Razin S V, Yarovaya O V
Exp Cell Res. 1985 May;158(1):273-5. doi: 10.1016/0014-4827(85)90451-3.
Several preparations of nuclear matrices containing varying amounts of DNA were obtained from mouse plasmocytoma P3-X63-Ag8.653 cells and tested for the presence of RNA polymerase II activity. It has been demonstrated that about 25% of RNA polymerase II activity detected in the original nuclei can be recovered in isolated nuclear matrices. Only DNA-bound RNA polymerase II was found in the isolated matrices, while both free and DNA-bound RNA polymerase II activities were detected in the original nuclei. RNA polymerase II activity found in the isolated matrices did not depend on the portion of DNA recovered in the nuclear matrices in a large interval between 91 and 1.5% of DNA content in the original nuclei. The conclusion has been drawn that initiated RNA polymerase II molecules are non-randomly distributed along DNA loops. They are concentrated near the points of DNA attachment to the nuclear skeleton.
从鼠浆细胞瘤P3-X63-Ag8.653细胞中获得了几种含有不同DNA量的核基质制剂,并检测了RNA聚合酶II活性的存在。已证明在原始细胞核中检测到的约25%的RNA聚合酶II活性可在分离的核基质中恢复。在分离的基质中仅发现了与DNA结合的RNA聚合酶II,而在原始细胞核中同时检测到了游离的和与DNA结合的RNA聚合酶II活性。在分离的基质中发现的RNA聚合酶II活性不依赖于在核基质中回收的DNA部分,该部分在原始细胞核DNA含量的91%至1.5%的较大区间内。得出的结论是,起始的RNA聚合酶II分子沿DNA环非随机分布。它们集中在DNA附着于核骨架的点附近。