TY - JOUR
T1 - Human-Specific ARHGAP11B Acts in Mitochondria to Expand Neocortical Progenitors by Glutaminolysis
AU - Namba, Takashi
AU - Dóczi, Judit
AU - Pinson, Anneline
AU - Xing, Lei
AU - Kalebic, Nereo
AU - Wilsch-Bräuninger, Michaela
AU - Long, Katherine R.
AU - Vaid, Samir
AU - Lauer, Janelle
AU - Bogdanova, Aliona
AU - Borgonovo, Barbara
AU - Shevchenko, Anna
AU - Keller, Patrick
AU - Drechsel, David
AU - Kurzchalia, Teymuras
AU - Wimberger, Pauline
AU - Chinopoulos, Christos
AU - Huttner, Wieland B.
PY - 2020/3/4
Y1 - 2020/3/4
N2 - Namba et al. demonstrate that increased glutaminolysis is essential for the ability of human-specific ARHGAP11B, which is localized in mitochondria, to increase cycling basal progenitor levels in developing neocortex, an effect implicated in the evolutionary expansion of the human neocortex.
AB - Namba et al. demonstrate that increased glutaminolysis is essential for the ability of human-specific ARHGAP11B, which is localized in mitochondria, to increase cycling basal progenitor levels in developing neocortex, an effect implicated in the evolutionary expansion of the human neocortex.
KW - evolution
KW - metabolism
KW - neocortex
KW - neural progenitor cells
UR - http://www.scopus.com/inward/record.url?scp=85080065568&partnerID=8YFLogxK
U2 - 10.1016/j.neuron.2019.11.027
DO - 10.1016/j.neuron.2019.11.027
M3 - Article
C2 - 31883789
AN - SCOPUS:85080065568
SN - 0896-6273
VL - 105
SP - 867-881.e9
JO - Neuron
JF - Neuron
IS - 5
ER -