TY - JOUR
T1 - NFIA controls telencephalic progenitor cell differentiation through repression of the Notch effector Hes1
AU - Piper, Michael
AU - Barry, Guy
AU - Hawkins, John
AU - Mason, Sharon
AU - Lindwall, Charlotta
AU - Little, Erica
AU - Sarkar, Anindita
AU - Smith, Aaron G.
AU - Moldrich, Randal X.
AU - Boyle, Glen M.
AU - Tole, Shubha
AU - Gronostajski, Richard M.
AU - Bailey, Timothy L.
AU - Richards, Linda J.
PY - 2010/7/7
Y1 - 2010/7/7
N2 - The balance between self-renewal and differentiation of neural progenitor cells is an absolute requirement for the correct formation of the nervous system. Much is known about both the pathways involved in progenitor cell self-renewal, such as Notch signaling, and the expression of genes that initiate progenitor differentiation. However, whether these fundamental processes are mechanistically linked, and specifically how repression of progenitor self-renewal pathways occurs, is poorly understood. Nuclear factor I A (Nfia), a gene known to regulate spinal cord and neocortical development, has recently been implicated as acting downstream of Notch to initiate the expression of astrocyte-specific genes within the cortex. Here we demonstrate that, in addition to activating the expression of astrocyte-specific genes, Nfia also downregulates the activity of the Notch signaling pathway via repression of the key Notch effector Hes1. These data provide a significant conceptual advance in our understanding of neural progenitor differentiation, revealing that a single transcription factor can control both the activation of differentiation genes and the repression of the self-renewal genes, thereby acting as a pivotal regulator of the balance between progenitor and differentiated cell states.
AB - The balance between self-renewal and differentiation of neural progenitor cells is an absolute requirement for the correct formation of the nervous system. Much is known about both the pathways involved in progenitor cell self-renewal, such as Notch signaling, and the expression of genes that initiate progenitor differentiation. However, whether these fundamental processes are mechanistically linked, and specifically how repression of progenitor self-renewal pathways occurs, is poorly understood. Nuclear factor I A (Nfia), a gene known to regulate spinal cord and neocortical development, has recently been implicated as acting downstream of Notch to initiate the expression of astrocyte-specific genes within the cortex. Here we demonstrate that, in addition to activating the expression of astrocyte-specific genes, Nfia also downregulates the activity of the Notch signaling pathway via repression of the key Notch effector Hes1. These data provide a significant conceptual advance in our understanding of neural progenitor differentiation, revealing that a single transcription factor can control both the activation of differentiation genes and the repression of the self-renewal genes, thereby acting as a pivotal regulator of the balance between progenitor and differentiated cell states.
UR - http://www.scopus.com/inward/record.url?scp=77954495752&partnerID=8YFLogxK
U2 - 10.1523/JNEUROSCI.6167-09.2010
DO - 10.1523/JNEUROSCI.6167-09.2010
M3 - Article
C2 - 20610746
AN - SCOPUS:77954495752
SN - 0270-6474
VL - 30
SP - 9127
EP - 9139
JO - Journal of Neuroscience
JF - Journal of Neuroscience
IS - 27
ER -