Pulvers Jeremy N, Journiac Nathalie, Arai Yoko, Nardelli Jeannette
Sydney Medical Program, University of Sydney Sydney, Australia.
U1141 Inserm Paris, France ; Université Paris Diderot, Sorbonne Paris Cité, UMRS 1141 Paris, France.
Front Cell Neurosci. 2015 Mar 27;9:92. doi: 10.3389/fncel.2015.00092. eCollection 2015.
The development of the mammalian cerebral cortex involves a series of mechanisms: from patterning, progenitor cell proliferation and differentiation, to neuronal migration. Many factors influence the development of the cerebral cortex to its normal size and neuronal composition. Of these, the mechanisms that influence the proliferation and differentiation of neural progenitor cells are of particular interest, as they may have the greatest consequence on brain size, not only during development but also in evolution. In this context, causative genes of human autosomal recessive primary microcephaly, such as ASPM and MCPH1, are attractive candidates, as many of them show positive selection during primate evolution. MCPH1 causes microcephaly in mice and humans and is involved in a diverse array of molecular functions beyond brain development, including DNA repair and chromosome condensation. Positive selection of MCPH1 in the primate lineage has led to much insight and discussion of its role in brain size evolution. In this review, we will present an overview of MCPH1 from these multiple angles, and whilst its specific role in brain size regulation during development and evolution remain elusive, the pieces of the puzzle will be discussed with the aim of putting together the full picture of this fascinating gene.
从模式形成、祖细胞增殖与分化到神经元迁移。许多因素影响大脑皮层发育至正常大小和神经元组成。其中,影响神经祖细胞增殖与分化的机制尤为引人关注,因为它们不仅在发育过程中,而且在进化过程中,可能对脑容量产生最大影响。在此背景下,人类常染色体隐性原发性小头畸形的致病基因,如ASPM和MCPH1,是有吸引力的候选基因,因为它们中的许多在灵长类进化过程中显示出正选择。MCPH1在小鼠和人类中导致小头畸形,并且除了大脑发育之外,还参与多种分子功能,包括DNA修复和染色体凝聚。MCPH1在灵长类谱系中的正选择引发了对其在脑容量进化中作用的诸多见解和讨论。在这篇综述中,我们将从这些多个角度对MCPH1进行概述,虽然其在发育和进化过程中脑容量调节中的具体作用仍不清楚,但我们将讨论这些谜团,以期拼凑出这个迷人基因的全貌。