Download Free Medical THE CHROMOSOMAL BASIS OF INHERITANCE PowerPoint Presentation

THE CHROMOSOMAL BASIS OF INHERITANCE PowerPoint Presentation

DOWNLOAD MEDICAL POWERPOINT PRESENTATION

About This Presentation

Description : Check out this medical presentation on Genetics, which is titled "THE CHROMOSOMAL BASIS OF INHERITANCE", to learn about the chromosomal basis of inheritance.

Tags : Genetics, chromosomal basis, inheritance

Published on : Aug 29, 2021 | Views : 2415 | Downloads : 0

Shareable Url :

Embed Code :

Comment

Transcript

Slide 1-

THE CHROMOSOMAL BASIS OF INHERITANCE CHAPTER 15
Slide 2-

Ch. 15 Warm-Up A white-eyed female fruit-fly is mated with a red-eyed male. What genotypes and phenotypes do you predict for the offspring? Neither Tim nor Rhoda has Duchenne muscular dystrophy (X-linked recessive disorder), but their firstborn son has it. What is the probability their 2nd child will have it? Colorblindness is a sex-linked recessive trait. A colorblind male and a female with normal vision have a son who is colorblind. What are the parents’ genotypes? Definitions: Sex-linked gene Barr body SRY gene Linked genes Linkage map
Slide 3-

Warm up What is a Barr body? How are linkage maps constructed? (See. Fig. 15.11 in Campbell 9th ed.) Determine the sequence of genes along a chromosome based on the following recombination frequencies: A-B, 8 map units; A-C, 19 map units; A-D, 20 map units; B-C, 11 map units; B-D, 28 map units. What does a frequency of recombination of 50% indicate?
Slide 4-

What is the pattern of inheritance of the trait (shaded square/circle) shown in the pedigree? How many chromosomes are in a human cell that is: a) Diploid? b) Triploid? c) Monosomic? d) Trisomic? Warm-Up
Slide 5-

What you must know: How the chromosome theory of inheritance connects the physical movement of chromosomes in meiosis to Mendel’s laws of inheritance. The unique pattern of inheritance in sex-linked genes. How alteration of chromosome number or structurally altered chromosomes (deletions, duplications, etc.) can cause genetic disorders. How genetic imprinting and inheritance of mitochondrial DNA are exceptions to standard Mendelian inheritance.
Slide 6-

Chromosome theory of inheritance: Genes have specific locations (loci) on chromosomes Chromosomes segregate and assort independently Chromosomes tagged to reveal a specific gene (yellow).
Slide 7-

Thomas Hunt Morgan Drosophila melanogaster – fruit fly Fast breeding, 4 prs. chromosomes (XX/XY) Sex-linked gene: located on X or Y chromosome Red-eyes = wild-type; white-eyes = mutant Specific gene carried on specific chromosome
Slide 8-

Sex determination varies between animals
Slide 9-

Sex-linked genes Sex-linked gene on X or Y Females (XX), male (XY) Eggs = X, sperm = X or Y Fathers pass X-linked genes to daughters, but not sons Males express recessive trait on the single X (hemizygous) Females can be affected or carrier
Slide 10-

Transmission of sex-linked recessive traits
Slide 11-

Sex-linked disorders Colorblindness Duchenne muscular dystrophy Hemophilia
Slide 12-

ppt slide no 12 content not found
Slide 13-

X-Inactivation Barr body = inactive X chromosome; regulate gene dosage in females during embryonic development Cats: allele for fur color is on X Only female cats can be tortoiseshell or calico.
Slide 14-

Human development Y chromosome required for development of testes Embryo gonads indifferent at 2 months SRY gene: sex-determining region of Y Codes for protein that regulates other genes
Slide 15-

Genetic Recombination: production of offspring with new combo of genes from parents If offspring look like parents  parental types If different from parents  recombinants
Slide 16-

If results do not follow Mendel’s Law of Independent Assortment, then the genes are probably linked
Slide 17-

Linked genes: located on same chromosome and tend to be inherited together during cell division
Slide 18-

Crossing over: explains why some linked genes get separated during meiosis the further apart 2 genes on same chromosome, the higher the probability of crossing over and the higher the recombination frequency
Slide 19-

Calculating recombination frequency
Slide 20-

Linkage Map: genetic map that is based on % of cross-over events 1 map unit = 1% recombination frequency Express relative distances along chromosome 50% recombination = far apart on same chromosome or on 2 different chromosomes
Slide 21-

Exceptions to Mendelian Inheritance
Slide 22-

Genomic Imprinting Genomic imprinting: phenotypic effect of gene depends on whether from M or F parent Methylation: silence genes by adding methyl groups to DNA
Slide 23-

Non-Nuclear DNA Some genes located in organelles Mitochondria, chloroplasts, plastids Contain small circular DNA Mitochondria = maternal inheritance (eggs) Variegated (striped or spotted) leaves result from mutations in pigment genes in plastids, which generally are inherited from the maternal parent.
Slide 24-

Genetic Testing Reasons for Genetic Tests: Diagnostic testing (genetic disorders) Presymptomatic & predictive testing Carrier testing (before having children) Pharmacogenetics (medication & dosage) Prenatal testing Newborn screening Preimplantation testing (embryos)
Slide 25-

Prenatal Testing May be used on a fetus to detect genetic disorders Amniocentesis: remove amniotic fluid around fetus to culture for karyotype Chorionic villus sampling: insert narrow tube in cervix to extract sample of placenta with fetal cells for karyotype
Slide 26-

ppt slide no 26 content not found
Slide 27-

Nondisjunction: chromosomes fail to separate properly in Meiosis I or Meiosis II
Slide 28-

Karyotyping can detect nondisjunctions. Down Syndrome = Trisomy 21
Slide 29-

Klinefelter Syndrome: 47XYY, 47XXY Nondisjunction
Slide 30-

Nondisjunction Turner Syndrome = 45XO
Slide 31-

Chromosomal Mutations
Slide 32-

Chromosomal Mutations
Slide 33-

Nondisjunction Aneuploidy: incorrect # chromosomes Monosomy (1 copy) or Trisomy (3 copies) Polyploidy: 2+ complete sets of chromosomes; 3n or 4n Rare in animals, frequent in plants A tetraploid mammal. Scientists think this species may have arisen when an ancestor doubled its chromosome # by errors in mitosis or meiosis.
Slide 34-

What is the pattern of inheritance of the trait (shaded square/circle) shown in the pedigree? How many chromosomes are in a human cell that is: a) Diploid? b) Triploid? c) Monosomic? d) Trisomic? Review Questions
Slide 35-

Chi-Square Analysis Practice Two true-breeding Drosophila are crossed: a normal-winged, red-eyed female and a miniature-winged, vermillion-eyed male. The F1 offspring all have normal wings and red eyes. When the F1 offspring are crossed with miniature-winged, vermillion-eyed flies, the following offspring resulted: 233 normal wing, red eye 247 miniature wing, vermillion eye 7 normal wing, vermillion eye 13 miniature wing, red eye What type of conclusions can you draw from this experiment? Explain your answer.