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可卡因诱导的DNA依赖性蛋白激酶通过促进TRIM28磷酸化来缓解RNA聚合酶II的暂停。

Cocaine-induced DNA-PK relieves RNAP II pausing by promoting TRIM28 phosphorylation.

作者信息

Sharma Adhikarimayum Lakhikumar, Tyagi Priya, Khumallambam Meenata, Tyagi Mudit

机构信息

Center for Translational Medicine, Thomas Jefferson University, 1020 Locust Street, Philadelphia, PA 19107, USA.

出版信息

bioRxiv. 2024 Aug 19:2024.08.19.608673. doi: 10.1101/2024.08.19.608673.

Abstract

Drug abuse continues to pose a significant challenge in HIV control efforts. In our investigation, we discovered that cocaine not only upregulates the expression of DNA-dependent protein kinase (DNA-PK) but also augments DNA-PK activation by enhancing its phosphorylation at S2056. Moreover, DNA-PK phosphorylation triggers the translocation of DNA-PK into the nucleus. The finding that cocaine promotes nuclear translocation of DNA-PK further validates our observation of enhanced DNA-PK recruitment at the HIV long terminal repeat (LTR) following cocaine exposure. By activating and facilitating the nuclear translocation of DNA-PK, cocaine effectively orchestrates multiple stages of HIV transcription, thereby promoting HIV replication. Additionally, our study indicates that cocaine-induced DNA-PK promotes hyper-phosphorylation of RNA polymerase II (RNAP II) carboxyl-terminal domain (CTD) at Ser5 and Ser2 sites, enhancing both initiation and elongation phases, respectively, of HIV transcription. Cocaine's enhancement of transcription initiation and elongation is further supported by its activation of cyclin-dependent kinase 7 (CDK7) and subsequent phosphorylation of CDK9, thereby promoting positive transcriptional elongation factor b (P-TEFb) activity. We demonstrate for the first time that cocaine, through DNA-PK activation, promotes the specific phosphorylation of TRIM28 at Serine 824 (p-TRIM28, S824). This modification converts TRIM28 from a transcriptional inhibitor to a transactivator for HIV transcription. Additionally, we observe that phosphorylation of TRIM28 (p-TRIM28, S824) promotes the transition from the pausing phase to the elongation phase of HIV transcription, thereby facilitating the production of full-length HIV genomic transcripts. This finding corroborates the observed enhanced RNAP II CTD phosphorylation at Ser2, a marker of transcriptional elongation, following cocaine exposure. Accordingly, upon cocaine treatment, we observed elevated recruitment of p-TRIM28-(S824) at the HIV LTR. Overall, our results have unraveled the intricate molecular mechanisms underlying cocaine-induced HIV transcription and gene expression. These findings hold promise for the development of highly targeted therapeutics aimed at mitigating the detrimental effects of cocaine in individuals living with HIV.

摘要

药物滥用在艾滋病毒防控工作中仍然构成重大挑战。在我们的调查中,我们发现可卡因不仅上调DNA依赖性蛋白激酶(DNA-PK)的表达,还通过增强其在S2056位点的磷酸化来增强DNA-PK的激活。此外,DNA-PK磷酸化触发DNA-PK向细胞核的转位。可卡因促进DNA-PK核转位这一发现进一步证实了我们的观察,即可卡因暴露后HIV长末端重复序列(LTR)处DNA-PK募集增强。通过激活并促进DNA-PK的核转位,可卡因有效地协调了HIV转录的多个阶段,从而促进HIV复制。此外,我们的研究表明,可卡因诱导的DNA-PK促进RNA聚合酶II(RNAP II)羧基末端结构域(CTD)在Ser5和Ser2位点的过度磷酸化,分别增强了HIV转录的起始和延伸阶段。可卡因对转录起始和延伸的增强作用还得到其对细胞周期蛋白依赖性激酶7(CDK7)的激活以及随后对CDK9的磷酸化的支持,从而促进正转录延伸因子b(P-TEFb)的活性。我们首次证明,可卡因通过激活DNA-PK,促进TRIM28在丝氨酸824位点(p-TRIM28,S824)的特异性磷酸化。这种修饰将TRIM28从转录抑制剂转变为HIV转录的反式激活因子。此外,我们观察到TRIM28(p-TRIM28,S824)的磷酸化促进了HIV转录从暂停阶段向延伸阶段的转变,从而促进全长HIV基因组转录本的产生。这一发现证实了在可卡因暴露后观察到的RNAP II CTD在Ser2位点磷酸化增强,这是转录延伸的一个标志。因此,在可卡因处理后,我们观察到p-TRIM28-(S824)在HIV LTR处的募集增加。总体而言,我们的结果揭示了可卡因诱导的HIV转录和基因表达背后复杂的分子机制。这些发现为开发旨在减轻可卡因对艾滋病毒感染者有害影响的高度靶向治疗方法带来了希望。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/969b/11370412/39cbacf4cfd9/nihpp-2024.08.19.608673v1-f0001.jpg

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