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Karyotyping

Karyotyping. CYTOGENETICS. Is the study of the structure and properties of chromosomes, chromosomal behaviour during mitosis and meiosis, chromosomal influence on the phenotype and the factors that cause chromosomal changes (Hare and Singh, 1979). . Human Chromosomes.

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Karyotyping

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  1. Karyotyping

  2. CYTOGENETICS • Is the study of the structure and properties of chromosomes, chromosomal behaviour during mitosis and meiosis, chromosomal influence on the phenotype and the factors that cause chromosomal changes (Hare and Singh, 1979).

  3. Human Chromosomes • A “normal” human carries 23 PAIRS of chromosomes (1 set came from the mother, 1 set came from the father) • 22 of these sets are called autosomes (or “self chromosomes”) • 1 set are the sex chromosomes • A female carries two X chromosomes (XX) • A male carries an X chromosome and a Y chromosome (XY)

  4. Why do scientists look at chromosomes? • Scientists can diagnose or predict genetic disorders by looking at chromosomes. • This kind of analysis is used in prenatal testing and in diagnosing certain disorders, such as • Down syndrome etc

  5. Chromosome abnormalities • Chromosome abnormalities can be • numerical, as in the presence of • extra • or missing chromosomes, • or structural as in translocations, inversions, large scale deletions or duplications.

  6. What is a Karyotype? • A display or photomicrograph of an individual’s somatic-cell metaphase chromosomes that are arranged in a standard sequence (usually based on number, size, and type)

  7. How Do Scientists Identify Chromosomes? • Three key features to identify their similarities and differences: • Size. This is the easiest way to tell two different chromosomes apart. • Banding pattern. The size and location of Giemsa bands on chromosomes make each chromosome pair unique. • Centromere position. Centromeres are regions in chromosomes that appear as a constriction. • Using these key features, scientists match up the 23 pairs

  8. Nomenclature of chromosomes

  9. In metacentric chromosomes, the centromere lies near the center of the chromosome.Submetacentric & very Submetacentric chromosomes, have a centromere that is off-center, so that one chromosome arm is longer than the other. In acrocentric chromosomes, the centromere resides very near one end. Mazen Zaharna Molecular Biology 1/2009

  10. PREPARATION OF CHROMOSOMES

  11. Normal Female

  12. Normal Male

  13. Chromosomal Abnormalities • Alterations in chromosome number. • Euploid - normal set (2n) • Polyploidy – extra set of the entire genome. • (3n, 4n etc) • Aneuploidy – the number of chromosomes is not a multiple of the normal haploid number. • Monosomy • one member of a chromosome pair is missing, (2n-1) • Trisomy • one chromosome set consists of 3 copies of a chromosome, (2n+1)

  14. Turner Syndrome

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