Literature DB >> 1899403

Evidence for the involvement of a pertussis toxin-insensitive G-protein in egg activation of the frog, Xenopus laevis.

D Kline1, G S Kopf, L F Muncy, L A Jaffe.   

Abstract

Activation responses of the frog egg at fertilization include the release of calcium from intracellular stores and the opening of calcium-dependent chloride channels, which produce the fertilization potential. To investigate the presence of guanine nucleotide-binding proteins (G-proteins), and their role in initiation of these events in the egg of the frog Xenopus laevis, we assayed for pertussis and cholera toxin substrates, and applied activators and inhibitors of G-proteins. Pertussis toxin catalyzed the [32P]ADP ribosylation of a Mr 40,000 component, but no cholera toxin substrates were demonstrated. Injection of greater than or equal to 25 pmole of guanosine-5'-O-(3-thiotriphosphate) GTP-gamma-S), an activator of G-proteins, produced a change in membrane potential that mimicked the fertilization potential and also caused cortical granule exocytosis and cortical contraction. Injections of up to 600 pmole of guanosine 3':5'-cyclic monophosphate or 9 nmole of guanosine-5'-(beta-gamma-imido)triphosphate did not active eggs. The membrane potential response to GTP-gamma-S injection showed the same peak and chloride dependence as the fertilization potential, although the duration of the GTP-gamma-S response was somewhat greater. GTP-gamma-S did not activate eggs if the calcium rise was prevented by prior injection of the calcium chelator BAPTA. Injection of up to 200 ng of cholera toxin did not activate eggs. However, eggs were activated by applying 1 nM serotonin to eggs that had been injected with a specific mRNA for the serotonin 1c receptor, a member of the class of receptors that act by way of G-proteins. Egg activation in response to either sperm or serotonin was not inhibited by pertussis toxin, under experimental conditions where approximately 80-90% of the toxin substrate was ADP-ribosylated. These results support the hypothesis that sperm activate Xenopus eggs at fertilization by way of a pertussis and cholera toxin-insensitive G-protein.

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Year:  1991        PMID: 1899403     DOI: 10.1016/0012-1606(91)90072-b

Source DB:  PubMed          Journal:  Dev Biol        ISSN: 0012-1606            Impact factor:   3.582


  7 in total

Review 1.  Calcium at fertilization and in early development.

Authors:  Michael Whitaker
Journal:  Physiol Rev       Date:  2006-01       Impact factor: 37.312

Review 2.  Phospholipase C and D regulation of Src, calcium release and membrane fusion during Xenopus laevis development.

Authors:  Bradley J Stith
Journal:  Dev Biol       Date:  2015-03-05       Impact factor: 3.582

3.  Activation of Src and release of intracellular calcium by phosphatidic acid during Xenopus laevis fertilization.

Authors:  Ryan C Bates; Colby P Fees; William L Holland; Courtney C Winger; Khulan Batbayar; Rachel Ancar; Todd Bergren; Douglas Petcoff; Bradley J Stith
Journal:  Dev Biol       Date:  2013-11-21       Impact factor: 3.582

4.  Inositol 1,4,5-trisphosphate mass changes from fertilization through first cleavage in Xenopus laevis.

Authors:  B J Stith; M Goalstone; S Silva; C Jaynes
Journal:  Mol Biol Cell       Date:  1993-04       Impact factor: 4.138

Review 5.  Calcium signaling and meiotic exit at fertilization in Xenopus egg.

Authors:  Alexander A Tokmakov; Vasily E Stefanov; Tetsushi Iwasaki; Ken-Ichi Sato; Yasuo Fukami
Journal:  Int J Mol Sci       Date:  2014-10-15       Impact factor: 5.923

6.  Reducing inositol lipid hydrolysis, Ins(1,4,5)P3 receptor availability, or Ca2+ gradients lengthens the duration of the cell cycle in Xenopus laevis blastomeres.

Authors:  J K Han; K Fukami; R Nuccitelli
Journal:  J Cell Biol       Date:  1992-01       Impact factor: 10.539

7.  Stimulation of Xenopus oocyte maturation by inhibition of the G-protein alpha S subunit, a component of the plasma membrane and yolk platelet membranes.

Authors:  C J Gallo; A R Hand; T L Jones; L A Jaffe
Journal:  J Cell Biol       Date:  1995-07       Impact factor: 10.539

  7 in total

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