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通过X射线微量分析确定的喹吖因在染色体上的分布。II. 小鼠染色体异染色质区和常染色质区的比较。

The distribution of quinacrine on chromosomes as determined by X-ray microanalysis. II. Comparison of heterochromatic and euchromatic regions of mouse chromosomes.

作者信息

Sumner A T

出版信息

Chromosoma. 1985;91(2):145-50. doi: 10.1007/BF00294059.

DOI:10.1007/BF00294059
PMID:3987440
Abstract

The distribution of quinacrine and protein sulphur has been compared with that of DNA in euchromatic and heterochromatic regions of mouse chromosomes stained with the fluorescent dye quinacrine, using X-ray microanalysis. Heterochromatin tends to bind relatively more quinacrine than euchromatin, and contains a greater concentration of sulphur. Measurements of quinacrine fluorescence, when compared with quinacrine binding, show that the excitation of fluorescence is more efficient when the dye is bound to euchromatin than when it is bound to heterochromatin. Although this observation is consistent with the hypothesis that the dull quinacrine fluorescence of mouse centromeres is due to quenching by guanine residues, two other factors should also be considered: the lower absolute amount of dye bound to the centromeres, and a concentration-dependent quenching of fluorescence.

摘要

利用X射线微量分析,将喹吖因和蛋白质硫的分布与用荧光染料喹吖因染色的小鼠染色体常染色质和异染色质区域中DNA的分布进行了比较。异染色质比常染色质倾向于结合相对更多的喹吖因,并且含有更高浓度的硫。与喹吖因结合相比,喹吖因荧光测量结果表明,当染料与常染色质结合时,荧光激发比与异染色质结合时更有效。尽管这一观察结果与小鼠着丝粒暗淡的喹吖因荧光是由于鸟嘌呤残基淬灭这一假设一致,但还应考虑另外两个因素:着丝粒结合的染料绝对量较低,以及荧光的浓度依赖性淬灭。

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引用本文的文献

1
Mechanisms of quinacrine binding and fluorescence in nuclei and chromosomes.喹吖因在细胞核和染色体中的结合及荧光机制。
Histochemistry. 1986;84(4-6):566-74. doi: 10.1007/BF00482993.
2
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本文引用的文献

1
The distribution of quinacrine on chromosomes as determined by X-ray microanalysis. I. Q-bands on CHO chromosomes.通过X射线微量分析确定的喹吖因在染色体上的分布。I. 中国仓鼠卵巢细胞(CHO)染色体上的Q带
Chromosoma. 1981;82(5):717-34. doi: 10.1007/BF00285777.
2
The longitudinal differentiation produced by photo-oxidation and acridine-orange staining in eukaryote chromosomes: role and involvement of DNA base composition.
Cytogenet Cell Genet. 1982;33(4):277-84. doi: 10.1159/000131773.
3
The nature and mechanisms of chromosome banding.染色体显带的本质与机制。
Cancer Genet Cytogenet. 1982 May;6(1):59-87. doi: 10.1016/0165-4608(82)90022-x.
4
X-ray microanalysis: a histochemical tool for elemental analysis.X射线微分析:一种用于元素分析的组织化学工具。
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Application of X-ray microanalysis to the study of histochemical staining reactions.
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Nuclear phosphoproteins. I. Isolation and characterization of a phosphoprotein fraction from calf thymus nuclei.核磷蛋白。I. 从小牛胸腺核中分离和鉴定一种磷蛋白组分。
Biochim Biophys Acta. 1969 Feb 4;175(1):123-35.
7
Quantum yield of acridines interacting with DNA of defined sequence. A basis for the explanation of acridine bands in chromosomes.与特定序列DNA相互作用的吖啶的量子产率。解释染色体中吖啶带的基础。
Exp Cell Res. 1972 Jun;72(2):602-8. doi: 10.1016/0014-4827(72)90045-6.
8
Optical studies of complexes of quinacrine with DNA and chromatin: implications for the fluorescence of cytological chromosome preparations.喹吖因与DNA和染色质复合物的光学研究:对细胞学染色体标本荧光的影响。
Chromosoma. 1974;49(1):17-40. doi: 10.1007/BF00284985.
9
Quinacrine fluorescence of Mus cervicolor chromosomes. Bright centrometric heterochromatin.赤麂染色体的喹吖因荧光。明亮的着丝粒异染色质。
Exp Cell Res. 1973 Jun;79(2):475-9. doi: 10.1016/0014-4827(73)90475-8.
10
Staining of human metaphase chromosomes with fluorescent conjugates of polylysine.
Exp Cell Res. 1973 Oct;81(2):401-6. doi: 10.1016/0014-4827(73)90529-6.