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Genetics -the scientific study of inheritance inheritance- the process in which genetic material is passed from parents to their offspring.

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Presentation on theme: "Genetics -the scientific study of inheritance inheritance- the process in which genetic material is passed from parents to their offspring."— Presentation transcript:

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2 Genetics -the scientific study of inheritance inheritance- the process in which genetic material is passed from parents to their offspring

3 Gregor Mendel  Austrian monk- studied pea plants  Mathematical basis for experiments  Kept careful records of numbers  Studied simple traits (seed color, shape, flower color, height, etc.)

4 Monohybrid Cross  A cross between two parents that are identical in all but one characteristic. Example: cross a short pea plant and a tall pea plant Example: cross a short pea plant and a tall pea plant P is parent generation, P is parent generation, F1 is first filial generation, F1 is first filial generation, F2 is second filial generation F2 is second filial generation Result of cross: F1-all tall, F2-3 tall:1 short Result of cross: F1-all tall, F2-3 tall:1 short

5 Modern Genetics  Allele: Alternate forms of the same gene. Each trait has two alleles: Dominant: masks the effects of the recessive (ex. T) Dominant: masks the effects of the recessive (ex. T) Recessive: is masked by the dominant (ex. t) Recessive: is masked by the dominant (ex. t)

6 Modern Genetics cont’d  Gene Locus: the place on a homologous pair of chromosomes where the alleles occur, one on each chromosome.  Homozygous (true-breeding): Both copies of the allele are identical (TT or tt)  Heterozygous: Each copy of the allele is unique (Tt)

7 Genotype vs. Phenotype  Genotype: the alleles an individual receives at fertilization. TT is homozygous dominant, tt is homozygous recessive, and Tt is heterozygous.  Phenotype: refers to the physical characteristics of an individual. Homozygous dominant and heterozygous individuals both show the dominant phenotype (tall), while homozygous recessive shows the recessive phenotype (short).

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12 autosomal chromosomes sex chromosomes Classes of chromosomes

13  In humans & other mammals, there are 2 sex chromosomes: X & Y 2 X chromosomes 2 X chromosomes develop as a female: XXdevelop as a female: XX an X & Y chromosome an X & Y chromosome develop as a male: XYdevelop as a male: XY Genetics of Sex XY X X XX XY 50% female : 50% male XX

14 Sex-Linked Traits  Sex-linked traits are produced by genes only on the X chromosome.  They can be Dominant or Recessive.  A = dominant a = recessive  What would be the genotypes of a male and female that have a Sex- linked Dominant trait and do not express the trait?  Expresses Trait: Male - X A Y Female - X A X A or X A X a  No Expression: Male - X a Y Female - X a X a  What would be the genotypes of a male and female that have a Sex- linked Recessive trait and do not express the trait?  Expresses Trait: Male - X a Y Female - X a X a  No Expression: Male - X A Y Female - X A X A or X A X a (Carrier) (Carrier)  Most Sex-linked traits are Recessive!

15 Dihybrid Cross  A cross between two individuals that differ from each other in regards to two traits. Ex: pod color and pea color: GGYY and ggyy. Ex: pod color and pea color: GGYY and ggyy. F1 generation will be GgYy.F1 generation will be GgYy.

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17 Polygenic Inheritance  phenotype determined by combination effects of 2 or more genes at a different loci on different chromosomes.  Phenotypes usually found on a bell-shaped curve a bell-shaped curve human traits human traits skin colorskin color heightheight weightweight intelligenceintelligence behaviorsbehaviors

18  Multiple alleles- more than 2 forms of a gene controlling the expression of a trait Ex: Blood type: Ex: Blood type: In humans, 3 alleles: A,B,OIn humans, 3 alleles: A,B,O  Co-dominance- A pattern of inheritance in which the phenotypic effect of two alleles in a heterozygous genotype express each phenotype of each allele fully and equally; a phenotype which would not be expressed in any other genotypic combination. Ex: Checkered chickens have both white and black feathers. Ex: Checkered chickens have both white and black feathers.

19 Environmental Effects  Phenotype is controlled by both environment & genes Color of Hydrangea flowers is influenced by soil pH Human skin color is influenced by both genetics & environmental conditions Coat color in arctic fox influenced by heat sensitive alleles

20 What are Chromosomal Mutations? Damage to chromosomes due to physical or chemical disturbances or errors during meiosis.   Mutations might also be inherited from the sex cells of your parents. If you inherit a mutation from your parent, all of your DNA will be made with the mutation already in it.   The only way to inherit mutations from your parent is through sex cells – not through other types of cells. Ex: Skin cancer is not passed on to your kid.   Mutations may cause certain types of diseases or make you susceptible to certain types of diseases.  Two Types of Chromosome Mutations: 1. Chromosome Structure 2. Chromosome Number

21 Problems with Chromosome Structure: 2 main types of chromosome structure mutations: 1. Point mutation - A point mutation is a simple change in one base of the gene sequence. This is equivalent to changing one letter in a sentence. 2. Frameshift mutation- a change in the bases that causes the sequence to be read in different sets of codons. Equivalent to changing the spacing of the sentence.

22 Gene Mutations  Nonsense substitution- a change in 1 base that changes an amino acid to a stop codon  Silent substitution- a change in 1 base that does not cause a change in the amino acid produced  Silent substitution- a change in 1 base that does not cause a change in the amino acid produced OR a change in the DNA that causes a change in the protein, but not the function of the protein.  Missense substitution- a change in 1 base that changes the amino acid produced  Deletion- a deletion of a base  Insertion- an addition of a base

23 Chromosomal Mutations  translocation- a portion of a chromosome breaks off and attaches to a non-homologous chromosome  inversion- a portion of a chromosome breaks off and reattaches “upside down”  deletion- a portion of a chromosome breaks off  duplication- a portion of a chromosome is duplicated

24 Problems with Chromosome Number nondisjunction – members of homologous chromosomes do not move apart in Meiosis I or sister chromatids do not separate during Meiosis II leaves one cell with too few chromosomes and one cell with too many. monosomy – only one of a particular type of chromosome (2n -1) trisomy – having three of a particular type of chromosome (2n + 1) polyploidy – having more than two sets of chromosomes; triploids (3n = 3 of each type of chromosome), tetraploids (4n = 4 of each type of chromosome).

25 Biotechnology  -any procedure or methodology that uses biological systems or living organisms to develop or modify either products or processes for specific use.  Genetic engineering- a technology that includes the process of manipulating or altering the genetic material of a cell resulting in desirable functions or outcomes that would not occur naturally. genetically modified organism- an organism whose genetic material has been altered through some genetic engineering technology or technique. genetically modified organism- an organism whose genetic material has been altered through some genetic engineering technology or technique.

26  gene therapy- the intentional insertion, alteration, or deletion of genes within an individual’s cells and tissues for the purpose of treating a disease.  gene splicing- a type of gene recombination in which the DNA is intentionally broken and recombined using laboratory techniques  Cloning- a process in which a cell, cell product, or organism is copied from an original source DNA cloning- making exact copy of a DNA fragment DNA cloning- making exact copy of a DNA fragment Reproductive cloning- transfer of genetic material from the nucleus of a donor adult cell to an egg that has had its nucleus removed ; the embryo is an exact genetic copy of the donor organism. Reproductive cloning- transfer of genetic material from the nucleus of a donor adult cell to an egg that has had its nucleus removed ; the embryo is an exact genetic copy of the donor organism. Therapeutic cloning- using STEM cells for use in research Therapeutic cloning- using STEM cells for use in research STEM cells- undifferentiated cells; have not decided “what they want to be” when they “grow up”STEM cells- undifferentiated cells; have not decided “what they want to be” when they “grow up”


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