Cytogenetics ‘2’ - KSU
Transcript of Cytogenetics ‘2’ - KSU
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CYTOGENETICS ‘2’Karyotyping, cell preparation and staining
9/8/2015NAHLA BAKHAMIS. MSc
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9/8/2015NAHLA BAKHAMIS. MSc
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Chromosomes
• 1970 Banding techniques
- identification of individual chromosomes
• Karyotype and FISH
- types of abnormalities;
. Extra copy of chromosome
. Missing copy of chromosome
. Structural abnormalities
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Chromosomes • Centromere
- movement during cell division
- divides the chromosomes into short (p) and long (q) arms
• Telomere - Tip of each chromosome
- seal chromosomes and retain chromosome integrity
- consists of tandem repeats TTAAGGG
- maintained by enzyme; telomerase
- telomerase & in tandem repeats imp in aging & cell death
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9/8/2015NAHLA BAKHAMIS. MSc
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Chromosomes Classified according to position of centromere ;
• Central centromere; metacentric
• Sub-terminal centromere ; acrocentric
- have satellites which contain multiple copies of genes for
ribosomal RNA
• Intermediate centromere; submetacentric
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Chromosomes
Chromosomes ideogram
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Chromosomes
• 22 autosomal, and sex chromosomes in pairs
• Classified according to:
- Length
- position of centromere
- presence or absence of satellites
• Chromosomes divided into groups labelled A-G
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Chromosomes
Chromosomes divided into groups labelled A-G
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Chromosomes
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Karyotyping
Staining method to identify chromosomes in a single cell
G banding .. Giemsa
Q banding .. Quinacrine, fluorescent stain (structural rearrangements)
R banding .. Reverse
C banding .. Centromeric (heterochromatin)
Ag-Nor stain .. Nucleolar Organizing Regions (active)
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Cell preparation
Required cell stage; metaphase
1. Culture cells until sufficient mitotic activity
2. Harvest protocol:
• Mitotic arrest
• Add hypotonic treatment
• Fixation with mix of methanol ; acetic acid
• Want long chromosomes with non-overlapping
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Harvest protocol
a. Mitotic arrest:
Colemid arrest cells at the equatorial plate by preventing
spindle fibres formation
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Mitosis
Studyblue.com
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Harvest protocol
b. Hypotonic treatment:
• Cells swell (osmotic potential):
reduce cytoplasm & allow chromosome spreading
• RBCs lysis
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Harvest protocol
c. fixation:• Prevent further swelling
• Maintain good morphology
Methamoglobin: brown supernatant formed after addition of fixative
Multiple fixative -- clear supernatant
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Harvest protocol
Harvesting procedure:
1. Add 100µ colemid to the culture 20min at 37C 2. Spin; 8 min at 1000 RPM
3. Discard supernatant, add 10ml hypotonic solution
4. Incubate 20min at 73C
5. Add 5 drops fixative 3:1 methanol:acetic acid, spin
6. Discard supernatant & resuspend pellets
7. Add 10ml fixative 30min at RT
8. Repeat until clear solution
9. Preserve at fridge (-4C) not freezer
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Dropping protocol
• 8 drops on slide
• dry in a controlled environmental evaporation chambers
• Observe mitotic index
• Aging: 60C over night Or 90C for 90min for better banding
pattern
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Dropping
• Residual cytoplasm staining quality
• Dark chromosomes with sharp borders
• No overlapping, no burst
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Natureprotocols IMSTARA.com glown.com
Burst overlapped good
Metaphase compactness
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Cell preparation
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Banding (staining)
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G banding
• Most common
• Chromosomes treated with trypsin;
- denatures protein
allow Gimsa react with exposed DNA (wang &Federoff)
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G banding Gimsa stain:
• Each chromosomes characterised by dark & light band
• 400 bands / haploid genome
• Dark bands are gene poor
• Appropriately stained chromosomes;
neither too dark nor too pale
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G banding
Under-trypsinized chromosomes:
Indistinct bands, little contrast and fuzzy
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G banding
Over-trypsinized chromosomes:
• Sharp bands and frazzled at the end
• Eventually become very pale (ghost-like) and very swollen
• Fetal calf serum immersion is recommended (α1-antitrypsin)
Broz. J et al, Scielo (2000)
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G banding
Staining procedure:
• Slides must cool down to RT• Immerse in trypsin solution 10-15 sec
• Wash in phosphate buffer or serum (stop trypsin activity)
• Transfer to Gimsa stain 90-120 sec
• Raines in d-water
• Dry
• Examine under microscope
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G banding
• Count chromosomes in 10-15 metaphases
• Count 30 if mosaicism suspected
• Detailed analysis of 3-5 metaphase
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• 13,18,21 gene poor (very dark chromosomes)
• 21 smaller than 22
• 21 (200 genes) twice as mane as 22 (400
genes)
• Bands stains darkly with Gimsa DNA rich in AT
pairs (genes poor)
• Pale bands (gene active)
G banding
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28Normal Male Karyotype Normal Female Karyotype
G banding
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Q banding
• Especially used for Y chromosome abnormalities or mosaicism
• similar to G band (exp. It can detect polymorphism)
• Need fluorescent microscope
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• Used to identify X chromosome
abnormality
• Heat chromosomes before treating
with Gimsa
• Light and dark bands are reversed
R banding
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C banding
• To identify centromere/ heterochromatin
• Heterochromatic region:- contains highly repetitive DNA sequence
- highly condense chromatin fibres
- genetically inactive (structural elements)
• Treated chromosomes:
- Acid
- Alkaline
- Then G band
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Karyotyping
Organization of the chromosomes, lined up according to:
• Size
• Location of centromere
• Banding pattern
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Karyotyping
Natureprotocols.com
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Karyotyping
Natureprotocols.com
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Ideogram
Is a schematic representation of
chromosomes
Show relative size of chromosomes
& their banding patterns
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ISCN
International System for Human Cytogenetic Nomenclature
• Each area of chromosome given number
• Lowest number (proximal) to centromere
• Highest number (distal to centromere)
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ISCN
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ISCN
, 46,XX,del(5p)
separates
- chromosome numbers
- Sex chromosomes
- Chromosome abnormalities
; 46,XX,t(2;4)(q21;q24)
Separates
- Altered chromosomes
- Break points structural rearrangement involving more than 1
chromosome
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ICSN
Normal Male
46,XY
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Normal Female
46,XX
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Karyotyping activity
• Make a karyotype:
http://mrforde.blogspot.com/2009/01/karyotype-game.html
Have fun ;)
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Thank You