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果蝇发育中眼睛的细胞命运特化。

Specification of cell fate in the developing eye of Drosophila.

作者信息

Basler K, Hafen E

机构信息

Howard Hughes Medical Institute, Columbia University College of Physicians and Surgeons, New York, N.Y. 10032.

出版信息

Bioessays. 1991 Dec;13(12):621-31. doi: 10.1002/bies.950131202.

Abstract

Determination of cell fate in the developing eye of Drosophila depends on a precise sequence of cellular interactions which generate the stereotypic array of ommatidia. In the eye imaginal disc, an initially unpatterned epithelial sheath of cells, the first step in this process may be the specification of R8 photoreceptor cells at regular intervals. Genes such as Notch and scabrous, known to be involved in bristle development, also participate in this process, suggesting that the specification of ommatidial founder cells and the formation of sensory organs in the adult epidermis may involve a similar mechanism, that of lateral inhibition. The subsequent steps of ommatidial assembly, following R8 assignment, involve a different mechanism: Undetermined cells read their position based on the contacts they make with neighbors that have already begun to differentiate. The development of the R7 photoreceptor cell, one of the eight photoreceptor cells in the ommatidium, is best understood. An important role seems to be played by sevenless, a receptor tyrosine kinase on the surface of the R7 precursor. It transmits the positional information--most likely encoded by the boss protein on the neighboring R8 cell membrane--into the cell via its tyrosine kinase, which activates a signal transduction cascade. Constitutive activation of the sevenless kinase by overexpression of an N-terminally truncated form results in the diversion of other ommatidial cells into the R7 pathway suggesting that activation of the sevenless signalling pathway is sufficient to specify R7 development. Genetic dissection of this pathway should therefore identify components of a signalling cascade activated by a tyrosine kinase.

摘要

果蝇发育中的眼睛中细胞命运的决定取决于一系列精确的细胞间相互作用,这些相互作用产生了小眼的定型排列。在眼成虫盘(一种最初无图案的细胞上皮鞘)中,这一过程的第一步可能是以规则的间隔指定R8感光细胞。已知参与刚毛发育的Notch和粗糙等基因也参与这一过程,这表明小眼奠基细胞的指定以及成虫表皮中感觉器官的形成可能涉及类似的机制,即侧向抑制。在指定R8之后,小眼组装的后续步骤涉及不同的机制:未确定的细胞根据它们与已经开始分化的邻居的接触来确定自己的位置。小眼的八个感光细胞之一R7感光细胞的发育得到了最好的理解。一种重要的作用似乎由sevenless发挥,它是R7前体细胞表面的一种受体酪氨酸激酶。它通过其酪氨酸激酶将位置信息(很可能由相邻R8细胞膜上的boss蛋白编码)传递到细胞内,从而激活信号转导级联反应。通过过度表达N端截短形式导致sevenless激酶的组成性激活,会使其他小眼细胞转入R7途径,这表明sevenless信号通路的激活足以指定R7的发育。因此,对该途径的遗传学剖析应该能够识别由酪氨酸激酶激活的信号级联反应的组成部分。

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