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Functional equivalents of interferon-mediated signals needed for induction of an mRNA can be generated by double-stranded RNA and growth factors.

作者信息

Tiwari R K, Kusari J, Sen G C

机构信息

Molecular Biology Program, Memorial Sloan-Kettering Cancer Center, New York, NY 10021.

出版信息

EMBO J. 1987 Nov;6(11):3373-8. doi: 10.1002/j.1460-2075.1987.tb02659.x.

DOI:10.1002/j.1460-2075.1987.tb02659.x
PMID:2828026
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC553793/
Abstract

In our earlier studies we demonstrated that in HeLaM cells, interferon-alpha produces two functionally distinguishable signals, both of which are needed for induced transcription of mRNA 561 and other inducible mRNAs. Interferon-gamma cannot induce mRNA 561 because it produces only signal 1. Here we report that platelet-derived growth factor or epidermal growth factor could also produce signal 1. On the other hand, signal 2, which can be produced by interferon-alpha but not by interferon-gamma, could be elicited also by double-stranded RNA. Several lines of evidence suggest that the production of signal 2 by double-stranded RNA was not mediated through interferon. Interferon-induced transcription of mRNA 561 in HeLaM cells or in human fibroblast GM2767 cells was transient. However, in interferon-alpha-treated GM2767 cells, which had ceased to synthesize mRNA 561, transcription of this mRNA could be induced effectively by double-stranded RNA suggesting that this induction process could bypass the interferon-mediated down-regulation of induced transcription. Unlike HeLaM and GM2767 cells, in Daudi cells, induction of mRNA 561 by interferon-alpha was not transient. Transcription of this and two other induced mRNAs continued at a high rate even after 18 h of interferon-alpha treatment of these cells. The lack of down-regulation of interferon-induced gene expression may be responsible for interferon's acute antigrowth effects on these cells.

摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3846/553793/5c472fc2dae7/emboj00251-0169-c.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3846/553793/1d6a27631ddd/emboj00251-0168-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3846/553793/7c593e1f4146/emboj00251-0168-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3846/553793/994a47cb8928/emboj00251-0168-c.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3846/553793/278f53b3560d/emboj00251-0169-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3846/553793/cd0ff1564db2/emboj00251-0169-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3846/553793/5c472fc2dae7/emboj00251-0169-c.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3846/553793/1d6a27631ddd/emboj00251-0168-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3846/553793/7c593e1f4146/emboj00251-0168-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3846/553793/994a47cb8928/emboj00251-0168-c.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3846/553793/278f53b3560d/emboj00251-0169-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3846/553793/cd0ff1564db2/emboj00251-0169-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3846/553793/5c472fc2dae7/emboj00251-0169-c.jpg

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本文引用的文献

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Transcriptional and posttranscriptional regulation of interferon-induced gene expression in human cells.人类细胞中干扰素诱导基因表达的转录和转录后调控。
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Transcriptional induction of two genes in human cells by beta interferon.β干扰素对人类细胞中两个基因的转录诱导作用。
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Comparative antiproliferative efficacies of human alpha and gamma interferons.
Nat Commun. 2022 Feb 25;13(1):1058. doi: 10.1038/s41467-022-28609-w.
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DDX5 potentiates HIV-1 transcription as a co-factor of Tat.DDX5作为Tat的辅助因子增强HIV-1转录。
Retrovirology. 2020 Mar 30;17(1):6. doi: 10.1186/s12977-020-00514-4.
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TAPBPR mediates peptide dissociation from MHC class I using a leucine lever.TAPBPR 通过亮氨酸杠杆介导肽从 MHC Ⅰ类解离。
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Utilizing TAPBPR to promote exogenous peptide loading onto cell surface MHC I molecules.利用 TAPBPR 促进外源性肽加载到细胞表面 MHC I 分子上。
Proc Natl Acad Sci U S A. 2018 Oct 2;115(40):E9353-E9361. doi: 10.1073/pnas.1809465115. Epub 2018 Sep 13.
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DDX17 Specifically, and Independently of DDX5, Controls Use of the HIV A4/5 Splice Acceptor Cluster and Is Essential for Efficient Replication of HIV.具体而言,DDX17 特异性地独立于 DDX5 控制 HIV A4/5 剪接受体位点簇的使用,并且对于 HIV 的有效复制是必需的。
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Preferential interaction of MHC class I with TAPBPR in the absence of glycosylation.在缺乏糖基化的情况下,MHC Ⅰ类与 TAPBPR 的优先相互作用。
Mol Immunol. 2019 Sep;113:58-66. doi: 10.1016/j.molimm.2018.06.269. Epub 2018 Aug 1.
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Inhibition of TBC1D5 activates Rab7a and can enhance the function of the retromer cargo-selective complex.抑制 TBC1D5 可激活 Rab7a,并能增强再循环 cargo 选择性复合物的功能。
J Cell Sci. 2018 Jun 21;131(12):jcs217398. doi: 10.1242/jcs.217398.
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Regulation of Human γδ T Cells by BTN3A1 Protein Stability and ATP-Binding Cassette Transporters.BTN3A1 蛋白稳定性和 ATP 结合盒转运蛋白对人 γδ T 细胞的调节。
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Down-regulation of the interferon receptor.
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Mechanisms of antiviral action of interferon.干扰素的抗病毒作用机制。
Interferon. 1983;5:23-42.
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Interferon induction by viruses: one molecule of dsRNA as the threshold for interferon induction.
Interferon. 1983;5:115-80.
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Mechanisms of interferon action: biochemical and genetic approaches.干扰素作用机制:生物化学与遗传学方法
Interferon. 1982;4:47-94.
9
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Nucleic Acids Res. 1983 Mar 11;11(5):1213-26. doi: 10.1093/nar/11.5.1213.
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Study of the plasma clearance of antibody--ricin-A-chain immunotoxins. Evidence for specific recognition sites on the A chain that mediate rapid clearance of the immunotoxin.抗体-蓖麻毒素A链免疫毒素的血浆清除研究。A链上介导免疫毒素快速清除的特异性识别位点的证据。
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