Chromosomes and Human Heredity

Slides:



Advertisements
Similar presentations
3.3 Review PBS.
Advertisements

Karyotypes and Sex-Linked Traits
Zoo-352 Principles of genetics Lecture 3 The cell cycle and its checkpoints.
Chapter 14: The Human Genome
Meiosis and Karyotypes
KARYOTYPE TESTS. KARYOTYPE =  Image of all the chromosomes from the nucleus of a cell  Can be done to identify genetic disorders.
MEIOSIS.
GENETICS I CHROMOSOMES GENETICS I CHROMOSOMES. A. CHROMOSOMES Chromosomes are found in the nucleus of the cell Chromosomes are found in the nucleus of.
How many chromosomes do you have?
 Human body cells have 46 paired chromosomes or 23 pairs of chromosomes.  Human gametes have 23 unpaired chromosomes  When a sperm and egg unite each.
Chromosome Theory & Heredity. Gene Linkage Where two or more genes occurs on the same chromosome – Located in close association with one another – Tend.
Functions and Pictures…
11.3 CHROMOSOMES & HUMAN HEREDITY
Compare Critical differences between Mitosis and Meiosis: Tetrads form (Pro I) Crossing over can occur (Pro I) Tetrads line up and are separated (Meta.
Meiosis and Human Reproduction
Meiosis and Reproduction Biology 1-2. Chromosomes Chromosomal theory of inheritance- genes have specific locations on chromosomes. Chromosomal theory.
KARYOTYPING Honors Biology. What and How? Used as a way to “see” the chromosomes Pairs up homologous chromosomes Allows for detection of several genetic.
The Human Genome Ch. 14. Human Chromosomes Karyotype = how chromosomes are arranged in pairs Humans have 46 chromosomes or 23 pairs The 23 rd pair are.
10.2 MEIOSIS Martin GENES, CHROMOSOMES, AND NUMBERS A. Dipolid and Haploid Cells: ▫Diploid Cells: cell that have two of each kind of chromosome.
Karyotypes.
 Autosome: the first 22 homologous pairs of chromosomes  Sex Chromosome: X and Y chromosome (the 23 rd set of chromosomes)  Female: XX  Male: XY.
What was your favorite thing about winter break? What is a karyotype? What is the purpose of a karyotype?
Mistakes in Meiosis. Non-Disjunction a type of mistake in meiosis that happens to the CHROMOSOME It is the failure of homologous chromosomes to separate.
1. DNA 2. Gene 4. Genome 5. Individual 3. Chromosome 7. Population 6. Family (pedigree) Cell Human Genetics.
2B: creating sperm and egg 2D: fertilization creates new genetic combinations 2E: each parent contributes half of their DNA 2F: sex chromosomes determine.
NOTES 21 - Sex-Linked Inheritance
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.
Catalyst 1. Hemophilia (h) is a recessive genetic disorder carried on the X chromosome. If a man with hemophilia marries a woman who doesn’t have the.
Karyotypes. How karyotypes are made… sist_safety_mode=1&safe=active.
Chapter 11-3 Chromosomes & Human Heredity. Focus Questions: How are Karyotypes used to study genetic disorders? What is the role of Telomeres? How is.
Chromosomes and Human Heredity Chapter Karyotype Studies  Scientists do not only study genes – they also like to look at the chromosome at a whole.
Meiosis Review.
Pedigrees and Karyotypes
Do Now Look at the karyotype below, what is the gender of the individual? How do you know? Is the karyotype considered normal? Why or why not?
Karyotypes.
Cell Division: sexual and asexual reproduction
Meiosis and Human Reproduction
Genetics: Karyotypes and X-linked traits
Chapter 11 Section 3: Chromosomes and Human Heredity
Chapter 14 Human Heredity.
Reproduction.
Meiosis and Sexual Reproduction
Tuesday March 28, 2017 I can: Agenda Catalyst HW: IP: Karyotypes
Copyright Pearson Prentice Hall
Meiosis & Mistakes Chapter 10.2.
The same genes, but different forms (alleles) of those genes
Chromosomes.
MEIOSIS & Abnormal Meiosis
The Human Genome Ch. 14.
Sex chromosomes AUTOSOMES
Title of notes: Karyotypes
Chromosomes.
Sources of Variation During Meiosis.
Start-up for 12/9/14 Refer to the karyotype on the right. Is this a male or female? Explain. What are autosomes? Which chromosomes in this karyotype.
Human Karyotypes and Heredity
3.3 Review PBS.
Meiosis.
Chromosomes.
What are they?? How do we use them?
You have body cells and gametes.
Fertilization The process of haploid gametes joining together to form a diploid cell with 2n chromosomes. n chromosomes come from the male parent and n.
How is gender determined?
Notes: When Mistakes Occur
8.3 Human Genetics and Mutations
Analyze how environmental factors can influence a persons phenotype?
Chromosomes.
What are they?? How do we use them?
DNA, Genes, and Chromosomes
Karyotypes Pages in textbook.
Presentation transcript:

Chromosomes and Human Heredity 11.3

Karyotype studies A karyotype is a diagram that shows all of the chromosomes that an organism has. Every colored bar on the chromsomes are different genes Notice how the chromosomes get smaller as you move towards the 22nd chromsome

Karyotype studies Humans have 23 pairs of chromosomes- 46 individual chromosomes The 23rd pair of chromosomes are the sex chromosomes The 23rd pair of chromosomes will either be an XY pair or an XX pair Females XX and males XY

Side B is from the other parent Karyotype studies The pairs of chromosomes, when lined up with the chromosome that has the same kinds of genes (when it is with the chromosome that looks just like itself) They’re called homologous chromosomes Homologous chromosomes- chromosomes that have the same types of genes on them, but not necessarily the same alleles for those genes Side A is from one parent

Chromosomes Telomere- protective end cap of a chromosome. Telomere are important because everytime chromosomes divide during mitosis or meiosis, it risks breakage and loss of DNA Telomeres protect the DNA

Chromosomes During Meiosis and Mitosis, there’s always the possibility that chromosomes won’t divide properly. When this happens, it’s called nondisjunction.

Chromosomes Remember, that all of the cells that result from Meiosis have the potential to be fertilized and become a baby. What do you think might become of the baby that results from either of the two cells that have been circled?

Genetic Diseases When nondisjunction occurs and those cells are fertilized, if the zygote survives to become a fetus and then a baby, that baby will most likely have a genetic disorder. Ex. Down’s Syndrome, Klinefelter’s, Patau Syndrome

Genetic Diseases There are certain types of tests that can be performed on pregnant women to see if their baby is at risk for these nondisjunction diseases. https://www.youtube.com/watch?v=oeR4jGNCnd4 Prenatal testing is good and bad. Good because it can inform you of health issues to expect with your baby. Also bad because you may discover that your baby is very unhealthy and you may have to face serious medical decisions for yourself and your baby.

Key points for 11.3 Humans have 23 chromosomes, as can be seen in a karyotype. The 23rd chromosomes in humans determine the biological sex (XX for women and XY for men) Nondisjunction is when chromosomes don’t properly divide during Mitosis or meiosis.