Human Karyotyping Lab #

Similar documents
4.2 Meiosis. Meiosis is a reduction division. Assessment statements. The process of meiosis

CHROMOSOMES Dr. Fern Tsien, Dept. of Genetics, LSUHSC, NO, LA

Each person normally has 23 pairs of chromosomes, or 46 in all. We inherit one chromosome per pair from our mother and one from our father.

CHROMOSOMES AND INHERITANCE

REI Pearls: Pitfalls of Genetic Testing in Miscarriage

Chapter 13: Meiosis and Sexual Life Cycles

Genetic Mutations. Indicator 4.8: Compare the consequences of mutations in body cells with those in gametes.

Chapter 13: Meiosis and Sexual Life Cycles

Chromosome Mapping Assignment INSTRUCTIONS

PSI Biology Mitosis & Meiosis

5. The cells of a multicellular organism, other than gametes and the germ cells from which it develops, are known as

Preimplantation Genetic Diagnosis (PGD) in Western Australia

Chromosomes, Karyotyping, and Abnormalities (Learning Objectives) Learn the components and parts of a metaphase chromosome.

Meiosis is a special form of cell division.

Cell Growth and Reproduction Module B, Anchor 1

The correct answer is c A. Answer a is incorrect. The white-eye gene must be recessive since heterozygous females have red eyes.

Bio EOC Topics for Cell Reproduction: Bio EOC Questions for Cell Reproduction:

The Huntington Library, Art Collections, and Botanical Gardens

Sexual Reproduction. The specialized cells that are required for sexual reproduction are known as. And come from the process of: GAMETES

Biology Behind the Crime Scene Week 4: Lab #4 Genetics Exercise (Meiosis) and RFLP Analysis of DNA

Reproductive System & Development: Practice Questions #1

Mitosis, Meiosis and Fertilization 1

Fluorescence in situ hybridisation (FISH)

LAB 8 EUKARYOTIC CELL DIVISION: MITOSIS AND MEIOSIS

Heredity - Patterns of Inheritance

What Is Genetic Counseling? Helping individuals and families understand how genetics affects their health and lives

Preimplantation genetic diagnosis new method of screening of 24 chromosomes with the Array CGH method...2

This fact sheet describes how genes affect our health when they follow a well understood pattern of genetic inheritance known as autosomal recessive.

In - Vitro Fertilization Handbook

1. When new cells are formed through the process of mitosis, the number of chromosomes in the new cells

The illustrations below reflect other scientists results in identifying and counting the stages of the onion root tip and the whitefish blastula.

Human Chromosomes lab 5

12.1 The Role of DNA in Heredity

List, describe, diagram, and identify the stages of meiosis.

Chromosomes, Mapping, and the Meiosis Inheritance Connection

National Down Syndrome Society

Chapter 3. Cell Division. Laboratory Activities Activity 3.1: Mock Mitosis Activity 3.2: Mitosis in Onion Cells Activity 3.

Cell Division CELL DIVISION. Mitosis. Designation of Number of Chromosomes. Homologous Chromosomes. Meiosis

Page The production of monoploid cells by spermatogenesis occurs in (1) zygotes (3) ovaries (2) testes (4) meristems

LEUKODYSTROPHY GENETICS AND REPRODUCTIVE OPTIONS FOR AFFECTED FAMILIES. Leila Jamal, ScM Kennedy Krieger Institute, Baltimore MD

1 Mutation and Genetic Change

CELL DIVISION. STAGES OF MITOTIC DIVISION (Diag. C1)

Science 10-Biology Activity 14 Worksheet on Sexual Reproduction

Genetics and Pregnancy Loss

The Cell Cycle: A series of modeling activities

Sex for the purposes of this class refers to 4 components

Fact Sheet 14 EPIGENETICS

Lecture 2: Mitosis and meiosis

Workshop: Cellular Reproduction via Mitosis & Meiosis

Reproductive Technology. Chapter 21

1. Why is mitosis alone insufficient for the life cycle of sexually reproducing eukaryotes?

Science 10-Biology Activity 15 The Development of the Human Embryo

Assisted Reproductive Technologies at IGO

Laboratory Observing the Cell Cycle of Onion Root Tip Cells

RECURRENT PREGNANCY LOSS DR.RAJALAKSHMI SRINIVASAN SPECIALIST GYNECOLOGIST ZULEKHA HOSPITAL DUBAI

Gene Therapy and Genetic Counseling. Chapter 20

A test your patients can trust.

14.3 Studying the Human Genome

CHROMOSOME STRUCTURE CHROMOSOME NUMBERS

Basic Human Genetics: Reproductive Health and Chromosome Abnormalities

The following chapter is called "Preimplantation Genetic Diagnosis (PGD)".

Array Comparative Genomic Hybridisation (CGH)

Cell Division Mitosis and the Cell Cycle

Preimplantation Genetic Diagnosis. Evaluation for single gene disorders

Genetics for the Novice

Practice Problems 4. (a) 19. (b) 36. (c) 17

Lecture 7 Mitosis & Meiosis

Biology 3201 Grading Standards June 2008

Unit 1 Higher Human Biology Summary Notes

CCR Biology - Chapter 7 Practice Test - Summer 2012

Chromosomal Basis of Inheritance. Ch. 3

Chapter 8: Variation in Chromosome Structure and Number


Biology 3A Laboratory MITOSIS Asexual Reproduction

Name: 4. A typical phenotypic ratio for a dihybrid cross is a) 9:1 b) 3:4 c) 9:3:3:1 d) 1:2:1:2:1 e) 6:3:3:6

FAMILY PLANNING AND PREGNANCY

Balanced. translocations. rarechromo.org. Support and Information

Germ cell formation / gametogenesis And Fertilisation

DNA Fingerprinting. Unless they are identical twins, individuals have unique DNA

Mitosis in Onion Root Tip Cells

Non-Invasive Prenatal Testing (NIPT) Factsheet

Cellular Reproduction

Consent to Perform Preimplantation Genetic Screening (PGS) using. Comparative Genomic Hybridization (acgh) or Next Generation Sequencing (NGS)

Reproductive System. from the Human Body System Series. catalog # Published & Distributed by AGC/UNITED LEARNING

Trisomy 13 (also called Patau s syndrome or T13)

DNA Determines Your Appearance!

Abortion and Stem Cell Debate Background Information

Preimplantation Genetic Diagnosis (PGD) for Fanconi Anemia and HLA matching

If you are signing for a minor child, you refers to your child throughout the consent document.

Objectives Role of Medical Genetics in Hearing Loss Evaluation. 5 y.o. boy with severe SNHL

Meio-Socks. Other Genetic Yarns HOW-TO-DO-IT A NTHEA M. STAVROULAKIS

MODEL FORM. [Program s SART Name and Number] INFORMED CONSENT FOR EGG DONORS

Lab 3: Testing Hypotheses about Mitosis

Genetics 1. Defective enzyme that does not make melanin. Very pale skin and hair color (albino)

AS Biology Unit 2 Key Terms and Definitions. Make sure you use these terms when answering exam questions!

Reebops. A model organism for teaching genetic concepts

B2 5 Inheritrance Genetic Crosses

X Linked Inheritance

FERTILITY AND AGE. Introduction. Fertility in the later 30's and 40's. Am I fertile?

The cell cycle, mitosis and meiosis

Transcription:

Human Karyotyping Lab # Background: Occasionally chromosomal material is lost or rearranged during the formation of gametes or during cell division of the early embryo. Such changes, primarily the result of nondisjunction or translocation, are so severe that the pregnancy ends in miscarriage or fertilization does not occur at all. It is estimated that one in 156 live births have some kind of chromosomal abnormality. Some of the abnormalities associated with chromosome structure and number can be detected by a test called a karyotype. A karyotype can show prospective parents whether they have certain abnormalities that could be passed on to their offspring, or it may be used to learn the cause of a child s disability. Karyotypes can also reveal the gender of a fetus or test for certain defects through examination of cells from uterine fluid a procedure called amniocentesis or through sampling of placental membranes. Over 400,000 karyotype analyses are performed each year in the U.S. and Canada. To create a karyotype, chromosomes from a cell are stained and photographed. The photograph is enlarged and cut up into individual chromosomes. The homologous pairs are identified and arranged in order by size (with the exception of the sex chromosomes; these appear last). These tests are typically done on a sample of blood, although any body cell could be used. The cell must be undergoing mitosis preferably in metaphase so that the chromosomes are replicated, condensed, and visible under a microscope. (adapted from: http://www.slic.wsu.edu/bios/biol107/107karyotypesp05.pdf) Purpose: The purpose of this laboratory experience is: -understand what a karyotype is and how it is performed. -understand the reason for performing a karyotype, especially for those with a higher risk of genetic defect in their lineage. -to determine what genetic defect is present in a chromosome sample. -to investigate a variety of genetic disorders that commonly occur and are studied in biology classes. Materials: The following materials are needed to perform this laboratory experience: -Scissors -tape -ruler -small envelope Procedure: The following procedure is utilized to perform this laboratory experience: 1. Using the attached sheets, complete four different karyotypes: One normal male, One normal female, two different disorders of your choice out of the four. Additional laboratory minutes may be granted for work above and beyond the four required karyotypes. 2. Working slowly and carefully, using scissors cut out the chromosome on one page labeled 1 and find its EXACT match elsewhere on the page (it will not be numbered). Cut out this chromosome and tape BOTH chromosomes side by side on a data page that has the heading filled out. 3. Continue this procedure until you have matched all chromosomes and taped each of them in the corresponding place on the data page. 4. If you are caught short of time, use the coin envelope to store any chromosomes you may have clipped out and not matched. DO NOT CUT OUT ALL CHROMOSOMES AND THEN ATTEMPT TO MATCH THEM!!! Cut out only one at a time or you will lose chromosomes. 5. In the event that you have an extra chromosome, DO NOT THROW IT OUT! It is the chromosome that causes your mutation/disorder and you must match it correctly. 6. Once your chromosomes are all cut out and included in the karyotypes, answer the questions and complete the lab.

Questions: Answer the following questions before turning in your lab. 1. What four karyotypes did you choose to complete? 2. How could you determine if your karyotype was male or female? 3. Complete the following table: Karyotype #1 Individual is a Number of chromosomes: What is the sex? Normal or Mutated (circle one) If mutated, name the disorder below: Karyotype #2 Individual is a Number of chromosomes: What is the sex? Normal or Mutated (circle one) If mutated, name the disorder below: Karyotype #3 Individual is a Number of chromosomes: What is the sex? Normal or Mutated (circle one) If mutated, name the disorder below: Karyotype #4 Individual is a Number of chromosomes: What is the sex? Normal or Mutated (circle one) If mutated, name the disorder below:

Chromosomes Picture #1

Chromosome Picture #2

Chromosome Picture #3

Chromosome Picture #4

Chromosome Picture #5

Chromosome Picture #6