Atomic force microscope imaging of chromatin assembled in Xenopus laevis egg extract

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發表在:Chromosoma vol. 120, no. 3 (Jun 2011), p. 245
主要作者: Fu, Hongxia
其他作者: Freedman, Benjamin S, Lim, Chwee Teck, Heald, Rebecca, Yan, Jie
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Springer Nature B.V.
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100 1 |a Fu, Hongxia 
245 1 |a Atomic force microscope imaging of chromatin assembled in Xenopus laevis egg extract 
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513 |a Feature Journal Article 
520 3 |a   Gaps persist in our understanding of chromatin lower- and higher-order structures. Xenopus egg extracts provide a way to study essential chromatin components which are difficult to manipulate in living cells, but nanoscale imaging of chromatin assembled in extracts poses a challenge. We describe a method for preparing chromatin assembled in extracts for atomic force microscopy (AFM) utilizing restriction enzyme digestion followed by transferring to a mica surface. Using this method, we find that buffer dilution of the chromatin assembly extract or incubation of chromatin in solutions of low ionic strength results in loosely compacted chromatin fibers that are prone to unraveling into naked DNA. We also describe a method for direct AFM imaging of chromatin which does not utilize restriction enzymes and reveals higher-order fibers of varying widths. Due to the capability of controlling chromatin assembly conditions, we believe these methods have broad potential for studying physiologically relevant chromatin structures.[PUBLICATION ABSTRACT]   Gaps persist in our understanding of chromatin lower- and higher-order structures. Xenopus egg extracts provide a way to study essential chromatin components which are difficult to manipulate in living cells, but nanoscale imaging of chromatin assembled in extracts poses a challenge. We describe a method for preparing chromatin assembled in extracts for atomic force microscopy (AFM) utilizing restriction enzyme digestion followed by transferring to a mica surface. Using this method, we find that buffer dilution of the chromatin assembly extract or incubation of chromatin in solutions of low ionic strength results in loosely compacted chromatin fibers that are prone to unraveling into naked DNA. We also describe a method for direct AFM imaging of chromatin which does not utilize restriction enzymes and reveals higher-order fibers of varying widths. Due to the capability of controlling chromatin assembly conditions, we believe these methods have broad potential for studying physiologically relevant chromatin structures. 
650 2 2 |a Animals 
650 1 2 |a Chromatin  |x ultrastructure 
650 2 2 |a Microscopy, Atomic Force 
650 2 2 |a Ovum  |x ultrastructure 
650 1 2 |a Xenopus laevis  |x genetics 
700 1 |a Freedman, Benjamin S 
700 1 |a Lim, Chwee Teck 
700 1 |a Heald, Rebecca 
700 1 |a Yan, Jie 
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