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经核酸酶处理的细胞核在低离子强度下提取会破坏转录活性DNA与核骨架的附着。

Low ionic strength extraction of nuclease-treated nuclei destroys the attachment of transcriptionally active DNA to the nuclear skeleton.

作者信息

Razin S V, Yarovaya O V, Georgiev G P

出版信息

Nucleic Acids Res. 1985 Oct 25;13(20):7427-44. doi: 10.1093/nar/13.20.7427.

Abstract

We have studied how the conditions in which the nuclear matrix is isolated influence the association of transcribing DNA with the nuclear matrix. Extraction of nuclease-treated nuclei with a low ionic strength solution before a high salt nuclei with a low ionic strength solution before a high salt extraction completely abolishes this association. However, RNA removal by RNAase treatment does not affect the binding of transcribing DNA to the nuclear matrix. The nature of the association of active genes with the nuclear matrix is discussed.

摘要

我们研究了分离核基质的条件如何影响正在转录的DNA与核基质的结合。在高盐提取之前先用低离子强度溶液提取经核酸酶处理的细胞核,会完全消除这种结合。然而,用核糖核酸酶处理去除RNA并不影响正在转录的DNA与核基质的结合。本文讨论了活性基因与核基质结合的性质。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e08b/322053/651b7ca2457e/nar00314-0265-a.jpg

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