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两例家族性异染色质缺乏症中组成型异染色质染色方法的比较。

A comparison of constitutive heterochromatin staining methods in two cases of familial heterochromatin deficiencies.

作者信息

Buys C H, Anders G J, Gouw W L, Borkent-Ypma J M, Blenkers-Platter J A

出版信息

Hum Genet. 1979 Nov 1;52(1):133-8. doi: 10.1007/BF00284607.

Abstract

Using DAPI staining after pretreatment with distamycin A we detected a familial deficiency of chromosome 16 heterochromatin. A distinct positively staining band, however, was seen after C-banding. Thus, by using these different heterochromatin staining methods, heterogeneity of the constitutive heterochromatin in the centromeric region of human chromosome 16 was indicated. The same C-banding procedure was also applied to a previously described familial deficiency of chromosome 9 heterochromatin evidenced using distamycin A/DAPI staining and G 11 staining (Buys et al., 1979). In this case a C-band appeared to be virtually absent on the relevant chromosome. These staining methods may be valuable tools in the study of chromosome polymorphisms.

摘要

在用偏端霉素A预处理后进行DAPI染色,我们检测到16号染色体异染色质的家族性缺陷。然而,在C显带后可见一条明显的阳性染色带。因此,通过使用这些不同的异染色质染色方法,表明人类16号染色体着丝粒区域组成型异染色质存在异质性。相同的C显带程序也应用于先前描述的9号染色体异染色质家族性缺陷,该缺陷通过偏端霉素A/DAPI染色和G11染色得以证实(Buys等人,1979年)。在这种情况下,相关染色体上几乎没有出现C带。这些染色方法可能是研究染色体多态性的有价值工具。

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