CYTOGENETICS CONCEPTS

Slides:



Advertisements
Similar presentations
DNA.
Advertisements

Human Genetics.
Cellular reproduction part 2
February 23, 2009 Objective: Discuss the effects of nondisjunction
Cytogenetics = The study of chromosome number, structure, function, and behavior in relation to gene inheritance, organization and expression.
Human Karyotypes and Chromosome Behavior
PowerPoint Presentation Materials to accompany
Chromosomal Structure and Chromosomal Mutations
Chromosomes.
Zoo-352 Principles of genetics Lecture 3 The cell cycle and its checkpoints.
Dr. Nasser A Elhawary Professor of Medical Genetics
CDC’s 2003 Science Ambassador Program
Human Chromosomes: Genotype/Phenotype Muhammad Faiyaz-Ul-Haque, PhD, FRCPath Human Chromosomes: Genotype/Phenotype Muhammad Faiyaz-Ul-Haque, PhD, FRCPath.
Human Medical Genetics LECTURE 1 Human Chromosomes Human Karyotype Muhammad Faiyaz-Ul-Haque, M.Phil, PhD Associate Professor and Consultant Molecular Genetics.
Human Chromosomes Human Karyotype M. Faiyaz-Ul-Haque, PhD, FRCPath
Karyotypes. I. What is a Karyotype? Karyotype = a test to identify and evaluate the size, shape, and number of chromosomes in a sample of body cells.
Section 6-1 Chromosomes. Cell division is the same as reproduction of the cell. Gametes – an organism’s reproductive cells Females – eggs Males – sperm.
Karyotyping. Karyotypes Chromosomes are distinguished by their appearance –size –position of centromere –pattern of bands (when stained) Karyotypes show.
Chromosomal Karyotypes. Chromosomes Definition Genetic structures of cells containing DNA Identification Each chromosome has a characteristic length and.
Human Medical Genetics
TIRUPATHI PICHIAH PhD., Student. Dept of Human Nutrition.
Human Medical Genetics LECTURE 1 Human Chromosomes Human Karyotype Muhammad Faiyaz-Ul-Haque, M.Phil, PhD Associate Professor and Consultant Molecular Genetics.
癌症生物學 1. 授課老師 : 生命科學系胡承波教授 辦公室 : 基礎科學實驗館 206A 電話 : 分機 2479 或 2480 手機 課程目的 : 瞭解癌症生物學的內涵、機制、及發展。 3. 授課方式 : a. 以 powerpoint.
Mitosis  Is a process of cell division which results in the production of two daughter cells from a single parent cell. The daughter cells are identical.
CHROMOSOMES AND CELL REPRODUCTION SECTION 1: CHROMOSOMES Chapter 6 Grade 10 Biology Fall 2010.
Chromosomes and Cell Reproduction Chromosome structure and role in development and reproduction.
BIOLOGY CONCEPTS & CONNECTIONS Fourth Edition Copyright © 2003 Pearson Education, Inc. publishing as Benjamin Cummings Neil A. Campbell Jane B. Reece Lawrence.
Karyotypes and Pedigrees
Cytogenetics Study of Chromosomes Chromosomes 23 pairs Numbered and arranged by size and position of centromere.
GENETICS . (DR.Kumar.k.v Professor, Anatomy 05/03/2012)
Javad Jamshidi Fasa University of Medical Sciences, October 2014 Session 3 Medical Genetics Chromosomes And Cell division.
Biology – Lecture 56 Karyotypes. Karyotype The number and appearance of chromosomes in the nucleus of a eukaryotic cell. The complete set of chromosomes.
Chromosomes and Cell Cycle. All genetic material of a cell is called the genome Genome is composed of DNA Long molecules of DNA organized for cell division.
Javad Jamshidi Fasa University of Medical Sciences, October 2014 Session 3 Medical Genetics Chromosomes And Cell division.
Genetics Lec.3. Chromosomal abnormalities Incidence is 1: 200 newborn, but it is much higher during pregnancy (50% in the first trimester abortions).
Copyright © 2003 Pearson Education, Inc. publishing as Benjamin Cummings To study human chromosomes microscopically, researchers stain and display them.
Clinical Cytogenetics Mohamad Nusier M.D., Ph.D..
Chapter 14 Human Heredity
Karyotypes.
Karyotyping.
Human Chromosomes, Human Karyotype
January 17, 2017 Journal: Why does DNA replicate?.
2/ Diseases caused by mutations in receptor proteins
Cytogenetics = The study of chromosome number, structure, function, and behavior in relation to gene inheritance, organization and expression.
Morgan Moritz, Noah Zhang, Shelleigh Harris, Palmer Moats
LECTURE – 3 Learning objectives
Karyotypes Objective: 6H - describe how techniques such as DNA fingerprinting, genetic modifications, and chromosomal analysis are used to study the genomes.
LECTURE 1 Human chromosomes: Genotype / Phenotype
Chromosomes Chapter 8.
Chromosomes Honors Biology.
Chromosomes.
Chromosomes and Karyotypes
Nondisjunction GT pg (Section 13.10) chromosomal mutation, p.408 (Last paragraph)?? Reg- p. 401, top 374.
Chapter 11 Section 3: Chromosomes and Human Heredity
Applications of DNA Analysis
Chromosome Structure and Mutations
Sexual Reproduction Meiosis.
CHROMOSOMES As a eukaryotic cell prepares to divide the DNA
The Nucleus and DNA.
CHAPTER 8 The Cellular Basis of Reproduction and Inheritance
Fishing for Chromosomes
CHAPTER 8 Chromosomes pp
MISTAKES IN MEIOSIS.
CHROMOSOMES As a eukaryotic cell prepares to divide the DNA
Linkage, crossing over and chromosomal mapping (2).
Cytogenetics Part 1 Dr. Mohammed Hussein
Cytogenetics Part 2 Dr. Mohammed Hussein
CHROMOSOMES As a eukaryotic cell prepares to divide the DNA
Presentation transcript:

CYTOGENETICS CONCEPTS Shaukat Iqbal Postdocs, UNC-CH & USEPA,NC Ph . D -Cancer Cytogenetics Associate Professor

PRINCIPLES OF CLINICAL CYTOGENETICS

Karyotyping is the process of pairing and ordering all the chromosomes of an organism, thus providing a genome-wide snapshot of an individual's chromosomes. Karyotypes are prepared using standardized staining procedures that reveal characteristic structural features for each chromosome. Clinical cytogeneticists analyze human karyotypes to detect gross genetic changes—anomalies What is a Chromosome? The DNA in an individual chromosome is one, long molecule which is highly coiled and condensed. The total number of bases in all the chromosomes of a human cell is approximately six billion and individual chromosomes range from 50 to 250 million bases.

BASIC GENETICS CONCEPTS  Hereditary Similarities Variations

Common chromosome structural disorders Chromosome banding Numerical Chromosome Abnormalities Structural Chromosome Abnormalities Aneuploidies: no disjunction Chromosome breakage syndromes; translocation Sex reversal

Introduction to Cytogenetics Cytogenetics is the study of chromosomes and chromosome abnormalities What is a Chromosome? Chromosomes, composed of protein and DNA, are distinct dense bodies found in the nucleus of cells. Genetic information is contained in the DNA of chromosomes in the form of linear sequences of bases (A,T,C,G).3.2 trillion

Human Chromosome Classification The human chromosome has been classified in to seven groups on the basis of their arm length and position of the centromers . A-1-3 B-4-5 C-6-8 D-9-12 E-13-15 F-16-18 G-19-22 XX, XY

Significance of CEHRDL Cytogenetics is a specialized laboratory test involving the study of normal and abnormal chromosomes. Cytogenetics studies are performed on blood, bone marrow, amniotic fluid, and solid tissue specimens. Cells from the specimen are cultured, harvested and banded then viewed under a microscope for numerical and structural abnormalities in chromosomes. Chromosome analysis is an important laboratory test for birth defects, mental retardation, miscarriage, infertility and cancer. A normal, female karyotype Fluorescent in situ hybridization

Chromosome Rejoin A rejoin is define as an area of chromosomes lying between two adjacent land marks . Land mark indicated the ends of the chromosomes arms, the centromer and certain bands . Banding Techniques: There are three banding technique(QG&R) (Q-AT Specific),(G-banding )(R- Reveres banding) ,where are C banding is used particularly for the identification of Y chromosome.

Designation of Region, Bands and Sub bands in Karyotyping Four items are required: The chromosome number The arm symbol The region number The band number within that region These items are given in order without spacing or punctuation. eg. 1P31 indicates chromosome1, short arm, region 3, band1 Whenever an existing band is subdivided, a decimal point is placed after the original band designation. eg. 1P31 is subdivided into three equal or unequal sub-bands and labeled. 1P31.1, 1P31.2 and 1P31.3 Sub-band 1P31.1 being proximal and 1P31.3 distal to the centromer.

Sister chromatid exchanges in Bloom syndrome When we need for SCEs Sister chromatid exchanges in Bloom syndrome

Clinical phenotype of Turner syndrome

46,XY,t(11;16)(q24;q23)

Translocation: non-random X-inactivation

Sex Reversal: Role of the sry gene

Sex reversal due to translocation of SRY from Y to X