Human Heredity. Parents give genes _______ reproductive cells -sperm & egg 23 chromosomes.

Slides:



Advertisements
Similar presentations
Inheritance Principles and Human Genetics
Advertisements

Mendelian Genetics.
Genetic Mutations & Pedigrees
Chromosomes and Inheritance
Human Genetics Phenotype: observed physical and functional traits
NOTES 24 – Genetic Disorders and Hereditary Diseases
Chapter 14- Human Genome.
I. Introduction A. 46 chromosomes in each cell (23 pairs) B. Autosomes: all chromosomes except sex chromosomes (22 pairs) C. Sex chromosomes: determine.
Changes in Chromosome Number
Mutations and other genetic issues
Chapter 12: Inheritance Patterns and Human Genetics
Ch 20 Lesson 2 From Generation to Generation. Things to do before we start class…  Take out Prenatal Development Worksheet.
Chapter 11 Human Heredity.
Chapter 14 – The Human Genome
Chapter 12.  Humans have 46 chromosomes  44 are autosomes  22 pairs of homologous chromosomes  2 are sex chromosomes: X and Y  Females have two X.
Sex linked genes.
Variations on Mendel’s principles Incomplete dominance Co-dominance Multiple alleles Sex-linked alleles.
Inheritance Patterns and Human Genetics. Sex Chromosomes and Autosomes Sex Chromosomes contain genes that determine the gender of an individual. Many.
Ch. 14 The Human Genome.
Chromosome Theory & Heredity. Gene Linkage Where two or more genes occurs on the same chromosome – Located in close association with one another – Tend.
Complex Inheritance and Human Heredity Chapter 11.
Human Inheritance Chapter 14 sec. 1 and 2. Pedigree Analysis Pedigree = a family record that shows how a trait is inherited over several generations.
Human Heredity Learning Target 14.1 Explain how human traits are inherited. Explain why human traits are not ideal for the study of genetics. Discuss.
Chapter 7 PowerPoint by Jacob Rondinella.
End Show Slide 1 of 43 Copyright Pearson Prentice Hall 14–1 Human Heredity 14-1 Human Heredity.
Human Genetics and the Pedigree. Section Objectives Understand how different mutations occur. Be able to identify different diseases and disorders.
 Studying humans requires alternative methods.  Human geneticists use.  Human are – Deduce the genotypes and phenotypes of individuals in.
HUMAN HEREDITY OBJECTIVES: 14.1
Genetic Disorders Things Can Go Wrong With DNA and Chromosomes.
Name 2 Genetic Diseases. Copyright Pearson Prentice Hall.
14-2 Human Chromosomes.
Human Genome. Karyotype – a picture of a cell’s chromosomes group in homologous pairs Humans have 46 chromosomes Two of these are sex chromosomes (XX.
Human Genetic Disorders
Heredity and Genetics. Every person inherits traits such as hair and eye color as well as the shape of their earlobes from their parents. Inherited traits.
Chapter 14 The Human Genome Pg. 341.
What determines are phenotypes? Autosomes- chromosomes 1-44, pairs 1-22 Sex chromosomes- 23 rd pair of chromosomes – Females have two copies of a large.
Chapter 11: Human Heredity
Human Genetics & Inheritance (p ) What do Geneticists use to study human traits & genetics diseases? Pedigrees: to analyze patterns of inheritance.
Heredity and Genetics (2:39) Click here to launch video Click here to download print activity.
Human Genetics Studying humans requires alternative methods – human geneticists use medical, historical and family records Human pedigrees – records extending.
Human Genetics Copyright © The McGraw-Hill Companies, Inc. Permission required for reproduction or display. Lecture Outline.
Human Genetics Inheritance in humans Male/female Multiple Alleles Inherited diseases Twins Sex-linked traits.
Mutations & Diseases. Nondisjunction: Missing 1 chromosome LETHAL! Results from non- disjunction –Chromosomes do not separate properly Miscarriage.
Ch. 14 The Human Genome.
The Human Genome Chapter 14. Human Heredity  Human chromosomes Karyotype – a picture of chromosomes arranged in pairs.
Chapter 14 Human Heredity. Human Chromosomes A picture of chromosomes arranged in this way (previous page) is know as a karyotype. This karyotype is.
Extending Mendelian Genetics Chapter 7 Mr. Scott.
Mutations & Diseases. Missing 1 chromosome LETHAL! Results from non- disjunction- _________________ _______________ Miscarriage Pg. 401.
1 Chapter 14- Human Genome Students know why approximately half of an individual ’ s DNA sequence comes from each parent. Students know the role of chromosomes.
Chapter 27 Human Genetics. Karyotype The arrangement of all the chromosomes found in a cell. Includes: 23 rd pair Female sex chromosomes X X Female =
~Please Staple Your Bibliography to your Rubric. ~If you present today keep everything at your desk and you will turn in when you present. ~If you present.
associated-331
Copyright © 2003 Pearson Education, Inc. publishing as Benjamin Cummings Inheritance.
Human Heredity. 1. condition : gender symptoms : male or female genetic cause : sex chromosomes genotypes/phenotypes : XX = female XY = male.
More Patterns of Inheritance Autosomal inheritance – genes are located on the autosomes, same for both male and female Sex-linked inheritance – genes located.
Human Heredity Chap 11 Lab Biology Mrs. Moon. Human Genetics Human chromosome # = 46 Human nucleotide pairs of DNA = 6 billion Gametes – reproductive.
Sex Determination Worksheet. A. COLOR-BLINDNESS, –Recessive trait on the X chromo. –Lack of pigments made in the eye which are for color vision –Most.
Human Genetics.
Chapter 11 Human Heredity.
Sex Determination Worksheet
Human Heredity.
Copy the chart: Quick Question 1/31
Chapter 14 The Human Heredity.
(Non-Mendelian Genetics)
Things Can Go Wrong With DNA and Chromosomes
Chapter 11 Human Heredity.
12-4 Mutations, blood types and pedigrees
12-4 Mutations, blood types and pedigress
Introduction to Genetics
Patterns of Heredity & Human Genetics
Presentation transcript:

Human Heredity

Parents give genes _______ reproductive cells -sperm & egg 23 chromosomes

Zygote- –Fertilized eggs 46 Chromosomes –23 pairs of chromosomes Male __ FemaleXX

Environmental effects ________ gene expression but are not inherited. ________ Twins Human Traits

Human Blood Groups ______ alleles –Gene with 3 or more alleles Ex. ABO blood

Blood Typing Karl __________ Types –A, B, AB, O Difference is the _______

A accepts A and O blood B accepts B and O blood __ accepts A,B&O blood O accepts O blood only –O is Universal donor

A, B, i 3 alleles code for blood types I A, I B, i O  ii  AA, A iA  I A I A, I A i B  BB, B iB  I B I B, I B i AB  ABAB  I A I B

Rh Blood Groups __ antigen- Named after Rhesus monkey _ & - Blood types + has it, - doesn’t

________ Disease _______ Gene that causes muscle loss and nervous cell ________ Gene is expressed only in 30’s and 40’s

A few are caused by dominant alleles –Examples: __________, Huntington’s disease

Polygenic Traits Traits controlled by a number of genes –Height –Skin Color

Sickle Cell Anemia Is it Good or Bad ?

Some Cells are _____ shaped not round

_______ Genes Cause Sickle Cell H A H A -normal cell H S H S - sickle cell H A H S - half/half

H A Person Lives out normal life

H S Sickle cells get stuck in capillaries Body parts die from lack of _____

H A H S Survive with _______ problems Have some _______ to Malaria -equatorial regions -Survive better

Sickle Cell Anemia Is it Good or Bad ?

Sex-Linked Inheritance

Non-disjunction Disorders Turner syndrome _________ syndrome Down syndrome

Turner syndrome Female ________ Sex organs never develop (Sterile) Abbrev. ___ or 45XO

Klinefelter syndrome ______ in appearance Sterile Abbr. _____

Down Syndrome Mentally disabled ______ 21 –Extra 21 st Chromosome –Stocky, smaller organs Die early

Down Syndrome

No baby has been born without at least one _ chromosome

If there is a Y chromosome present the appearance of the child is Male Ex. 48XXXY __________

Sex-Linked Disorders Genes carried on X or Y chromosome

Color Blindness ___________ Muscular Dystrophy

Color Blindness 8% of males, 1% of females Allele is carried on X

Hemophilia Males-1 in 10,000 Females-_____________ Blood doesn’t clot

A high incidence of hemophilia has plagued the ____ families of Europe Queen Victoria Albert AliceLouis AlexandraCzar Nicholas II of Russia Alexis

Muscular ________ Skeletal muscle wastes away. Dystrophin protein is defective Usually die by adulthood

Sex-______ Traits Baldness –Normal hair B –Baldb –Females only get thin hair

Diagnosis of Genetic Disorders

Before Birth Microscope matchup ___________ –Uses fluid from around baby Chorionic villus biopsy

Before Birth Amniocentesis –Uses _____ from around baby Chorionic villus biopsy –Uses cells from the ______ around the baby

Karyotyping and biochemical tests of fetal cells and molecules can help people make reproductive decisions –Fetal cells can be obtained through amniocentesis Connection: Fetal testing can spot many inherited disorders early in pregnancy Amniotic fluid Fetus (14-20 weeks) Placenta Amniotic fluid withdrawn Centrifugation Fetal cells Fluid UterusCervix Cell culture Several weeks later Karyotyping Biochemical tests

Chorionic villus sampling is another procedure that obtains fetal cells for karyotyping Fetus (10-12 weeks) Placenta Chorionic villi Suction Several hours later Fetal cells (from chorionic villi) Karyotyping Some biochemical tests

Ethical Issues Should genetic counseling be a cause for abortion?

Family pedigrees are used to determine patterns of inheritance and individual genotypes Dd Joshua Lambert Dd Abigail Linnell D_ Abigail Lambert Female Dd Elizabeth Eddy D_ John Eddy ?D_ Hepzibah Daggett ? ? ddDd ddDd Male Deaf Hearing dd Jonathan Lambert