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人类染色体组成型异染色质的特征分析

Characterization of human chromosomal constitutive heterochromatin.

作者信息

Babu A, Verma R S

出版信息

Can J Genet Cytol. 1986 Oct;28(5):631-44. doi: 10.1139/g86-093.

DOI:10.1139/g86-093
PMID:2433008
Abstract

The constitutive heterochromatin of human chromosomes is evaluated by various selective staining techniques, i.e., CBG, G-11, distamycin A plus 4,6-diamidino-2-phenylindole-2-HCl (DA/DAPI), the fluorochrome D287/170, and Giemsa staining following the treatments with restriction endonucleases AluI and HaeIII. It is suggested that the constitutive heterochromatin could be arbitrarily divided into at least seven types depending on the staining profiles expressed by different regions of C-bands. The pericentromeric C-bands of chromosomes 1, 5, 7, 9, 13-18, and 20-22 consist of more than one type of chromatin, of which chromosome 1 presents the highest degree of heterogeneity. Chromosomes 3 and 4 show relatively less consistent heterogeneous fractions in their C-bands. The C-bands of chromosomes 10, 19, and the Y do not have much heterogeneity but have characteristic patterns with other methods using restriction endonucleases. Chromosomes 2, 6, 8, 11, 12, and X have homogeneous bands stained by the CBG technique only. Among the chromosomes with smaller pericentric C-bands, chromosome 18 shows frequent heteromorphic variants for the size and position (inversions) of the AluI resistant fraction of C-band. The analysis of various types of heterochromatin with respect to specific satellite and nonsatellite DNA sequences suggest that the staining profiles are probably related to sequence diversity.

摘要

通过各种选择性染色技术,即CBG、G-11、放线菌素A加4,6-二脒基-2-苯基吲哚-2-盐酸盐(DA/DAPI)、荧光染料D287/170以及用限制性内切酶AluI和HaeIII处理后的吉姆萨染色,对人类染色体的组成型异染色质进行评估。结果表明,根据C带不同区域所表现出的染色模式,组成型异染色质可任意分为至少七种类型。染色体1、5、7、9、13 - 18以及20 - 22的着丝粒周围C带由不止一种类型的染色质组成,其中染色体1表现出最高程度的异质性。染色体3和4在其C带中显示出相对不太一致的异质部分。染色体10、19和Y的C带没有太多异质性,但在用限制性内切酶的其他方法中具有特征性模式。染色体2、6、8、11、12和X仅通过CBG技术染成均匀带。在着丝粒周围C带较小的染色体中,染色体18在C带的AluI抗性部分的大小和位置(倒位)方面显示出频繁的异形变体。对各种类型异染色质与特定卫星和非卫星DNA序列的分析表明,染色模式可能与序列多样性有关。

相似文献

1
Characterization of human chromosomal constitutive heterochromatin.人类染色体组成型异染色质的特征分析
Can J Genet Cytol. 1986 Oct;28(5):631-44. doi: 10.1139/g86-093.
2
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Demonstration of specific heterochromatic segments in the orangutan (Pongo pygmaeus) by a distamycin/DAPI double staining technique.利用偏端霉素/4',6-二脒基-2-苯基吲哚双重染色技术对红毛猩猩(婆罗洲猩猩)特定异染色质区段的显示
Cytogenet Cell Genet. 1979;24(1):7-14. doi: 10.1159/000131351.

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Chromosomal abnormality in men with impaired spermatogenesis.精子发生受损男性的染色体异常。
Int J Fertil Steril. 2014 Apr;8(1):35-42. Epub 2014 Mar 9.
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Chromosomal polymorphisms involved in reproductive failure in the romanian population.罗马尼亚人群中与生殖失败相关的染色体多态性
Balkan J Med Genet. 2012 Dec;15(2):23-8. doi: 10.2478/bjmg-2013-0003.
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Association of pericentric inversion of chromosome 9 and infertility in romanian population.罗马尼亚人群中9号染色体臂间倒位与不孕的关联。
Maedica (Bucur). 2012 Jan;7(1):25-9.
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Chromosome heteromorphisms: an impact on infertility.染色体异态性:对不孕的影响。
J Assist Reprod Genet. 2008 May;25(5):191-5. doi: 10.1007/s10815-008-9216-3. Epub 2008 May 7.
6
Breakpoints in alpha, beta, and satellite III DNA sequences of chromosome 9 result in a variety of pericentric inversions.9号染色体的α、β和卫星III DNA序列中的断点会导致多种臂间倒位。
J Med Genet. 1996 May;33(5):395-8. doi: 10.1136/jmg.33.5.395.
7
Small metacentric marker chromosomes, particularly isochromosomes, in cancer.癌症中的小中着丝粒标记染色体,尤其是等臂染色体。
Hum Genet. 1988 Jun;79(2):96-102. doi: 10.1007/BF00280545.
8
AluI-resistant chromatin of chromosome 18: classification, frequencies and implications.18号染色体的抗AluI染色质:分类、频率及意义
Chromosoma. 1987;95(3):163-6. doi: 10.1007/BF00330345.
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Restriction endonuclease resistant chromatin in human chromosomes.人类染色体中抗限制性内切酶的染色质
Mol Gen Genet. 1988 Feb;211(2):367-8. doi: 10.1007/BF00330618.