BIO113 Exam 2 Ch 4, 10, 13

Similar documents
CELLS. Some human cells

Patterns of Inheritance

Essential Questions. Basic Patterns of Human Inheritance. Copyright McGraw-Hill Education

Human Genetic Disorders

Human Genetics (Learning Objectives)

Mendel. The pea plant was ideal to work with and Mendel s results were so accurate because: 1) Many. Purple versus flowers, yellow versus seeds, etc.

Genetics, Mendel and Units of Heredity

Patterns of Heredity - Genetics - Sections: 10.2, 11.1, 11.2, & 11.3

Genes and Inheritance (11-12)

12.1 X-linked Inheritance in Humans. Units of Heredity: Chromosomes and Inheritance Ch. 12. X-linked Inheritance. X-linked Inheritance

Genetic Disorders. PART ONE: Detecting Genetic Disorders. Amniocentesis Chorionic villus sampling Karyotype Triple Screen Blood Test

Two copies of each autosomal gene affect phenotype.

GENETICS NOTES. Chapters 12, 13, 14, 15 16

Honors Biology Review Sheet to Chapter 9 Test

Unit 3 Chapter 16 Genetics & Heredity. Biology 3201

Patterns of Heredity Genetics

Semester 2- Unit 2: Inheritance

What You ll Learn. Genetics Since Mendel. ! Explain how traits are inherited by incomplete dominance

Patterns of Inheritance

Unit 7 Section 2 and 3

The passing of traits from parents to offspring. The scientific study of the inheritance

Genetics. The study of heredity. Father of Genetics: Gregor Mendel (mid 1800 s) Developed set of laws that explain how heredity works

NOTES: : HUMAN HEREDITY

Chapter 28 Modern Mendelian Genetics

Gene Expression and Mutation

GENETIC VARIATION AND PATTERNS OF INHERITANCE. SOURCES OF GENETIC VARIATION How siblings / families can be so different

Ch 7 Extending Mendelian Genetics

Name Period. Keystone Vocabulary: genetics fertilization trait hybrid gene allele Principle of dominance segregation gamete probability

Genetics Practice Test. A. phenylketonuria B. Tay-Sachs C. hemophilia D. color blindness

Genetics: CH9 Patterns of Inheritance

REVIEW SHEET: Units 11 Meiosis, Fertilization, & Genetics

REVIEW SHEET: Units 11 Meiosis, Fertilization, & Genetics

Figure 1: Transmission of Wing Shape & Body Color Alleles: F0 Mating. Figure 1.1: Transmission of Wing Shape & Body Color Alleles: Expected F1 Outcome

Pre-AP Biology Unit 7 Genetics Review Outline

Meiotic Mistakes and Abnormalities Learning Outcomes

Genetics. the of an organism. The traits of that organism can then be passed on to, on

Recessive Genetic Disorders! A recessive trait is expressed when the individual is homozygous recessive for the trait.

Genetics. by their offspring. The study of the inheritance of traits is called.

THE CHROMOSOMAL BASIS OF INHERITANCE CHAPTER 15

Extra Review Practice Biology Test Genetics

Semester 2- Unit 2: Inheritance

Patterns in Inheritance. Chapter 10

Mendelian Genetics. KEY CONCEPT Mendel s research showed that traits are inherited as discrete units.

Lesson Overview. Human Genetic Disorders. Lesson Overview Human Genetic Disorders

Principles of Genetics Biology 204 Marilyn M. Shannon, M.A.

Introduction to Genetics and Heredity

UNIT 6 GENETICS 12/30/16

By Mir Mohammed Abbas II PCMB 'A' CHAPTER CONCEPT NOTES

B1 Revision You and Your Genes. You and Your Genes (B1) Revision for Exam

Chapter 17 Genetics Crosses:

TECHNIQUE. Parental generation (P) Stamens Carpel 3. RESULTS First filial. offspring (F 1 )

Genetics All somatic cells contain 23 pairs of chromosomes 22 pairs of autosomes 1 pair of sex chromosomes Genes contained in each pair of chromosomes

Unit 5: Genetics Guided Notes

Lab Activity 36. Principles of Heredity. Portland Community College BI 233

8.1 Human Chromosomes and Genes

Chapter 13: Patterns of Inheritance

Section Objectives: Pedigrees illustrate inheritance. Pedigrees illustrate inheritance

The Chromosomal Basis Of Inheritance

Human Genetic Mutations

MULTIPLE CHOICE QUESTIONS

You are who you are because of a combination of HEREDITY and ENVIRONMENT. ENVIRONMENT: all outside forces that act on an organism.

Chapter 15 Notes 15.1: Mendelian inheritance chromosome theory of inheritance wild type 15.2: Sex-linked genes

Heredity and Genetics (8%)

Genes are found on Chromosomes! Genes are found on Chromosomes! I. Types of Mutations

Genetics & The Work of Mendel. AP Biology

I. Classical Genetics. 1. What makes these parakeets so varied in color?

Genetic Variation Junior Science

Gregor Mendel Father of Genetics

GENETICS PREDICTING HEREDITY

Biology. Chapter 13. Observing Patterns in Inherited Traits. Concepts and Applications 9e Starr Evers Starr. Cengage Learning 2015

Human Genetic Diseases (Ch. 15)

BSC 2010C SI EXAM 3 REVIEW REVIEW SESSION AT: Wednesday, 12 2 PM In CB2 Room 105

B1 You and Your Genes Q3 Question: What are alleles?

Pedigree Analysis. Genetic disorders. Dominant inheritance. Recessive inheritance. Autosomal vs. sex-linked traits. X-linked recessive inheritance

Genetics and Heredity

The Discovery of Chromosomes and Sex-Linked Traits

Chapter 11 Gene Expression

Mendelian Genetics & Inheritance Patterns. Practice Questions. Slide 1 / 116. Slide 2 / 116. Slide 3 / 116

Progressive Science Initiative. Click to go to website:

Mendelian Genetics. Gregor Mendel. Father of modern genetics

Lesson Overview Human Chromosomes

Genetic Disorders. Students must provide an explanation for all problems. Students must have parent signature prior to submission.

Human Genetic Disorders. Lesson Overview. Lesson Overview Human Genetic Disorders

Mendelian Genetics & Inheritance Patterns. Multiple Choice Review. Slide 1 / 47. Slide 2 / 47. Slide 4 / 47. Slide 3 / 47. Slide 5 / 47.

Ch 10 Genetics Mendelian and Post-Medelian Teacher Version.notebook. October 20, * Trait- a character/gene. self-pollination or crosspollination

The Work of Gregor Mendel. Guided Reading

PREDICTING INHERITED TRAITS & PUNNETT SQUARE ANALYSIS

LECTURE 12 B: GENETIC AND INHERITANCE

The Chromosomal Basis of Inheritance

Human Heredity: The genetic transmission of characteristics from parent to offspring.

Mendelian Genetics & Inheritance Patterns. Multiple Choice Review. Slide 1 / 47. Slide 2 / 47. Slide 3 / 47

Mendelian Genetics & Inheritance Patterns. Multiple Choice Review. Slide 2 / 47. Slide 1 / 47. Slide 3 (Answer) / 47. Slide 3 / 47.

Human Genetics Notes:

Biology 12. Mendelian Genetics

Chapter 10 Notes Patterns of Inheritance, Part 1

Genetics & The Work of Mendel

15/12/2011. You and your genes (OCR)

Chromosomal Mutations

Each person has a unique set of characteristics, such as eye colour, height and blood group.

Lesson Overview. Human Chromosomes. Lesson Overview. Human Chromosomes

Transcription:

BIO113 Exam 2 Ch 4, 10, 13 See course outline for specific reading assignments Study notes and focus on terms and concepts The images in the textbook are useful

CELLS (pg. 37) The basic unit of life living things are composed of at least one cell cells metabolize (obtain energy, use energy, make waste) cells can reproduce cells sense and respond to the environment red blood cell brain cell sperm egg Some human cells

Cells need a large surface area to volume ratio

3 parts of the eukaryotic cell Cheek epithelial cells

1. plasma (cell) membrane Selectively permeable Lipid bilayer hydrophilic outer/inner portions hydrophobic within

The membrane determines what can get into and out of the cell such as..

Fluid mosaic model Dynamic!

membrane proteins Transporters, Channels ferry substances Example: glucose transporters Example: chloride ion channel

Cystic fibrosis (CF) and cell membrane most common serious genetic disease in the US A single gene mutation causes a cell membrane Cl- transport protein to malfunction

Cells produce thick, sticky mucus that clogs the lungs infections

2. DNA

Eukaryotic cells have a nucleus that contains DNA Why is DNA important? DNA in nucleus

DNA = instructions for cells to manufacture proteins DNA = genetic material

DNA is in the form of chromosomes 46 long strands of DNA per cell (23 in egg and sperm)

3. cytoplasm (fluid-like interior) Contains ORGANELLES

2 Organelles found in the cytoplasm of the eukaryotic cell 1. lysosomes Bags of enzymes that clean old parts, digest foreign matter

Microscopic view of affected brain Tay Sach s disease and lysosomes Mutation in a single gene results in a malfunctioning lysosomal enzyme Lysosomes fill up with lipid (fatty substance) Normal until ~ 1year, brain deteriorates, fatal ~age 3

Lysosomes and apoptosis Apoptosis = programmed cell death Ex. Tadpole tail, fingers during human embryonic development

2. mitochondria produce energy (ATP) use oxygen and fuel (sugar)

The human life cycle DNA has the instructions

These instructions are on chromosomes which contain units of information called genes

Gregor Mendel (~1850) the father of genetics Worked out the transmission of traits from parent to offspring using pea plants What makes peas good genetic subjects (compared to humans)?

Pisum sativum Single gene traits

Start with true-breeding varieties Cross or self pollination Keep detailed records Statistical analysis

1. Particulate theory of inheritance Modern version: Genes are physical units passed from parent to offspring

The monohybrid (one gene) cross

2. Principle of dominance : For each gene we have 2 alleles Dominant allele observed in phenotype (appearance) B = brown eye allele G = yellow pea allele

recessive allele is masked by a dominant allele b = blue eye allele g = green pea allele BUT, each individual has two alleles per gene. What are the 3 possible GENOTYPES?

Fill in for eye color Genotype Genotype Phenotype Homozygous dominant Homozygous Recessive Heterozygous

3. Principle of segregation Modern version: each sperm and egg randomly gets one allele per trait and fertilization gives the new individual 2 alleles per trait

Sickle cell disease S = normal allele s = sickle cell allele Mutation in the gene for hemoglobin Red blood cells form a sickle shape when oxygen is low

The sickled red blood cells cannot fit through capillaries Causes joint pain, anemia why? Over time stresses kidneys, heart, other organs An example of pleiotropy = single gene, multiple effects

Harmful recessive alleles: Bedouin intermarriage Bedoin intermarriage

Continuous variation results from many genes (polygenic) Examples:

Bell shaped curve shows continuous variation

IQ is polygenic

phenotype also affected by environment -Skin color melanin production increased by sun -Height is ~90% genetic

X-linked genes genes that are ONLY on the X chromosome Females have 2 allele Males have 1 allele

Other single gene disorders Hemophilia mutation in X-linked gene Lack of protein required for blood clotting

Use this notation ONLY for X-linked genes X H X H = X H Y = X H X h = X h Y = X h X h =

Chromosomes = strands of DNA in nucleus Gene = unit of information on a chromosome DNA = molecule that composes chromosomes/genes

Genes (and alleles) are located on chromosomes Humans have 46 chromosomes in each somatic cell nucleus Somatic cell = body cell (not sperm or egg) A human chromosome in nucleus

Chromosomes are copied before a cell divides into 2 cells so that each new cell has a full set

Humans have 2 sets of chromosomes in each cell 23 from egg 23 from sperm Fertilized egg

Homologous chromosomes Chromosomes of (most) animals are in pairs Homologues have same genes at same positions Each chromosome has 100s or 1000s of genes

Chromosomes and genetics Human 46 Chimpanzee 48 Dog 78 Cat 72 Alligator 32 Goldfish 94 Mosquito 6 Potato 48 Baker s yeast 34 The more complex the organism the more chromosomes?

Karyotype photo of chromosomes arranged according to? Pairs 1 through 22 = autosomes Sex chromosomes are X and Y Note the homologous pairs Cant see individual genes!

Fig. 10.14 Autosomes are the same in male and female The Y chromosome determines sex! What genes are on the Y? The X?

Look at the pairs, what is different about these two karyotypes? Female = XX Male = XY

Chromosomal number disorders 47, XX, 21+ Down syndrome Page 136 (ch 9)

Klinefelter syndrome Chromosomal notation?

Chromosomal changes Translocation = portion of one chromosome another

C. Deletion small piece of a chromosome lost Example: Cri du Chat

D. Inversion a piece of a chromosome inverts (flips) 16 year old with leukemia (AML) Note this karyotype is from the cancerous cells only

Genetic testing 1. Of children and adults Obtain chromosomes/dna from cells for testing

2. Prenatal testing 1. ultrasound for fetal anatomy, age, size, twins Can pick up defects such as spina bifida

2. Fetal testing Test fetus in utero

A. amniocentesis Obtain fluid from sac via needle through uterus - contains fetal cells

B. Chorionic villus sampling Tube through vagina into uterus Obtain cells from placenta Greater risk of miscarriage

3. Embryo testing In vitro fertilization (IVF) - > Remove one cell from an early embryo > why? Implant embryo in uterus

Genetic profiling What type of genes would you like to know about? Predisposition genes Predict health risk for: Diabetes, cancer, Alzheimer, etc Metabolic profile How a person handles a drug Disease gene carrier status Monitor work place dangers