Welcome What is a dihybrid cross?. Agenda Quiz Sex Linked Traits Mutations.

Slides:



Advertisements
Similar presentations
Question of the Day 5-17 What are chromosomes composed of?
Advertisements

Chapter 12 Table of Contents Section 1 Chromosomes and Inheritance
Linkage, Sex linkage, Pedigrees. Linked genes We know two traits should assort independently. Why? So, offspring phenotype ratios should be: –9:3:3:1.
Chapter 15~ The Chromosomal Basis of Inheritance
Chapter 15: The Chromosomal Basis of Inheritance
Sex-Linked Genes and Pedigrees. Linked Genes Some genes are linked because they are on the SAME chromosome. A chromosome is a set of linked genes. Remember:
Chromosomes and Inheritance
Chapter 12-1 Chromosomes and Inheritance patterns
The Chromosomal Basis of Inheritance
The Chromosomal Basis of Inheritance Connecting Mendel's Work to Chromosomes.
1 2 Gregor Mendel 3 Vocabulary 4 Pisum sativum.
Genetics Chapters 9 and 12.
Chapter 12-Inheritance Patterns and Human Genetics
Inheritance Patterns & Human Genetics
The Chromosomal Basis of Inheritance Chapter 15. Review Mitosis Meiosis Chromosome Genotype and Phenotype Mendelian Genetics.
Inheritance & Human Genetic Patterns
Human Genetics Unit.
Human Heredity. Human Chromosomes Humans have 46 total chromosomes Two Categories –Autosomes- first 22 pairs –Sex Chromosomes- 23rd pair, determine sex.
The Chromosomal Basis of Inheritance Chapter 15. The importance of chromosomes In 1902, the chromosomal theory of inheritance began to take form, stating:
Inheritance Patterns and Human Genetics. Sex Chromosomes and Autosomes Sex Chromosomes contain genes that determine the gender of an individual. Many.
Chapter 15: The Chromosomal Basis of Inheritance.
Let’s think about it… What are autosomes? What are sex chromosomes?
Chromosomal Basis of Inheritance Featuring fruit fly: Drosophila Melanogaster.
Humans have 23 pairs of chromosomes. One pair of chromosomes is related to the sex of an individual, these chromosomes are called sex chromosomes.
Cross a homozygous dominant green plant with a heterozygous green plant. What are the genotypic and phenotypic ratios. Agenda for Tuesday Jan 3 rd 1.Test.
What’s the difference between a phenotype and a genotype? Agenda for Friday Jan 30 th 1.Go over HW (Dihybrid) 2.Incomplete and codominance.
Cross a homozygous dominant green plant with a heterozygous green plant. What are the genotypic and phenotypic ratios. Agenda for Monday April 11 th 1.
How to Use This Presentation
The Chromosomal Basis of Inheritance Chapter 15. The Chromosomal Theory of Inheritance chromosomes and genes are present as pairs in diploid cells homologous.
 IN  What are the probabilities of a monohybrid cross between two heterozygous parents?  Flower color R=redr=white.
CHAPTER 12 SEX-LINKED TRAITS
Chapter 15 notes The Chromosomal Basis of Inheritance.
Chromosomes and Heredity. When Gregor Mendel formulated his laws of inheritance of traits, he did not know about meiosis or the existence of chromosomes.
Chapter 12 Inheritance Patterns and Human Genetics.
Vocabulary Review Chapter 14 & 15. Mendel’s true breeding generation P or parental generation.
1/14/15 Objective: How do sex-linked genes produce different inheritance patterns in males and females? Do Now: Take out assigned homework.
Chapter 10.
Genetic Linkage Chapter 11, Section 5.
MUTATIONS pp , 231. MUTATION  A change in a genetic trait  Either 1) chromosomal or 2) gene mutation  Germ cell (gametes) or somatic cell (body)
Chapter 12 Inheritance Patterns and Human Genetics.
Chapter 12 Mutations, Xs, and Inheritance. Mutations= changes in organisms DNA Beneficial- lead to adaptations and aid evolution of a species Harmful-
Welcome What is a dihybrid cross?. Agenda Quiz Sex Linked Traits Mutations.
Chapter 12 Inheritance Patterns and Human Genetics.
Chapter 12 Objectives Distinguish between sex chromosomes and autosomes. Explain the role of sex chromosomes in sex determination. Describe how an X- or.
Chapter 15: The chromosomal basis of inheritance Chromosome Theory of inheritance Chromosome Theory of inheritance Genes have specific loci on chromosomes.
What was your favorite thing about winter break? What is a karyotype? What is the purpose of a karyotype?
Mutations Mutations – heritable changes in genetic information (changes to the DNA sequence) Two types - gene and chromosomal mutations Remember mutations.
Genes in Action Chapter 14. Sex Linked Traits Another way for traits to be passed on is by being sex linked Female Chromosomes: XX Male Chromosomes: Xy.
Pedigree Chart Symbols Male Female Person with trait.
Beyond Mendel… I.Mutations,Mutations II.Gene Linkage,Gene Linkage III.Gene-Mapping,Gene-Mapping IV.X-linked Traits,X-linked Traits V.Polygenic Traits,Polygenic.
Cross a homozygous dominant green plant with a heterozygous green plant. What are the genotypic and phenotypic ratios. Agenda for Monday April 11 th 1.
Copyright © by Holt, Rinehart and Winston. All rights reserved. ResourcesChapter menu To View the presentation as a slideshow with effects select “View”
Chromosomal Inheritance and Human Heredity. Human Chromosomes Karyotype – a picture of an organism’s chromosomes We take pictures during mitosis when.
Chapter 12: Inheritance Patterns and Human Genetics.
THOMAS MORGAN. Morgan’s DISCOVERY of LINKED GENES Characteristics of linked genes 1.WHEN GENES ARE CLOSE TOGETHER ON A CHROMOSOME THEY TEND TO BE INHERITED.
Inheritance Patterns and Human Genetics
Mutations.
12.1 Sex Linkage Thomas Hunt Morgan: Sex Determination:
Chapter 10.
Please pick up the notes, yeti sheet, and x-linked traits sheet.
Genetic Linkage Chapter 11, Section 5.
Chromosomes and inheritance.
Human Genetics Biology Waggy
Chapter 10.
what are autosomes? What are sex chromosomes?
Effects of Gene Location
Genetics – Types of Inheritance
12-4 Mutations, blood types and pedigrees
12-4 Mutations, blood types and pedigress
Gregor Mendel. Gregor Mendel Vocabulary Pisum sativum.
Presentation transcript:

Welcome What is a dihybrid cross?

Agenda Quiz Sex Linked Traits Mutations

Sex Determination Thomas Hunt Morgan – studied fruit flies in the early 1900’s

Sex Determination Observed that one pair of chromosomes was different between males and females –Large one named “X” chromosome –Smaller one named “Y” chromosome –XX = female; XY = male

XY XX X Y X X X X X Y Female XX Female XY Male XY Male 50% Female; 50% Male

Sex Linkage Sex Linkage: the presence of a gene on a sex chromosome (X or Y)

Sex Linkage X-linked genes: genes found on the X chromosome –X chromosome carries more genes Y-linked genes: genes found on the Y chromosome

Fruit Fly Eye Color Fruit flies normally have red eyes A few males have white eyes Red is dominant; white is recessive

Morgan’s Fruit Fly Experiments Red-eyed female (X R X R) x White-eyed male (X r Y) XRXR XRXR XrXr Y XRXrXRXr XRXrXRXr XRYXRYXRYXRY RESULTS: F 1 generation – all red-eyed

Morgan’s Fruit Fly Experiments Red-eyed female (X R X r) x Red-eyed male (X R Y) XRXR XrXr XRXR Y XRXRXRXR XRXrXRXr XRYXRYXrYXrY RESULTS: F 2 generation – 3 red-eyed and 1 white-eyed ** all white-eyed where males…why?

Morgan’s Conclusions Gene for eye color is carried on the X chromosome = eye color is an X-linked trait Y chromosome does not carry a gene for eye color Red-eyed = X R X R, X R X r, X R Y White-eyed = X r X r, X r Y

In humans colorblindness (b) is an example of a sex-linked recessive trait. A male with colorblindness marries a female who is not colorblind but carries the (b) allele. Using a Punnett square, determine the genotypic and phenotypic probabilities for their potential offspring.

In fruit flies red eye color (R) is dominant to white eyes (r). In a cross between two flies, 50% of the male and 50% of the female offspring had red eyes. The other half of the males and females had white eyes. What are the phenotype, and all possible genotypes, of the offspring?

Worksheet

Linkage Groups 2 or more genes that are on the same chromosome are “linked” Linked genes tend to be inherited together

More Fruit Fly Experiment Gray, long-winged (GGLL) x black, short-winged (ggll) F 1 generation = all heterozygous gray, long-winged (GgLl)

Morgan’s Fruit Fly Experiment Cross F 1 flies: GgLl x GgLl F 2 generation –If alleles on different chromosomes, they assort independently and get a 9:3:3:1 ratio –If alleles on same chromosome, get 3 gray, long- winged: 1 black, short-winged ratio –Morgan saw roughly the 3:1 ratio

Morgan’s Fruit Fly Experiment Unexpected results –Some gray, short-winged (Ggll) –Some black, long-winged (ggLl)

Morgan’s Fruit Fly Experiment How were these alleles separated? –Alleles were rearranged through crossing-over during meiosis Genes that are farther apart are more likely to be separated by crossovers

Chromosome Mapping Chromosome Map: diagram that shows the possible genes on a chromosome Made using crossing-over data

Chromosome Mapping The percentage of crossing-over between the genes for 2 traits is equal to the distance between them on a chromosome This distance is measured in map units

MUTATIONS

Mutations Mutation: change in DNA VIDEO

Mutations Germ-cell mutation: occurs in sex cells –Affect the offspring –Example – Down Syndrome Somatic mutation: occurs in body cells –Affect the individual –Example - Cancer

Possible Effects of Mutations Lethal mutations: cause death, often before birth Beneficial mutations: provide variation needed for evolution No effect

Chromosome Mutations Chromosome Mutations: a change in the chromosome structure or loss/addition of entire chromosome

Chromosome Mutations Deletion: loss of piece of chromosome due to breakage

Chromosome Mutations Deletion: loss of piece of chromosome due to breakage –Example – Cri du chat; deletion of part of chromosome 5

Chromosome Mutations Duplication: part of chromosome is duplicated/copied

Chromosome Mutations Duplication: part of chromosome is duplicated/copied –Example – Charcot-Marie Tooth Disease

Chromosome Mutations Inversion: piece breaks off and reattaches to SAME chromosome in wrong order

Chromosome Mutations Inversion: piece breaks off and reattaches to SAME chromosome in wrong order –Example – Hemophilia (this disorder is also X linked)

Chromosome Mutations Translocation: piece breaks off and reattaches to DIFFERENT chromosome

Chromosome Mutations Translocation: piece breaks off and reattaches to DIFFERENT chromosome –Example – Cancer

Chromosome Mutations Nondisjunction: chromosomes do not separate during meiosis

Chromosome Mutations Nondisjunction: chromosomes do not separate during meiosis –Example – trisomy, monosomy

Gene Mutations Gene Mutations: involve large segments of DNA (genes) or a single nucleotide –Causes possible changes in the amino acid sequence

Gene Mutations Point Mutation: substitution, addition, or deletion of a single nucleotide

Gene Mutations Point Mutation: substitution, addition, or deletion of a single nucleotide –Example – sickle cell anemia

Gene Mutations Frame Shift Mutation: occurs when the number of nucleotides inserted or deleted is not a multiple of 3