Chromosomal Basis of Inheritance Chapter 15. Genetic work done on fruit flies - takes little time to...
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Transcript of Chromosomal Basis of Inheritance Chapter 15. Genetic work done on fruit flies - takes little time to...
• Genetic work done on fruit flies - takes little time to observe many generations.
• Thomas Morgan - fruit fly eye color.
• Wild type (normal) - red.• Mutant - white.
• Discovered mutant eye color appeared more often in males, leading him to discover some traits sex-linked (carried on sex chromosomes).
• Chromosomes - hundreds or thousands of genes.
• Genes located on same chromosome, linked genes, inherited together because chromosome is passed along as unit.
http://faculty.clintoncc.suny.edu/faculty/Michael.Gregory/files/Bio%20101/Bio%20101%20Lectures/genetics-%20chromosomes/img003.gif
• Genetic recombination- Production of offspring with new combinations of traits inherited from two parents.
• Can occur during crossing over - sections of homologous chromosomes are exchanged during meiosis I.
• Genetic map - list of loci along chromosomes.
• Further apart genes are, higher probability that they will switch places.
Sex chromosomes
• 2 sex chromosomes X and Y.• Males – XY; females - XX. • Other species have other systems
- X-0 system, Z-W system, haplo-diploid system.
• X-Y system behaves like normal chromosomes - 50/50 chance of having male or female.
• Sex chromosomes, also have genes for traits.
• Trait recessive - female will only inherit it if both parents pass it on.
• Males have 50% chance of inheriting it -only have 1 X chromosome.
• Males have higher rate of inheriting sex-linked diseases than females.
• Muscular dystrophy - sex-linked disease.
• Affects more males than females.
• Hemophilia, excessive bleeding, - sex-linked.
• Though females have two X chromosomes, 1 turned on.
• Other - Barr body - reactivated in ovaries during egg production (to pass genes on).
• Females exhibit characteristics from their mother and some from their father (sex chromosomes only).
• Pattern responsible for mosaic of effects like patterns seen in tortoiseshell cats.
• Occurs due to patches of cells expressing orange allele while others have nonorange allele.
Errors
• Errors can occur in DNA and in chromosomes.
• Nondisjunction - homologous chromosomes fail to separate during meiosis I, or chromatids fail to separate during meiosis II.
• Some gametes receive 2 of same type of chromosome, another gamete receives no copy.
• Abnormal number of chromosomes - aneuploidy.
• Trisomy - gamete receives 3 of same chromosomes (2n + 1).
• Monosomy - gamete receives only 1 of same chromosome (2n – 1).
• Earlier in development this occurs more profound effect because cells will go through mitosis.
• Organisms with more than 2 complete sets of chromosomes - polyploidy.
• Happens more often in plants than animals.
• Species with polyploidy - more normal than aneuploidy because not missing chromosomes.
• Deletion - piece of chromosome broken off during cell division.
• Duplication - fragment becomes attached as extra segment to sister chromatid.
• Inversion - piece breaks off, turns around, reattaches (backwards).
• Translocation - chromosomal fragment joins nonhomologous chromosome.
• Down syndrome - trisomy (Trisomy 21).
• Chromosome 21 smallest chromosome, individual with this abnormality can survive.
• Aneuploidy can occur in sex chromosomes.
• Klinefelter’s syndrome - male is XXY because of nondisjunction.
• Trisomy X (XXX) - females.• Monosomy X - Turner syndrome -
example of nondisjunction.
• Deletion - cri-du-chat found on chromosome 5.
• Chronic myologenous leukemia - translocation between chromosome 9 and chromosome 22.
• Some traits dependent on who passes on alleles, mother or father.
• Prader-Willi syndrome - deletion on chromosome 15 inherited by father.
• Same deletion from mother - Angelman syndrome.
• Genomic imprinting - gene on 1 homologous chromosome silenced - allele on homologous chromosome expressed.
• Some eukaryotic genes located in mitochondria.
• These passed from mother to offspring; none of father’s mitochondrial genes passed on.