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5-氮杂胞苷(5-ACR)诱导的人类染色体分割

Segmentation of human chromosomes induced by 5-ACR (5-azacytidine).

作者信息

Viegas-Péquignot E, Dutrillaux B

出版信息

Hum Genet. 1976 Dec 15;34(3):247-54. doi: 10.1007/BF00295287.

Abstract

The 5-ACR (5-azacytidine) introduced in human lymphocyte cultures induces a lack or a delay of condensation of some chromosome segments corresponding to the G-bands. The resulting R-banding is very similar to that obtained with a 7-h treatment by BrdU, although the segmentation may be much stronger (pulverization) with high doses. However, the 5-ACR does not induce chromatid asymmetry, as BrdU does. This constitutes a new argument for considering that the segmentation and the asymmetry of chromatids depend, at least partly, on two different mechanisms, where proteins are probably involved. Another effect of 5-ACR is to increase chromosome associations by satellites, secondary constrictions, and telomeric regions.

摘要

在人类淋巴细胞培养物中引入的5-氮杂胞苷(5-ACR)会导致某些与G带相对应的染色体片段出现凝聚缺失或延迟。由此产生的R带与用溴脱氧尿苷(BrdU)处理7小时所获得的R带非常相似,尽管高剂量时的染色体分段可能更强(染色体粉碎)。然而,5-ACR不像BrdU那样诱导染色单体不对称。这构成了一个新的论据,支持认为染色单体的分段和不对称至少部分取决于两种不同机制,其中可能涉及蛋白质。5-ACR的另一个作用是增加通过卫星、次缢痕和端粒区域形成的染色体关联。

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