Chromosomes and Karyotypes

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

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

PSI Biology Mitosis & Meiosis

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

Heredity - Patterns of Inheritance

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

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

Chapter 13: Meiosis and Sexual Life Cycles

BioSci 2200 General Genetics Problem Set 1 Answer Key Introduction and Mitosis/ Meiosis

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

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

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.

Sex for the purposes of this class refers to 4 components

Lecture 2: Mitosis and meiosis

Chapter 13: Meiosis and Sexual Life Cycles

Meiosis is a special form of cell division.

Mitosis, Meiosis and Fertilization 1

Basic Human Genetics: Reproductive Health and Chromosome Abnormalities

CHROMOSOME STRUCTURE CHROMOSOME NUMBERS

CHROMOSOMES AND INHERITANCE

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

Chromosomes, Mapping, and the Meiosis Inheritance Connection

Fluorescence in situ hybridisation (FISH)

12.1 The Role of DNA in Heredity

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

The Developing Person Through the Life Span 8e by Kathleen Stassen Berger

Chromosome Mapping Assignment INSTRUCTIONS

Human Chromosomes lab 5

Chapter 8: Variation in Chromosome Structure and Number

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

Human Blood Types: Codominance and Multiple Alleles. Codominance: both alleles in the heterozygous genotype express themselves fully

*Please consult the online schedule for this course for the definitive date and time for this lecture.

Trisomy 13 (also called Patau s syndrome or T13)

Fact Sheet 14 EPIGENETICS

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

your questions answered the reassurance of knowing A guide for parents-to-be on noninvasive prenatal testing.

Name: Class: Date: ID: A

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

Chromosomal Basis of Inheritance. Ch. 3

Biology Final Exam Study Guide: Semester 2

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

A test your patients can trust.

Chapter 9 Patterns of Inheritance

REI Pearls: Pitfalls of Genetic Testing in Miscarriage

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

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

UNIT 13 (OPTION) Genetic Abnormalities

Science 10-Biology Activity 14 Worksheet on Sexual Reproduction

Lecture 7 Mitosis & Meiosis

LAB 8 EUKARYOTIC CELL DIVISION: MITOSIS AND MEIOSIS

Abortion and Stem Cell Debate Background Information

Genetics and Pregnancy Loss

Reebops. A model organism for teaching genetic concepts

X-Plain Low Testosterone Reference Summary

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

CHAPTER 15 THE CHROMOSOMAL BASIS OF INHERITANCE. Section B: Sex Chromosomes

MCB41: Second Midterm Spring 2009

Sexual Reproduction. and Meiosis. Sexual Reproduction

National Down Syndrome Society

Marrying a relative. Is there an increased chance that a child will have genetic problems if its parents are related to each other?

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

Cell Growth and Reproduction Module B, Anchor 1

CCR Biology - Chapter 7 Practice Test - Summer 2012

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

Female Reproductive System. Unit 8 Lesson 2 Continued

Cell Division Mitosis and the Cell Cycle

A test your patients can trust. A company you know and trust.

DRAGON GENETICS LAB -- Principles of Mendelian Genetics

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

Respiration occurs in the mitochondria in cells.

Biology 1406 Exam 4 Notes Cell Division and Genetics Ch. 8, 9

( ).

First Trimester Screening for Down Syndrome

Lecture 11 The Cell Cycle and Mitosis

4 SEX CHROMOSOMES AND SEX DETERMINATION

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

Chapter 3. Chapter Outline. Chapter Outline 9/11/10. Heredity and Evolu4on

Classify chromosomes in a karyotype according to size and centromere position. Identify metacentric, submetacentric and acrocentric chromosomes

Appendix C DNA Replication & Mitosis

Reproductive System & Development: Practice Questions #1

X Linked Inheritance

Influence of Sex on Genetics. Chapter Six

Forensic DNA Testing Terminology

Introduction Breast cancer is cancer that starts in the cells of the breast. Breast cancer happens mainly in women. But men can get it too.

TERATOGENESIS ONTOGENESIS

LAB : PAPER PET GENETICS. male (hat) female (hair bow) Skin color green or orange Eyes round or square Nose triangle or oval Teeth pointed or square

3 VARIATION IN CHROMOSOME NUMBER & STRUCTURE

Men s Health: Testicular & Breast. September 2012

Workshop: Cellular Reproduction via Mitosis & Meiosis

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

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

Executive summary. Current prenatal screening

17. A testcross A.is used to determine if an organism that is displaying a recessive trait is heterozygous or homozygous for that trait. B.

A trait is a variation of a particular character (e.g. color, height). Traits are passed from parents to offspring through genes.

The cell cycle, mitosis and meiosis

Von Mäusen und Menschen E - 1

Array Comparative Genomic Hybridisation (CGH)

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

HUMAN CHROMOSOMES. Using this criterion, human chromosomes are divided in: metacentric, submetacentric, and acrocentric.

Causes of Birth Defects

Transcription:

Chromosomes and Karyotypes

Review of Chromosomes Super coiled DNA Structure: It may be A single coiled DNA molecule

Chromosomes Or after replication, it may be two coiled DNA molecules held together at the center. The area it is held together is called the centromere. Chromatid: Each DNA molecule in a double stranded chromosome (therefore, each replicated chromosome has 2 chromatids).

Chromosomes Humans have 46 chromosomes 23 chromosomes from Mom 23 chromosomes from Dad Two Types of Chromosomes: 1. Autosomes ALL chromosomes except the sex chromosomes 22 pairs (Chromosomes #1-22)

Two Types of Chromosomes: 2. Sex Chromosomes: 1 pair (human chromosome #23) Determine the sex of an organism In mammals & fruit flies XX is female, XY is male Female Male In birds ZZ is male, ZW female *FIX IN NOTE TEMPLATE

Two Types of Cells 1. Somatic Cells: All cells of the body 2. Sex Cells: Egg and Sperm

1. Somatic Cells: Chromosomes are Homologues: Homo means same. Homologous chromosomes are the same size and shape, and carry genes for the same traits. Called a homologous pair

Homologous Chromosomes Humans have 23 homologous pairs in all cells except sex cells Cells with 23 homologous pairs care called DIPLOID or 2N N stands for number of unique chromosomes Cells with 23 homologous pairs are called somatic cells In humans, all cells except sperm and egg are somatic cells

2. Sex cells (sperm and egg) only have one of each chromosome No homologous pairs Called HAPLOID or N (think half ) Sex Cells are called GAMETES.

Karyotypes A picture of the chromosomes in which the chromosomes arranged in matching (homologous) pairs

Karyotypes Arranged in size order from largest pair to smallest pair The sex chromosomes (X and Y) are usually the last pair, though they are not the smallest.

Karyotypes How are they used? They are used for diagnosis of genetic abnormality based on the number of chromosomes. They are used to determine the sex of an unborn child.

Karyotypes How are they prepared? Cells are collected from a variety of sources: Amniotic fluid via a pre-natal amniocentesis Blood Sample

Karyotypes How are they prepared? Sample of cells are allowed to continue dividing Cells are stopped when in METAPHASE of MITOSIS.

Karyotypes A photograph of the chromosomes is taken and enlarged. A trained technician matches the chromosomes into the homologous pairs based on three characteristics: Size Banding Centromere position

Chromosomal Disorders Normal: Have 2 matching chromosomes for each of the 23 pairs Aneuploidy: Having one more or one less of one of the chromosomes of the 23 pairs.

Chromosomal Disorders Monosomy: Missing one chromosome of one of the pairs Turner s syndrome; Monosomy 23 Missing one of the X chromosomes Female who is X0 instead of XX

Chromosomal Disorders Symptoms: Short stature Webbed neck Lack of secondary sex characteristics A hollow appearance to the chest Lack of menstruation Low hairline "Droopy" eyelids

Chromosomal Disorders Trisomy: An extra chromosome of one of the pairs Down syndrome; Trisomy 21 Extra chromosome #21 (so, there are 3 chromosome #21)

Chromosomal Disorders Incidence One of the most common chromosomal abnormalities Frequency varies a lot according to the age of the mother. The rate is only 1 in 2,000 for women 20 years old In those 40 or older, it is 1 birth in 100.

Genetic Disorders Symptoms: Small head, flattened in the back Broad, flat face Relatively small eyes, turned up at the outer corners Oversize tongue in a small mouth Single horizontal line across the palm, instead of the usual "head" and "heart" lines Short stature, with short limbs and stubby fingers

Genetic Disorders Kleinfelter s Syndrome; Trisomy 23 Extra sex chromosome Male who is XXY instead of XY The most common sex chromosome abnormality in males

Genetic Disorders Symptoms: Arm span exceeds height by more that an inch. No or very little body hair and no facial hair. High voice Minimal muscle growth in arms/legs Small testicles Breast Tissue (not just fat, but actually firm breasts) Low Testosterone Level