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- W126272185 abstract "In ascidians the cell cycle machinery has been studied mainly in oocytes while ascidian embryos have been used to dissect the mechanism that controls asymmetric cell division (ACD). Here we overview the most specific and often exceptional points and events in cell cycle control in ascidian oocytes and early embryos. Mature stage IV eggs are arrested at metaphase I due to cytostatic factor (CSF). In vertebrates, unfertilized eggs are arrested at metaphase II by CSF. Meta II-CSF is mediated by the Mos/MEK/MAPK/Erp1 pathway, which inhibits the ubiquitin ligase APC/C(cdc20) preventing cyclin B destruction thus stabilizing MPF activity. CSF is inactivated by the fertilization Ca(2+) transient that stimulates the destruction of Erp1 thus releasing APC/C(cdc20) from inhibition. Although many of the components of CSF are conserved between the ascidian and the vertebrates, the lack of Erp1 in the ascidians (and indeed other invertebrates) is notable since the Mos/MAPK pathway nonetheless mediates Meta I-CSF. Moreover, since the fertilization Ca(2+) transient targets Erp1, it is not clear how the sperm-triggered Ca(2+) transient in ascidians (and again other invertebrates) stimulates cyclin B destruction in the absence of Erp1. Nonetheless, like mammalian eggs, sperm trigger a series of Ca(2+) oscillations that increases the rate of cyclin B destruction and the subsequent loss of MAPK activity leading to meiotic exit in ascidians. Positive feedback from MPF maintains the Ca(2+) oscillations in fertilized ascidian eggs ensuring the eventual loss of MPF stimulating the egg-to-embryo transition. Embryonic cell cycles in the ascidian are highly stereotyped where both the rate of cell division and the orientation of cell division planes are precisely controlled. Three successive rounds of ACD generate two small posterior germ cell precursors at the 64 cell stage. The centrosome-attracting body (CAB) is a macroscopic cortical structure visible by light microscopy that causes these three rounds of ACD. Entry into mitosis activates the CAB causing the whole mitotic spindle to rotate and migrate toward the cortical CAB leading to a highly ACD whereby one small cell is formed that inherits the CAB and approximately 40 maternal postplasmic/PEM RNAs including the germ cell marker vasa." @default.
- W126272185 created "2016-06-24" @default.
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- W126272185 date "2011-01-01" @default.
- W126272185 modified "2023-10-10" @default.
- W126272185 title "Cell Cycle in Ascidian Eggs and Embryos" @default.
- W126272185 cites W1486920532 @default.
- W126272185 cites W1547794316 @default.
- W126272185 cites W1830166812 @default.
- W126272185 cites W1931124483 @default.
- W126272185 cites W1965027896 @default.
- W126272185 cites W1965991185 @default.
- W126272185 cites W1967796034 @default.
- W126272185 cites W1970894617 @default.
- W126272185 cites W1972979813 @default.
- W126272185 cites W1973025143 @default.
- W126272185 cites W1974708640 @default.
- W126272185 cites W1979186312 @default.
- W126272185 cites W1988813675 @default.
- W126272185 cites W1997923583 @default.
- W126272185 cites W2001056871 @default.
- W126272185 cites W2002656407 @default.
- W126272185 cites W2004346300 @default.
- W126272185 cites W2005249317 @default.
- W126272185 cites W2006200936 @default.
- W126272185 cites W2007278837 @default.
- W126272185 cites W2009371644 @default.
- W126272185 cites W2009725639 @default.
- W126272185 cites W2013843350 @default.
- W126272185 cites W2024681690 @default.
- W126272185 cites W2029356159 @default.
- W126272185 cites W2032736669 @default.
- W126272185 cites W2032840077 @default.
- W126272185 cites W2034761252 @default.
- W126272185 cites W2036496205 @default.
- W126272185 cites W2039669035 @default.
- W126272185 cites W2040392785 @default.
- W126272185 cites W2043270554 @default.
- W126272185 cites W2045843159 @default.
- W126272185 cites W2047361983 @default.
- W126272185 cites W2050103288 @default.
- W126272185 cites W2056631203 @default.
- W126272185 cites W2057495884 @default.
- W126272185 cites W2058777636 @default.
- W126272185 cites W2059623287 @default.
- W126272185 cites W2060050992 @default.
- W126272185 cites W2062906922 @default.
- W126272185 cites W2068065491 @default.
- W126272185 cites W2068234279 @default.
- W126272185 cites W2068344177 @default.
- W126272185 cites W2068799271 @default.
- W126272185 cites W2077285952 @default.
- W126272185 cites W2079223456 @default.
- W126272185 cites W2083128930 @default.
- W126272185 cites W2087334554 @default.
- W126272185 cites W2088303309 @default.
- W126272185 cites W2089394002 @default.
- W126272185 cites W2093460132 @default.
- W126272185 cites W2093916262 @default.
- W126272185 cites W2094577119 @default.
- W126272185 cites W2098479948 @default.
- W126272185 cites W2101031857 @default.
- W126272185 cites W2102975710 @default.
- W126272185 cites W2102988868 @default.
- W126272185 cites W2103431676 @default.
- W126272185 cites W2107332774 @default.
- W126272185 cites W2108772416 @default.
- W126272185 cites W2114802821 @default.
- W126272185 cites W2115358069 @default.
- W126272185 cites W2117035204 @default.
- W126272185 cites W2128211797 @default.
- W126272185 cites W2128832587 @default.
- W126272185 cites W2129723437 @default.
- W126272185 cites W2132204920 @default.
- W126272185 cites W2140558722 @default.
- W126272185 cites W2145332903 @default.
- W126272185 cites W2155652476 @default.
- W126272185 cites W2158179580 @default.
- W126272185 cites W2166457341 @default.
- W126272185 cites W2170258388 @default.
- W126272185 cites W2172257350 @default.
- W126272185 cites W2238313648 @default.
- W126272185 cites W98119722 @default.
- W126272185 doi "https://doi.org/10.1007/978-3-642-19065-0_8" @default.
- W126272185 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/21630145" @default.
- W126272185 hasPublicationYear "2011" @default.
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