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黑腹果蝇折叠间期基因组的分离、表征及结构

Isolation, characterization, and structure of the folded interphase genome of Drosophila melanogaster.

作者信息

Benyajati C, Worcel A

出版信息

Cell. 1976 Nov;9(3):393-407. doi: 10.1016/0092-8674(76)90084-2.

Abstract

The intact interphase genome of Drosophila melanogaster has been isolated by sucrose gradient centrifugation after gentle lysis of tissue culture cells in 0.9 M NaCl-0.4% nonidet P40. The non-viscous folded DNA sediments as a single broad 5000S peak in a complex with RNA (a fraction of the nuclear nascent RNA) and protein (all of the four intranuclesome histones: H2A, H2B, H3, and H4). The folded DNA is supercoiled and can be relaxed to slower sedimenting forms either by intercalating ethidium or by nicking with DNAase I. Incomplete DNAase treatment gives partially relaxed complexes, indicating that each nick relaxes only a stretch of DNA (defined as a supercoiled DNA loop) without affecting the superhelical content of the rest of the genome. The concentration of superhelices in the Drosophila folded DNA is the same as in the E. coli and SV40 closed circular DNAs-that is, about one negative turn every 200 base pairs (bp) in 0.15 M NaCl at 26 degrees C. The estimated average size of the supercoiled DNA loops, about 85,000 bp, equals the size of the larger Drosophila chromomeres. Ethidium intercalation in 0.9 M NaCl both removes the negative superhelical turns and dissociates the four histones from the DNA. The four histones are dissociated in equimolar concentrations, and the relative proportion of histones displaced from the DNA is a function of ethidium concentration. The histones are completely dissociated from the folded DNA at the ethidium concentration. The histones are completely dissociated from the folded DNA at the ethidium concentration which removes all of the negative superhelices. Thus the data strongly suggest that the rotation of the Watson Crick helix which accompanies ethidium intercalation causes the loss of nucleosomes from the DNA. The results are interpreted in terms of a model for the folded Drosophila genome which has the DNA constrained (by both protein-DNA and RNA- DNA interactions) into independent supercoiled loops containing on the average 400 nucleosomes per loop. Each nucleosome is composed of a histone core with the DNA wound around it in a 360 degrees left-handed toroidal supercoil; each nucleosome toroidal supercoil plus its relaxed internucleosome DNA contains, on the average, 200 bp.

摘要

在0.9M NaCl - 0.4% 非离子去污剂P40中轻柔裂解组织培养细胞后,通过蔗糖梯度离心法分离出了黑腹果蝇完整的间期基因组。非粘性折叠DNA与RNA(核新生RNA的一部分)和蛋白质(四种核小体组蛋白:H2A、H2B、H3和H4全部)形成复合物,以单一宽峰的形式沉降,沉降系数为5000S。折叠DNA是超螺旋的,通过插入溴化乙锭或用DNA酶I切口可使其松弛为沉降较慢的形式。不完全的DNA酶处理会产生部分松弛的复合物,这表明每个切口仅使一段DNA(定义为一个超螺旋DNA环)松弛,而不影响基因组其余部分的超螺旋含量。果蝇折叠DNA中超螺旋圈的浓度与大肠杆菌和SV40闭环DNA中的相同,即在26℃、0.15M NaCl条件下,大约每200个碱基对(bp)有一个负超螺旋圈。估计超螺旋DNA环的平均大小约为85,000bp,与较大的果蝇染色粒大小相当。在0.9M NaCl中插入溴化乙锭既能去除负超螺旋圈,又能使四种组蛋白与DNA解离。四种组蛋白以等摩尔浓度解离,从DNA上置换下来的组蛋白的相对比例是溴化乙锭浓度的函数。在使所有负超螺旋圈都被去除的溴化乙锭浓度下,组蛋白完全从折叠DNA上解离。因此,这些数据有力地表明,伴随溴化乙锭插入而发生的沃森-克里克螺旋的旋转导致了核小体从DNA上丢失。根据果蝇折叠基因组的模型对结果进行了解释,该模型中DNA通过蛋白质-DNA和RNA-DNA相互作用被限制在独立的超螺旋环中,每个环平均包含400个核小体。每个核小体由一个组蛋白核心组成,并带有在其周围以360度左手环形超螺旋缠绕的DNA;每个核小体环形超螺旋加上其松弛的核小体间DNA平均包含200bp。

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