t( 15;17 )

Molecular Haematology


Description

The chromosomal translocation t( 15;17 ) has been shown to be important in clinical practice. This aberration is specific for acute promyelocytic leukaemia, and indicates the specific treatment by the differentiative agent all-trans retinoic acid ( ATRA ). The molecular consequence of this translocation is PML-RARa gene fusion. The are 3 breakpoint cluster regions, one at the 5'end and 2 at the 3' end of the PML gene, requiring amplification of 2 separate PCR's with different primers and Mg2+ concentrations. The polymerase chain reaction ( PCR ) is a rapid and powerful method for detection of cDNA after reverse transcription of mRNA. PCR efficiently detects the chromosomal translocation t( 15;17 ) and may also be used to detect minimal residual disease.


Indications

Used to monitor cases known to have t( 15;17 ).


Sample Type

5ml EDTA blood or bone marrow, less than 48 hrs old.


Turnaround Time

Within 4 weeks


Testing Frequency

As required.


External Notes

Level of detection 1 leukaemic cell in 103 normal cells.


Please note: the above information is subject to change and we endeavour to keep this website up to date wherever necessary.

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t( 15;17 )