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Purification of 14C-labelled deoxyribonuclease II from HeLa S3 lysosomes and its use as a marker for the study of nuclear deoxyribonuclease II

机译:从HeLa S3溶酶体中纯化14C标记的脱氧核糖核酸酶II及其作为研究核脱氧核糖核酸酶II的标记物的用途

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摘要

Deoxyribonuclease II (DNAase II) in mammalian cells has generally been considered to be located in the lysosomes. Several recent studies have indicated that some DNAase II activity is present in purified nuclei; this, however, could have been due to some contamination of the nuclear fraction by lysosomes, or alternatively, it could have been caused by specific binding of lysosomal DNAase II to the nuclear fraction during isolation. Our previous studies have eliminated the possibility that lysosomal contamination was the cause of the presence of DNAase II in isolated nuclei. In this study I have purified 14C-labelled lysosomal DNAase II and added it to cells during isolation of their nuclei. This study demonstrates that there is no specific binding of lysosomal DNAase II to the nuclear fraction and concludes that DNAase II activity observed in isolated nuclei represents an intrinsic activity that might be involved in nuclear DNA metabolism.
机译:通常认为哺乳动物细胞中的脱氧核糖核酸酶II(DNAase II)位于溶酶体中。最近的一些研究表明,纯化的核中存在某些DNAase II活性。然而,这可能是由于溶酶体对核部分的某种污染,或者可能是由于在分离过程中溶酶体DNAase II与核部分的特异性结合所致。我们以前的研究消除了溶酶体污染是DNAase II存在于分离核中的原因。在这项研究中,我纯化了14C标记的溶酶体DNAase II,并在分离细胞核的过程中将其添加到细胞中。这项研究表明溶酶体DNAase II与核部分没有特异性结合,并得出结论,在分离的核中观察到的DNAase II活性代表了可能参与核DNA代谢的固有活性。

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    Slor, Hanoch;

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  • 年度 1973
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  • 原文格式 PDF
  • 正文语种 en
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