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Non-Mendelian Genetics Honors Biology Ms. Day
Lecture #26 Non-Mendelian Genetics Honors Biology Ms. Day
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RECALL… Complete dominance Heterozygote (Hh) and dominant homozygote (HH) look identical Demonstrates or follows “Mendelian Genetics” inheritance pattern
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“Non-Mendelian Genetics”
Incomplete (intermediate) Dominance 1 allele is not completely dominant over the other, so heterozygote (Hh) has intermediate (or mixed) phenotype between 2 alleles (like snapdragon flowers)
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Figure 14.10 1⁄2 P Generation White CWCW Red CRCR Gametes Pink CRCW
F1 Generation F2 Generation Red CRCR Gametes CR CW White CWCW Pink CRCW Sperm Cw 1⁄2 Eggs CR CR CR CW CW CW Figure 14.10
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“Non-Mendelian Genetics”
Codominance 2 dominant alleles affect phenotype in separate, distinguishable ways BOTH phenotypes are present in heterzygote Ex’s of codominance Some flowers and Roan animals (cattle & horses)
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Multiple Alleles A type of codominance
When there is 3+ alleles (genes) for a single trait Ex: Human Blood type, human hair color
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The ABO blood group in humans Is determined by multiple alleles
Table 14.2 The ABO blood group in humans Is determined by multiple alleles
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Multiple Alleles (Codominance)
Blood Type Genotypes A IAIA, or IAi B IBIB, or IBi AB IAIB O ii
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Polygenic Inheritance
Many genes (2+) determine one (1) phenotype Many human traits Vary in the population along a continuum Few genes actually follow a simple Mendelian inheritance pattern Examples: Height, eye color, intelligence, body build and skin color
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Polygenic Inheritance
AaBbCc aabbcc Aabbcc AaBbcc AABbCc AABBCc AABBCC 20⁄64 15⁄64 6⁄64 1⁄64 Fraction of progeny
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Nature and Nurture: The Environmental Impact on Phenotype
Departs from simple Mendelian genetics phenotype depends on environment as well as on genotype Called multifactorial inheritance Ex: human fingerprints hydrangea flowers Add P to soil; need HIGHERpH Al in soil; need LOW pH
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Lecture #27 Honors Biology Ms. Day
The Chromosomal Basis of Inheritance Introduction to Sex Linkage Honors Biology Ms. Day
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Gene Linkage Linked genes
Usually inherited together because located near each other on the SAME chromosome Genes closer together on the same chromosome are more often inherited together Each chromosome Has 100’s or 1000’s of genes Sex-linked genes exhibit unique patterns of inheritance; genes on the X or Y chromosome
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Morgan’s Experimental Evidence
Thomas Hunt Morgan Provided convincing evidence that chromosomes are the location of Mendel’s heritable alleles
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Sex linkage explained Thomas Hunt Morgan (Columbia University 1910)
Thomas Hunt Morgan (Columbia University 1910) Fruit Flies (Drosophila) melanogaster) © 2007 Paul Billiet ODWS
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Morgan’s Choice of Experimental Organism
Morgan worked with fruit flies Lots of offspring A new generation can be bred every two weeks They have only 5 pairs of chromosomes
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Morgan and Fruit Flies w+ w Morgan first observed and noted
Wild type (most common) phenotypes that were common in the fly populations Traits alternative to the wild type are called mutant phenotypes WILDTYPE w+ w MUTANT
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The case of the white-eyed mutant
Character Traits Eye color Red eye (wild type) White eye (mutant) P Phenotypes Wild type (red-eyed) female x White-eyed male F1 Phenotypes All red-eyed Red eye is dominant to white eye
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So far so good Hypothesis
A cross between the F1 flies should give us: 3 red eye : 1 white eye F2 Phenotypes Red eye White eye Numbers 3470 82% 782 18% So far so good
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An interesting observation
The F2 generation showed the 3:1 red: white eye ratio, but only males had white eyes F2 Phenotypes Red-eyed males Red-eyed females White-eyed males White-eyed females Numbers 1011 2459 782 24% 58% 18% 0%
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A reciprocal cross Morgan tried the cross the other way round white-eyed female x red-eyed male Result All red-eyed females and all white-eyed males This confirmed what Morgan suspected The gene for eye color is linked to the X chromosome
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Morgan’s Discovery: Sex Linked Traits
Eye color is linked on X Chromosome Females carry 2 copies of gene; males have only 1 copy If mutant allele is recessive, white eyed female has the trait on both X’s White eyed male can not hide the trait since he has only one X.
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The Chromosomal Basis of Sex
An organism’s sex Is an inherited phenotype determined by the presence or absence of certain chromosomes XX = girl XY = boy
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Inheritance of Sex-Linked Genes
The sex chromosomes Have genes for many characters unrelated to sex (especially the X chromosome) A gene located on either sex chromosome Is called a sex-linked gene (Usually on X chromosome)
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What genes are on the X chromosome?
carries a couple thousand genes but few, if any, of these have anything to do directly with sex determination Larger and more active than Y chromosome
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What genes are on the Y chromosome?
Gene called SRY triggers testis development, which determines male sex characteristics This gene is turned “on” ~6 weeks into the development of a male embryo Y-Chromosome-linked diseases are rare
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Sex-linked genes follow specific patterns of inheritance
Fathers pass sex-linked alleles to ALL their daughters but NONE to their sons XY (Father) XX (daughter) XY (Father) XY (son) Mothers can pass sex-linked alleles to BOTH sons and daughters XX (Mother) XX (daughter) XX (Mother) XY (son)
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Sex Linkage If sex-linked recessive on Xn Females have to be Xn Xn to show sex-linked trait Xn X Females do NOT show sex-linked trait Males have to be Xn Y to show sex-linked trait **Most sex-linked disorders affect males; sometimes females
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Sex-Linked Disorders Some recessive alleles found on the X chromosome in humans cause certain types of disorders Color blindness Duchenne muscular dystrophy Hemophilia Male pattern baldness
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X-Linked Trait = Male Pattern Baldness
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Another X-Linked Trait = Hemophilia
About 85% of hemophiliacs suffer from classic hemophilia 1 male in cannot produce factor VIII The rest show Christmas disease where they can’t make factor IX The genes for both forms of hemophilia are sex linked Hemophiliacs have trouble clotting their blood
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Another X-Linked Trait = Red-Green Colorblindness
Normal vision Color blind simulation
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Another X-Linked Trait = Duchenne Muscular Dystrophy
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