The Sarco-Endoplasmic Reticulum Ca2+ ATPase Is Required for Development and Muscle Function in Caenorhabditis elegans

The sarco-endoplasmic reticulum Ca2+-transport ATPase (SERCA) loads intracellular releasable Ca2+ stores by transporting cytosolic Ca2+ into the endoplasmic (ER) or sarcoplasmic reticulum (SR). We characterized the only SERCA homologue of the nematode Caenorhabditis elegans, which is encoded by the...

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Bibliographic Details
Published in:The Journal of biological chemistry 2001-11, Vol.276 (47), p.43557-43563
Main Authors: Zwaal, Richard R., Van Baelen, Kurt, Groenen, José T.M., van Geel, Anton, Rottiers, Veerle, Kaletta, Titus, Dode, Leonard, Raeymaekers, Luc, Wuytack, Frank, Bogaert, Thierry
Format: Article
Language:English
Subjects:
Animals
Base Sequence
Caenorhabditis elegans - enzymology
Caenorhabditis elegans - growth & development
Caenorhabditis elegans - physiology
Calcium-Transporting ATPases - antagonists & inhibitors
Calcium-Transporting ATPases - metabolism
COS Cells
DNA Primers
Enzyme Inhibitors - pharmacology
Larva - growth & development
Muscles - physiology
Sarcoplasmic Reticulum Calcium-Transporting ATPases
Thapsigargin - pharmacology
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Summary:The sarco-endoplasmic reticulum Ca2+-transport ATPase (SERCA) loads intracellular releasable Ca2+ stores by transporting cytosolic Ca2+ into the endoplasmic (ER) or sarcoplasmic reticulum (SR). We characterized the only SERCA homologue of the nematode Caenorhabditis elegans, which is encoded by the sca-1 gene. The sca-1 transcript is alternatively spliced in a similar mode as the vertebrate SERCA2 transcript, giving rise to two protein variants: CeSERCAa and CeSERCAb. These proteins showed structural and functional conservation to the vertebrate SERCA2a/b proteins. The CeSERCAs were primarily expressed in contractile tissues. Loss of CeSERCA through gene ablation or RNA interference resulted in contractile dysfunctioning and in early larval or embryonic lethality, respectively. Similar defects could be induced pharmacologically using the SERCA-specific inhibitor thapsigargin, which bound CeSERCA at a conserved site. The conservation of SERCA2 homologues in C. elegans will allow genetic and chemical suppressor analyses to identify promising drug targets and lead molecules for treatment of SERCA-related diseases such as heart disease.
ISSN:0021-9258
1083-351X
DOI:10.1074/jbc.M104693200