Cloning, Characterization, and Mapping of a Murine Promiscuous Chemokine Receptor Gene: Homolog of the Human Duffy Gene

  1. Hong Luo1,
  2. Asok Chaudhuri1,
  3. Kenneth R. Johnson2,
  4. Kuldeep Neote3,
  5. Valerie Zbrzezna1,
  6. Yu He2, and
  7. A. Oscar Pogo1,4
  1. 1Laboratory of Cell Biology, Lindsley F. Kimball Research Institute of the New York Blood Center, New York, New York NY 10021; 2The Jackson Laboratory, Bar Harbor, Maine 04609; 3Pfizer Central Research, Groton, Connecticut 06340

Abstract

We report here the isolation and genomic organization of the orthologous mouse Duffy gene, named Dfy. It is a single copy gene located in chromosome 1 in a region homologous to the human Duffy gene (FY). Sequence analyses indicate that Dfyconsists of two exons: exon 1 of 55 nucleotides, which encodes 7 amino acid residues; and exon 2 of 1038 nucleotides, which encodes 327 residues. The single intron consists of 462 nucleotides. The 5′-end promoter region contains motifs involved in vertebrate development in addition to potential binding sites of factors for globin transcription. The open reading frame (ORF) shows 60% homology with the human Duffy protein. However, mouse erythrocytes are serologically Duffy-negative and mouse erythrocyte membrane proteins do not cross-react with two Duffy-specific rabbit polyclonal antibodies. The deduced protein predicts a M r of 36,692 and carries three potential N-glycosylation sites to asparagine residues. Hydropathy analysis predicts an exocellular amino-terminal domain of 57 residues, seven transmembrane α-helices, and an endocellular carboxy-terminal domain of 29 residues. In bone marrow and spleen,Dfy expresses a major 1.4-kb and a minor 1.8-kb mRNA. Contrary to humans, Dfy is expressed in liver, synthesizing a 1.4-kb mRNA, and is repressed in kidney. Dfy is highly expressed in mouse brain and produces a major 8.5-kb and a minor 10.2-kb mRNA. The human erythroleukemia K562 cells, transfected with cDNA encoding the mouse Duffy-like protein and mouse erythrocytes, have the same chemokine binding profiles indicating that they contain the same protein.

[The sequence data described in this paper have been submitted to GenBank under accession nos. AF016584 and AF016697.]

Footnotes

  • 4 Corresponding author.

  • E-MAIL opogo{at}nybc.org; FAX (212) 570-3195.

    • Received May 5, 1997.
    • Accepted July 25, 1997.
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