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猿猴病毒40肿瘤抗原与猿猴病毒40染色质的特异性关联。

Specific association of simian virus 40 tumor antigen with simian virus 40 chromatin.

作者信息

Reiser J, Renart J, Crawford L V, Stark G R

出版信息

J Virol. 1980 Jan;33(1):78-87. doi: 10.1128/JVI.33.1.78-87.1980.

Abstract

Simian virus 40 tumor antigen (SV40 T antigen) was bound to both replicating and fully replicated SV40 chromatin extracted with a low-salt buffer from the nuclei of infected cells, and at least a part of the association was tight specific. T antigen cosedimented on sucrose gradients with SV40 chromatin, and T antigen-chromatin complexes could be precipitated from the nuclear extract specifically with anti-T serum. From 10 to 20% of viral DNA labeled to steady state with [3H]thymidine for 12 h late in infection or 40 to 50% of replicating viral DNA pulse-labeled for 5 min was associated with T antigen in such immunoprecipitates. After reaction with antibody, most of the T antigen-chromatin complex was stable to washing with 0.5 M NaCl, but only about 20% of the DNA label remained in the precipitate after washing with 0.5 M NaCl-0.4% Sarkosyl. This tightly bound class of T antigen was associated preferentially with a subfraction of pulse-labeled replicating DNA which comigrated with an SV40 form I marker. A tight binding site for T antigen was identified tentatively by removing the histones with dextran sulfate and heparin from immunoprecipitated chromatin labeled with [32P]phosphate to steady state and then digesting the DNA with restriction endonucleases HinfI and HpaII. The site was within the fragment spanning the origin of replication, 0.641 to 0.725 on the SV40 map.

摘要

猿猴病毒40肿瘤抗原(SV40 T抗原)与用低盐缓冲液从受感染细胞核中提取的正在复制和已完全复制的SV40染色质结合,并且至少部分结合是紧密且特异的。T抗原与SV40染色质在蔗糖梯度中共沉降,并且T抗原 - 染色质复合物可以用抗T血清从核提取物中特异性沉淀出来。在感染后期用[3H]胸苷标记12小时达到稳态的病毒DNA的10%至20%,或脉冲标记5分钟的正在复制的病毒DNA的40%至50%,在这种免疫沉淀中与T抗原相关联。与抗体反应后,大多数T抗原 - 染色质复合物在用0.5M NaCl洗涤时是稳定的,但在用0.5M NaCl - 0.4% Sarkosyl洗涤后,沉淀中仅约20%的DNA标记物保留下来。这种紧密结合的T抗原类别优先与与SV40 I型标记物共迁移的脉冲标记的正在复制的DNA的一个亚组分相关联。通过用硫酸葡聚糖和肝素从用[32P]磷酸盐标记至稳态的免疫沉淀染色质中去除组蛋白,然后用限制性内切酶HinfI和HpaII消化DNA,初步鉴定了T抗原的一个紧密结合位点。该位点位于SV40图谱上跨越复制起点的片段内,位置在0.641至0.725处。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5e37/288525/ef502667e5e6/jvirol00169-0103-a.jpg

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