Tatchell K, Van Holde K E
Biochemistry. 1979 Jun 26;18(13):2871-80. doi: 10.1021/bi00580a031.
Core histones (H2A, H2B, H3, and H4) are reconstituted by salt gradient dialysis with DNA molecules ranging in length from 177 bp down to 50 bp. While reconstituted particles containing 125 bp are very similar to native particles, those particles containing a single piece of shorter DNA tend to aggregate. The aggregation depends on the ionic strength and DNA length. The DNA placement on the histone core is not random as determined by pancreatic DNase I digestions of particles containing 32P 5'-end-labeled DNA. Rather, it is found that all DNA molecules, up to 161 bp in length, reassociate with core histones in such a way as to produce defined patterns of DNase I cutting with respect to the 5' ends. Particles were made that contained two pieces of 65-bp DNA. These particles are very similar to native particles under most conditions but tended to dissociation results in the production of two half-nucleosomes (hemisones).
核心组蛋白(H2A、H2B、H3和H4)通过盐梯度透析与长度从177 bp到50 bp不等的DNA分子进行重构。虽然含有125 bp的重构颗粒与天然颗粒非常相似,但那些含有单条较短DNA的颗粒往往会聚集。聚集取决于离子强度和DNA长度。通过对含有32P 5'-末端标记DNA的颗粒进行胰脱氧核糖核酸酶I消化确定,DNA在组蛋白核心上的放置并非随机。相反,发现所有长度达161 bp的DNA分子与核心组蛋白重新结合的方式,使得相对于5'末端产生确定的脱氧核糖核酸酶I切割模式。制备了含有两条65-bp DNA的颗粒。在大多数条件下,这些颗粒与天然颗粒非常相似,但倾向于解离,导致产生两个半核小体(半体)。