TY - JOUR
T1 - Oligodendrocyte specification in zebrafish requires notch-regulated cyclin-dependent kinase inhibitor function
AU - Park, Hae Chul
AU - Boyce, Janene
AU - Shin, Jimann
AU - Appel, Bruce
PY - 2005/7/20
Y1 - 2005/7/20
N2 - Cyclin-dependent kinase inhibitors (Cdkis) influence both cell-cycle progression and differentiation of neural cells. However, the precise roles of Cdkis in coordinating formation of neurons and glia and the mechanisms that regulate expression of genes that encode Cdkis in the vertebrate CNS remain unknown. Here, we report that, in zebrafish, expression of the Cdki gene cyclin-dependent kinase inhibitor 1c (cdkn1c), a p57 homolog, is negatively regulated by Delta-Notch signaling and that Cdkn1c function is required for neural plate cells to stop dividing and differentiate as neurons on schedule, even in the absence of Notch signaling activity. Furthermore, Cdkn1c function is required for specification of oligodendrocytes from ventral spinal cord precursors. We propose that levels of cdkn1c expression are an important factor in regulating neural development: high levels of Cdkn1c promote cell-cycle exit and neuronal development, whereas, during late embryogenesis, neural cells that have low but functional levels of Cdkn1c, regulated by Notch activity, are specified for oligodendrocyte fate.
AB - Cyclin-dependent kinase inhibitors (Cdkis) influence both cell-cycle progression and differentiation of neural cells. However, the precise roles of Cdkis in coordinating formation of neurons and glia and the mechanisms that regulate expression of genes that encode Cdkis in the vertebrate CNS remain unknown. Here, we report that, in zebrafish, expression of the Cdki gene cyclin-dependent kinase inhibitor 1c (cdkn1c), a p57 homolog, is negatively regulated by Delta-Notch signaling and that Cdkn1c function is required for neural plate cells to stop dividing and differentiate as neurons on schedule, even in the absence of Notch signaling activity. Furthermore, Cdkn1c function is required for specification of oligodendrocytes from ventral spinal cord precursors. We propose that levels of cdkn1c expression are an important factor in regulating neural development: high levels of Cdkn1c promote cell-cycle exit and neuronal development, whereas, during late embryogenesis, neural cells that have low but functional levels of Cdkn1c, regulated by Notch activity, are specified for oligodendrocyte fate.
KW - Cell cycle
KW - Cell fate
KW - Neural precursor
KW - Neurogenesis
KW - Oligodendrocyte
KW - Spinal cord
UR - http://www.scopus.com/inward/record.url?scp=22544443908&partnerID=8YFLogxK
U2 - 10.1523/JNEUROSCI.0981-05.2005
DO - 10.1523/JNEUROSCI.0981-05.2005
M3 - Article
C2 - 16033893
AN - SCOPUS:22544443908
SN - 0270-6474
VL - 25
SP - 6836
EP - 6844
JO - Journal of Neuroscience
JF - Journal of Neuroscience
IS - 29
ER -