Injection of a Sperm Extract Triggers Egg Activation in the Newt Cynops pyrrhogaster
Developmental Biology, ISSN: 0012-1606, Vol: 230, Issue: 1, Page: 89-99
2001
- 27Citations
- 11Captures
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Example: if you select the 1-year option for an article published in 2019 and a metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019. If you select the 3-year option for the same article published in 2019 and the metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019, 2018 and 2017.
Citation Benchmarking is provided by Scopus and SciVal and is different from the metrics context provided by PlumX Metrics.
Metrics Details
- Citations27
- Citation Indexes27
- 27
- CrossRef24
- Captures11
- Readers11
- 11
Article Description
Unfertilized eggs of the newt Cynops pyrrhogaster are arrested at the second meiotic metaphase. The primary signal for egg activation is a transient increase in [Ca 2+ ] i, which is triggered by the fertilizing sperm and propagates over the egg cortex as a Ca 2+ wave. We injected an extract of Cynops sperm (SE) into unfertilized eggs and induced a wave-like [Ca 2+ ] i increase which resulted in activation and resumption of meiosis. The SE-injected eggs showed degradation of cyclin B1 and DNA replication. When SE was boiled or treated with proteinase K before injection, it was unable to cause egg activation. Preinjection of Ca 2+ -chelator BAPTA before SE injection inhibited egg activation. These results indicate that a heat-labile and proteinaceous factor in the sperm cytoplasm induces a transient increase in [Ca 2+ ] i which is required for egg activation. Injection of IP 3 into unfertilized eggs caused an increase in [Ca 2+ ] i and egg activation, but injection of cADP-ribose did not. These results support the hypothesis that Ca 2+ release at fertilization occurs via IP 3 receptors.
Bibliographic Details
http://www.sciencedirect.com/science/article/pii/S0012160600999494; http://dx.doi.org/10.1006/dbio.2000.9949; http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=0035253395&origin=inward; http://www.ncbi.nlm.nih.gov/pubmed/11161564; https://linkinghub.elsevier.com/retrieve/pii/S0012160600999494; https://dx.doi.org/10.1006/dbio.2000.9949
Elsevier BV
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