Organization of Genetics Course Molecular Genetics Cytogenetics Transmission Genetics Population Genetics.

Slides:



Advertisements
Similar presentations
Lecture 41 Prof Duncan Shaw. Genetic Variation Already know that genes have different alleles - how do these arise? Process of mutation - an alteration/change.
Advertisements

DNA molecule Gene 1 Gene 2 Gene 3 DNA template strand TRANSCRIPTION TRANSLATION mRNA Protein Codon Amino acid 1.
More on Genetics.  ______________________- use desired traits to produce the next generation-example-selectively breeding dogs,horses,plants  ______________________crossing.
Allele Important Genetic Concepts Genotype Phenotype Gene.
Chapters 11 Reading , 11.2, 11.10, 11.12, 11.15, 11.17, 11.18, 11.19, 11.20, , 27.10, 27.11, Important Concepts Molecular.
Chromatin Remodeling DNA is wrapped around histones to form nucleosomes DNA is wrapped around histones to form nucleosomes Chromosome packaging Chromosome.
N C Fig. 13-1, Page 307 Gene Expression. Pg. 242 Deoxyribonucleotide.
Unit 4 Genetics Ch. 14 The Human Genome.
Human Genetic Mutations
3.1 Genes Understanding: -A gene is a heritable factor that consists of a length of DNA and influences a specific characteristic -A gene occupies a specific.
FROM GENE TO PROTEIN: TRANSLATION & MUTATIONS Chapter 17.
Applications of genome sequencing projects 4) Bioarchaeology, anthropology, human evolution, human migration.
Mutations.
Genes as DNA: How Genes Encode Proteins
Answers: Genes, alleles, nucleotide sequence Questions: – You share 99% of your ___________ with a chimpanzee. – You share 60% of your ___________ with.
Genetics SQ3R’s. SQ3R Ch. 1, section 2 1.Cell Wall 2.Cell Membrane 3.Nucleus 4.Organelles in the cytoplasm 5. Bacterial Cells 6. Specialized Cells Answer.
Chapter # - Chapter Title $100 $200 $300 $400 $500 $100$100$100 $200 $300 $400 $500 Human Heredity Human Chromosomes Human Molecular Genetics Human Heredity.
Heredity Review. Heredity – Mitosis/Cell Division Cell Cycle Mitosis..structure of chromosome Regulation –Density Dependent –Density Independent –G o,
HUMAN MOLECULAR GENETICS Lecture Genetic testing Genetic tests are now available for hundreds of disorders. Parents can find out if they carry defective.
Genetics and Inheritance Part 1
Small Scale Mutations & Gene Expression. LARGE MUTATIONS & GENETICS Quick Review.
Topic 4.1 Chromosomes, Genes, Alleles and Mutations.
Chapter 14 Homework is due on Sunday, January 25 at 11:59 pm The Chapter 13 and 14 test is on Monday.
CRUNCH TIME 90 minute power review! Get ready to exercise your brain!!!
Gene Mutations. O A mutation is a permanent change in the DNA sequence of a gene. O Any change in this sequence is likely to change the message transcribed.
Class 22 DNA Polymorphisms Based on Chapter 10 Recombinant DNA Technology Copyright © 2010 Pearson Education Inc.
Review 4: Heredity & Molecular Genetics AP Biology.
Molecular Basis for Relationship between Genotype and Phenotype DNA RNA protein genotype function organism phenotype DNA sequence amino acid sequence transcription.
11 Gene function: genes in action. Sea in the blood Various kinds of haemoglobin are found in red blood cells. Each kind of haemoglobin consists of four.
the Genetic Code Shown as mRNA 5′ → 3′ 64 codons Redundant
GENETICS Dr. Samar Saleh Assiss. Lecturer Mosul Medical College Pathology3 rd year.
Regents Biology Mutations Changes to DNA.
Rate of mutations in the Human Genome A study published in Current Biology in 2009, shows that in total, we all carry new mutations in our DNA.
Mutations Csaba Bödör, Semmelweis University, 1 st Dept. of Pathology.
zUWlK5s-94A&sns=em.
Genetics 3.1 Genes. Essential Idea: Every living organism inherits a blueprint for life from its parents.
Human Genetic Mutations. 2 Main Types of Mutations 1.) Chromosomal Mutations 2.) Gene Mutations.
FROM GENE TO PROTEIN: TRANSLATION & MUTATIONS Chapter
 Structural genes: genes that contain the information to make a protein.  Regulatory genes: guide the expression of structural genes, without coding.
Restriction Fragment Length Polymorphism. Definition The variation in the length of DNA fragments produced by a restriction endonuclease that cuts at.
Warm-Up (1/27) Answer the following questions, and explain in a complete sentence why each answer is correct. Name Date Period If a paramecium (a one-celled.
Chapter 14: Human Heredity
13.2 – Human Genetic Disorders
Exam #3 W 12/5 at 7-8:30pm in ETC for the 9am class and ECJ 1
From Gene to Protein: Translation & Mutations
Protein on Normal Red Blood Cells
Every living organism inherits a blueprint for life from its parents.
Mendel & the gene idea Chapter 14.
Genes 3.1.
CHROMOSOMES, ALLELES, GENES & MUTATIONS
Mendel & the gene idea Chapter 14.
Chapter 14 – The Human Genome Human Chromosome 3 Suzanna Macedo 2010
THE HUMAN GENOME Molecular Genetics.
Relationship between Genotype and Phenotype
More on Genetics.
Interphase (G1, S, G2) Chromosomes M-Phase Chromosome.
Genes 3.1.
Mutations.
Today: Mendelian Genetics
Mendel & the gene idea Chapter 14.
Chapter # - Chapter Title
INTRODUCTION TO MOLECULAR GENETICS
KEY CONCEPT Human inheritance patterns are more complex.
Single Gene Disorders.
Gene Protein Genome Proteome Genomics Proteomics.
INTRODUCTION TO MOLECULAR GENETICS
Relationship between Genotype and Phenotype
Relationship between Genotype and Phenotype
Relationship between Genotype and Phenotype
Tools for Molecular Biology
Presentation transcript:

Organization of Genetics Course Molecular Genetics Cytogenetics Transmission Genetics Population Genetics

Molecular Genetics Identification of DNA as the genetic material Structure of DNA Function of Genes Gene (DNA) RNA PROTEIN Gene Regulation Mutation and Genetic Variation (origin of alleles) Linking diseases to specific alleles Genetic Technologies Genetic testing Gene Therapy

Genomics Identification, sequencing and mapping of all human genes Evolution of the human genome

Cytogenetics Meiosis Chromosome Theory of Inheritance Karyotypes Identification of Chromosome Abnormalities

Transmission Genetics Mendelian Principles Alleles, Dominant/Recessive Genotype Determines Phenotype Extensions to Mendelian Principles Multiple alleles Lethal alleles Additive alleles Co-dominance Partial dominance Epistasis Linkage and Genetic Mapping

Population Genetics Mendelian and Molecular Genetics of Populations Frequency of alleles (e.g., “disease” alleles) How allele frequency changes over time DNA Fingerprinting p 2 + pq + q 2 = 1

Normal Red Blood Cell Sickle Cell Anemia Red Blood Cell

Hemoglobin

Allele (DNA) RNA Protein Genotype/Phenotype

N C Fig. 13-1, Page 307 Flow of Genetic Information

DNA Structure 5’ 3’ 5’ 3’ Fig. 1-8,Page 5

Fig. 13-7,Page 314

Possible Reading Frames for RNA

Fig. 13-7,Page 314

Normal Red Blood Cell Sickle Cell Anemia Red Blood Cell

ATG GTG CAC TTG ACC CCC GAG GAG met - val - his - leu - thr - pro - glu - glu 5’ 3’ (N) (C) Hb A Molecular Genetics of Sickle-Cell Anemia HbA

ATG GTG CAC TTG ACC CCC GAG GAG met - val - his - leu - thr - pro - glu - glu 5’ 3’ (N) (C) ATG GTG CAC TTG ACC CCC GTG GAG met - val - his - leu - thr - pro - val - glu 5’ 3’ (C)(N) Hb A Hb S Molecular Genetics of Sickle-Cell Anemia HbA HbS

Pg. 350 Fig. 350

Hemoglobin

Healthy Lung Lung epithelial cells Lung epithelial cells

Lung epithelial cells Lung epithelial cells Cystic Fibrosis Lung

Chloride Ion Channel gene and protein involved in Cystic Fibrosis Missense mutation Nonsense mutation Frame-shift mutation Deletion, in-frame CFCTR Gene Mutations

Healthy Lung Lung epithelial cells Lung epithelial cells AA or Aa

Lung epithelial cells Lung epithelial cells Cystic Fibrosis Lung aa

Chromosome genes 158 million bp of DNA CFCTR Gene

Chromosome genes 158 million bp of DNA CFCTR Genotype AA A A Phenotype Healthy

Chromosome genes 158 million bp of DNA CFCTR Genotype Aa A a Phenotype Healthy

Chromosome genes 158 million bp of DNA CFCTR Genotype aa a a Phenotype Cystic Fibrosis

Huntington’s Disease

Cell from “Hh” individual Huntingtin protein aggregates

Trinucleotide Repeat Diseases

Fig Pg. 459 Restriction Enzymes

Chloride Ion Channel gene and protein involved in Cystic Fibrosis Missense mutation Nonsense mutation Frame-shift mutation Deletion, in-frame CFCTR Gene Mutations

Amniocentesis Genetic testing weeks Fig Pg. 555

Early Embryonic Development (~ 7 days)

8 cell Embryo from IVF Remove one cell for genetic testing Pre-Implantation Genetic Diagnosis

Genetic Testing for Sickle Cell Anemia Embryos Made by IVF Parents Hb S Hb A Fig Pg. 556

Genetic Testing for Sickle Cell Anemia Embryos Made by IVF Parents Implant embyro #1 Hb S Hb A Fig Pg. 556

Early Embryonic Development (~ 7 days)

Fig Pg. 559

Microarray (“gene chip”) Normal B-Cell Purify mRNA Label mRNA with “green” dye Diffuse Large B-Cell Lymphoma Purify mRNA Label mRNA with “red” dye Hybridize to Microarray

DLBCL Individuals Microarray Analysis of Diffuse Large B-Cell Lymphoma Genes (~ 18,000)

Gene Therapy for Severe Combined Immunodeficiency Fig Pg. 561 “aa” individual “aa” cells Virus with “A” allele “Aaa” cells Cloned “A” allele

DNA Sequencing: How it works Products separated By gel electrophoresis Fig Pg. 477

Fig Pg. 486

“Raw” DNA sequence Where are the genes?

Fig Pg. 488 ORF scanning in all reading frames and both strands ORFs are in brown

Fig. 13-7,Page 314

Pg. 494

Function of Human Genes Fig Pg. 497

Gene Genes comprise ~ 5% of genome Repeated DNA comprises ~ 50% of genome Unique (“junk”) DNA comprises the rest Organization of Human Genome Fig Pg. 494 (~ 50 kbp)

Comparative Genomics Pg. 499

Genome Transcriptome Proteome All of the DNA of a cell Methods: DNA sequencing, computer analysis All of the mRNA produced by a cell Method: Microarray analysis (gene chips) All of the proteins produced by a cell Methods: 2-dimensional gel eletrophoresis

Eukaryotic Cell

Electron Micrograph of Mitochondrial DNA Fig. 9-7 Pg. 219

13 proteins encoded by human mitochondrial genome

Heteroplasmy Mutant Normal

Interphase and M-Phase Chromosomes

Chromosome genes 158 million bp of DNA

Histone Structure

Fig. 12-9

Interphase and M-Phase Chromosomes

Core Promoter Fig. 17-4

Leucine Zipper Transcription Factor DNA Binding Domain Activation Domain Fig

Formation of the Pre-initiation Complex Fig