Jin Y J, Cole R D
J Biol Chem. 1986 Mar 5;261(7):3420-7.
Chromatin fragments produced by mild nuclease digestion were chromatographed on Bio-Gel A-50m to give fractions ranging in size from 0.4 to 30 kilobase pair-DNA. The fragments that were larger than about 8-10 nucleosomes accounted for 80% of the chromatin, and the H1/core histone ratio was constant throughout these fractions. When adjusted to 150 mM NaCl, aggregates precipitated in each fraction, the largest fragments yielding 60% and the smallest 25%. In all of these fractions, after aggregation was induced by NaCl, the H1/core histone ratio in the aggregation-resistant chromatin (S) was 0.7 that in the aggregated chromatin (P). To show that the H1 deficiency and aggregation resistance were not produced by transfer of H1 from little fragments to bigger one, big aggregation-resistant fragments were incubated with little aggregation-prone fragments in 75 mM NaCl for 2 h, and readjusted to 150 mM. The little aggregation-prone fragments retained their aggregatibility after exposure to big aggregation-resistant fragments. By mixing [3H]P with [14C]S and vice versa, incubating at 75 mM NaCl for 2 h, and separating P from S with 150 mM NaCl, it was demonstrated that H1 histone did not equilibrate between S and P. Similarly, mixing combinations of radioactive and unlabeled, big and little, S and P fractions, and fractionating by size after 2 h or more incubation at 75 mM NaCl, it was shown that H1 equilibrates between different S fragments, and between different P fragments, but not between S and P. The distribution of H1 variants between S and P fractions was not correlated with the affinity of the variants for DNA. The order of binding affinities was H10 greater than H1ab = H1c, but the deficits of H1's in the aggregation-resistant S fractions were ranked H1ab greater than H1c greater than H10. It is suggested that chromatin is a mosaic of aggregation-resistant and aggregation-prone regions which differ in H1 content quantitatively and qualitatively.
经温和核酸酶消化产生的染色质片段在Bio-Gel A-50m上进行色谱分析,得到大小范围为0.4至30千碱基对DNA的组分。大于约8 - 10个核小体的片段占染色质的80%,并且在这些组分中H1/核心组蛋白的比例是恒定的。当调整至150 mM NaCl时,每个组分中都会有聚集体沉淀,最大的片段产生60%的沉淀,最小的片段产生25%的沉淀。在所有这些组分中,NaCl诱导聚集后,抗聚集染色质(S)中的H1/核心组蛋白比例是聚集染色质(P)中的0.7倍。为了表明H1缺乏和抗聚集性不是由H1从小片段转移到大片段所产生的,将大的抗聚集片段与小的易聚集片段在75 mM NaCl中孵育2小时,然后重新调整至150 mM。小的易聚集片段在与大的抗聚集片段接触后仍保留其聚集能力。通过将[3H]P与[14C]S混合(反之亦然),在75 mM NaCl中孵育2小时,并用150 mM NaCl将P与S分离,证明H1组蛋白在S和P之间不会达到平衡。同样,将放射性和未标记的、大的和小的、S和P组分进行混合组合,在75 mM NaCl中孵育2小时或更长时间后按大小进行分级分离,结果表明H1在不同的S片段之间以及不同的P片段之间会达到平衡,但在S和P之间不会。H1变体在S和P组分之间的分布与变体对DNA的亲和力无关。结合亲和力的顺序是H10大于H1ab = H1c,但抗聚集S组分中H1的缺乏程度排序为H1ab大于H1c大于H10。有人提出染色质是抗聚集区域和易聚集区域的镶嵌体,它们在H1含量上在数量和质量上都有所不同。