Musich P R, Brown F L, Maio J J
Proc Natl Acad Sci U S A. 1977 Aug;74(8):3297-301. doi: 10.1073/pnas.74.8.3297.
Component alpha DNA is a homogeneous, highly repetitive fraction that comprises nearly a quarter of the African green monkey (Cercopithecus aethiops) genome. By restriction enzyme analysis, it has a repeat periodicity of 176 +/- 4 nucleotide base pairs, corresponding closely with the length of DNA contained within a nucleosome. The sequence is organized into large blocks of constitutive heterochromatin. A method is described here for the isolation of intact polynucleosomal arrays containing only component alpha sequences. Isolated monkey nuclei are treated with EcoRI, which releases only component alpha nucleosomal arrays; the arrays are then fractionated and purified by sedimentation in sucrose gradients. The method permits a compositional analysis of the proteins associated with a constitutively repressed, heterochromatic sequence. The major differences in the proteins associated with component alpha nucleosomes that distinguish them from the bulk DNA nucleosomes are a decrease in the content of the H1 histones in the component alpha nucleosomes and a concomitant increase in the amount of certain nonhistone proteins. The specific observations are: (i) In the component alpha nucleosomes, 65-70% of the proteins were nonhistone proteins; this contrasts with the value, 40%, for nonhistone proteins associated with nucleosomes containing bulk DNA. (ii) The amount of H1 histone in chromatin containing predominantly bulk DNA was about 13.7%. However, the H1 histone was depleted and possibly absent in component alpha oligonucleosomes. (iii) Coincident with the decrease in the H1 histones and in the same molecular weight range (24,000-43,000), there appeared five minor nonhistone proteins. The minor, low-molecular-weight, nonhistone proteins were not detected in chromatin containing bulk DNA but they represented nearly 12% of the protein in component alpha nucleosomes. The resistance to salt extraction (0.6-2.0 M NaCl) indicates that the low-molecular-weight nonhistone proteins are tenaciously bound to the component alpha nucleosomes. In addition, a class of high-molecular-weight (>100,000) nonhistone proteins was enriched 5- or 6-fold in component alpha oligonucleosomes. The relative amounts of the nucleosome core histones were not changed.
α-DNA组分是一种均匀的、高度重复的片段,占非洲绿猴(长尾黑颚猴)基因组的近四分之一。通过限制性酶切分析,其重复周期为176±4个核苷酸碱基对,与核小体中所含DNA的长度密切对应。该序列被组织成组成型异染色质的大片段。本文描述了一种分离仅包含α-DNA组分序列的完整多核小体阵列的方法。将分离的猴细胞核用EcoRI处理,该酶仅释放α-DNA组分核小体阵列;然后通过蔗糖梯度沉降对这些阵列进行分级分离和纯化。该方法允许对与组成型抑制的异染色质序列相关的蛋白质进行成分分析。与α-DNA组分核小体相关的蛋白质与大量DNA核小体的主要区别在于,α-DNA组分核小体中H1组蛋白的含量减少,同时某些非组蛋白的量增加。具体观察结果如下:(i)在α-DNA组分核小体中,65%-70%的蛋白质是非组蛋白;这与与包含大量DNA的核小体相关的非组蛋白的40%的值形成对比。(ii)主要包含大量DNA的染色质中H1组蛋白的量约为13.7%。然而,α-DNA组分寡核小体中H1组蛋白减少,甚至可能不存在。(iii)与H1组蛋白的减少同时且在相同分子量范围(24,000-43,000)内,出现了五种次要的非组蛋白。这些低分子量的次要非组蛋白在包含大量DNA的染色质中未检测到,但它们占α-DNA组分核小体中蛋白质的近12%。对盐提取(0.6-2.0 M NaCl)的抗性表明,低分子量非组蛋白与α-DNA组分核小体紧密结合。此外,一类高分子量(>100,000)的非组蛋白在α-DNA组分寡核小体中富集了5至6倍。核小体核心组蛋白的相对量没有变化。