“…Kambadur et al, 1998;Karlsson et al, 2010;Reichert, 2011;Touma et al, 2012;Tran and Doe, 2008). Indeed, many of the basic cellular processes and molecular mechanisms that operate in asymmetric stem cell division have been elucidated in the Drosophila neuroblast models (Januschke and Gonzalez, 2008;Schaefer and Knoblich, 2001;Wu et al, 2008;Zhong and Chia, 2008). While type I and type II neuroblasts differ in some aspects of their asymmetric cell division modes, a fundamental property of the asymmetric divisions manifested by these neuroblasts is the unequal segregation of proteins that assign cell polarity and cell fate to the two asymmetric daughter cells, the selfrenewing neuroblast and the more differentiated daughter cell (GMC or INP) (Doe, 2008;Homem and Knoblich, 2012;Neumuller and Knoblich, 2009).…”