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无调性基因是果蝇光感受器的原神经基因。

Atonal is the proneural gene for Drosophila photoreceptors.

作者信息

Jarman A P, Grell E H, Ackerman L, Jan L Y, Jan Y N

机构信息

Howard Hughes Medical Institute, University of California at San Francisco 94143-0724.

出版信息

Nature. 1994 Jun 2;369(6479):398-400. doi: 10.1038/369398a0.

Abstract

The Drosophila peripheral nervous system comprises four major types of sensory element: external sense organs (such as mechano-sensory bristles), chordotonal organs (internal stretch receptors), multiple dendritic neurons, and photoreceptors. During development, the selection of neural precursors for external sense organs requires the proneural genes of the achaete-scute complex, which encode basic-helix-loop-helix transcription factors. These genes do not, however, control precursor selection for chordotonal organs or photoreceptors, raising the question of whether other proneural genes exist or a different mechanism of neurogenesis operates. Here we show that atonal (ato), originally isolated as a proneural gene for chordotonal organs, is also the proneural gene for photoreceptors. Pattern formation in the Drosophila eye involves a succession of cell fate specifications. Of the eight photoreceptors within each ommatidium of the compound eye, the photoreceptor R8 is the first to appear in the eye imaginal disc, right behind the morphogenetic furrow. The appearance of other photoreceptors (R1-7) follows in a defined sequence that is thought to arise by induction from R8 (refs 8, 9, 11, 12). We find that photoreceptor formation requires the function of atonal at the morphogenetic furrow and that atonal is specifically required for R8 selection. Formation of other photoreceptors does not directly require atonal function, but does depend on R8 selection by atonal. Thus, photoreceptors are selected by two mechanisms: R8 by a proneural mechanism, and R1-7 by local recruitment.

摘要

果蝇的外周神经系统由四种主要类型的感觉元件组成

外部感觉器官(如机械感觉刚毛)、弦音器官(内部拉伸感受器)、多树突神经元和光感受器。在发育过程中,外部感觉器官神经前体的选择需要achaete - scute复合体的原神经基因,这些基因编码基本螺旋-环-螺旋转录因子。然而,这些基因并不控制弦音器官或光感受器的前体选择,这就提出了是否存在其他原神经基因或是否存在不同的神经发生机制的问题。在这里,我们表明,最初作为弦音器官的原神经基因分离出来的无调性(ato)基因,也是光感受器的原神经基因。果蝇眼睛中的模式形成涉及一系列细胞命运的特化。在复眼中每个小眼的八个光感受器中,光感受器R8是第一个出现在眼成虫盘上的,就在形态发生沟的后面。其他光感受器(R1 - 7)按确定的顺序出现,据认为这是由R8诱导产生的(参考文献8、9、11、12)。我们发现光感受器的形成需要无调性基因在形态发生沟处发挥作用,并且无调性基因对于R8的选择是特异性必需的。其他光感受器的形成并不直接需要无调性基因的功能,但确实依赖于无调性基因对R8的选择。因此,光感受器通过两种机制被选择:R8通过原神经机制,R1 - 7通过局部募集。

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