Hydrophobicity of methylated DNA as a possible mechanism for gene silencing

被引:34
作者
Kaur, Parminder [1 ,2 ]
Plochberger, Birgit [3 ]
Costa, Peter [2 ]
Cope, Stephanie M. [2 ,4 ]
Vaiana, Sara M. [2 ,4 ]
Lindsay, Stuart [1 ,2 ,4 ,5 ]
机构
[1] Arizona State Univ, Biodesign Inst, Tempe, AZ 85287 USA
[2] Arizona State Univ, Dept Phys, Tempe, AZ 85287 USA
[3] Vienna Univ Technol, Inst Appl Phys, A-1040 Vienna, Austria
[4] Arizona State Univ, Ctr Biol Phys, Tempe, AZ 85287 USA
[5] Arizona State Univ, Dept Chem & Biochem, Tempe, AZ 85287 USA
关键词
CYTOSINE METHYLATION; FORCE MICROSCOPY; CHROMATIN; FLEXIBILITY; COMPACTION; TRANSITION; HYDRATION;
D O I
10.1088/1478-3975/9/6/065001
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
AFM images show that chromatin reconstituted on methylated DNA (meDNA) is compacted when imaged under water. Chromatin reconstituted on unmethylated DNA is less compacted and less sensitive to hydration. These differences must reflect changes in the physical properties of DNA on methylation, but prior studies have not revealed large differences between methylated and unmethylated DNA. Quasi-elastic light scattering studies of solutions of methylated and unmethylated DNA support this view. In contrast, AFM images of molecules at a water/solid interface yield a persistence length that nearly doubles (to 92.5 +/- 4 nm) when 9% of the total DNA is methylated. This increase in persistence length is accompanied by a decrease in contour length, suggesting that a significant fraction of the meDNA changes into the stiffer A form as the more hydrophobic meDNA is dehydrated at the interface. This suggests a simple mechanism for gene silencing as the stiffer meDNA is more difficult to remove from nucleosomes.
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页数:8
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