Drinkwater R D, Wilson P J, Skinner J D, Burgoyne L A
Flinders Medical Centre, Adelaide, SA, Australia.
Nucleic Acids Res. 1987 Oct 12;15(19):8087-103. doi: 10.1093/nar/15.19.8087.
Four separate features could be distinguished in Fe-DNAase-1 digestions of human lymphoblast nuclei: a di-nucleosomal (2N) repeat, a mono-nucleosomal (1N) repeat, a component of "random" DNA, and triple splitting of major peaks. The random component is major, is unlikely to be completely artifactual, and is what would be expected from the face to face layering model of Subirana et. al., (1). The 2N pattern appeared to be associated with compact, metaphase-type chromatin, whereas the 1N pattern was associated with more exposed chromatin. These two modes are explained in terms of orderly back-to-back folding of zig-zag nucleofilaments, and face-to-face folding respectively. Hybridization studies indicated that the centromeric classes of repetitive DNA had the same digestion spectra as the major interspersed classes of repetitive DNA, and DNA enriched in transcriptionally active sequences. It is suggested that current coil models are all inadequate explanations of higher order chromatin packing.
在人淋巴母细胞核的铁-脱氧核糖核酸酶-1消化过程中可区分出四个不同的特征:双核小体(2N)重复序列、单核小体(1N)重复序列、“随机”DNA成分以及主峰的三重分裂。随机成分占主要部分,不太可能完全是人为造成的,这是苏比拉纳等人(1)的面对面分层模型所预期的。2N模式似乎与紧密的中期型染色质相关,而1N模式与更暴露的染色质相关。这两种模式分别用锯齿状核丝有序的背对背折叠和面对面折叠来解释。杂交研究表明,着丝粒类重复DNA与主要的散布类重复DNA以及富含转录活性序列的DNA具有相同的消化谱。有人提出,目前的螺旋模型都不足以解释高阶染色质包装。