在Tribolium中,神经母细胞定时基因结节蛋白显示出与间隙基因的功能冗余,以调节节段识别

O. Tidswell, Matthew A. Benton, M. Akam
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引用次数: 2

摘要

在果蝇中,gap类的片段基因形成了一个定位片段边界和分配片段身份的调控网络。这个基因网络显示出与另一个被称为神经母细胞定时器系列的基因网络惊人的相似之处。神经母细胞定时器基因hunchback、kr ppel、nubbin和castor在神经干细胞中按时间顺序表达,以调节其后代的命运。这四种基因沿果蝇胚皮按相应的空间序列表达。前两个,hunchback和kr ppel,是典型的间隙基因,但nubbin和castor在果蝇的分割中作用有限或没有作用。是否结节蛋白和蓖麻调节昆虫的分割与祖先,顺序模式的分割仍在很大程度上未被探索。我们研究了小块蛋白和蓖麻蛋白在三角甲虫节理过程中的表达和功能。通过多重荧光原位杂交,我们发现Tc-hunchback、tc - kr ppel、Tc-nubbin和Tc-castor在Tribolium的片段添加区依次表达,与它们在果蝇神经母细胞中的表达顺序相同。此外,同时破坏多个基因表明Tc-nubbin调节片段身份,但与两个先前描述的gap/gap样基因,Tc-giant和tc - knps冗余。敲除其中两个或更多的基因会导致腹部部分形成多达七对异位腿。我们发现,这种同体转化是由腹部Hox基因表达的缺失引起的,可能是由于tc - kr ppel表达的增加。我们的研究结果支持了神经母细胞计时器系列被用于昆虫片段模式的理论,并有助于我们对果蝇外间隙基因网络的进化和功能的理解。
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The neuroblast timer gene nubbin exhibits functional redundancy with gap genes to regulate segment identity in Tribolium
In Drosophila, segmentation genes of the gap class form a regulatory network that positions segment boundaries and assigns segment identities. This gene network shows striking parallels with another gene network known as the neuroblast timer series. The neuroblast timer genes hunchback, Krüppel, nubbin, and castor are expressed in temporal sequence in neural stem cells to regulate the fate of their progeny. These same four genes are expressed in corresponding spatial sequence along the Drosophila blastoderm. The first two, hunchback and Krüppel, are canonical gap genes, but nubbin and castor have limited or no roles in Drosophila segmentation. Whether nubbin and castor regulate segmentation in insects with the ancestral, sequential mode of segmentation remains largely unexplored. We have investigated the expression and functions of nubbin and castor during segment patterning in the sequentially-segmenting beetle Tribolium. Using multiplex fluorescent in situ hybridisation, we show that Tc-hunchback, Tc-Krüppel, Tc-nubbin and Tc-castor are expressed sequentially in the segment addition zone of Tribolium, in the same order as they are expressed in Drosophila neuroblasts. Furthermore, simultaneous disruption of multiple genes reveals that Tc-nubbin regulates segment identity, but does so redundantly with two previously described gap/gap-like genes, Tc-giant and Tc-knirps. Knockdown of two or more of these genes results in the formation of up to seven pairs of ectopic legs on abdominal segments. We show that this homeotic transformation is caused by loss of abdominal Hox gene expression, likely due to expanded Tc-Krüppel expression. Our findings support the theory that the neuroblast timer series was co-opted for use in insect segment patterning, and contribute to our growing understanding of the evolution and function of the gap gene network outside of Drosophila.
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