BPIFB9P

Vomeromodulin/BPIFB9/BPIFB9A is a member of the BPI fold protein superfamily defined by the presence of the bactericidal/permeability-increasing protein fold (BPI fold) which is formed by two similar domains in a "boomerang" shape.[9] This superfamily is also known as the BPI/LBP/PLUNC family or the BPI/LPB/CETP family.[10] The BPI fold creates apolar binding pockets that can interact with hydrophobic and amphipathic molecules, such as the acyl carbon chains of lipopolysaccharide found on Gram-negative bacteria, but members of this family may have many other functions.

BPIFB9P is a human pseudogene member the BPI-fold gene family and the transcribed protein in other species is a member of the BPI/LBP/PLUNC protein superfamily

Genes for the BPI/LBP/PLUNC superfamily are found in all vertebrate species, including distant homologs in non-vertebrate species such as insects, mollusks, and roundworms.[11][12] Within that broad grouping is the BPIF gene family whose members encode the BPI fold structural motif and are found clustered on a single chromosome, e.g., Chromosome 20 in humans, Chromosome 2 in mouse, Chromosome 3 in rat, Chromosome 17 in pig, Chromosome 13 in cow. The BPIF gene family is split into two groupings, BPIFA (SPLUNC) and BPIFB (LPLUNC). In humans, BIPFA consists of 3 protein encoding genes BPIFA1, BPIFA2, BPIFA3, and 1 pseudogene BPIFA4P; while BPIFB consists of 5 protein encoding genes BPIFB1, BPIFB2, BPIFB3, BPIFB4, BPIFB6 and 2 pseudogenes BPIFB5P, BPIFB9P. What appears as pseudogenes in humans may appear as fully functional genes in other species.

The PIFB9P pseduogene in humans was first reported in 2011 as a member of the BPI/LBP/PLUNC family,[13][12] but clones containing PIFB9P had been detected in 1999 genomic screening by the Welcome Trust Sanger Institute.[14]

In humans, the expression of the BPIFB9P pseudogene into functional BPIFB9 protein is unclear. Although identified multiple times by independent scientists as a pseudogene not capable of coding for a protein, its gene sequence may predict two transcripts (splice variants) [15] and RNA transcripts detected by RNA-Seq screens have been observed in brain tissues, striated muscle, white blood cells (granulocytes, monocytes), and esophageal mucosa.[16] Yet, definitive evidence for human BPIFB9 protein has never been produced and is unlikely to happen.

The non-human version of this protein, however, is well known. Vomeromodulin is highly expressed in nasal mucosa, particularly within a structure known as the Vomeronasal organ.[17] The vomeronasal organ is present and well-developed in many mammals to process pheromone odors into neural signals to the brain, but the chemical and neural components of the vomeronasal system have been completely inactivated in most primates, including humans. [18][19] In this context, BPIFB9-type proteins are thought to be similar to odorant binding proteins which presents odorant molecules to chemical odorant receptor molecules.[20] Those odorant receptors, in turn, are associated with nasal epithelial cells integrated with olfactory neurons that project back to the brain's oflactory areas and hypothalamus. It has been established that the genes and proteins for these components are present and active in many mammal species, but in higher primates the genes are found to be mutated and appear as non-functional pseudogenes, like BPIFB9P.

• Human BPIFB9P genome location and BPIFB9P gene details page in the UCSC Genome Browser.