PRY/SPRY/B30.2 Domain of Butyrophilin 1A1 (BTN1A1) Binds to Xanthine Oxidoreductase: IMPLICATIONS FOR THE FUNCTION OF BTN1A1 IN THE MAMMARY GLAND AND OTHER TISSUES

• Published in: The Journal of biological chemistry Vol. 284; no. 33; pp. 22444 - 22456
• Main Authors: Jeong, Jaekwang, Rao, Anita U, Xu, Jinling, Ogg, Sherry L, Hathout, Yetrib, Fenselau, Catherine, Mather, Ian H
• Format: Journal Article
• Language: English
• Published: United States American Society for Biochemistry and Molecular Biology 14-08-2009
• Subjects: Animals; Butyrophilins; Cattle; Cytoplasm - metabolism; Dimerization; Female; Humans; Hydrogen-Ion Concentration; Mammary Glands, Animal - metabolism; Membrane Glycoproteins - chemistry; Membrane Glycoproteins - metabolism; Mice; Mice, Inbred C3H; Milk; Molecular Basis of Cell and Developmental Biology; Protein Binding; Protein Structure, Tertiary; Xanthine Dehydrogenase - chemistry
• ISSN: 0021-9258; 1083-351X
• DOI: 10.1074/jbc.M109.020446

Butyrophilin 1A1 (BTN1A1) and xanthine oxidoreductase (XOR) are highly expressed in the lactating mammary gland and are secreted into milk associated with the milk fat globule membrane (MFGM). Ablation of the genes encoding either protein causes severe defects in the secretion of milk lipid droplets, suggesting that the two proteins may function in the same pathway. Therefore, we determined whether BTN1A1 and XOR directly interact using protein binding assays, surface plasmon resonance analysis, and gel filtration. Bovine XOR bound with high affinity in a pH- and salt-sensitive manner (KD = 101 ± 31 nM in 10 mM HEPES, 150 mM NaCl, pH 7.4) to the PRY/SPRY/B30.2 domain in the cytoplasmic region of bovine BTN1A1. Binding was stoichiometric, with one XOR dimer binding to either two BTN1A1 monomers or one dimer. XOR bound to BTN1A1 orthologs from mice, humans, or cows but not to the cytoplasmic domains of the closely related human paralogs, BTN2A1 or BTN3A1, or to the B30.2 domain of human RoRet (TRIM 38), a protein in the TRIM family. Analysis of the protein composition of the MFGM of wild type and BTN1A1 null mice showed that most of the XOR in mice lacking BTN1A1 was released from the MFGM in a soluble form when the milk lipid droplets were disrupted to prepare membrane, compared with wild-type mice, in which most of the XOR remained membrane-bound. Thus BTN1A1 functions in vivo to stabilize the association of XOR with the MFGM by direct interactions through the PRY/SPRY/B30.2 domain. The potential significance of BTN1A1/XOR interactions in the mammary gland and other tissues is discussed.