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将抗拓扑异构酶I免疫球蛋白G显微注射到摇蚊唾液腺细胞核中会导致转录延伸受阻。

Microinjection of anti-topoisomerase I immunoglobulin G into nuclei of Chironomus tentans salivary gland cells leads to blockage of transcription elongation.

作者信息

Egyházi E, Durban E

机构信息

Department of Medical Cell Biology, Karolinska Institutet, Stockholm, Sweden.

出版信息

Mol Cell Biol. 1987 Dec;7(12):4308-16. doi: 10.1128/mcb.7.12.4308-4316.1987.

DOI:10.1128/mcb.7.12.4308-4316.1987
PMID:2449604
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC368113/
Abstract

Purified anti-topoisomerase I immunoglobulin G (IgG) was microinjected into nuclei of Chironomus tentans salivary gland cells, and the effect on DNA transcription was investigated. Synthesis of nucleolar preribosomal 38S RNA by RNA polymerase I and of chromosomal Balbiani ring RNA by RNA polymerase II was inhibited by about 80%. The inhibitory action of anti-topoisomerase I IgG could be reversed by the addition of exogenous topoisomerase I. Anti-topoisomerase I IgG had less effect on RNA polymerase II-promoted activity of other less efficiently transcribing heterogeneous nuclear RNA genes. The pattern of inhibition of growing nascent Balbiani ring chains indicated that the transcriptional process was interrupted at the level of chain elongation. The highly decondensed state of active Balbiani ring chromatin, however, remained unaffected after injection of topoisomerase I antibodies. These data are consistent with the interpretation that topoisomerase I is an essential component in the transcriptional process but not in the maintenance of the decondensed state of active chromatin.

摘要

将纯化的抗拓扑异构酶I免疫球蛋白G(IgG)显微注射到摇蚊唾液腺细胞的细胞核中,研究其对DNA转录的影响。RNA聚合酶I合成核仁前体核糖体38S RNA以及RNA聚合酶II合成染色体巴尔比亚尼环RNA的过程受到约80%的抑制。添加外源性拓扑异构酶I可逆转抗拓扑异构酶I IgG的抑制作用。抗拓扑异构酶I IgG对RNA聚合酶II促进的其他转录效率较低的不均一核RNA基因的活性影响较小。对正在生长的新生巴尔比亚尼环链的抑制模式表明,转录过程在链延伸水平被中断。然而,注射拓扑异构酶I抗体后,活跃的巴尔比亚尼环染色质的高度解聚状态并未受到影响。这些数据与以下解释一致:拓扑异构酶I是转录过程中的必需成分,但不是维持活跃染色质解聚状态的必需成分。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2f66/368113/5c72ccf496e5/molcellb00084-0171-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2f66/368113/7171616eda69/molcellb00084-0170-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2f66/368113/1ab681bd3747/molcellb00084-0170-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2f66/368113/dfd21afb4efe/molcellb00084-0170-c.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2f66/368113/5c72ccf496e5/molcellb00084-0171-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2f66/368113/7171616eda69/molcellb00084-0170-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2f66/368113/1ab681bd3747/molcellb00084-0170-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2f66/368113/dfd21afb4efe/molcellb00084-0170-c.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2f66/368113/5c72ccf496e5/molcellb00084-0171-a.jpg

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Cancer Res. 1981 Feb;41(2):537-45.
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