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Novel tools for unbiased DNA differential methylation screening
被引:2
|作者:
Tanas, Alexander S.
[1
]
Shkarupo, Viktoria V.
[1
,2
]
Kuznetsova, Ekaterina B.
[1
,2
]
Zaletayev, Dmitry V.
[1
,2
]
Strelnikov, Vladimir V.
[1
,2
]
机构:
[1] Russian Acad Med Sci, Med Genet Res Ctr, Moscow 115478, Russia
[2] IM Sechenov Moscow Med Acad, Moscow, Russia
来源:
基金:
俄罗斯基础研究基金会;
关键词:
amplification of intermethylated sites;
capillary electrophoresis;
differential methylation screening;
in silico tool;
methylation-sensitive arbitrarily primed PCR;
virtual imaging;
GENOME;
AMPLIFICATION;
GENES;
AIMS;
D O I:
10.2217/EPI.10.3
中图分类号:
Q3 [遗传学];
学科分类号:
071007 ;
090102 ;
摘要:
DNA differential methylation screening approaches may be hypothesis driven (preselection of the loci to screen) or unbiased (screening precedes mapping of differentially methylated loci). The latter allow for the identification of sequences demonstrating 'nonclassical' methylation behavior in cancer and, thus, widen our concept of tumor biology. Extensive employment of unbiased screening methods is hampered by the troublesome procedures involved in physically mapping the identified differentially methylated DNA fragments. In this special report, we describe a positive experience of optimizing two screening methods, methylation-sensitive arbitrarily primed PCR and amplification of intermethylated sites, with a special focus on simplification, or even exclusion, of sequencing procedures. With our modifications, unbiased screening of DNA differential methylation acquires an easy-to-use workflow, including sophisticated experimental design, high-resolution analysis and simple genomic mapping of the fragments of interest.
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页码:325 / 333
页数:9
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