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  Cloning of a novel phospholipase C-delta isoform from Pacific purple sea urchin (Strongylocentrotus purpuratus) gametes and its expression during early embryonic development

Coward, K., Owen, H., Poustka, A. J., Hibbitt, O., Tunwell, R., Kubota, H., et al. (2004). Cloning of a novel phospholipase C-delta isoform from Pacific purple sea urchin (Strongylocentrotus purpuratus) gametes and its expression during early embryonic development. Biochemical and Biophysical Research Communications, 313(4), 894-901. doi:10.1016/j.bbrc.2003.12.029.

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Genre: Journal Article
Alternative Title : Biochem Biophys Res Commun

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 Creators:
Coward, Kevin, Author
Owen, Helen, Author
Poustka, Albert J.1, Author              
Hibbitt, Olivia, Author
Tunwell, Richard, Author
Kubota, Hiroki, Author
Swann, Karl, Author
Parrington, John, Author
Affiliations:
1Evolution and Development (Albert Poustka), Dept. of Vertebrate Genomics (Head: Hans Lehrach), Max Planck Institute for Molecular Genetics, Max Planck Society, ou_1479650              

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Free keywords: Fertilization; Calcium; Phospholipase C; PLCsmall delta, Greek; Egg; Sperm; Embryo; Sea urchin
 Abstract: Calcium (Ca2+) is a ubiquitous intracellular messenger, controlling a diverse range of cellular processes, including fertilization and development of the embryo. One of the key mechanisms involved in triggering intracellular calcium release is the generation of the second messenger inositol-1,4,5-phosphate (IP3) by the phospholipase C (PLC) class of enzymes. Although five distinct forms of PLC have been identified in mammals (, , , , and ), only one, PLC, has thus far been detected in echinoderms. In the present study, we describe the isolation of a cDNA encoding a novel PLC isoform of the delta () subclass, PLC-su, from the egg of the Pacific purple sea urchin Strongylocentrotus purpuratus. We also demonstrate the presence of this PLC within the sperm and in the early embryo. The PLC-su cDNA (2.44 kb) encodes a 742 amino acid polypeptide with an open reading frame of 84.6 kDa and a pI of 6.04. All of the characteristic domains found in mammalian PLC isoforms (PH domain, EF hands, an X–Y catalytic region, and a C2 domain) are present in PLC-su. A homology search revealed that PLC-su shares most sequence identity with bovine PLC2 (39%). We present evidence that PLC-su is expressed in unfertilized eggs, fertilized eggs, and in the early embryo. In addition to Northern and polymerase chain reaction (PCR) analyses, in situ hybridization experiments further demonstrated that the embryonic regions within which the PLC-su transcript can be detected during early embryonic development are associated with the highest levels of proliferative activity, suggesting a possible involvement with metabolism or cell cycle regulation.

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Language(s): eng - English
 Dates: 2004-01-23
 Publication Status: Published in print
 Pages: -
 Publishing info: -
 Table of Contents: -
 Rev. Type: -
 Identifiers: eDoc: 173716
DOI: 10.1016/j.bbrc.2003.12.029
 Degree: -

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Title: Biochemical and Biophysical Research Communications
  Alternative Title : Biochem Biophys Res Commun
Source Genre: Journal
 Creator(s):
Affiliations:
Publ. Info: -
Pages: - Volume / Issue: 313 (4) Sequence Number: - Start / End Page: 894 - 901 Identifier: ISSN: 0006-291X