Asymmetric cell division and apoptosis (programmed cell death) are two fundamental processes important for the development and function of 
  multi-cellular organisms. Asymmetric cell division creates daughter cells of different fates, and this is critical for the generation of cellular 
  diversity. 
Apoptosis eliminates superfluous cells from the organism, and this is critical for cellular homeostasis. In this week's  PLoS Biology 
  Julia Hatzold and Barbara Conradt find that the processes of asymmetric cell division and apoptosis can be functionally linked. Specifically, they 
  show that asymmetric cell division in the nematode Caenorhabditis elegans is mediated by a pathway involving three genes, dnj-11 MIDA1, ces-2 HLF and 
  ces-1 Snail, that directly control the enzymatic machinery responsible for  apoptosis. Interestingly, the role of this pathway in asymmetric cell 
  division and the control of apoptosis might be evolutionarily conserved. 
Furthermore, it might have an unexpected role in stem cell biology: the 
  process of asymmetric cell division plays an essential role in the ability of stem cells to self renew and the mammalian counterparts of two 
  components of the dnj-11 MIDA1, ces-2 HLF, ces-1 Snail pathway have recently been implicated in stem cell function. For this reason, they speculate 
  that a dnj-11 MIDA1, ces-2 HLF, ces-1 Snail-like pathway might function in stem cells to coordinate self-renewal and apoptosis and, hence, the number 
  of stem cells.
Control of apoptosis by asymmetric cell division 
Hatzold J, Conradt B (2008) 
PLoS Biol 6(4): e84. doi:10.1371/journal.pbio.0060084 
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 PLoS Biology
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