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在果蝇中进行的一项遗传筛选,用于鉴定刺猬信号通路的新成分。

A genetic screen in Drosophila for identifying novel components of the hedgehog signaling pathway.

作者信息

Collins Russell T, Cohen Stephen M

机构信息

Developmental Biology Programme, European Molecular Biology Laboratory, Heidelberg, Germany.

出版信息

Genetics. 2005 May;170(1):173-84. doi: 10.1534/genetics.104.039420. Epub 2005 Mar 2.

Abstract

The Hedgehog signaling pathway plays an essential role in the pattern formation and development of metazoan animals. Misregulation of Hedgehog signaling has also been associated with the formation of multiple types of cancer. For these reasons, the Hedgehog pathway has attracted considerable interest. Many proteins required in the Hedgehog pathway have been identified, and while much has been learned about their function in signal transduction, it is clear that this complement of proteins does not comprise the full set necessary for Hedgehog signal transduction. Because significant gaps remain in our knowledge of the molecules required for Hedgehog signaling, we performed an enhancer/suppressor screen in Drosophila melanogaster to identify novel components of the pathway. In addition to the isolation of new alleles of the known pathway components patched and smoothened, this screen identified 14 novel complementation groups and a larger number of loci represented by single alleles. These groups include mutations in the genes encoding the translation factors eRF1 and eIF1A and the kinesin-like protein Pavarotti. It also identified mutations in a gene whose product is necessary for the movement of Hedgehog protein through tissues.

摘要

刺猬信号通路在多细胞动物的模式形成和发育过程中起着至关重要的作用。刺猬信号通路的失调也与多种癌症的形成有关。基于这些原因,刺猬信号通路引起了广泛关注。刺猬信号通路中所需的许多蛋白质已被鉴定出来,虽然我们对它们在信号转导中的功能已经有了很多了解,但很明显,这些蛋白质并不构成刺猬信号转导所需的全部分子。由于我们对刺猬信号转导所需分子的认识仍存在重大空白,我们在黑腹果蝇中进行了增强子/抑制子筛选,以鉴定该信号通路的新成分。除了分离出已知信号通路成分“patched”和“smoothened”的新等位基因外,该筛选还鉴定出了14个新的互补群以及大量由单个等位基因代表的基因座。这些互补群包括编码翻译因子eRF1和eIF1A以及类驱动蛋白Pavarotti的基因突变。它还鉴定出一个基因的突变,该基因的产物是刺猬蛋白在组织中移动所必需的。

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