Title

The Caenorhabditis elegans IMPAS gene, imp-2, is essential for development and is functionally distinct from related presenilins

UMMS Affiliation

Brudnick Neuropsychiatric Research Institute, Department of Psychiatry; Program in Molecular Medicine

Date

10-8-2004

Document Type

Article

Subjects

Animals; Caenorhabditis elegans; Caenorhabditis elegans Proteins; Cloning, Molecular; Endopeptidases; Gene Expression Regulation, Developmental; Membrane Proteins; RNA Interference; RNA, Double-Stranded; Recombinant Proteins

Disciplines

Life Sciences | Medicine and Health Sciences

Abstract

Presenilins (PSs) are required for Notch signaling in the development of vertebrates and invertebrates. Mutations in human PS1 and PS2 homologs are a cause of familial Alzheimer's disease (AD). The function of the recently identified ancient family of IMPAS proteins (IMP/SPP/PSH) homologous to PSs is not yet known. We show here that, unlike PSs, IMPs (orthologous C. elegans Ce-imp-2 and human hIMP1/SPP) do not promote Notch (C. elegans lin-12,glp-1) proteolysis or signaling. The knock-down of Ce-imp-2 leads to embryonic death and an abnormal molting phenotype in Caenorhabditis elegans. The molting defect induced by Ce-imp-2 deficiency was mimicked by depleting cholesterol or disrupting Ce-lrp-1 and suppressed, in part, by expression of the Ce-lrp-1 derivate. C. elegans lrp-1 is a homolog of mammalian megalin, lipoprotein receptor-related protein (LRP) receptors essential for cholesterol and lipoprotein endocytosis and signaling. These data suggest that IMPs are functionally distinct from related PSs and implicate IMPs as critical regulators of development that may potentially interact with the lipid-lipoprotein receptor-mediated pathway.

Rights and Permissions

Citation: Proc Natl Acad Sci U S A. 2004 Oct 12;101(41):14955-60. Epub 2004 Oct 6. Link to article on publisher's site

DOI of Published Version

10.1073/pnas.0406462101

Related Resources

Link to Article in PubMed

Journal Title

Proceedings of the National Academy of Sciences of the United States of America

PubMed ID

15469912