Barboric M, Nissen R M, Kanazawa S, Jabrane-Ferrat N, Peterlin B M
Howard Hughes Medical Institute Departments of Medicine, Microbiology, and Immunology University of California at San Francisco 94143, USA.
Mol Cell. 2001 Aug;8(2):327-37. doi: 10.1016/s1097-2765(01)00314-8.
To stimulate transcriptional elongation of HIV-1 genes, the transactivator Tat recruits the positive transcription elongation factor b (P-TEFb) to the initiating RNA polymerase II (RNAPII). We found that the activation of transcription by RelA also depends on P-TEFb. Similar to Tat, RelA activated transcription when tethered to RNA. Moreover, TNF-alpha triggered the recruitment of P-TEFb to the NF-kappaB-regulated IL-8 gene. While the formation of the transcription preinitiation complex (PIC) remained unaffected, DRB, an inhibitor of P-TEFb, prevented RNAPII from elongating on the IL-8 gene. Remarkably, DRB inhibition sensitized cells to TNF-alpha-induced apoptosis. Thus, NF-kappaB requires P-TEFb to stimulate the elongation of transcription and P-TEFb plays an unexpected role in regulating apoptosis.
为了刺激HIV-1基因的转录延伸,反式激活因子Tat将正性转录延伸因子b(P-TEFb)募集到起始的RNA聚合酶II(RNAPII)上。我们发现RelA介导的转录激活也依赖于P-TEFb。与Tat相似,RelA与RNA相连时可激活转录。此外,肿瘤坏死因子-α(TNF-α)促使P-TEFb募集到NF-κB调控的白细胞介素-8(IL-8)基因上。虽然转录前起始复合物(PIC)的形成未受影响,但P-TEFb的抑制剂5,6-二氯-1-β-D-呋喃核糖基苯并咪唑(DRB)可阻止RNAPII在IL-8基因上延伸。值得注意的是,DRB抑制使细胞对TNF-α诱导的凋亡敏感。因此,NF-κB需要P-TEFb来刺激转录延伸,且P-TEFb在调节细胞凋亡中发挥了意想不到的作用。