McGhee J D, Felsenfeld G
Cell. 1983 Apr;32(4):1205-15. doi: 10.1016/0092-8674(83)90303-3.
We show that, contrary to expectations, restriction enzyme cleavage of chicken erythrocyte nucleosome core particle DNA generates a series of distinct subnucleosome fragments. These fragments do not result from bulk nucleosome phasing in vivo, but arise from micrococcal nuclease cleavages internal to the core particle, at roughly 10-base pair intervals and at AT-rich sequences. Those 145-base pair DNA fragments remaining intact are a biased population in which the guanine content can fluctuate by as much as 10%, with a 10-base pair period. We suggest that these same considerations, when applied to a unique DNA sequence, are the true explanation for several previous claims for nucleosome phasing.
我们发现,与预期相反,鸡红细胞核小体核心颗粒DNA经限制性内切酶切割会产生一系列不同的亚核小体片段。这些片段并非体内大量核小体相位排列的结果,而是由核心颗粒内部微球菌核酸酶的切割产生的,切割间隔约为10个碱基对,且发生在富含AT的序列处。那些保持完整的145个碱基对的DNA片段是一个有偏向性的群体,其中鸟嘌呤含量可波动高达10%,呈现10个碱基对的周期。我们认为,当将这些相同的因素应用于独特的DNA序列时,就能真正解释之前关于核小体相位排列的若干说法。