Functional Studies of CCAAT/Enhancer Binding Protein Site Located Downstream of the Transcriptional Start Site.
Previous studies have identified a CCAAT/enhancer binding protein (C/EBP) site located downstream of the transcriptional start site (DS3). The role of the DS3 element with respect to HIV-1 transactivation by Tat and viral replication has not been characterized. We have demonstrated that DS3 was a functional C/EBPβ binding site and mutation of this site to the C/EBP knockout DS3-9C variant showed lower HIV-1 long terminal repeat (LTR) transactivation by C/EBPβ. However, it was able to exhibit similar or even higher transcription levels by Tat compared to the parental LTR. C/EBPβ and Tat together further enhanced the transcription level of the parental LAI-LTR and DS3-9C LTR, with higher levels in the DS3-9C LTR. HIV molecular clone viruses carrying the DS3-9C variant LTR demonstrated a decreased replication capacity and delayed rate of replication. These results suggest that DS3 plays a role in virus transcriptional initiation and provides new insight into C/EBP regulation of HIV-1.
Liu, Yujie; Nonnemacher, Michael R.; Alexaki, Aikaterini; Pirrone, Vanessa; Banerjee, Anupam; Li, Luna; Kilareski, Evelyn; and Wigdahl, Brian, "Functional Studies of CCAAT/Enhancer Binding Protein Site Located Downstream of the Transcriptional Start Site." (2017). Kimmel Cancer Center Papers, Presentations, and Grand Rounds. Paper 60.
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This article has been peer reviewed. It is the author’s final published version in Clinical Medicine Insights: Pathology, Volume 10, March 2017, Pages 1-10.
The published version is available at https://doi.org/10.1177/1179555717694556 . Copyright © Liu et al.