Suppr超能文献

一名患有新发13号、14号染色体易位个体中的卫星DNA缺失与核仁组织区活性

Satellite DNA loss and nucleolar organiser activity in an individual with a de novo chromosome 13,14 translocation.

作者信息

Gosden J R, Gosden C M, Lawrie S S, Buckton K E

出版信息

Clin Genet. 1979 Jun;15(6):518-29. doi: 10.1111/j.1399-0004.1979.tb00836.x.

Abstract

The distribution of satellite DNA and nucleolar organiser activity have been studied in a female with a new dicentric translocation chromosome derived from the maternal chromosomes 13 and 14. More than half the satellite DNA (60.5%) was lost in the translocation, together with both the nucleolar organiser regions (NOR'S). However, at least one NOR (chromosome 21) which was inactive in the mother (by the AgI reaction) is active in the subject, and this may be an example of functional compensation. The somatic cells of the mother of the subject, which do not have the translocation, show a high frequency of acrocentric associations, but these do not include any obvious excess of associations involving chromosomes 13 and 14, indicating that the high frequency of association in somatic cells is not in itself a predisposition to Robertsonian translocation in germ line cells. The father's chromosomes 9 both have more satellite DNA in the secondary constriction than normal, but this is not reflected in any obviously larger size of the C-band in this region.

摘要

在一位患有源自母本13号和14号染色体的新型双着丝粒易位染色体的女性中,研究了卫星DNA的分布和核仁组织区活性。超过一半的卫星DNA(60.5%)在易位中丢失,同时核仁组织区(NOR)也全部丢失。然而,至少有一个在母亲体内无活性(通过银染反应判断)的NOR(21号染色体)在该个体中具有活性,这可能是功能补偿的一个例子。该个体母亲的体细胞没有这种易位,显示出较高频率的近端着丝粒联合,但其中并不包括涉及13号和14号染色体的明显过多联合,这表明体细胞中联合的高频率本身并非生殖系细胞中罗伯逊易位的易感性因素。父亲的两条9号染色体在次缢痕处的卫星DNA都比正常情况更多,但这并未在该区域的C带尺寸上体现出明显更大。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验