CONCEPT 4: APPLYING THE CHROMOSOMAL BASIS OF INHERITANCE TO ANALYSIS THE EFFECTS OF ALTERATIONS IN CHROMOSOME NUMBER OR STRUCTURE. Campbell: Chapter 15.

Slides:



Advertisements
Similar presentations
The Chromosomal Basis of Inheritance
Advertisements

CHAPTER 15.
Lecture #6 Date ________
THE CHROMOSOMAL BASIS OF INHERITANCE
Chromosomal Basis of Inheritance
Chapter 11 Mendel & The Gene Idea.
Concept 15.2: Sex-linked genes exhibit unique patterns of inheritance
Chapter 15~ The Chromosomal Basis of Inheritance
THE CHROMOSOMAL BASIS OF INHERITANCE
 Chapter 15~ The Chromosomal Basis of Inheritance.
Introduction to Human Genetics
Introduction to Human Genetics
The Chromosomal Basis of Inheritance Chapter 15. Review Mitosis Meiosis Chromosome Genotype and Phenotype Mendelian Genetics.
Chapter 15: Chromosomal Basis of Inheritance AP Biology.
AP Review Chapters
The Chromosomal Basis of Inheritance Chapter 15. The importance of chromosomes In 1902, the chromosomal theory of inheritance began to take form, stating:
Chapter 15. Chromosome Theory of Inheritance Chromosomes actually segregate (homologs) and assort (nonhomologous) in meiosis Compare with dihybrid cross.
AP Biology Test Return/Lab return/Study guide return Chapter 13-15
Copyright © 2008 Pearson Education, Inc., publishing as Pearson Benjamin Cummings PowerPoint ® Lecture Presentations for Biology Eighth Edition Neil Campbell.
Copyright © 2008 Pearson Education, Inc., publishing as Pearson Benjamin Cummings PowerPoint ® Lecture Presentations for Biology Eighth Edition Neil Campbell.
Chapter 15 notes The Chromosomal Basis of Inheritance.
Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings Chapter 15 Overview: Locating Genes on Chromosomes Genes – Are located on chromosomes.
Vocabulary Review Chapter 14 & 15. Mendel’s true breeding generation P or parental generation.
Chapter 15 Chromosomal Basis of Inheritance
Chromosomal Basis of Inheritance Chapter 15. Slide 2 of 36 Mendel & Chromosomes  Today we know that Mendel’s “hereditary factors” are located on chromosomes.
Chromosomal Basis of Inheritance Chapter 15. Genetic work done on fruit flies - takes little time to observe many generations. Thomas Morgan - fruit fly.
Chapter 15 The Chromosomal Basis of Inheritance. Concept 15.2: Sex-linked genes exhibit unique patterns of inheritance In humans and some other animals,
Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings PowerPoint Lectures for Biology, Seventh Edition Neil Campbell and Jane Reece.
Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings PowerPoint Lectures for Biology, Seventh Edition Neil Campbell and Jane Reece.
Chapter 15 The Chromosomal Basis of Inheritance. Fig The location of a particular gene can be seen by tagging isolated chromosomes with a fluorescent.
Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings Concept 15.1: Mendelian inheritance has its physical basis in the behavior of.
The Chromosomal Basis of Inheritance Chapter 15 Biology – Campbell Reece.
THE CHROMOSOMAL BASIS OF INHERITANCE CHAPTER 15. Warm up 1.What is the probability of the following? a.) Aabb X AaBb -> Aabb b.) AaBB X AaBb -> aaBB c.)
Introduction to Human Genetics But what happens when meiosis goes wrong? What when wrong? Happens meiosis wrong? When wrong? What meiosis goes wrong? Boehm.
Chapter 15: The chromosomal basis of inheritance Chromosome Theory of inheritance Chromosome Theory of inheritance Genes have specific loci on chromosomes.
Chapter 15 The Chromosomal Basis of Inheritance.
Slide 1 Chapter 15: The Chromosomal Basis of Inheritance.
Chapter 13 Raven & Johnson Chapter 15 Campbell Chromosomes & Inheritance.
4 Chapter 15~ The Chromosomal Basis of Inheritance.
CAMPBELL BIOLOGY IN FOCUS © 2014 Pearson Education, Inc. Urry Cain Wasserman Minorsky Jackson Reece Lecture Presentations by Kathleen Fitzpatrick and Nicole.
CAMPBELL BIOLOGY IN FOCUS © 2014 Pearson Education, Inc. Urry Cain Wasserman Minorsky Jackson Reece Lecture Presentations by Kathleen Fitzpatrick and Nicole.
Nondisjunction Alterations of Chromosomes Chapter 15 Section 4 Pgs Objective: I can predict how the number of chromosomes will change based off.
Chapter 15 The Chromosomal Basis of Inheritance
The Chromosomal Basis of Inheritance
Presentation of Genetics
Chromosomal Basis of Inheritance Lecture 13 Fall 2008
Human Genetics and Disorders
Human Genetics and Disorders
The chromosomal basis of inheritance
The Chromosomal Basis of Inheritance
Lecture #6 Date ________
Concept 15.3: Sex-linked genes exhibit unique patterns of inheritance
Chapter 15 Overview: Locating Genes Along Chromosomes.
The Chromosomal Basis of Inheritance
The Chromosomal Basis of Inheritance
The Chromosomal Basis of Inheritance
Chapter 15: The Chromosomal Basis of Inheritance
Genes and Chromosomes The behavior of chromosomes in meiosis and fertilization explains Mendel’s rules of inheritance. Genes on different chromosomes assort.
THE CHROMOSOMAL BASIS OF INHERITANCE
The Chromosomal Basis of Inheritance
The Chromosomal Basis of Inheritance
The Chromosomal Basis of Inheritance
Human Genetics and Disorders
The Chromosomal Basis of Inheritance
Chapter 12 Linkage Maps. Chapter 12 Linkage Maps.
Human Genetics and Disorders
The Chromosomal Basis of Inheritance
The Chromosomal Basis of Inheritance
Chapter 15: The Chromosomal Basis of Inheritance
Presentation transcript:

CONCEPT 4: APPLYING THE CHROMOSOMAL BASIS OF INHERITANCE TO ANALYSIS THE EFFECTS OF ALTERATIONS IN CHROMOSOME NUMBER OR STRUCTURE. Campbell: Chapter 15 Holtzclaw: pg 111 Please do the following activities on the student media (Chapter 15): - MP3 tutor: Chromosomal Basis of Inheritance - Activity: Polyploid Plants (relate to speciation (sympatric)!!)

But First… Linked Genes from last class… A blue fly with silver spots is mated with a wild type fly (grey, no spots) and all of the F1 generation are phenotypically wild (grey, no spots). The F1 fly is mated with a blue fly with silver spots (test cross) with the following results for the testcross offspring: 1025 wild type 1002 blue with silver spots 352 grey with silver spots 366 blue with no spots Are the genes for blue and silver spots linked? How do you know? If so, what is the recombination frequency for the genes for blue and silver spots?

But First… Linked Genes from last class… 1025 wild type PARENTAL TYPE 1002 blue with silver spots PARENTAL TYPE 352 grey with silver spots RECOMBINANT 366 blue with no spots RECOMBINANT Are the genes for blue and silver spots linked? YES How do you know? BECAUSE IF IT WAS TRUE INDEPENDENT ASSORTMENT, THE TEST CROSS OF A DOUBLE HETEROZYGOTE AND THE DOUBLE HOMOZYGOUS RECESSIVE WOULD HAVE PRODUCED A 1:1:1:1 RATIO However, the genes are not completely linked… in other words, since some recombinants exist… the chromosomes must have recombined via crossing over…

Video Clip

But First… Linked Genes from last class… 1025 wild type PARENTAL TYPE 1002 blue with silver spots PARENTAL TYPE 352 grey with silver spots RECOMBINANT 366 blue with no spots RECOMBINANT If so, what is the recombination frequency for the genes for blue and silver spots? Recombination frequency = #recombinants/total # of offspring = ( )/( ) = (731)/(2738) = This means that the genes recombine via crossing over 26.6% of the time!

Try This!  Genes A, B, and C are located on the same chromosome. Testcrosses show that the recombination frequency between A and B is 28% and between A and C is 12%. A’s in the middle! Can you determine the linear order of these genes are their relative distance from each other in map units?

Try This!  Genes A, B, and C are located on the same chromosome. Testcrosses show that the recombination frequency between A and B is 28% and between A and C is 12%. Can you determine the linear order of these genes are their relative distance from each other in map units? 40 mu 28mu12mu B A C

Learning Intentions Goal: to analyze mechanisms of chromosomal inheritance  You must know:  How the chromosome theory of inheritance connects the physical movement of chromosomes in meiosis to Mendel’s laws of inheritance  How alteration of chromosome number or structurally altered chromosomes can cause genetic disorders

Alteration of Chromosome Number  How? Nondisjuction  Occurs when homologous chromosomes do not separate properly during meiosis II.  Result? Aneuploidy  Incorrect number of a chromosome Trisomic: three copies of the chromosome Monosomic: one copy of the chromosome  OR: Result? Polyploidy  More than two complete sets of chromosomes

What happens next? What would the haploid gametes look like?

Down’s Syndrome: aneuploidy

 Is this individual trisomic or monosomic?

Tetraploid Mammal! Polyploidy

Rearrangement of Chromosome Structure  Portions of a chromosomes may be lost or rearranged during crossing over  Deletion Fragment is lost. Missing genes.  Duplication Extra fragment. Extra genes.  Inversion Backwards section! May affect genes.  Translocation Moving a piece to a nonhomologous chromosome

Translocation

Chromosaomal Deletion  Example: Cris du Chat  Deletion in chromosome 5 in humans  Small head, unusual facial features, has a cry that sounds like mewing of a distressed cat  Death in infancy or early childhood  Affects 1 in 20,000 or 50,000 of live births

Try This! A spermatocyte produces the following four sperm cells: n + 1 n + 1n – 1n – 1 1) These cells are the result of which process? 2) When would this happen?

Try This! A spermatocyte produces the following four sperm cells: n + 1 n + 1n – 1n – 1 1) These cells are the result of which process? NONDISJUNCTION 2) When would this happen? DURING MEIOSIS I

Learning Intentions Goal: to analyze mechanisms of chromosomal inheritance  You must know: How the chromosome theory of inheritance connects the physical movement of chromosomes in meiosis to Mendel’s laws of inheritance How alteration of chromosome number or structurally altered chromosomes can cause genetic disorders  Try Worksheet!  You should be able to answer all questions on pg in Holtzclaw