Kuzmina Alona, Krasnopolsky Simona, Taube Ran
a The Shraga Segal Department of Microbiology Immunology and Genetics Faculty of Health Sciences , Ben-Gurion University of the Negev , Israel.
Transcription. 2017 May 27;8(3):133-149. doi: 10.1080/21541264.2017.1295831. Epub 2017 Feb 17.
Early work on the control of transcription of the human immunodeficiency virus (HIV) laid the foundation for our current knowledge of how RNA Polymerase II is released from promoter-proximal pausing sites and transcription elongation is enhanced. The viral Tat activator recruits Positive Transcription Elongation Factor b (P-TEFb) and Super Elongation Complex (SEC) that jointly drive transcription elongation. While substantial progress in understanding the role of SEC in HIV gene transcription elongation has been obtained, defining of the mechanisms that govern SEC functions is still limited, and the role of SEC in controlling HIV transcription in the absence of Tat is less clear. Here we revisit the contribution of SEC in early steps of HIV gene transcription. In the absence of Tat, the AF4/FMR2 Family member 4 (AFF4) of SEC efficiently activates HIV transcription, while gene activation by its homolog AFF1 is substantially lower. Differential recruitment to the HIV promoter and association with Human Polymerase-Associated Factor complex (PAFc) play key role in this functional distinction between AFF4 and AFF1. Moreover, while depletion of cyclin T1 expression has subtle effects on HIV gene transcription in the absence of Tat, knockout (KO) of AFF1, AFF4, or both proteins slightly repress this early step of viral transcription. Upon Tat expression, HIV transcription reaches optimal levels despite KO of AFF1 or AFF4 expression. However, double AFF1/AFF4 KO completely diminishes Tat trans-activation. Significantly, our results show that P-TEFb phosphorylates AFF4 and modulates SEC assembly, AFF1/4 dimerization and recruitment to the viral promoter. We conclude that SEC promotes both early steps of HIV transcription in the absence of Tat, as well as elongation of transcription, when Tat is expressed. Significantly, SEC functions are modulated by P-TEFb.
早期关于人类免疫缺陷病毒(HIV)转录调控的研究为我们当前对RNA聚合酶II如何从启动子近端暂停位点释放以及转录延伸如何增强的认识奠定了基础。病毒Tat激活剂招募正转录延伸因子b(P-TEFb)和超级延伸复合物(SEC),它们共同驱动转录延伸。虽然在理解SEC在HIV基因转录延伸中的作用方面取得了重大进展,但对调控SEC功能的机制的定义仍然有限,并且在没有Tat的情况下SEC在控制HIV转录中的作用尚不清楚。在这里,我们重新审视SEC在HIV基因转录早期步骤中的作用。在没有Tat的情况下,SEC的AF4/FMR2家族成员4(AFF4)有效地激活HIV转录,而其同源物AFF1的基因激活作用则低得多。对HIV启动子的差异招募以及与人类聚合酶相关因子复合物(PAFc)的结合在AFF4和AFF1之间的这种功能差异中起关键作用。此外,虽然在没有Tat的情况下细胞周期蛋白T1表达的缺失对HIV基因转录有微妙影响,但AFF1、AFF4或这两种蛋白的敲除(KO)会轻微抑制病毒转录的这一早期步骤。在Tat表达后,尽管AFF1或AFF4表达被敲除,HIV转录仍达到最佳水平。然而,AFF1/AFF4双敲除完全消除了Tat的反式激活作用。值得注意的是,我们的结果表明P-TEFb使AFF4磷酸化并调节SEC组装、AFF1/4二聚化以及对病毒启动子的招募。我们得出结论,SEC在没有Tat时促进HIV转录的早期步骤,以及在Tat表达时促进转录延伸。值得注意的是,SEC的功能受到P-TEFb的调节。