CRACM1 Is a Plasma Membrane Protein Essential for Store-Operated Ca 2+ Entry

Author:

Vig M.12,Peinelt C.12,Beck A.12,Koomoa D. L.12,Rabah D.12,Koblan-Huberson M.12,Kraft S.12,Turner H.12,Fleig A.12,Penner R.12,Kinet J.-P.12

Affiliation:

1. Department of Pathology, Beth Israel Deaconess Medical Center and Harvard Medical School, Boston, MA 02215, USA.

2. Center for Biomedical Research at The Queen's Medical Center and John A. Burns School of Medicine at the University of Hawaii, Honolulu, HI 96813, USA.

Abstract

Store-operated Ca 2+ entry is mediated by Ca 2+ release–activated Ca 2+ (CRAC) channels following Ca 2+ release from intracellular stores. We performed a genome-wide RNA interference (RNAi) screen in Drosophila cells to identify proteins that inhibit store-operated Ca 2+ influx. A secondary patch-clamp screen identified CRACM1 and CRACM2 (CRAC modulators 1 and 2) as modulators of Drosophila CRAC currents. We characterized the human ortholog of CRACM1, a plasma membrane–resident protein encoded by gene FLJ14466 . Although overexpression of CRACM1 did not affect CRAC currents, RNAi-mediated knockdown disrupted its activation. CRACM1 could be the CRAC channel itself, a subunit of it, or a component of the CRAC signaling machinery.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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