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Today: some things Mendel did not tell us... Exam #3 T 12/2 in class, Final Sat. 12/6
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Single genes controlling a single trait are unusual. Inheritance of most genes/traits is much more complex… Dom.Rec. Dom.
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PhenotypeGenotype Genes code for proteins (or RNA). These gene products give rise to traits… It is rarely this simple.
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Fig 4.4
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Fig 4.7 Sickle-cell anemia is caused by a point mutation
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Sickle and normal red blood cells Fig 4.7
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Mom = HSDad = HS H or S HH HSSS HS possible offspring 75% Normal 25% Sickle-cell Mom Dad S=sickle-cell H=normal Sickle-Cell Anemia: A dominant or recessive allele? Fig 4.7
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Coincidence of malaria and sickle-cell anemia Fig 24.14
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Mom = HSDad = HS H or S HH HSSS HS possible offspring Oxygen transport: 75% Normal 25% Sickle-cell Malaria resistance: 75% resistant 25% susceptible Mom Dad Sickle-Cell Anemia: A dominant or recessive allele? S=sickle-cell H=normal Fig 4.7
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The relationship between genes and traits is often complex Complexities include: Complex relationships between alleles
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Sex determination is normally inherited by whole chromosomes or by number of chromosomes. Fig 3.18
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X/Y chromosomes in humans
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The X chromosome has many genes; the Y chromosome only has genes for maleness.
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Human sex chromosomes (includes Mic2 gene) Fig 4.14
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Sex-linked traits are genes located on the X chromosome
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Color Blind Test
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Sex-linked traits: Genes on the X chromosome No one affected, female carriers A= normal; a= colorblind colorblind normal similar to Fig 4.13
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Sex-linked traits: Genes on the X chromosome 50% of males affected, 0 % females affected A= normal; a= colorblind normal similar to Fig 4.13
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Sex-linked traits: Genes on the X chromosome 50% males affected, 50% females affected A= normal; a= colorblind colorblind normal similar to Fig 4.13
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Sex-linked traits: Genes on the X chromosome No one affected, female carriers 50% of males affected, 0 % female affected 50% males affected, 50% females affected A= normal ; a= colorblind similar to Fig 4.13
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males and females may have different numbers of chromosomes Fig 3.18
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Tbl 7.1 dosage compensation
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At an early stage of embryonic development The epithelial cells derived from this embryonic cell will produce a patch of white fur While those from this will produce a patch of black fur Fig 7.4
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Promotes compaction Prevents compaction Mammalian X-inactivation involves the interaction of 2 overlapping genes.
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The Barr body is replicated and both copies remain compacted Barr body compaction is heritable within an individual
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A few genes on the inactivated X chromosome are expressed in the somatic cells of adult female mammals –Pseudoautosomal genes (Dosage compensation in this case is unnecessary because these genes are located both on the X and Y) –Up to a 25% of X genes in humans may escape full inactivation The mechanism is not understood
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Epigenetics: http://www.pbs.org/wgbh/nova/sciencenow/3411/02.html http://www.pbs.org/wgbh/nova/sciencenow/3411/02.html Lamarck was right? Sort of… Image from: http://www.sparknotes.com/biology/evolution/lamarck/section2.rhtml
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Genomic Imprinting Genomic imprinting is a phenomenon in which expression of a gene depends on whether it is inherited from the male or the female parent Imprinted genes follow a non-Mendelian pattern of inheritance –Depending on how the genes are “marked”, the offspring expresses either the maternally- inherited or the paternally-inherited allele ** Not both
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Genomic Imprinting: Methylation of genes during gamete production.
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A hypothetical example of imprinting A=curly hair a=straight hair B=beady eyes b=normal *=methylation A* in males B* in females a B* a B* A* b A* b
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A hypothetical example of imprinting A=curly hair a=straight hair B=beady eyes b=normal *=methylation A* in males B* in females A*a bB* A*a bB* a B* a B* A* b A* b
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A hypothetical example of imprinting A=curly hair a=straight hair B=beady eyes b=normal *=methylation A* in males B* in females A*a bB* A*a bB* A*a bB Aa bB* a B* a B* A* b A* b
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A hypothetical example of imprinting A=curly hair a=straight hair B=beady eyes b=normal *=methylation A* in males B* in females A*a bB* A*a bB* A*a bB Aa bB* A*b, A*B, ab, aB Ab, AB*, ab, aB* a B* a B* A* b A* b similar to Fig 7.10
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Thus genomic imprinting is permanent in the somatic cells of an animal –However, the marking of alleles can be altered from generation to generation
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Genomic imprinting must involve a marking process At the molecular level, the imprinting is known to involve differentially methylated regions –They are methylated either in the oocyte or sperm Not both Imprinting and DNA Methylation
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