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黑腹果蝇中的体节极性:在融合抑制子背景下对融合基因的遗传剖析揭示了与肋节-2的相互作用。

Segmental polarity in Drosophila melanogaster: genetic dissection of fused in a Suppressor of fused background reveals interaction with costal-2.

作者信息

Préat T, Thérond P, Limbourg-Bouchon B, Pham A, Tricoire H, 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

Genetics. 1993 Dec;135(4):1047-62. doi: 10.1093/genetics/135.4.1047.

Abstract

fused (fu) is a segment polarity gene that encodes a putative serine/threonine kinase. A complete suppressor of the embryonic and adult phenotypes of fu mutants, Suppressor of fused (Su(fu)), was previously described. The amorphic Su(fu) mutation is viable and displays no phenotype by itself. We have used this suppressor as a tool to perform a genetic dissection of the fu gene. Analysis of the interaction between Su(fu) and 33 fu alleles shows that they belong to three different classes. Defects due to class I fu alleles are fully suppressed by Su(fu). Class II fu alleles lead to a new segment polarity phenotype in interaction with Su(fu). This phenotype corresponds to embryonic and adult anomalies similar to those displayed by the segment polarity mutant costal-2 (cos-2). Class II alleles are recessive to class I alleles in a fu[I]/fu[II];Su(fu)/Su(fu) combination. Class 0 alleles, like class I alleles, confer a normal segmentation phenotype in interaction with Su(fu). However class II alleles are dominant over class 0 alleles in a fu[0]/fu[II];Su(fu)/Su(fu) combination. Alleles of class I and II correspond to small molecular events, which may leave part of the Fu protein intact. On the contrary, class 0 alleles correspond to large deletions. Several class I and class II fu mutations have been mapped, and three mutant alleles were sequenced. These data suggest that class I mutations affect the catalytic domain of the putative Fu kinase and leave the carboxy terminal domain intact, whereas predicted class II proteins have an abnormal carboxy terminal domain. Su(fu) enhances the cos-2 phenotype and cos-2 mutations interact with fu in a way similar to Su(fu). All together these results suggest that a close relationship might exist between fu, Su(fu) and cos-2 throughout development. We thus propose a model where the Fu+ kinase is a posterior inhibitor of Costal-2+ while Su(fu)+ is an activator of Costal-2+. The expression pattern of wingless and engrailed in fu and fu;Su(fu) embryos is in accordance with this interpretation.

摘要

融合基因(fu)是一个节段极性基因,编码一种假定的丝氨酸/苏氨酸激酶。之前已描述了融合基因(fu)突变体胚胎和成体表型的完全抑制子,即融合抑制子(Su(fu))。无义的Su(fu)突变是可行的,其自身不表现出表型。我们利用这个抑制子作为工具对fu基因进行遗传剖析。对Su(fu)与33个fu等位基因之间相互作用的分析表明,它们可分为三个不同的类别。I类fu等位基因导致的缺陷被Su(fu)完全抑制。II类fu等位基因与Su(fu)相互作用时会导致一种新的节段极性表型。这种表型对应于胚胎和成体的异常,类似于节段极性突变体肋-2(cos-2)所表现出的异常。在fu[I]/fu[II];Su(fu)/Su(fu)组合中,II类等位基因相对于I类等位基因为隐性。0类等位基因与I类等位基因一样,在与Su(fu)相互作用时赋予正常的分节表型。然而,在fu[0]/fu[II];Su(fu)/Su(fu)组合中,II类等位基因相对于0类等位基因为显性。I类和II类等位基因对应于小的分子事件,这可能使部分Fu蛋白保持完整。相反,0类等位基因对应于大的缺失。已对几个I类和II类fu突变进行了定位,并对三个突变等位基因进行了测序。这些数据表明,I类突变影响假定的Fu激酶的催化结构域,而使羧基末端结构域保持完整,而预测的II类蛋白具有异常的羧基末端结构域。Su(fu)增强了cos-2表型,并且cos-2突变与fu相互作用的方式类似于Su(fu)。所有这些结果共同表明,在整个发育过程中,fu、Su(fu)和cos-2之间可能存在密切关系。因此,我们提出一个模型,其中Fu+激酶是肋-2+的后部抑制剂,而Su(fu)+是肋-2+的激活剂。无翅基因和 engrailed基因在fu和fu;Su(fu)胚胎中的表达模式符合这种解释。

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