Biology 112 Chromosomal Basis of Inheritance. Locating Genes Along Chromosomes Mendel’s...
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![Page 1: Biology 112 Chromosomal Basis of Inheritance. Locating Genes Along Chromosomes Mendel’s “hereditary factors” were genes, though this wasn’t known during.](https://reader036.fdocuments.in/reader036/viewer/2022062407/56649cda5503460f949a41e0/html5/thumbnails/1.jpg)
Biology 112
Chromosomal Basis of Inheritance
![Page 2: Biology 112 Chromosomal Basis of Inheritance. Locating Genes Along Chromosomes Mendel’s “hereditary factors” were genes, though this wasn’t known during.](https://reader036.fdocuments.in/reader036/viewer/2022062407/56649cda5503460f949a41e0/html5/thumbnails/2.jpg)
Locating Genes Along ChromosomesMendel’s “hereditary factors” were genes,
though this wasn’t known during his timeToday know that genes are located on
chromosomesThe location of a particular gene can be
seen by tagging isolated chromosomes with a fluorescent dye that highlights the gene
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Mendelian inheritance has its physical basis in the behavior of chromosomes
The chromosome theory of inheritance states:Mendelian genes have specific loci (positions) on
chromosomes
Chromosomes undergo segregation and independent assortment
The behavior of chromosomes during meiosis can be said to account for Mendel’s laws of segregation and independent assortment
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Fig. 15-2P Generation Yellow-round
seeds (YYRR)
Y
F1 Generation
Y
R R
R Y
r
r
r
y
y
y
Meiosis
Fertilization
Gametes
Green-wrinkledseeds ( yyrr)
All F1 plants produceyellow-round seeds (YyRr)
R R
YY
r ry y
Meiosis
R R
Y Y
r r
y y
Metaphase I
Y Y
R Rrr
y y
Anaphase I
r r
y Y
Metaphase IIR
Y
R
y
yyy
RR
YY
rrrr
yYY
R R
yRYryrYR1/41/4
1/41/4
F2 Generation
Gametes
An F1 F1 cross-fertilization
9 : 3 : 3 : 1
LAW OF INDEPENDENTASSORTMENT Alleles of geneson nonhomologouschromosomes assortindependently during gameteformation.
LAW OF SEGREGATIONThe two alleles for each geneseparate during gameteformation.
1
2
33
2
1
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Thomas Hunt MorganDrosophila melanogaster
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Morgan’s Experimental EvidenceThe first solid evidence associating a specific
gene with a specific chromosome came from Thomas Hunt Morgan
Morgan’s experiments with fruit flies provided convincing evidence that chromosomes are the location of Mendel’s heritable factors
Several characteristics make fruit flies a convenient organism for genetic studies: They breed at a high rate A generation can be bred every two weeksThey have only four pairs of chromosomes
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Morgan noted wild type, or normal, phenotypes that were common in the fly populations
Traits alternative to the wild type are called mutant phenotypes
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Sex-Linked Genes
Sex-Linked genes: Genes located on sex chromosomes.This term is commonly applied to genes on the X
chromosome
In one experiment, Morgan mated male flies with white eyes (mutant) with female flies with red eyes (wild type)The F1 generation all had red eyesThe F2 generation showed the 3:1 red:white eye ratio,
but only males had white eyes
Morgan determined that the white-eyed mutant allele must be located on the X chromosome
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Fig. 15-4
PGeneration
Generation
Generation
Generation
Generation
Generation
F1
F2
All offspring had red eyes
Sperm
EggsF1
F2
P
Sperm
Eggs
XX
XY
CONCLUSION
EXPERIMENT
RESULTS
w
w
w
w
ww
w w
+
+
++ +
w
ww w
w
w
w
ww
+
+
+
+ +
+
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Each chromosome has hundreds or thousands of genes
Genes located on the same chromosome that tend to be inherited together are called linked genes
Linked genes tend to be inherited together because they are located near each other on the same chromosome
Linked genes
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Linkage Affects Inheritance
Morgan did some experiments with fruit flies to see how linkage affects inheritance of two characters
Morgan crossed flies that differed in traits of body color and wing size
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Morgan found that body color and wing size are usually inherited together in specific combinations (parental phenotypes)
He noted that these genes do not assort independently, and reasoned that they were on the same chromosome
However, nonparental phenotypes were also produced
Genetic recombinationoccured: the production of offspring with combinations of traits differing from either parent
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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
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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+ vg
PREDICTED 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 Unlinked Genes: Independent Assortment of Chromosomes
Mendel observed that combinations of traits in some offspring differ from either parent
Offspring with a phenotype matching one of the parental phenotypes are called parental types
Offspring with nonparental phenotypes (new combinations of traits) are called recombinant types, or recombinants
A 50% frequency of recombination is observed for any two genes on different chromosomes
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Recombination of Linked Genes: Crossing Over
Morgan discovered that genes can be linked, but the linkage was incomplete, as evident from recombinant phenotypes
Morgan proposed that some process must sometimes break the physical connection between genes on the same chromosome
That mechanism was the crossing over of homologous chromosomes
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Fig. 15-10Testcrossparents
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 vgb vg
b vg
b+ vg+
b+ vg
b vg+
b vg
Recombinantchromosomes
Meiosis I and II
Meiosis I
Meiosis II
b vg+b+ vgb vgb+ vg+
Eggs
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+
Sperm
b vg
Parental-type offspringRecombinant offspring
Recombinationfrequency =
391 recombinants2,300 total offspring
100 = 17%
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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 offspringRecombinant offspring
Recombinationfrequency =
391 recombinants2,300 total offspring
100 = 17%
b vg
b+ vg b vg+
b vg+
Eggs
Recombinantchromosomes
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Mapping the Distance Between Genes Using Recombination Data
Genetic map, an ordered list of the genetic loci along a particular chromosome
The farther apart two genes are, the higher the probability that a crossover will occur between them and therefore the higher the recombination frequency
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A linkage map is a genetic map of a chromosome based on recombination frequencies
Distances between genes can be expressed as map units; one map unit, or centimorgan, represents a 1% recombination frequency
Map units indicate relative distance and order, not precise locations of genes
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Fig. 15-11
RESULTS
Recombinationfrequencies
Chromosome9% 9.5%
17%
b cn vg
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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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Genes that are far apart on the same chromosome can have a recombination frequency near 50%
Such genes are physically linked, but genetically unlinked, and behave as if found on different chromosomes
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Using methods like chromosomal banding, geneticists can develop cytogenetic maps of chromosomes
Cytogenetic maps indicate the positions of genes with respect to chromosomal features
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Sex systems in animals
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Fig. 15-6
44 + XY Parents 44 +
XX
22 + X
22 +X
22 + Yor +
44 + XX or
Sperm Egg
44 + XY
Zygotes (offspring)
(a) The X-Y system
22 + XX
22 + X
(b) The X-0 system
76 + ZW
76 + ZZ
(c) The Z-W system
32(Diploid)
16(Haploid)
(d) The haplo-diploid system
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Inheritance of Sex-Linked Genes
The sex chromosomes have genes for many characters unrelated to sex
A gene located on either sex chromosome is called a sex-linked gene
In humans, sex-linked usually refers to a gene on the larger X chromosome
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Sex-linked genes follow specific patterns of inheritance
For a recessive sex-linked trait to be expressedA female needs two copies of the alleleA male needs only one copy of the allele
Sex-linked recessive disorders are much more common in males than in females
Some disorders caused by recessive alleles on the X chromosome in humans:Color blindnessDuchenne muscular dystrophyHemophilia
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Fig. 15-7
(a) (b) (c)
XNXN XnY XNXn XNY XNXn XnY
YXnSpermYXNSpermYXnSperm
XNXnEggsXN
XN XNXn
XNY
XNY
EggsXN
Xn
XNXN
XnXN
XNY
XnY
EggsXN
Xn
XNXn
XnXn
XNY
XnY
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Some disorders caused by recessive alleles on the X chromosome in humans:Color blindnessDuchenne muscular dystrophyHemophilia
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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
DNA Methylation is the mechanism for X-inactivation(methyl groups added to cytosine nucleotide in the
DNA molecule)
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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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Chromosomal AlterationsLarge-scale chromosomal alterations often lead
to spontaneous abortions (miscarriages) or cause a variety of developmental disorders…bad news!
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Abnormal Chromosome Number
In nondisjunction, pairs of homologous chromosomes do not separate normally during meiosis
As a result, one gamete receives two of the same type of chromosome, and another gamete receives no copy
Nondisjunction can also occur in mitosis
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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
Nondisjunction video
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Aneuploidy
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
Polyploidy is a condition in which an organism has more than two complete sets of chromosomesTriploidy (3n) is three sets of chromosomesTetraploidy (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 segmentInversion 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.
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Aneuploidy of Sex Chromosomes
Nondisjunction of sex chromosomes produces a variety of aneuploid conditions
MalesKlinefelter syndrome is the result of an extra
chromosome in a male, producing sterile XXY individuals (1 in 2000 births?)
Extra Y (XYY)…apparently normal males (1 in 1000 births?)
FemalesMonosomy X, called Turner syndrome, produces
X0 females, who are sterile; it is the only known viable monosomy in humans (1 in 5000 births?)
Triple X Syndrome (XXX)…apparently normal females (1 in 1000 births?)
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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 productionCauses certain genes to be differently expressed in
the offspring depending upon whether the alleles were inherited from the ovum or from the sperm cell.
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Triplet Repeats
Fragile-X syndrome (CGG)
Huntington’s disease (CAG)
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Extranuclear Genes
Extranuclear genes (or cytoplasmic genes) are genes found in organelles in the cytoplasm
Mitochondria, chloroplasts carry small circular DNA molecules
Extranuclear genes are inherited maternally because the zygote’s cytoplasm comes from the egg