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无调性、粗糙以及果蝇发育中的视网膜中神经前体细胞簇的分化

Atonal, rough and the resolution of proneural clusters in the developing Drosophila retina.

作者信息

Dokucu M E, Zipursky S L, Cagan R L

机构信息

Department of Molecular Biology and Pharmacology, Washington University School of Medicine, St Louis, Missouri 63110, USA.

出版信息

Development. 1996 Dec;122(12):4139-47. doi: 10.1242/dev.122.12.4139.

Abstract

In the developing Drosophila retina, the proneural gene for photoreceptor neurons is atonal, a basic helix-loop-helix transcription factor. Using atonal as a marker for proneural maturation, we examine the stepwise resolution of proneural clusters during the initiation of ommatidial differentiation in the developing eye disc. In addition, evidence is provided that atonal is negatively regulated by rough, a homeobox-containing transcription factor expressed exclusively in the retina. This interaction leads to the refinement of proneural clusters to specify R8, the first neuron to emerge in the retinal neuroepithelium. Ectopic expression of atonal or removal of rough results in the transformation of a discrete 'equivalence group' of cells into R8s. In addition, ectopic expression of rough blocks atonal expression and proneural cluster formation within the morphogenetic furrow. Thus, rough provides retina-specific regulation to the more general atonal-mediated proneural differentiation pathway. The opposing roles of atonal and rough are not mediated through the Notch pathway, as their expression remains complementary when Notch activity is reduced. These observations suggest that homeobox-containing genes can provide tissue-specific regulation to bHLH factors.

摘要

在发育中的果蝇视网膜中,感光神经元的原神经基因是无调性基因(atonal),它是一种碱性螺旋-环-螺旋转录因子。我们以无调性基因为原神经成熟的标志物,研究了发育中的眼盘小眼分化起始过程中原神经簇的逐步解析。此外,有证据表明,无调性基因受到粗糙基因(rough)的负调控,粗糙基因是一种仅在视网膜中表达的含同源异型框的转录因子。这种相互作用导致原神经簇的细化,从而确定R8,即视网膜神经上皮中最早出现的神经元。无调性基因的异位表达或粗糙基因的缺失会导致离散的“等效细胞群”转变为R8细胞。此外,粗糙基因的异位表达会阻断形态发生沟内无调性基因的表达和原神经簇的形成。因此,粗糙基因为更普遍的无调性基因介导的原神经分化途径提供了视网膜特异性调控。无调性基因和粗糙基因的相反作用并非通过Notch信号通路介导,因为当Notch活性降低时,它们的表达仍然互补。这些观察结果表明,含同源异型框的基因可以为bHLH因子提供组织特异性调控。

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