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人类前中期染色体上高分辨率胰蛋白酶-吉姆萨带的定量分析。

Quantitative analysis of high-resolution trypsin-giemsa bands on human prometaphase chromosomes.

作者信息

Francke U, Oliver N

出版信息

Hum Genet. 1978 Dec 18;45(2):137-65. doi: 10.1007/BF00286957.

Abstract

We have constructed ideograms of human prometaphase chromosomes from synchronized and from standard 72-h lymphocyte cultures. G banding was achieved by a trypsin-Giemsa (or Wright's stain) method. In addition to light (white) and dark (black) bands, we have distinguished three different shades of grey. This distinction is essential for proper identification of the increasing number of bands displayed by high-resolution chromosomes. The relative amount of chromatin in each category of staining intensity has been calculated and expressed as 'light value.' The ideograms represent the maximal number of bands discernible with some consistency on prometaphase chromosomes, i.e., 721 euchromatic and 62 'variable' heterochromatic or heteromorphic bands. The ideograms are based on measurements. On selected printed copies of each chromosome derived from different cells and different individuals, the relative width of each band was measured in relation to the length of the respective chromosome arm. The measurements per chromosome were averaged and used for construction of the ideograms. The distance of each border between bands or sub-bands from the centromere has been calculated on a relative scale, with positions 0 at the centromere and 1.0 at the p terminus of q terminus. The numbering system for bands and sub-bands follows the Paris Conference (1971) recommendations.

摘要

我们从同步化的以及标准的72小时淋巴细胞培养物中构建了人类前中期染色体的 ideogram。通过胰蛋白酶 - 吉姆萨(或瑞氏染色)方法实现了G带染色。除了浅(白色)带和深(黑色)带外,我们还区分出三种不同深浅的灰色带。这种区分对于正确识别高分辨率染色体所显示的越来越多的带至关重要。已计算出每种染色强度类别中染色质的相对量,并表示为“光值”。这些ideogram代表在前中期染色体上能以一定一致性分辨出的最大带数,即721条常染色质带和62条“可变”异染色质或异形带。这些ideogram基于测量结果。在从不同细胞和不同个体获得的每个染色体的选定打印副本上,相对于相应染色体臂的长度测量每个带的相对宽度。对每个染色体的测量值进行平均,并用于构建ideogram。已在相对尺度上计算了带或子带之间每个边界与着丝粒的距离,着丝粒位置为0,p末端或q末端为1.0。带和子带的编号系统遵循巴黎会议(1971年)的建议。

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