Team:Imperial College London/M3/DamMethylation

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=[[Image:II09_Thumb_m3.png|40px]]<font size='5'><b>Module 3: Genome Deletion Overview</b></font>=
=[[Image:II09_Thumb_m3.png|40px]]<font size='5'><b>Module 3: Genome Deletion Overview</b></font>=
==Dam methylation==
==Dam methylation==
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Restriction enzymes often come together with methylation enzymes to form a restriction-modification system.  This prevents the genome of the cell from being cleaved by the restriction enzyme. <br>
To protect against DNA destruction due to basal levels of restriction enzyme production, we have made use of the native E. coli Dam methylase protection system. <br>
To protect against DNA destruction due to basal levels of restriction enzyme production, we have made use of the native E. coli Dam methylase protection system. <br>

Revision as of 22:46, 11 October 2009

Contents

II09 Thumb m3.pngModule 3: Genome Deletion Overview

Dam methylation

Restriction enzymes often come together with methylation enzymes to form a restriction-modification system. This prevents the genome of the cell from being cleaved by the restriction enzyme.

To protect against DNA destruction due to basal levels of restriction enzyme production, we have made use of the native E. coli Dam methylase protection system.

II09 Dpn meth.jpg


Dam methylases recognise the sequence GATC and methylate the Adenine base. This prevents the restriction enzymes from recognising the sequence and cleaving it. Therefore, only high levels of restriction enzyme (ie. after thermal triggering) will cleave the DNA.

There is an asymmetry between the function of restriction enzymes and methylases. Restriction enzymes can cause just one cleavage, which if unrepaired, kills the cell. However, to effectively protect the cell, methylases need to methylate all the recognition sites.

The methylase protection system has been used with its native promoter to prevent basal levels of restriction enzyme expression from killing the cell. The use of a native promoter shows the highly sensitive balance that exist between restriction enzymes and methylases.


References

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