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果蝇中一个体节极性基因fused与其他体节基因之间的相互作用。

Interactions between fused, a segment-polarity gene in Drosophila, and other segmentation genes.

作者信息

Limbourg-Bouchon B, Busson D, Lamour-Isnard C

机构信息

Centre de Génétique Moléculaire, C.N.R.S., Gif-sur-Yvette, France.

出版信息

Development. 1991 Jun;112(2):417-29. doi: 10.1242/dev.112.2.417.

Abstract

Fused (fu) is a segment polarity gene whose product is maternally required in the posterior part of each segment. To define further the role of fused and determine how it interacts with other segmentation genes, we examined the phenotypes obtained by combining fused with mutations of pair rule, homeotic and other segment polarity loci. When it was possible, we also looked at the distribution of corresponding proteins in fused mutant embryos. We observed that fused-naked (fu;nkd) double mutant embryos display a phenotypic suppression of simple mutant phenotypes: both naked cuticle and denticle belts, which would normally have been deleted by one of the two mutants alone, were restored. In fused mutant embryos, engrailed (en) and wingless (wg) expression was normal until germ band extension, but partially and completely disappeared respectively during germ band retraction. In the fu;nkd double mutant embryo, en was expressed as in nkd mutant at germ band extension, but later this expression was restricted and became normal at germ band retraction. On the contrary, wg expression disappeared as in fu simple mutant embryos. We conclude that the requirements for fused, naked and wingless activities for normal segmental patterning are not absolute, and propose mechanisms by which these genes interact to specify anterior and posterior cell fates.

摘要

融合基因(fu)是一种体节极性基因,其产物在每个体节的后部是母体必需的。为了进一步确定融合基因的作用,并确定它如何与其他体节划分基因相互作用,我们研究了将融合基因与配对规则、同源异型和其他体节极性位点的突变相结合所获得的表型。在可能的情况下,我们还观察了融合突变胚胎中相应蛋白质的分布。我们观察到融合-裸基因(fu;nkd)双突变胚胎表现出对简单突变体表型的抑制:通常会被两个突变体之一单独删除的裸表皮和齿带都恢复了。在融合突变胚胎中,配对规则基因(en)和无翅基因(wg)的表达在胚带延伸之前是正常的,但在胚带回缩期间分别部分和完全消失。在fu;nkd双突变胚胎中,en在胚带延伸时如在nkd突变体中一样表达,但后来这种表达受到限制并在胚带回缩时恢复正常。相反,wg的表达如在fu简单突变胚胎中一样消失。我们得出结论,正常体节模式形成对融合基因、裸基因和无翅基因活性的要求不是绝对的,并提出了这些基因相互作用以指定前后细胞命运的机制。

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