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Nonmendelian Genetics

Epistasis and gene interactions

  • Epistasis - one gene modifies the expression of another gene (usually one gene blocking another)

    • This will usually show up in questions involving pigmentation - one gene codes for the production of a pigment, another may block the laying down of this pigment (recall albino cat question - this affects phenotypic ratio!! don’t just accept 9:3:3:1 for these)

    • ex) some chicken coloring is influenced by 2 genes, C and I

      • C codes for a dark pigment production, c codes for no pigment production

      • I inhibits pigment production, i does not

      • A dihybrid cross will result in 13 white chickens and 3 dark chickens - only those with CCii or Ccii genotypes will lay down pigment

    • If we had assumed independent assortment for this cross, a X^2 test would require rejecting of the null hypothesis - genes C and I do NOT assort independently of each other

    • Epistasis can also include more subtle alterations rather than complete blockage, such as with horse coat color (chestnut, palomino, cremello)

Sex-linked traits

  • sex genotypes showing up frequently: XX(F) and XY(M) in most mammals, ZW(F) and ZZ(M or F) common in birds and reptiles

  • dark blue shows common genes between X and Y

  • X and Y chromosomes don’t share many common genes, so don’t typically cross over (recall that crossing over only involves swapping of different versions of the same gene)

  • Crossing over on sex chromosomes usually leads to defects

  • Law of segregation applies to whole chromosomes as well -- eggs will have 50/50 maternal or paternal X, sperm will have 50/50 maternal X and paternal Y → zygotes will be 50/50 XX and XY

Inheritance of X-linked traits

  • Male offspring always inherit their X chromosome from their mother and Y from their father

  • Males only have one X chromosome - they only need to inherit one recessive allele to express the recessive phenotype - this is why you’ll see disproportionate numbers of male offspring with recessive X-linked conditions

    • Fathers pass down Y chromosomes to their sons - the son of a colorblind man will not be colorblind unless his mother also passes down a recessive allele

  • Daughters with an X-linked recessive condition (i.e. RG colorblindness) must inherit a recessive X-chromosome from both parents (a colorblind girl has to have a colorblind father)

Y-linked gene inheritance

  • This won’t show up often b/c there aren’t many genes on the Y chromosome

  • Most genes on the Y affect male fertility or sex traits - mutations on the Y can cause infertility/low sperm ct

  • Fathers transmit mutant alleles to sons only - all sons of affected fathers are also affected

  • Daughters of affected fathers cannot inherit or transmit Y-linked genes, and affected females are impossible

Linked Genes

  • Genes located on the same chromosome do not assort independently of one another - typical ratios assuming this do not work

    • This is why we often see combos like blue eyes/blond hai

  • Genes become unlinked when recombination happens in between two genes

  • Vast majority of progeny will have parental genotypes b/c there is a relatively low probability of recombination always

  • Percent of progeny with recombined chromosomes depends on how close together the genes are on the chromosome - higher percent = farther apart, greater probability that chromosome will split/recombine somewhere between the two

    • We can determine how close together genes are by tracking frequency of recombination - 1% corresponds to 1 map unit of distance between

    • One entire chromosome is 50 map units → If frequency of recombination is greater than 50%, the genes are on separate chromosomes and independent assortment likely applies

Mitochondrial and Chloroplast DNA

  • DNA from mitochondria and chloroplasts is maternally inherited

  • Recall differences in male/female meiosis - mature sperm only have enough mitochondria to power its movement into the egg, and these disintegrate when fertilization happens - the mitochondria that are in the zygote and then in the organism are from the egg, which contains all the vital organelles

  • exception: giant redwoods have paternal inheritance, some fern species have biparental inheritance - these patterns are very rare compared to maternal inheritance

  • Mitochondrial diseases are also maternally inherited - all children of women affected by a mitochondrial disease will also be affected, even males

    • But males cannot pass on mitochondrial diseases

Nonmendelian Genetics

Epistasis and gene interactions

  • Epistasis - one gene modifies the expression of another gene (usually one gene blocking another)

    • This will usually show up in questions involving pigmentation - one gene codes for the production of a pigment, another may block the laying down of this pigment (recall albino cat question - this affects phenotypic ratio!! don’t just accept 9:3:3:1 for these)

    • ex) some chicken coloring is influenced by 2 genes, C and I

      • C codes for a dark pigment production, c codes for no pigment production

      • I inhibits pigment production, i does not

      • A dihybrid cross will result in 13 white chickens and 3 dark chickens - only those with CCii or Ccii genotypes will lay down pigment

    • If we had assumed independent assortment for this cross, a X^2 test would require rejecting of the null hypothesis - genes C and I do NOT assort independently of each other

    • Epistasis can also include more subtle alterations rather than complete blockage, such as with horse coat color (chestnut, palomino, cremello)

Sex-linked traits

  • sex genotypes showing up frequently: XX(F) and XY(M) in most mammals, ZW(F) and ZZ(M or F) common in birds and reptiles

  • dark blue shows common genes between X and Y

  • X and Y chromosomes don’t share many common genes, so don’t typically cross over (recall that crossing over only involves swapping of different versions of the same gene)

  • Crossing over on sex chromosomes usually leads to defects

  • Law of segregation applies to whole chromosomes as well -- eggs will have 50/50 maternal or paternal X, sperm will have 50/50 maternal X and paternal Y → zygotes will be 50/50 XX and XY

Inheritance of X-linked traits

  • Male offspring always inherit their X chromosome from their mother and Y from their father

  • Males only have one X chromosome - they only need to inherit one recessive allele to express the recessive phenotype - this is why you’ll see disproportionate numbers of male offspring with recessive X-linked conditions

    • Fathers pass down Y chromosomes to their sons - the son of a colorblind man will not be colorblind unless his mother also passes down a recessive allele

  • Daughters with an X-linked recessive condition (i.e. RG colorblindness) must inherit a recessive X-chromosome from both parents (a colorblind girl has to have a colorblind father)

Y-linked gene inheritance

  • This won’t show up often b/c there aren’t many genes on the Y chromosome

  • Most genes on the Y affect male fertility or sex traits - mutations on the Y can cause infertility/low sperm ct

  • Fathers transmit mutant alleles to sons only - all sons of affected fathers are also affected

  • Daughters of affected fathers cannot inherit or transmit Y-linked genes, and affected females are impossible

Linked Genes

  • Genes located on the same chromosome do not assort independently of one another - typical ratios assuming this do not work

    • This is why we often see combos like blue eyes/blond hai

  • Genes become unlinked when recombination happens in between two genes

  • Vast majority of progeny will have parental genotypes b/c there is a relatively low probability of recombination always

  • Percent of progeny with recombined chromosomes depends on how close together the genes are on the chromosome - higher percent = farther apart, greater probability that chromosome will split/recombine somewhere between the two

    • We can determine how close together genes are by tracking frequency of recombination - 1% corresponds to 1 map unit of distance between

    • One entire chromosome is 50 map units → If frequency of recombination is greater than 50%, the genes are on separate chromosomes and independent assortment likely applies

Mitochondrial and Chloroplast DNA

  • DNA from mitochondria and chloroplasts is maternally inherited

  • Recall differences in male/female meiosis - mature sperm only have enough mitochondria to power its movement into the egg, and these disintegrate when fertilization happens - the mitochondria that are in the zygote and then in the organism are from the egg, which contains all the vital organelles

  • exception: giant redwoods have paternal inheritance, some fern species have biparental inheritance - these patterns are very rare compared to maternal inheritance

  • Mitochondrial diseases are also maternally inherited - all children of women affected by a mitochondrial disease will also be affected, even males

    • But males cannot pass on mitochondrial diseases