Title: Chromosomes:%20Vessels%20For%20The%20Genes
1ChromosomesVessels For The Genes
- Timothy G. Standish, Ph. D.
2Reasons Mendels Work Was Ignored
- There was no Physical element in which Mendels
inherited particles could be identified. - By the turn of the century, chromosomes had been
discovered (physical particles) and biologists
were better at math.
3ChromosomesThe Physical Basis of Inheritance
- 1866 Mendel published his work
- 1875 Mitosis was first described
- 1890s Meiosis was described
- 1900 Mendel's work was rediscovered
- 1902 Walter Sutton, Theodore Boveri and others
noted parallels between behavior of chromosomes
and alleles.
4Chromosomal Theory of Inheritance
- Genes have specific loci on chromosomes.
- Chromosomes undergo segregation (meiosis) and
independent assortment, - Thus alleles of genes are independently assorted.
5Chromosomal Theory of Inheritance
Telophase II
6Independent Assortment
As long as genes are on different chromosomes,
they will assort independently
7Two Genes On One Chromosome
Telophase II
As long as genes on the same chromosome are
located a long distance apart, they will assort
independently due to crossing over during
prophase I of meiosis
8Thomas Hunt Morgan
- First to associate a trait (gene) with a
chromosome. - Worked with fruit flies (Drosophila melanogaster)
- Why fruit flies?
- Short generation time ( 2 weeks)
- Survives and breeds well in the lab
- Very large chromosomes in some cells
- Many aspects of phenotype are genetically
controlled.
9Drosophila Mutations
10More Drosophila Mutations
Wild Type
ebony body ee
white eyes ww
11X Chromosome Human and Drosphila Genes Are Easy
To Find
- In humans and Drosophila, males are XY
- Thus males are haploid for the X chromosome
- Because of this, recessive genes on the X
chromosome show up far more commonly in male than
female phenotypes
12Morgans Discovery Of An X-Linked Drosophila Gene
A white-eyed male was discovered
13The Key To Morgans Discovery
- The key to Morgans discovery was the observation
that all the white eyed individuals in the F2
generation were males - Without this vital data on the association of
white eyes with being male, the gene for white
eyes could have been seen as a simple recessive
trait on an autosome - This illustrates the importance of recording all
the data possible and being alert to the
possibility of interesting things being present
in the data - Fate favors the prepared mind (Louis Pasture)
14Human X-linked Recessive Genes
- Brown enamel - Tooth enamel appears brown rather
than white - Hemophilia - Two types
- A - Classic hemophilia, deficiency of blood
clotting factor VIII - B - Christmas disease, deficincy of blood
clotting factor IX
15X-linked Recessive GenesRelated to sight
- Coloboma iridis - A fissure in the eyes iris
- Color Blindness - Two types
- Deutan - Decreased sensitivity to green light
- Protan - Decreased sensitivity to red light
- Congenital night blindness - Not due to a
deficency of vitimin A - Mocrophthalmia - Eyes fail to develop
- Optic atrophy - Degeneration of the optic nerves
16Royal Pedigree
Edward Duke of Kent (1767-1820)
Victoria Princess of Saxe-Coburg (1786-1861)
Albert of Saxe-Coburg (18XX-18XX)
Victoria Queen of England (1819-1910)
17Variation In Chromosome Number - Polyploidy
- Polyploid individuals have more than two sets of
chromosomes - Many important commercial plants are polyploid
- Roses
- Navel oranges
- Seedless watermelons
- Polyploid individuals usually result from some
sort of interruption during meiosis
18Variation In Chromosome Number - Aneuploidy
- Polyploid humans are unknown, but individuals
with extra individual chromosomes are known. - Having extra chromosomes or lacking some
chromosomes is called aneuploidy - Aneuploid individuals result from nondisjunction
during meiosis
19Aneuploidy In Humans
- Most human aneuploids spontaneously abort
- The most viable variations in chromosome number
are those that deal with the sex chromosomes - XO - Turners Syndrome - Phenotypically females
- XXX- Super females
- XYY - Super Males - On average tend to be
larger and less intelligent - XXY - Klinefelters Syndrome - Phenotypically
male - Of the non-sex chromosome aneuploidys, Downs
Syndrome, extra chromosome 21, tends to be the
most viable - Downs Syndrome is more common in children of
mothers who gave birth after age 40
20Gene Dosage
- There seem to be elegant mechanisms for
maintaining the correct dosage of genetic
material in each cell - When aneuploidy causes a change in the relative
dose of one chromosome, problems result
21The Lyon Hypothesis
- Having extra chromosomes causes problems (ie
Downs Syndrome) - Men have only one X chromosome and they are
normal (at least they think so) - Women have two X chomosomes and they are normal
- Mary Lyon proposed that the extra dosage of X
chromosome that women have is compensated for by
turning off one of the X chromosomes. - This turned off chromosome can be observed as a
Bar Body in metaphase female nuclei
22Consequences of X Chromosome Dosage Compensation
- Early during development, X chromosomes are
randomly turned off in female cells - All daughter cells have the same X chromosome
inactivated as their parental cell. - Thus, females are a mosaic of patches of cells
some patches expressing the genes on the paternal
X chromosome, other patches expressing the
maternal X chromosome
23Consequences of X Chromosome Dosage Compensation
At some pont (probably later than the 4 cell
stage) half the X chromosomes are turned off
Daughter cells inherit the mother cells
combination off and on X chromosomes
Because of dosage compensation, females are
thought to be a mosaic of patches of cells with
each patch expressing the same X chromosome, but
none expressing both chromosomes
Different patches of cells inherit different act
X chromosomes
24Why Calico Cats Are Usually Female
- Orange coat color is a sex-linked trait in cats
(it is on the X chromosome) - A female cat heterozygous for orange, has skin
patches expressing the orange X with the other X
chromosome turned off. In other patches the
opposite occurs.
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