chapter 15 the chromosomal basis of inheritance. fig. 15-2b 0.5 mm meiosis metaphase i anaphase i...
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Chapter 15
The Chromosomal Basis of Inheritance
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Fig. 15-2b
0.5 mm
Meiosis
Metaphase I
Anaphase I
Metaphase II
Gametes
LAW OF SEGREGATIONThe two alleles for each gene separate during gamete formation.
LAW OF INDEPENDENTASSORTMENT Alleles of genes on nonhomologous chromosomes assort independently during gamete formation.
14
yr 1 4Yr1
4 YR
3 3
F1 Generation
14
yR
R
R
R
R
RR
R
R R R R
R
Y
Y
Y Y
Y
YY
Y
YY
YY
yr r
rr
r r
rr
r r r r
y
y
y
y
y
y y
yyyy
All F1 plants produceyellow-round seeds (YyRr)
1
2 2
1
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Fig. 15-3
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EXPERIMENT
PGeneration
GenerationF1 All offspring
had red eyes
RESULTS
GenerationF2
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Fig. 15-4c
EggsF1
CONCLUSION
Generation
Generation
P XX
w
Sperm
XY
+
+
++ +
Eggs
Sperm+
++ +
+
GenerationF2
w
w
w
ww
w
w
w
ww
w
w
w
ww
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Fig. 15-7
(a) (b) (c)
XNXN XnY XNXn XNY XNXn XnY
YXnSpermYXNSpermYXnSperm
XNXnEggs XN
XN XNXn
XNY
XNY
Eggs XN
Xn
XNXN
XnXN
XNY
XnY
Eggs XN
Xn
XNXn
XnXn
XNY
XnY
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X Inactivation in Female Mammals
• In mammalian females, one of the two X chromosomes in each cell is randomly inactivated during embryonic development
• The inactive X condenses into a Barr body• If a female is heterozygous for a particular
gene located on the X chromosome, she will be a mosaic for that character
Copyright © 2008 Pearson Education Inc., publishing as Pearson Benjamin Cummings
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Fig. 15-8X chromosomes
Early embryo:
Allele fororange fur
Allele forblack fur
Cell division andX chromosomeinactivationTwo cell
populationsin adult cat:
Active XActive X
Inactive X
Black fur Orange fur
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Fig. 15-UN1
b+ vg+
Parents in testcross
Most offspring
b+ vg+
b vg
b vg
b vg
b vg
b vg
b vg
or
How Linkage Affects Inheritance
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Fig. 15-9-4
EXPERIMENTP Generation (homozygous)
RESULTS
Wild type(gray body,normal wings)
Double mutant(black body,vestigial wings)
b b vg vg
b b vg vg
Double mutantTESTCROSS
b+ b+ vg+ vg+
F1 dihybrid(wild type)
b+ b vg+ vg
Testcrossoffspring Eggs b+ vg+ b vg b+ vg b vg+
Black-normal
Gray-vestigial
Black-vestigial
Wild type(gray-normal)
b vg
Sperm
b+ b vg+ vg b b vg vg b+ b vg vg b b vg+ vgPREDICTED RATIOS
If genes are located on different chromosomes:
If genes are located on the same chromosome andparental alleles are always inherited together:
1
1
1
1
1 1
0 0
965 944 206 185
:
:
:
:
:
:
:
:
:
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Recombination of Linked Genes: Crossing Over
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Fig. 15-10aTestcrossparents
Replicationof chromo-somes
Gray body, normal wings(F1 dihybrid)
Black body, vestigial wings(double mutant)
Replicationof chromo-somes
b+ vg+
b+ vg+
b+ vg+
b vg
b vg
b vg
b vg
b vg
b vg
b vg
b vg
b vg
b+ vg+
b+ vg
b vg+
b vg
Recombinantchromosomes
Meiosis I and II
Meiosis I
Meiosis II
Eggs Sperm
b+ vg+ b vg b+ vg b vgb vg+
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Fig. 15-10b
Testcrossoffspring
965Wild type
(gray-normal)
944Black-
vestigial
206Gray-
vestigial
185Black-normal
b+ vg+
b vg b vg
b vg b+ vg
b vg
b vg
b+ vg+
Spermb vg
Parental-type offspring Recombinant offspring
Recombinationfrequency =
391 recombinants2,300 total offspring
100 = 17%
b vg
b+ vg b vg+
b vg+
Eggs
Recombinantchromosomes
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Fig. 15-11
Recombinationfrequencies
Chromosome
9% 9.5%
17%
b cn vg
Cytogenetic maps
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Fig. 15-12
Mutant phenotypes
Shortaristae
Blackbody
Cinnabareyes
Vestigialwings
Browneyes
Redeyes
Normalwings
Redeyes
Graybody
Long aristae(appendageson head)
Wild-type phenotypes
0 48.5 57.5 67.0 104.5
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Concept 15.4: Alterations of chromosome number or structure cause some genetic
disorders
– spontaneous abortions (miscarriages)
developmental disorders• Abnormal Chromosome Number: nondisj
unction: Aneuploidy and Polyploidy
• Alterations of Chromosome Structure
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Fig. 15-13-1
Meiosis I
(a) Nondisjunction of homologous chromosomes in meiosis I
(b) Nondisjunction of sister chromatids in meiosis II
Nondisjunction
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Fig. 15-13-2
Meiosis I
Nondisjunction
(a) Nondisjunction of homologous chromosomes in meiosis I
(b) Nondisjunction of sister chromatids in meiosis II
Meiosis II
Nondisjunction
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Fig. 15-13-3
Meiosis I
Nondisjunction
(a) Nondisjunction of homologous chromosomes in meiosis I
(b) Nondisjunction of sister chromatids in meiosis II
Meiosis II
Nondisjunction
Gametes
Number of chromosomes
n + 1 n + 1 n + 1n – 1 n – 1 n – 1 n n
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• Aneuploidy results from the fertilization of gametes in which nondisjunction occurred
• Offspring with this condition have an abnormal number of a particular chromosome– A monosomic zygote has only one copy of
a particular chromosome
– A trisomic zygote has three copies of a particular chromosome
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• Polyploidy is a condition in which an organism has more than two complete sets of chromosomes– Triploidy (3n) is three sets of chromosomes– Tetraploidy (4n) is four sets of chromosomes
• Polyploidy is common in plants, but not animals
• Polyploids are more normal in appearance than aneuploids
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Alterations of Chromosome Structure
• Breakage of a chromosome can lead to four types of changes in chromosome structure:– Deletion removes a chromosomal segment– Duplication repeats a segment– Inversion reverses a segment within a
chromosome– Translocation moves a segment from one
chromosome to another
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Fig. 15-15
DeletionA B C D E F G H A B C E F G H(a)
(b)
(c)
(d)
Duplication
Inversion
Reciprocaltranslocation
A B C D E F G H
A B C D E F G H
A B C D E F G H
A B C B C D E F G H
A D C B E F G H
M N O C D E F G H
M N O P Q R A B P Q R
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Human Disorders Due to Chromosomal Alterations
• Alterations of chromosome number and structure are associated with some serious disorders
• Some types of aneuploidy appear to upset the genetic balance less than others, resulting in individuals surviving to birth and beyond
• These surviving individuals have a set of symptoms, or syndrome, characteristic of the type of aneuploidy
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Down Syndrome (Trisomy 21)
• Down syndrome is an aneuploid condition that results from three copies of chromosome 21
• It affects about one out of every 700 children born in the United States
• The frequency of Down syndrome increases with the age of the mother, a correlation that has not been explained
Copyright © 2008 Pearson Education Inc., publishing as Pearson Benjamin Cummings
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Fig. 15-16
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Aneuploidy of Sex Chromosomes
• Nondisjunction of sex chromosomes produces a variety of aneuploid conditions
• Klinefelter syndrome is the result of an extra chromosome in a male, producing XXY individuals
• Monosomy X, called Turner syndrome, produces X0 females, who are sterile; it is the only known viable monosomy in humans
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Disorders Caused by Structurally Altered Chromosomes
• The syndrome cri du chat (“cry of the cat”), results from a specific deletion in chromosome 5
• Certain cancers, including chronic myelogenous leukemia (CML), are caused by translocations of chromosomes
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Fig. 15-17
Normal chromosome 9
Normal chromosome 22
Reciprocaltranslocation Translocated chromosome 9
Translocated chromosome 22(Philadelphia chromosome)
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Concept 15.5: Some inheritance patterns are exceptions to the standard chromosome theory• There are two normal exceptions to
Mendelian genetics• One exception involves genes located in
the nucleus, and the other exception involves genes located outside the nucleus
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Genomic Imprinting
• For a few mammalian traits, the phenotype depends on which parent passed along the alleles for those traits
• Such variation in phenotype is called genomic imprinting
• Genomic imprinting involves the silencing of certain genes that are “stamped” with an imprint during gamete production
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Fig. 15-18a
Normal Igf2 alleleis expressed
Paternalchromosome
Maternalchromosome
(a) Homozygote
Wild-type mouse(normal size)
Normal Igf2 alleleis not expressed
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Fig. 15-18b
Mutant Igf2 alleleinherited from mother
Mutant Igf2 alleleinherited from father
Normal size mouse(wild type)
Dwarf mouse(mutant)
Normal Igf2 alleleis expressed
Mutant Igf2 alleleis expressed
Mutant Igf2 alleleis not expressed
Normal Igf2 alleleis not expressed
(b) Heterozygotes
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• It appears that imprinting is the result of the methylation (addition of –CH3) of DNA
• Genomic imprinting is thought to affect only a small fraction of mammalian genes
• Most imprinted genes are critical for embryonic development
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Inheritance of Organelle Genes
• Extranuclear genes (or cytoplasmic genes) are genes found in organelles in the cytoplasm
• Mitochondria, chloroplasts, and other plant plastids carry small circular DNA molecules
• Extranuclear genes are inherited maternally because the zygote’s cytoplasm comes from the egg
• The first evidence of extranuclear genes came from studies on the inheritance of yellow or white patches on leaves of an otherwise green plant
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Fig. 15-19
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• Some defects in mitochondrial genes prevent cells from making enough ATP and result in diseases that affect the muscular and nervous systems – For example, mitochondrial myopathy and Leb
er’s hereditary optic neuropathy
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You should now be able to:1. Explain how meiosis accounts for recombinan
t phenotypes
2. Explain how linkage maps are constructed
3. Explain how nondisjunction can lead to aneuploidy
4. Define trisomy, triploidy, and polyploidy
5. Distinguish among deletions, duplications, inversions, and translocations
6. Explain genomic imprinting
7. Explain why extranuclear genes are not inherited in a Mendelian fashion