Knockout of the BRAP homolog in mice leads to abnormal tracheal cilia

Abstract

Both bombesin receptor‐activated protein (BRAP) and its mouse homolog have been found to be expressed in bronchial epithelia but with unclear functions. Using electron microscopy combined with histological assays, we found that BRAP homolog deficiency in mice led to abnormal tracheal cilia. Rab‐3A‐interacting protein (Rabin8), a protein that might play a role in cilia development, was screened by yeast two‐hybrid and further verified to have interaction with human BRAP by co‐immunoprecipitation and pulldown assays. The expression levels of Rabin8, together with acetylated α‐tubulin, a marker of cilia, were either downregulated by knockdown of BRAP or upregulated by overexpression of BRAP in cultured immortalized human bronchial epithelial cells. These results reveal a role for BRAP in airway cilia formation.