BBSome Interacting Protein 1 (BBIP1)

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BBIP10; BBSome-Interacting Protein Of 10 kDa

BBSome Interacting Protein 1 (BBIP1)
Primary cilium dysfunction affects the development and homeostasis of many organs in Bardet-Biedl syndrome (BBS). Seven highly conserved BBS proteins form a stable complex, the BBSome, that functions in membrane trafficking to and inside the primary cilium.Similar to other BBSome subunits, BBIP10 localizes to the primary cilium, BBIP10 is present exclusively in ciliated organisms, and depletion of BBIP10 yields characteristic BBS phenotypes in zebrafish. Unexpectedly, BBIP10 is required for cytoplasmic microtubule polymerization and acetylation, two functions not shared with any other BBSome subunits. Strikingly, inhibition of the tubulin deacetylase HDAC6 restores microtubule acetylation in BBIP10-depleted cells, and BBIP10 physically interacts with HDAC6. BBSome-bound BBIP10 may therefore function to couple acetylation of axonemal microtubules and ciliary membrane growth.

Organism species: Homo sapiens (Human)

CATALOG NO. PRODUCT NAME APPLICATIONS
Proteins n/a Recombinant BBSome Interacting Protein 1 (BBIP1) Recombinant Protein Customized Service Offer
Antibodies n/a Monoclonal Antibody to BBSome Interacting Protein 1 (BBIP1) Monoclonal Antibody Customized Service Offer
n/a Polyclonal Antibody to BBSome Interacting Protein 1 (BBIP1) Polyclonal Antibody Customized Service Offer
Assay Kits n/a CLIA Kit for BBSome Interacting Protein 1 (BBIP1) CLIA Kit Customized Service Offer
n/a ELISA Kit for BBSome Interacting Protein 1 (BBIP1) ELISA Kit Customized Service Offer
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  2. "The DNA sequence and comparative analysis of human chromosome 10." Nature 429:375-381(2004) [PubMed] [Europe PMC] [Abstract]
  3. "The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC)."Genome Res. 14:2121-2127(2004) [PubMed] [Europe PMC] [Abstract]
  4. "A BBSome subunit links ciliogenesis, microtubule stability and acetylation."Dev. Cell 15:854-865(2008)
  5. "Exome sequencing of Bardet-Biedl syndrome patient identifies a null mutation in the BBSome subunit BBIP1 (BBS18)."J. Med. Genet. 51:132-136(2014) [PubMed] [Europe PMC] [Abstract]