is a nematode-specific gene that encodes a type II transmembrane protein containing the BRICHOS domain. The gene was isolated as a heat-sensitive mutant， but the function of the protein remained unclear. We examined the expression pattern and subcellular localization of C09F5.1 as well as its roles in thermotolerance and chaperone function. Expression of under heat shock conditions was induced in a heat shock factor 1 (HSF-1)-dependent manner. However， under normal growth conditions， most cells types exposed to mechanical stimuli expressed . Knockdown of expression or deletion of the N-terminal domain decreased thermotolerance. The BRICHOS domain of C09F5.1 did not exhibit chaperone function unlike thos... More
is a nematode-specific gene that encodes a type II transmembrane protein containing the BRICHOS domain. The gene was isolated as a heat-sensitive mutant， but the function of the protein remained unclear. We examined the expression pattern and subcellular localization of C09F5.1 as well as its roles in thermotolerance and chaperone function. Expression of under heat shock conditions was induced in a heat shock factor 1 (HSF-1)-dependent manner. However， under normal growth conditions， most cells types exposed to mechanical stimuli expressed . Knockdown of expression or deletion of the N-terminal domain decreased thermotolerance. The BRICHOS domain of C09F5.1 did not exhibit chaperone function unlike those of other proteins containing this domain， but the domain was essential for the proper subcellular localization of the protein. Intact C09F5.1 was localized to the Golgi body， but the N-terminal domain of C09F5.1 (C09F5.1-NTD) was retained in the ER. C09F5.1-NTD delayed paralysis by beta-amyloid (1-42) protein (Aβ) in Alzheimer's disease model worms (CL4176) and activated the unfolded protein response (UPR) by interacting with Aβ. An intrinsically disordered region (IDR) located at the N-terminus of C09F5.1 may be responsible for the chaperone function of C09F5.1-NTD. Taken together， the data suggest that C09F5.1 triggers the UPR by interacting with abnormal proteins.
