PT  - JOURNAL ARTICLE
AU  - Laurie R. Gray
AU  - Rachel E. Jackson
AU  - Patrick E. H. Jackson
AU  - Stefan Bekiranov
AU  - David Rekosh
AU  - Marie-Louise Hammarskjöld
TI  - HIV-1 Rev interacts with HERV-K RcREs present in the human genome and promotes export of unspliced HERV-K proviral RNA
AID  - 10.1101/822619
DP  - 2019 Jan 01
TA  - bioRxiv
PG  - 822619
4099  - http://biorxiv.org/content/early/2019/12/01/822619.short
4100  - http://biorxiv.org/content/early/2019/12/01/822619.full
AB  - Background The HERV-K (HML-2) viruses are the youngest of the human endogenous retroviruses. They are present as several almost complete proviral copies and numerous fragments in the human genome. Many HERV-K proviruses express a regulatory protein Rec, which binds to an element present in HERV-K mRNAs called the RcRE. This interaction is necessary for the nucleo-cytoplasmic export and expression of HERV-K mRNAs that retain introns and plays a role analogous to that of Rev and the RRE in HIV replication. There are over 900 HERV-K RcREs distributed throughout the human genome. Thus, it was of interest to determine if Rev could functionally interact with selected RcRE elements that map either to HERV-K proviruses or human gene regions. This interaction would have the potential to alter the expression of both HERV-K mRNAs and cellular mRNAs during HIV-1 infection.Results In this study we employed a combination of RNAseq, bioinformatics and cell-based functional assays. Potential RcREs were identified through a number of bioinformatic approaches. They were then tested for their ability to promote export and translation of a reporter mRNA with a retained intron in conjunction with Rev or Rec. Some of the selected elements functioned well with either Rev, Rec or both, whereas some showed little or no function. Rev function on individual RcREs varied and was also dependent on the Rev sequence. We also performed RNAseq on total and cytoplasmic RNA isolated from SupT1 cells expressing HIV Rev, with or without Tat, or HERV-K Rec. Proviral mRNA from three HERV-K loci (4p16.1b, 22q11.23 and most significantly 3q12.3) accumulated in the cytoplasm in the presence of Rev or Tat and Rev, but not Rec. Consistent with this, the 3’ RcRE from 3q12.3 functioned well with HIV-Rev in our reporter assay. In contrast, this RcRE showed little or no function with Rec.Conclusions The HIV Rev protein can functionally interact with many RcREs present in the human genome, depending on the RcRE sequence, as well as the Rev sequence. This leads to export of some of the HERV-K proviral mRNAs and also has the potential to change the expression of non-viral genes.HERVhuman endogenous retrovirusHML-2human MMTV-likeLTRlong terminal repeatORFopen reading frameprRcREprototype RcREprRecprototype RecEVempty vectorIRESinternal ribosome entry siteSEAPsecreted placental alkaline phosphataseGTFgene transfer format