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Ganglion mother cell information


Type I neuroblast gives rise to a GMC and an identical neuroblast, as opposed to type II whose daughter cells are known as intermediate neural progenitors (INPs). The GMC then differentiates into two neurons.[1]

Ganglion mother cells (GMCs) are cells involved in neurogenesis, in non-mammals, that divide only once to give rise to two neurons, or one neuron and one glial cell or two glial cells,[2] and are present only in the central nervous system. They are also responsible for transcription factor expression. While each ganglion mother cell necessarily gives rise to two neurons, a neuroblast can asymmetrically divide multiple times.[3] GMCs are the progeny of type I neuroblasts. Neuroblasts asymmetrically divide during embryogenesis to create GMCs.[4] GMCs are only present in certain species and only during the embryonic and larval stages of life. Recent research has shown that there is an intermediate stage between a GMC and two neurons. The GMC forms two ganglion cells which then develop into neurons or glial cells.[5] Embryonic neurogenesis has been extensively studied in Drosophila melanogaster embryos and larvae.

the signal protein Notch is exposed to both daughter cells of a neuroblast (another neuroblast and a GMC). Because Numb (represented by the blue line) is a Notch suppressor and only present in the GMC, the GMC will behave differently from the other daughter cell, the neuroblast.
  1. ^ Bayraktar, Boone, Drummond, Doe (2010). Drosophila type II neuroblast lineages keep Prospero levels low to generate large clones that contribute to the adult brain central complex. Neural Development, 5:26.
  2. ^ Cite error: The named reference Karcavich was invoked but never defined (see the help page).
  3. ^ Doe, C. Q. et al (2008). Identification of Drosophila type II neuroblast lineages containing transit amplifying ganglion mother cells. PMC 2804867.
  4. ^ Doe, C. Q. (1992). Molecular markers for identified neuroblasts and ganglion mother cells in the Drosophila central nervous system. Development, 116(4), 855-863.
  5. ^ Colonques, Jordi, Ceron, Julian, Reichert, Heinrich, & Tejedor, Francisco J. (2011). A transient expression of Prospero promotes cell cycle exit of Drosophila postembryonic neurons through the regulation of Dacapo. PLoS ONE, 6(4), e19342-e19342.

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