A specific and unusual nuclear localization signal in the DNA binding domain of the Rev-erb orphan receptors

Abstract

The orphan receptors Rev-erbα and Rev-erβ are members of the nuclear receptors superfamily and act as transcriptional repressors. Rev-erbα is expressed with a robust circadian rhythm and is involved in liver metabolism through repression of the ApoA1 gene, but no role has been yet defined for Rev-erbβ. To gain better understanding of their function and mode of action, we characterized the proteins encoded by these two genes. Both Rev-erbα and Rev-erbβ proteins were nuclear when transiently transfected in COS-1 cells. The major nuclear location signal (NLS) of Rev-erbα is in the amino-terminal region of the protein. Fusion of green fluorescent protein (GFP) to the amino terminus of Rev-erbα deletion mutants showed that the NLS is located whithin a 53 amino acid segment of the DNA binding domain (DBD). The homologous region of Rev-erbβ fused to GFP also targeted the fusion protein to the nucleus, suggesting that the location of this NLS is conserved among all the Rev-erb group members. Interestingly, members of the phylogenetically closest nuclear orphan receptor group (ROR), which exhibit 58% amino acid identity with Rev-erb in the DBD, do not have their NLS located whithin the DBD. GFP/DBD.RORα or GFP/DBD.RORβ remained cytoplasmic, in contrast to GFP/DBD.Rev-erb fusion proteins. Alignment of human Rev-erb and ROR DBD amino acid sequences predicted that the two basic residues, K167 and R168, located just upstream from the second zinc finger, could play a critical part in the nuclear localization of Rev-erb proteins. Substitution of these two residues with those found in ROR, in the GFP/DBD.Rev-erb context, resulted in cytoplasmic proteins. In contrast, the reverse mutation of the GFP/DBD.RORα towards the Rev-erbα residues targeted the fusion protein to the nucleus. Our data demonstrate that Rev-erb proteins contain a functional NLS in the DBD. Its location is unusual within the nuclear receptor superfamily and suggests that Rev-erb orphan receptors control their intracellular localization via a mechanism different from that of other nuclear receptors.