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| {{familytree | | | |A11| | | | |A11 =Molecular<br>pathology}} | | {{familytree | | | |A11| | | | |A11 =Molecular<br>pathology}} |
| {{familytree | |,|-|-|^|-|-|.|}} | | {{familytree | |,|-|-|^|-|-|.|}} |
| {{familytree | B11 | | | | B12 |B11=Molecular<br>techniques|B12=Cytogenetics}} | | {{familytree | B11 | | | | B12 |B11=Molecular<br>techniques|B12=[[Cytogenetics]]}} |
| {{familytree/end}} | | {{familytree/end}} |
| </center> | | </center> |
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| ==Cytogenetics== | | ==Cytogenetics== |
| ===General===
| | {{Main|Cytogenetics}} |
| *Large changes (chromosomal).
| | This deals with karyotyping and ISH. |
| **Maximum resolution 3-4 megabase pairs (3-4 million base pairs); may be less - dependent on band density.<ref>{{Ref WMSP|695}}</ref>
| |
| *Morphologic data.
| |
| | |
| ===Techniques===
| |
| *ISH = in situ hybridization.
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| **FISH = fluorescent in situ hybridization.
| |
| **SISH = silver in situ hybridization.<ref>URL: [http://www.immunoportal.com/modules.php?name=News&file=article&sid=186 http://www.immunoportal.com/modules.php?name=News&file=article&sid=186]. Accessed on: 2 May 2011.</ref>
| |
| *Karyotyping.
| |
| | |
| ====Karyotyping====
| |
| What?
| |
| *Metaphase nuclei.
| |
| | |
| How?
| |
| *Chromosomes are identified by:
| |
| **Size (chromosome 1 = largest, chromosome 22 = smallest).
| |
| **Position of centromere.
| |
| **Banding pattern - using (special) stains:
| |
| ***Several different techniques (stains) are used:<ref>URL: [http://www.ncbi.nlm.nih.gov/pmc/articles/PMC355922/ http://www.ncbi.nlm.nih.gov/pmc/articles/PMC355922/]. Accessed on: 10 May 2011.</ref>
| |
| ****Examples: Q-banding (Q=Quinacrine), C-banding (C=constitutive heterchromatin), G-banding (G=Giemsa), R-banding (R=reverse).
| |
| *****Q-banding is the standard at UHN.
| |
| | |
| Image:
| |
| *[http://commons.wikimedia.org/wiki/File:NHGRI_human_male_karyotype.png Karyotype (WC)].
| |
| | |
| Notes:
| |
| *Quinacrine dye - AT-rich regions brighter than GC-rich regions.
| |
| | |
| ====ISH====
| |
| *Usu. interphase nuclei.
| |
| | |
| May be prepared from:
| |
| *In situ paraffin sections (section 4 micrometers thick).
| |
| *Isolated nuclei (section 10 micrometers thick).
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| *Cytospin.
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| *Cultured cells.
| |
| | |
| =====Probe types=====
| |
| Types:
| |
| *Fusion (two colours).
| |
| *Breakapart (two colours).
| |
| *Deletion/duplication (e.g. trisomy).
| |
| | |
| Image:
| |
| *[http://commons.wikimedia.org/wiki/File:Bcrablmet.jpg Bcr-Abl translocation (WC)].
| |
|
| |
|
| ==Other garbage== | | ==Other garbage== |