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HpaII [[enzyme]] can cleave a DNA only when C is protected by [[methylation]].<ref>{{cite journal |author1=Waalwijk, C|author2=Flavell, R A|pages=3231–6|volume=5|pmc=342244|title=MspI, an isoschizomer of hpaII which cleaves both unmethylated and methylated hpaII sites|doi=10.1093/nar/5.9.3231|pmid=704354|year=1978|journal=Nucleic Acids Res.}}</ref> This feature is exploited for determination of the clonal origin of a [[mammalian]] female tumor through [[HUMARA assay]].
HpaII will not cut sites that have been methylated by SssI methyltransferase or HpaII methyltransferase. When the sites have been methylated by MspI methyltransferase, the enzyme will cut 300 times slower than unmethylated DNA and 50 times slower if the DNA is hemi-methylated.<ref>McClelland, M., Nelson, M., Raschke, E. (1994). Nucleic Acids Research 22, No. 17, 3640-3659.</ref> This feature is exploited for determination of the clonal origin of a [[mammalian]] female tumor through [[HUMARA assay]].


== References ==
== References ==

Revision as of 01:06, 22 March 2017

HpaII (IntEnz: EC 3.1.21.4) is a restriction enzyme obtained from the microorganism called Haemophilus parainfluenzae. It is a DNA restriction enzyme, therefore it has the ability to cut the DNA from certain region as demonstrated below.[1] It has the ability to produce cohesive ends, which are rather useful in constructing plasmids.

Recognition sequence Cut results
5' CCGG
3' GGCC
5' C  CGG
3' GGC  C

HpaII will not cut sites that have been methylated by SssI methyltransferase or HpaII methyltransferase. When the sites have been methylated by MspI methyltransferase, the enzyme will cut 300 times slower than unmethylated DNA and 50 times slower if the DNA is hemi-methylated.[2] This feature is exploited for determination of the clonal origin of a mammalian female tumor through HUMARA assay.

References

  1. ^ InterProIPR019062
  2. ^ McClelland, M., Nelson, M., Raschke, E. (1994). Nucleic Acids Research 22, No. 17, 3640-3659.