1 4 Chapter 15~ The Chromosomal Basis of Inheritance.
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Transcript of 1 4 Chapter 15~ The Chromosomal Basis of Inheritance.
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Chapter 15~ The Chromosomal Basis of Inheritance
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Mendel’s Inheritance w/ Independent Assortment
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The Chromosomal Theory of Inheritance
Genes have specific loci on chromosomes and chromosomes undergo segregation and independent assortment
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Chromosomal Linkage Morgan- used Drosophilia melanogaster
» XX (female) vs. XY (male) Discovered: Sex-linkage: genes located on a sex chromosome Linked genes: genes located on the same chromosome that tend
to be inherited together
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Chromosomal Linkage
Sex - Linked– Genes on the X
chromosome will only have 1 copy in males
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Genetic recombination
Crossing over
– Genes that DO NOT assort independently of each other
Genetic maps
– The further apart 2 genes are, the higher the probability that a crossover will occur between them and therefore the higher the recombination frequency
Linkage maps
– Genetic map based on recombination frequencies
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Recombination Calculations
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Human sex-linkage SRY gene: gene on Y chromosome that triggers the development of testes
Fathers= pass X-linked alleles to all daughters only (but not to sons)
Mothers= pass X-linked alleles to both sons & daughters
Sex-Linked Disorders: Color-blindness; Duchenne muscular dystropy (MD); hemophilia
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Sex-Linked Disorders
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X- inactivation X-inactivation: 2nd X chromosome in females condenses into a Barr body (e.g.,
tortoiseshell gene gene in cats)
A different X will be randomly be inactive in different cells. (The Barr body can be viewed in the nucleus.)
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Chromosomal errors, I Nondisjunction:
members of a pair of homologous chromosomes do not separate properly during meiosis I or sister chromatids fail to separate during meiosis II
Aneuploidy: chromosome number is abnormal
– • Monosomy~ missing chromosome
– • Trisomy ~ extra chromosome (Down syndrome)
– • Polyploidy~ extra sets of chromosomes
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Chromosomal Errors - Turner’s (XO)
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Chromosomal Errors - Metafemale
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Chromosomal Errors -Klinefelter (XXY) or (XXXY)
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Chromosomal Errors - Down’s syndrome (Trisomy 21)
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Chromosomal errors, II Alterations of chromosomal structure:
Deletion: removal of a chromosomal segment
Duplication: repeats a chromosomal segment
Inversion: segment reversal in a chromosome
Translocation: movement of a chromosomal segment to another
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Genomic imprinting
Def: a parental effect on gene expression
Identical alleles may have different effects on offspring, depending on whether they arrive in the zygote via the ovum or via the sperm.
Fragile X syndrome: higher prevalence of disorder and retardation in males (partially caused by maternal imprint)
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Mitochondrial DNA
Small circular DNA located in mitochondria
Inherited from the mother (maternally)
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