| Our nervous system is   made up of an astonishing diversity of neurons. And yet only a very small   number of proteins are needed to generate and determine the identity of these   billions of neurons. An even smaller number of proteins, called proneural   proteins, initiate and regulate brain development and neurogenesis (i.e. the   manufacture of functional neurons from neural stem cells). These proneural   proteins are transcription factors, meaning they control the expression of   other proteins. They are expressed   very transiently during early neurogenesis. A key aspect of this system that   remains to be elucidated is the precise temporal regulation of the activity   of the proneural proteins and the manner in which this regulation contributes   to neural differentiation. How does a very small set of proteins expressed   over a very limited period of time control the generation of such a high and   diverse number of neurons? What are the causes and effects of the transient   expression of these proteins? And finally, is this mechanism, which enables   the development of the nervous system, conserved between species? Previous studies in Drosophila,   or fruit flies, and in mice have shown that the expression of proneural   proteins begins at very low levels in neural stem cells, thereafter   increasing by self-activation. This sudden increase stops very quickly. The   activity of proneural proteins thus has two characteristics: significant   amplitude – easily explained by auto-activation – and a limited duration. How   can a protein that auto-activates its own expression disappear at the peak of   that expression? The results suggest the existence of an unknown mechanism   that overrides the auto-activation and synchronises the amplitude and   duration of proneural protein expression.  To answer these   questions, Bassem Hassan’s team studied the control and the mechanism of   proneural protein expression during retinal development in Drosophila.   The proteins in question control the differentiation of retinal neurons from   neural stem cells.   The researchers   discovered a binary "all-or-nothing" mechanism that can inactivate   proneural proteins: a reversible chemical modification (phosphorylation) in a   part of the protein that is highly conserved among different species, from   fruit flies to mice to humans. It is this mechanism that enables the   establishment of a network of functional neurons. In fact, the   suppression of this phosphorylation alters the activity of proneural   proteins, causing changes in the expression of target genes, which prevents   normal brain development. These changes interfere with signaling between   neurons and have a negative impact on their number and diversity.   Interestingly, the inhibition of this "all-or-nothing" mechanism   produces quantitative changes in the expression of target genes. The delicate   and precise temporal control of neurogenesis is seemingly regulated by the   balance between quantities of active and inactive proneural proteins. These results,   confirmed in another experimental model, thus reveal the existence of a   mechanism that is both highly conserved between species and universal, and   which regulates neurogenesis and the generation of a sufficient and diverse   number of neurons during brain development.  Mutations that   prevent this chemical modification cause diseases that affect the development   of the nervous system. The elucidation of the mechanism could therefore   eventually enable the development of therapeutic solutions. Moreover,   throughout their lives, adults generate new neurons that help maintain all   their cognitive abilities and play a key role in memory. Understanding the   role of this mechanism during neurogenesis in adults would open up a   promising pathway in the fight against degenerative diseases.  *Bassem Hassan   currently works at Institut du Cerveau et de la Moelle épinière. |