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Chapter 10
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10.1 The Chromosome Theory of Heredity
Chromosomes are located in the nucleus Factors (genes) are found on chromosomes Sutton discovered that genes are on chromosomes in 1902
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Chromosome Theory of Heredity
States that genes are located on chromosomes and each gene occupies a specific place on a chromosome Only one allele is on a chromosome
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Independent Assortment
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Gene Linkage Genes on a chromosome are linked together
Inherited together – THEREFORE they do not undergo independent assortment
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Linked Genes- genes on the same chromosome – inherited as a package
Height Gene A Flower color gene B Flower position gene C
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Thomas Hunt Morgan Studied fruit flies – Drosophilia melanogaster
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Fruit Flies are excellent for genetic studies because:
Reproduce quickly Easy to raise Many mutations Have 8 chromosomes (n=4)
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Fruit Fly Mutations
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Thomas Hunt Morgan began to carry out experiments with
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Morgan looked at TWO traits
Gray bodies – G Normal Wings - W Black bodies – g Small wings – w
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The flies mated….
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The female laid eggs
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GGWW ggww P1 x F1 GgWw 100%
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Morgan then mated the F1 back to the recessive parent
GgWw x ggww Expected ratio – 1:1:1:1 25% GgWw % Ggww 25% ggWw % ggww
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Morgan’s Actual Results
41.5% gray normal 41.5% black small 8.5 % black normal 8.5% gray small
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Conclusion Gene for body size and wing color were somehow connected or linked Can’t undergo independent assortment
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Linkage Groups Package of genes that are always inherited together
Chromosome One linkage group for each homologous pair Fruit flies – 4 linkage groups Humans – 23 linkage groups Corn – 10 linkage groups
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So linkage groups explain the high percentages (41.5%) but
What about the 8.5%??????
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The combinations that were expected would be:
17% had new combinations The combinations that were expected would be: Gray normal – GW or Black small - gw
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P1 G G g g W W w w Dad Mom
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F1 G g W w
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g G g g W w w w F1 F1 F1 X Recessive Fruit Fly Heterozygous
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The Offspring of the Cross
and W w w w F1 F1 41.5 % 41.5 %
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Genes of the Heterozygous Parent
W W w w The homologous pair copied
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The homolgous pairs pair up in Prophase and form a tetrad
W W w w
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When they are lined up they can become twisted and switch genes
Crossing Over
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So you could then have ….. G G g g W w W w switch
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The other offspring of the cross
and w w W w F1 F1 8.5 % 8.5 %
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The 17% that had new combinations are known as
Recombinants – individuals with new combinations of genes Crossing Over – gives rise to new combinations – Prophase I
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Gene Mapping Sturtevant – associate of Morgan
Crossing over occurs at random The distance between two genes determines how often they cross over Genes that are close do not crossover often Genes that are far apart – cross over often
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So…… If you know the frequency with which crossing over occurs then you can use that to map the position of the genes on the chromosome
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Frequency of crossover exchange...
is GREATER the FARTHER apart 2 genes are is proportional to relative distance between 2 linked genes Relative distance is established as... 1% crossover frequency = 1 map unit of map distance 1% CrossOver Freq = 1 centiMorgan
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Sex Linkage Stevens – made observations of meal worm chromosomes
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Sex Chromosomes One pair Female – XX Male – XY
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Autosomes All the chromosomes except the sex chromosomes
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Sex Determination
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Genes on Sex Chromosomes
Sex chromosomes determine a person’s sex Sex chromosomes also contain genes
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Sex Linked A gene located on a sex chromosome Usually X
Example – Fruit Fly Eye Color So the gene for eye color is on the X chromosome and not the Y
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Fruit Fly Sex Chromosomes
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Females Males XRY XrY XRXR XRXr XrXr Red Eyed White Eyed
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Mutations
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A change in the DNA of an organism
Can involve an entire chromosome or a single DNA nucleotide and they may take place in any cell
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Germ Cell Mutation Occur in an organism’s germ cells (gametes)- can only affect offpsring
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Somatic Mutations Take place in an organisms body cells and can affect the organism
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Lethal Mutation Cause death, often before birth
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Good Mutations Some mutations can be beneficial – these organisms have a better chance to reproduce and therefore have an evolutionary advantage Provide the variation on which natural selection acts
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Chromosome Mutations
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Are either changes in the structure of a chromosome or the loss of an entire chromosome or an addition Four Types (duplication, deletion, inversion and translocation)
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Duplication – segment of a chromosome is repeated
Deletion – the loss of a chromosome or part due to chromosomal breakage – that information is lost
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Inversion – a chromosomal segment breaks off and then reattached in reverse orientation to the same chromosome Translocation – a chromosome breaks off and reattaches to another nonhomologous chromosome
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Nondisjunction Some chromosome mutations alter the number of chromosomes found in a cell Nondisjunction – the failure of a chromosome to separate from its homologue during meiosis
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Gene Mutations
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May involve large segments of DNA or a single nucleotide within a codon
Involve individual genes
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Point Mutations – 3 types
The substitution, addition or removal of a single nucleotide Substitution – a point mutation where one nucleotide in a codon is replaced with a different nucleotide, resulting in a new codon Ex. Sickle Cell Anemia – sub. Of A for T in a single codon
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2 & 3. Insertion and Deletions – one or more nucleotides is lost or added – have more serious effects
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Frameshift Mutation When a nucleotide is lost or added so that the remaining codons are grouped incorrectly Insertions and deletions are frameshift mutations
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THE FAT CAT ATE THE RAT
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Polyploidy Condition in which an organism has an extra set of chromosomes 3N, 4N Usually fatal in animals Plants – usually more robust Caused by - Nondisjunction
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10-3 Regulation of Gene Expression
As biologists have intensified their studies of gene activity, it has become clear that interactions between different genes and between genes and their environment are critically important
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Gene Interactions Gene – piece of DNA – DNA codes for proteins
In many cases the dominant allele codes for a protein that works and the recessive allele codes for a protein that does not work
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Incomplete Dominance When offspring have a phenotype that is in-between the two parents Occurs when two or more alleles influence the phenotype Example – flowers – four o’ clocks, snapdragons Alleles – R/R’, R/r, R/W, FR F r
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Red Flower
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White Flower
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Pink Flower Red mixed with white makes pink
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Incomplete Dominance Example #2
Incomplete dominance is a half way between point. Halfway to dark blue is light blue.
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Incomplete Dominance is not a blending.
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RR rr Rr
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Phenotypic Ratio: 1:2:1 Genotypic Ratio: 1:2:1
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Codominace Occurs when both alleles for a gene are expressed in a heterozygous offspring Neither allele is dominant or recessive Example – horse coat color
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Horse Coat Color Red – HR HR White – HWHW Roan – HR HW
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Roan – red and white hairs
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Blue roan - The coat has white hairs and blue hairs
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Polygenic Inheritance
Traits controlled by two or more genes Examples – height, skin color, coat patterns Phenotypes are seen in a range
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Polygenic Inheritance
AB Ab aB ab AABB AABb AaBB AaBb AAbb Aabb aaBB aaBb aabb
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Gene Expression in Prokaryotes
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Genes serve as a pattern for the production of mRNA
mRNA serves as the instructions to make a protein All the genes of an organism can’t be active all the time
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When a cell needs a product it must be able to make it fast
When the product of a gene is being made we say the gene is being expressed
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Genes are: Rarely expressed Constantly expressed Turn on and off
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The Operon
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Genes that work together are clustered together
Some genes in the cluster do not code for proteins instead they are involved in regulation and expression
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Operon Genes that work together Operator Promotor
There is slight overlap between the operator and the promotor
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Inducer Molecule that causes the production of a protein
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To Make a Protein RNA polymerase must attach to the promoter (“Start here”) Moves along to the genes mRNA
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The Repressor Special protein
Attaches itself to the RNA between the promotor and the genes Does not let RNA polymerase make a protein Turns off genes
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Each repressor has a special shape that allows it to attach to a specific piece of RNA
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Gene Activation When an inducer enters a cell it binds to the repressor The repressor changes shape and can no longer bond RNA polymerase can then attach
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Proteins eats up the inducer repressor attaches again
Ex. Lactose – sugar – food for bacteria
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Gene Expression in Eukaryotes
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More complex than Eukaryotes
More DNA in a nucleus 1976 – Sharp and Berget Discovered mRNA produced during transcription may be altered before it is used to make a protein
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DNA mRNA not an exact copy as was thought – not complementary
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Exons Sequences that code for a protein Expressed sequences
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Introns Segments that do not code for a protein Intervening sequences
IN the way
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