh bad gene.)
Dominant disorders in human:
Achondroplasia (a kind of dwarfism)
Huntingtin disease (a neurodegenerative disorder) even if your a heterozygote you are
going to show all of the features! Even if you have a good copy! The bad copy is dominant!
Most people who are Achondroplasia dwarf don't have parents with the disease?! Could be
caused by spontaneous mutation.
Huntington disease parents can now use genetic engineering to stop their kids form getting
the disease. Once you have it there is no cure but you can stop it before it even starts.
If you have Huntington disease in your family, generations are never skipped as it is
dominant!
Strange things with inheritance: Was medel wrong?
Snap dragons: They were red and white so wanted to cross it to see which is dominant, but
tis time they got pink!!! This wasn't meant to happen as his is blending inheritance!! 9white,
pink, red)
When the heterozygous pink plants were crossed there was 3 phenotypes, expressed
1:2:1... white, pink, red) ... This is what we call incomplete dominance. When teh two are
present you get a third phenotype. They aren't a mix of teh 2 phenotypes, red and white,
they are their own thing!
Human blood groups:
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Document Summary

Mendel"s observations were used as the first process to actually numerically analyse inheritance. Not everyone will have the same trait but everybody will have teh same genes this is showed in alleles as you may have defend traits on the gene thus having differences. One will be dominant and one will be recessive. Everybody has a little finger but the aren"t always the same. If 2 alternative forms of the gene are present, one is fully expressed (dominant) and the other completely hidden (recessive) There are two genes for teh one trait in humans as we are 2n. If one ancestor has a recessive trait, they have 2 copy"s of the bad allele If it skips a generation it is thought that one person from the parents would have homozygous dominant genes. Because the other parent had a recessive allele, all teh kids will be heterozygous (you cant dodge it)

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