Touchette N A, Cole R D
Journal of NIH Research, Washington, D.C. 20037.
Biochemistry. 1992 Feb 18;31(6):1842-9. doi: 10.1021/bi00121a037.
The effects of increasing NaCl concentrations on the melting profiles of chromatin in isolated nuclei contradicted published claims that structural transitions near 76 degrees C (Tn-7), near 89 degrees C (Tn-8), and near 105 degrees C (Tn-10) were respectively the melting of linker DNA, the melting of extended nucleosomal strands, and the collapse of nucleosomes in the 300-A fiber. Contrary to expectations of such an interpretation, decreases in salt concentration stabilized Tn-7 and failed to eliminate Tn-10. Moreover, nuclei depleted of H1 histone, which is known to be essential for the formation of the 300-A fiber, gave the same melting profile as intact nuclei with regard to the relative magnitudes of Tn-8 and Tn-10. The effect of salt concentration on the melting profiles and the insensitivity of Tn-8 and Tn-10 to H1 histone removal supports the notion that Tn-7 is the collapse of the nucleosome while Tn-8 and Tn-10 are respectively the unstacking of nucleotide bases in relaxed chromatin and supercoiled chromatin. The identification of Tn-8 as the unstacking of bases in relaxed DNA, and Tn-10 as unstacking in supercoiled DNA, shows that scanning calorimetry can be used to measure the state of repair of DNA in the nucleus. The gain in Tn-8 at the expense of Tn-10 that is seen as the mitotic index drops and differentiation occurs suggests that nicks accumulate in the DNA, perhaps because the gross aggregation of the inactive majority of the chromatin makes it inaccessible to repair enzymes.
增加氯化钠浓度对分离细胞核中染色质解链曲线的影响与已发表的观点相悖,即76℃(Tn-7)附近、89℃(Tn-8)附近和105℃(Tn-10)附近的结构转变分别是连接DNA的解链、延伸核小体链的解链以及300埃纤维中核小体的解体。与这种解释的预期相反,盐浓度降低使Tn-7稳定,且未能消除Tn-10。此外,已知对300埃纤维形成至关重要的H1组蛋白缺失的细胞核,在Tn-8和Tn-10的相对大小方面,其解链曲线与完整细胞核相同。盐浓度对解链曲线的影响以及Tn-8和Tn-10对H1组蛋白去除的不敏感性支持了这样一种观点,即Tn-7是核小体的解体,而Tn-8和Tn-10分别是松弛染色质和超螺旋染色质中核苷酸碱基的解堆叠。将Tn-8鉴定为松弛DNA中碱基的解堆叠,将Tn-10鉴定为超螺旋DNA中碱基的解堆叠,表明扫描量热法可用于测量细胞核中DNA的修复状态。随着有丝分裂指数下降和分化发生,以Tn-10为代价的Tn-8增加表明DNA中积累了切口,这可能是因为大部分无活性染色质的总体聚集使其无法被修复酶接近。