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果蝇胚胎分节过程中基因活性的局部需求:嵌合胚胎中犰狳、融合、巨人和无配对基因突变的分析

Localized requirements for gene activity in segmentation of Drosophila embryos: analysis of armadillo, fused, giant and unpaired mutations in mosaic embryos.

作者信息

Gergen J Peter, Wieschaus Eric F

机构信息

Department of Biology, Princeton University, 08544, Princeton, New Jersey, USA.

出版信息

Rouxs Arch Dev Biol. 1986 Jan;195(1):49-62. doi: 10.1007/BF00444041.

Abstract

In order to investigate the localized requirements for the activity of genes that are required in a Drosophila embryo for segmentation, we have analyzed the patterns in genetic mosaics. In this paper, we describe our results with four different X-chromosome linked segmentation loci: armadillo, fused, giant and unpaired. For each locus, we first describe in detail the cuticle phenotype of mutant embryos. We then describe the segmentation patterns in embryos mosaic for these mutations, in each case utilizing the shavenbaby (svb) larval cuticle marker mutation to identify the regions of pattern made by genetically mutant cells. For all four loci, we can identify embryos containing large regions of both mutant and wildtype pattern. In these mosaics the regions of mutant pattern are marked with svb and the genetically wildtype (svb ) cells make wildtype pattern. The interpretations of the patterns in embryos mosaic for fused and unpaired are complicated by the variability of the phenotypes. However, after taking these complications into account, our principal conclusion is that the requirement for embryonic gene activity seems to be primarily cell autonomous. Based on the descriptions of the mutant phenotypes of these four loci and the analysis of the mosaics, we speculate on the possible roles these genes play in the process of segmentation.

摘要

为了研究果蝇胚胎分节所需基因活性的局部需求,我们分析了基因嵌合体中的模式。在本文中,我们描述了四个不同的X染色体连锁分节位点的研究结果:犰狳、融合、巨型和无配对。对于每个位点,我们首先详细描述突变胚胎的表皮表型。然后,我们描述这些突变的胚胎嵌合体中的分节模式,每种情况下利用无毛幼虫(svb)表皮标记突变来识别由基因变异细胞形成的模式区域。对于所有四个位点,我们都能鉴定出同时含有大片突变模式区域和野生型模式区域的胚胎。在这些嵌合体中,突变模式区域用svb标记,基因野生型(svb)细胞形成野生型模式。融合和无配对的胚胎嵌合体模式的解释因表型的变异性而变得复杂。然而,在考虑了这些复杂因素之后,我们的主要结论是胚胎基因活性的需求似乎主要是细胞自主性的。基于对这四个位点突变表型的描述以及嵌合体分析,我们推测了这些基因在分节过程中可能发挥的作用。

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