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Functional interaction of nuclear transport-defective simian virus 40 large T antigen with chromatin and nuclear matrix.

机译:核运输缺陷性猿猴病毒40大T抗原与染色质和核基质的功能相互作用。

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摘要

We analyzed the subcellular distribution of nuclear transport-defective simian virus 40 Lys-128-mutant (cT-3 [R. E. Lanford and J. S. Butel, Cell 37:801-813, 1984] and d10 [D. Kalderon, W. D. Richardson, A. F. Markham, and A. E. Smith, Nature (London) 311:33-38, 1984]) large T antigens in various Lys-128-mutant-transformed rodent cells and in Lys-128-mutant d10-infected TC7 cells. Small but significant amounts of the mutant large T antigens were found in association with nuclear substructures, both in mutant-transformed and in mutant-infected cells. Experiments with TC7 cells made incompetent for cell division by 60Co irradiation supported the assumption that Lys-128-mutant large T antigen did not associate with nuclear components during mitosis but most likely was transported into the nucleus because the Lys-128 mutation was leaky for nuclear transport. Low-level simian virus 40 DNA replication and production of infectious mutant virus progeny in TC7 cells indicated that the association of Lys-128-mutant large T antigen with nuclear substructures is functional.
机译:我们分析了核转运缺陷性猿猴病毒40 Lys-128突变体(cT-3 [RE Lanford和JS Butel,Cell 37:801-813,1984]和d10 [D. Kalderon,WD Richardson,AF Markham)的亚细胞分布,以及AE Smith,Nature(London)311:33-38,1984])在各种经Lys-128突变体转化的啮齿动物细胞和经Lys-128突变体d10感染的TC7细胞中的大T抗原。在突变体转化的细胞和突变体感染的细胞中均发现少量但大量的突变体大T抗原与核亚结构相关。 TC7细胞无法通过60Co辐射进行细胞分裂的实验支持这样的假设:Lys-128突变的大T抗原在有丝分裂过程中不与核成分相关,但最有可能被转运到细胞核中,因为Lys-128突变对于核泄漏运输。在TC7细胞中低水平的猿猴病毒40 DNA复制和传染性突变病毒后代的产生表明Lys-128突变的大T抗原与核亚结构的联系是有功能的。

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