HERV-Derived Ervpb1 Is Conserved in Simiiformes, Exhibiting Expression in Hematopoietic Cell Lineages Including Macrophages

Int J Mol Sci. 2021 Apr 26;22(9):4504. doi: 10.3390/ijms22094504.

Abstract

(1) Background: The ERVPb1 gene in humans is derived from an envelope (Env) gene of a human endogenous retrovirus group, HERV-P(b). The ERVPb1 gene reportedly has a conserved open reading frame (ORF) in Old World monkeys. Although its forced expression led to cell-fusion in an ex vivo cell culture system, like other Env-derived genes such as syncytin-1 and -2, its mRNA expression is not placenta-specific, but almost ubiquitous, albeit being quite low in human tissues and organs, implying a distinct role for ERVPb1. (2) Methods: To elucidate the cell lineage(s) in which the ERVPb1 protein is translated in human development, we developed a novel, highly sensitive system for detecting HERV-derived proteins/peptides expressed in the tissue differentiation process of human induced pluripotent stem cells (iPSCs). (3) Results: We first determined that ERVPb1 is also conserved in New World monkeys. Then, we showed that the ERVPb1 protein is translated from a uniquely spliced ERVPb1 transcript in hematopoietic cell lineages, including a subset of macrophages, and further showed that its mRNA expression is upregulated by lipopolysaccharide (LPS) stimulation in primary human monocytes. (4) Conclusions: ERVPb1 is unique to Simiiformes and actually translated in hematopoietic cell lineages, including a subset of macrophages.

Keywords: a simiiforme-specific gene; an Env-derived ERVPb1 gene; hemangioblast cells; hematopoietic cells; human genome; human iPSCs; macrophages; organoid generation; retrovirus-derived genes (RVDs).

MeSH terms

  • Animals
  • CRISPR-Cas Systems
  • Cell Differentiation
  • Cell Line
  • Endogenous Retroviruses* / genetics
  • Endogenous Retroviruses* / isolation & purification
  • Endogenous Retroviruses* / metabolism
  • Fluorescent Dyes
  • Gene Editing / methods
  • Genes, Viral
  • Haplorhini / virology*
  • Humans
  • Induced Pluripotent Stem Cells / metabolism
  • Macrophages / metabolism
  • Macrophages / virology*
  • Viral Fusion Proteins / genetics
  • Viral Fusion Proteins / metabolism
  • Viral Proteins / genetics
  • Viral Proteins / metabolism

Substances

  • Fluorescent Dyes
  • Viral Fusion Proteins
  • Viral Proteins