Literature DB >> 14605367

Suspended animation in C. elegans requires the spindle checkpoint.

Todd G Nystul1, Jesse P Goldmark, Pamela A Padilla, Mark B Roth.   

Abstract

In response to environmental signals such as anoxia, many organisms enter a state of suspended animation, an extreme form of quiescence in which microscopically visible movement ceases. We have identified a gene, san-1, that is required for suspended animation in Caenorhabditis elegans embryos. We show that san-1 functions as a spindle checkpoint component in C. elegans. During anoxia-induced suspended animation, embryos lacking functional SAN-1 or a second spindle checkpoint component, MDF-2, failed to arrest the cell cycle, exhibited chromosome missegregation, and showed reduced viability. These data provide a model for how a dynamic biological process is arrested in suspended animation.

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Year:  2003        PMID: 14605367     DOI: 10.1126/science.1089705

Source DB:  PubMed          Journal:  Science        ISSN: 0036-8075            Impact factor:   47.728


  49 in total

Review 1.  The spindle checkpoint: a quality control mechanism which ensures accurate chromosome segregation.

Authors:  Stephen S Taylor; Maria I F Scott; Andrew J Holland
Journal:  Chromosome Res       Date:  2004       Impact factor: 5.239

2.  The Caenorhabditis elegans kinetochore reorganizes at prometaphase and in response to checkpoint stimuli.

Authors:  Jeffrey H Stear; Mark B Roth
Journal:  Mol Biol Cell       Date:  2004-09-15       Impact factor: 4.138

3.  Human pharmacology of hydrogen sulfide, putative gaseous mediator.

Authors:  J M Ritter
Journal:  Br J Clin Pharmacol       Date:  2010-06       Impact factor: 4.335

4.  A spindle checkpoint functions during mitosis in the early Caenorhabditis elegans embryo.

Authors:  Sandra E Encalada; John Willis; Rebecca Lyczak; Bruce Bowerman
Journal:  Mol Biol Cell       Date:  2004-12-22       Impact factor: 4.138

5.  Systematic analysis in Caenorhabditis elegans reveals that the spindle checkpoint is composed of two largely independent branches.

Authors:  Anthony Essex; Alexander Dammermann; Lindsay Lewellyn; Karen Oegema; Arshad Desai
Journal:  Mol Biol Cell       Date:  2008-12-24       Impact factor: 4.138

6.  Systematic identification of gene activities promoting hypoxic death.

Authors:  Meghann E Mabon; Xianrong Mao; York Jiao; Barbara A Scott; C Michael Crowder
Journal:  Genetics       Date:  2008-12-01       Impact factor: 4.562

7.  The spindle assembly checkpoint in Caenorhabditis elegans: one who lacks Mad1 becomes mad one.

Authors:  Risa Kitagawa
Journal:  Cell Cycle       Date:  2009-02-17       Impact factor: 4.534

8.  Down-regulation of tricarboxylic acid (TCA) cycle genes blocks progression through the first mitotic division in Caenorhabditis elegans embryos.

Authors:  Mohammad M Rahman; Simona Rosu; Daphna Joseph-Strauss; Orna Cohen-Fix
Journal:  Proc Natl Acad Sci U S A       Date:  2014-02-03       Impact factor: 11.205

9.  Cyclin B3 and dynein heavy chain cooperate to increase fitness in the absence of mdf-1/MAD1 in Caenorhabditis elegans.

Authors:  Maja Tarailo-Graovac; Tammy Wong; Zhaozhao Qin; Stephane Flibotte; Jon Taylor; Donald G Moerman; Ann M Rose; Nansheng Chen
Journal:  Cell Cycle       Date:  2014       Impact factor: 4.534

10.  Use of time lapse microscopy to visualize anoxia-induced suspended animation in C. elegans embryos.

Authors:  Anastacia M Garcia; Mary L Ladage; Pamela A Padilla
Journal:  J Vis Exp       Date:  2012-12-03       Impact factor: 1.355

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