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通过与补骨脂素衍生物氨甲基三氧杂补骨脂素交联,在活的HeLa细胞中探测到的异质核RNA双链区域。

Heterogeneous nuclear RNA double-stranded regions probed in living HeLa cells by crosslinking with the psoralen derivative aminomethyltrioxsalen.

作者信息

Calvet J P, Pederson T

出版信息

Proc Natl Acad Sci U S A. 1979 Feb;76(2):755-9. doi: 10.1073/pnas.76.2.755.

Abstract

The psoralen derivative aminomethyltrioxsalen (AMT, 4'-aminomethyl-4,5',8-trimethylpsoralen) has been employed as a probe for heterogeneous nuclear RNA (hnRNA) double-stranded regions in experiments with living HeLa cells. hnRNA ribonucleoprotein (hnRNP) particles were purified from untreated or AMT-treated cells after irradiation with 365-nm light, and double-stranded hnRNA regions (dsRNA) were isolated by RNase A + T1 digestion of hnRNP, followed by preparative Cs2SO4 isopycnic centrifugation. The purified, hnRNP-derived dsRNA was then assayed for interstrand crosslinks by measurement of its "snapback" to RNase-resistant form after thermal denaturation. By this procedure, the amount of crosslinked dsRNA was found to be increased 3- to 7-fold in cells exposed to AMT in vivo. The levels of crosslinking in vivo compared favorably with those observed in model experiments with pure dsRNA in vitro. These results establish that double-stranded hnRNA regions exist in the living cell, and they further demonstrate that these base-paired regions are organized as rather accessible sites within the nucleus.

摘要

补骨脂素衍生物氨甲基三氧补骨脂素(AMT,4'-氨甲基-4,5',8-三甲基补骨脂素)已被用作在活的HeLa细胞实验中探测异质核RNA(hnRNA)双链区域的探针。在用365纳米光照射后,从未经处理或经AMT处理的细胞中纯化hnRNA核糖核蛋白(hnRNP)颗粒,然后通过用核糖核酸酶A + T1消化hnRNP来分离双链hnRNA区域(dsRNA),接着进行制备性硫酸铯等密度离心。然后通过测量热变性后其“回折”成抗核糖核酸酶形式来检测纯化的、源自hnRNP的dsRNA的链间交联。通过该程序,发现体内暴露于AMT的细胞中交联的dsRNA量增加了3至7倍。体内的交联水平与体外纯dsRNA模型实验中观察到的水平相当。这些结果证实活细胞中存在双链hnRNA区域,并且进一步证明这些碱基配对区域在细胞核内被组织成相当容易接近的位点。

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