Contribution of calumin to embryogenesis through participation in the endoplasmic reticulum-associated degradation activity

Dev Biol. 2014 Sep 1;393(1):33-43. doi: 10.1016/j.ydbio.2014.06.024. Epub 2014 Jul 8.


Calumin is an endoplasmic reticulum (ER)-transmembrane protein, and little is known about its physiological roles. Here we showed that calumin homozygous mutant embryos die at embryonic days (E) 10.5-11.5. At mid-gestation, calumin was expressed predominantly in the yolk sac. Apoptosis was enhanced in calumin homozygous mutant yolk sacs at E9.5, pointing to a possible link to the embryonic lethality. Calumin co-immunoprecipitated with ERAD components such as p97, BIP, derlin-1, derlin-2 and VIMP, suggesting its involvement in ERAD. Indeed, calumin knockdown in HEK 293 cells resulted in ERAD being less efficient, as demonstrated by attenuation in both degradations of a misfolded α1-antitrypsin variant and the ER-to-cytosol dislocation of cholera toxin A1 subunit. In calumin homozygous mutant yolk sac endoderm cells, ER stress-associated alterations were observed, including lipid droplet accumulation, fragmentation of the ER and dissociation of ribosomes from the ER. In this context, the ER-overload response, assumed to be cytoprotective, was also triggered in the mutant endoderm cells, but seemed to fully counteract the excessive ER stress generated due to defective ERAD. Taken together, our findings suggested that calumin serves to maintain the yolk sac integrity through participation in the ERAD activity, contributing to embryonic development.

Keywords: CCDC47; Calumin; ER stress; ERAD; Embryogenesis; Secretory cells.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Apoptosis / genetics
  • Cell Line
  • Cholera Toxin / metabolism
  • Embryonic Development / genetics
  • Endoderm / cytology
  • Endoderm / pathology
  • Endoplasmic Reticulum / metabolism*
  • Endoplasmic Reticulum Stress / genetics
  • Endoplasmic Reticulum-Associated Degradation / genetics*
  • HEK293 Cells
  • Humans
  • Membrane Proteins / genetics
  • Membrane Proteins / physiology*
  • Mice
  • Mice, Inbred C57BL
  • Mice, Transgenic
  • Mutation
  • Protein Folding
  • RNA Interference
  • RNA, Small Interfering
  • Yolk Sac / metabolism*
  • alpha 1-Antitrypsin / metabolism


  • CCDC47 protein, human
  • Membrane Proteins
  • RNA, Small Interfering
  • alpha 1-Antitrypsin
  • calumin protein, mouse
  • Cholera Toxin