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实验性凝聚不足染色体区域的特异性银染

Specific silver staining of experimentally undercondensed chromosome regions.

作者信息

Haaf T, Weis H, Schindler D, Schmid M

出版信息

Chromosoma. 1984;90(2):149-55. doi: 10.1007/BF00292452.

Abstract

Treatment of human and mouse cell cultures with DNA binding AT-specific compounds and with some base analogues induced distinct undercondensations in several heterochromatic chromosome regions. All those heterochromatic regions undercondensed by AT-specific DNA ligands (distamycin A, DAPI, Hoechst 33258) could be heavily labeled with the silver(Ag)-staining technique; but the heterochromatic regions undercondensed with the cytidine analogue 5-azacytidine were Ag-negative. In metaphase chromosomes from BrdU-treated human cell cultures, the bifilarly substituted chromatids, which show a slight undercondensation, were also Ag-negative. Cytochemical analyses of the Ag-stained undercondensed heterochromatic regions showed that the Ag-stainable material consisted of nonhistone proteins. The mechanism of Ag staining in the undercondensed heterochromatic regions was compared with Ag staining of the nucleolus organizer regions.

摘要

用与DNA结合的AT特异性化合物以及一些碱基类似物处理人和小鼠细胞培养物,在几个异染色质染色体区域诱导出明显的凝聚不足。所有被AT特异性DNA配体(放线菌素D、DAPI、Hoechst 33258)诱导凝聚不足的异染色质区域,都能用银(Ag)染色技术进行强烈标记;但用胞苷类似物5-氮杂胞苷诱导凝聚不足的异染色质区域是Ag阴性的。在经BrdU处理的人细胞培养物的中期染色体中,显示出轻微凝聚不足的双股取代染色单体也是Ag阴性的。对经Ag染色的凝聚不足的异染色质区域进行细胞化学分析表明,可被Ag染色的物质由非组蛋白组成。将凝聚不足的异染色质区域中Ag染色的机制与核仁组织区的Ag染色进行了比较。

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