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中断多瘤病毒DNA的早期区域会增强致瘤性。

Interrupting the early region of polyoma virus DNA enhances tumorigenicity.

作者信息

Israel M A, Simmons D T, Hourihan S L, Rowe W P, Martin M A

出版信息

Proc Natl Acad Sci U S A. 1979 Aug;76(8):3713-6. doi: 10.1073/pnas.76.8.3713.

Abstract

The tumorigenicity of DNA from polyoma virus after cleavage with a variety of restriction enzymes was evaluated in suckling hamsters. Cleavage with enzymes that interrupt the region of the genome coding for the large tumor (T) antigen of polyoma virus markedly enhanced the tumorigenicity above that observed with DNA I of the virus. Cell lines established in vitro from tumors induced by polyoma virions, polyoma virus DNA I, or polyoma virus DNA that had been cleaved with restriction endonucleases in the early region all contain the polyoma virus middle and small T antigens but not the large T antigen of polyoma virus is not required for maintenance of the transformed state and probably not for initiation of tumorigenesis by viral DNA.

摘要

用多种限制性内切酶切割后的多瘤病毒DNA的致瘤性在乳鼠中进行了评估。用能中断多瘤病毒基因组中编码大肿瘤(T)抗原区域的酶进行切割,可使致瘤性显著增强,高于用病毒DNA I所观察到的情况。从由多瘤病毒颗粒、多瘤病毒DNA I或早期区域经限制性内切酶切割的多瘤病毒DNA诱导产生的肿瘤中体外建立的细胞系,均含有多瘤病毒中、小T抗原,但不含有多瘤病毒大T抗原。维持转化状态可能不需要多瘤病毒大T抗原,病毒DNA引发肿瘤发生可能也不需要该抗原。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5ea9/383903/8351dafd43dc/pnas00008-0150-a.jpg

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