Bellefroid E J, Bourguignon C, Hollemann T, Ma Q, Anderson D J, Kintner C, Pieler T
Institut für Biochemie und Molekulare Zellbiologie, Göttingen, Germany.
Cell. 1996 Dec 27;87(7):1191-202. doi: 10.1016/s0092-8674(00)81815-2.
X-MyT1 is a C2HC-type zinc finger protein that we find to be involved in the primary selection of neuronal precursor cells in Xenopus. Expression of this gene is positively regulated by the bHLH protein X-NGNR-1 and negatively regulated by the Notch/Delta signal transduction pathway. X-MyT1 is able to promote ectopic neuronal differentiation and to confer insensitivity to lateral inhibition, but only in cooperation with bHLH transcription factors. Inhibition of X-MyT1 function inhibits normal neurogenesis as well as ectopic neurogenesis caused by overexpression of X-NGNR-1. On the basis of these findings, we suggest that X-MyT1 is a novel, essential element in the cascade of events that allows cells to escape lateral inhibition and to enter the pathway that leads to terminal neuronal differentiation.
X-MyT1是一种C2HC型锌指蛋白,我们发现它参与非洲爪蟾神经元前体细胞的初始选择。该基因的表达受bHLH蛋白X-NGNR-1的正向调控,受Notch/Delta信号转导通路的负向调控。X-MyT1能够促进异位神经元分化并赋予对侧向抑制的不敏感性,但仅在与bHLH转录因子协同作用时才如此。抑制X-MyT1功能会抑制正常神经发生以及由X-NGNR-1过表达引起的异位神经发生。基于这些发现,我们认为X-MyT1是一系列事件中的一个新的关键要素,这些事件使细胞能够逃避侧向抑制并进入导致终末神经元分化的途径。