Molecular Cloning and Characterization of Rat Genes Encoding Homologues of Human β-Defensins

ABSTRACT β-Defensins are cationic peptides with broad-spectrum antimicrobial activity that may play a role in mucosal defenses of several organs. They have been isolated in several species, and in humans, two β-defensins have been identified. Here, we report the identification of two genes encoding β-defensin homologues in the rat. Partial cDNAs were found by searching the expressed-sequence-tag database, and primers were designed to generate full-length mRNA coding sequences. One gene was highly similar to the human β-defensin-1 (HBD-1) gene and mouse β-defensin-1 gene at both the nucleic acid and amino acid levels and was termed rat β-defensin-1 (RBD-1). The other gene, named RBD-2, was homologous to the HBD-2 and bovine tracheal antimicrobial peptide (TAP) genes. The predicted prepropeptides were strongly cationic, were 69 and 63 residues in length for RBD-1 and RBD-2, respectively, and contained the six-cysteine motif characteristic of β-defensins. The β-defensin genes mapped closely on rat chromosome 16 and were closely linked to the α-defensins genes, suggesting that they are part of a gene cluster, similar to the organization reported for humans. Northern blot analysis showed that both RBD-1 and RBD-2 mRNA transcripts were ∼0.5 kb in length; RBD-1 mRNA was abundantly transcribed in the rat kidney, while RBD-2 was prevalent in the lung. Reverse transcription-PCR indicated that RBD-1 and RBD-2 mRNAs were distributed in a variety of other tissues. In the lung, RBD-1 mRNA expression localized to the tracheal epithelium while RBD-2 was expressed in alveolar type II cells. In conclusion, we characterized two novel β-defensin homologues in the rat. The rat may be a useful model to investigate the function and contribution of β-defensins to host defense in the lung, kidney, and other tissues.

[1]  E. Greenberg,et al.  Production of β-defensins by human airway epithelia , 1998 .

[2]  J. Stokes,et al.  Developmental regulation of epithelial sodium channel subunit mRNA expression in rat colon and lung. , 1998, American journal of physiology. Gastrointestinal and liver physiology.

[3]  H. Heng,et al.  Structure and mapping of the human beta-defensin HBD-2 gene and its expression at sites of inflammation. , 1998, Gene.

[4]  V. Bafna,et al.  Human beta-defensin 2 is a salt-sensitive peptide antibiotic expressed in human lung. , 1998, The Journal of clinical investigation.

[5]  G. Diamond,et al.  β-defensins: Endogenous antibiotics of the innate host defense response , 1998 .

[6]  M. Schrader,et al.  Human beta-defensin-1: A urinary peptide present in variant molecular forms and its putative functional implication. , 1998, European journal of medical research.

[7]  D. Davidson,et al.  Mouse beta defensin-1 is a functional homolog of human beta defensin-1 , 1998, Mammalian Genome.

[8]  V. Sheffield,et al.  The forkhead transcription factor gene FKHL7 is responsible for glaucoma phenotypes which map to 6p25 , 1998, Nature Genetics.

[9]  Christina H. Park,et al.  Human beta-defensin-1: an antimicrobial peptide of urogenital tissues. , 1998, The Journal of clinical investigation.

[10]  T. Ganz,et al.  Molecular cloning and tissue expression of porcine β‐defensin‐1 , 1998 .

[11]  James M. Wilson,et al.  Mouse β-Defensin 1 Is a Salt-Sensitive Antimicrobial Peptide Present in Epithelia of the Lung and Urogenital Tract , 1998, Infection and Immunity.

[12]  Douglas E. Jones,et al.  Enteric β-Defensin: Molecular Cloning and Characterization of a Gene with Inducible Intestinal Epithelial Cell Expression Associated with Cryptosporidium parvumInfection , 1998, Infection and Immunity.

[13]  G. Diamond,et al.  Antimicrobial peptide expression is developmentally regulated in the ovine gastrointestinal tract. , 1998, The Journal of nutrition.

[14]  D. Burkin,et al.  Localization and genomic organization of sheep antimicrobial peptide genes. , 1998, Gene.

[15]  D. Clark,et al.  Enteric beta-defensin: molecular cloning and characterization of a gene with inducible intestinal epithelial cell expression associated with Cryptosporidium parvum infection. , 1998, Infection and immunity.

[16]  R. Siebert,et al.  Mapping of the gene encoding human beta-defensin-2 (DEFB2) to chromosome region 8p22-p23.1. , 1997, Genomics.

[17]  C. Kozak,et al.  The mouse genome encodes a single homolog of the antimicrobial peptide human β‐defensin 1 , 1997, FEBS letters.

[18]  H. Heng,et al.  The human β-defensin-1 and α-defensins are encoded by adjacent genes : Two peptide families with differing disulfide topology share a common ancestry , 1997 .

[19]  J. Schröder,et al.  A peptide antibiotic from human skin , 1997, Nature.

[20]  R. Mallampalli,et al.  Sphingomyelin metabolism is developmentally regulated in rat lung. , 1997, American journal of respiratory cell and molecular biology.

[21]  P. McCray,et al.  Human airway epithelia express a beta-defensin. , 1997, American journal of respiratory cell and molecular biology.

[22]  James M. Wilson,et al.  Human β-Defensin-1 Is a Salt-Sensitive Antibiotic in Lung That Is Inactivated in Cystic Fibrosis , 1997, Cell.

[23]  Lucio Luzzatto,et al.  Somatic Mutations in Paroxysmal Nocturnal Hemoglobinuria: A Blessing in Disguise? , 1997, Cell.

[24]  G. Steffens,et al.  Antibacterial activity of antileukoprotease , 1996, Infection and immunity.

[25]  E. Greenberg,et al.  Cystic Fibrosis Airway Epithelia Fail to Kill Bacteria Because of Abnormal Airway Surface Fluid , 1996, Cell.

[26]  A. Dutra,et al.  Human enteric defensin genes: chromosomal map position and a model for possible evolutionary relationships. , 1996, Genomics.

[27]  B. Schonwetter,et al.  Epithelial antibiotics induced at sites of inflammation. , 1995, Science.

[28]  J. Whitsett,et al.  Human surfactant protein B: structure, function, regulation, and genetic disease. , 1995, Physiological reviews.

[29]  H. O'brodovich,et al.  Lung epithelial Na channel subunits are differentially regulated during development and by steroids. , 1995, The American journal of physiology.

[30]  M. Raida,et al.  hBD‐1: a novel β‐defensin from human plasma , 1995 .

[31]  M. Raida,et al.  hBD-1: a novel beta-defensin from human plasma. , 1995, FEBS letters.

[32]  K. Gibson,et al.  Intracellular distribution of lysozyme in rat alveolar type II epithelial cells. , 1994, Experimental lung research.

[33]  J. Wilcox Fundamental principles of in situ hybridization. , 1993, The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society.

[34]  Douglas E. Jones,et al.  Airway epithelial cells are the site of expression of a mammalian antimicrobial peptide gene. , 1993, Proceedings of the National Academy of Sciences of the United States of America.

[35]  R. Ellison,et al.  Killing of gram-negative bacteria by lactoferrin and lysozyme. , 1991, The Journal of clinical investigation.

[36]  J. Bourbon Pulmonary Surfactant: Biochemical, Functional, Regulatory, and Clinical Concepts , 1991 .

[37]  M. Zasloff,et al.  Tracheal antimicrobial peptide, a cysteine-rich peptide from mammalian tracheal mucosa: peptide isolation and cloning of a cDNA. , 1991, Proceedings of the National Academy of Sciences of the United States of America.

[38]  K. Nealson,et al.  Cloning, organization, and expression of the bioluminescence genes of Xenorhabdus luminescens , 1990, Journal of bacteriology.

[39]  M. Millar The susceptibility to lysozyme of beta-lactamase-producing and non-producing derivatives of Staphylococcus aureus strain 1030. , 1987, Journal of medical microbiology.

[40]  M. Williams,et al.  An improved method for isolating type II cells in high yield and purity. , 2015, The American review of respiratory disease.

[41]  R. C. Davies,et al.  The dependence of lysozyme activity on pH and ionic strength. , 1969, Biochimica et biophysica acta.

[42]  A. Fleming On a Remarkable Bacteriolytic Element Found in Tissues and Secretions , 1922 .