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The Drosophila fork head factor directly controls larval salivary gland-specific expression of the glue protein gene Sgs3.

机译:果蝇叉头因子直接控制胶蛋白基因Sgs3的幼虫唾液腺特异性表达。

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摘要

The Drosophila Fork head protein participates in salivary gland formation, since salivary glands are missing in fork head embryos. Here we show that the fork head encoded protein binds to an upstream regulatory region of the larval salivary gland glue protein gene Sgs3. Mobility shift assay in the presence of an anti-Fork head antibody demonstrated that the Fork head factor interacts with the TGTTTGC box shown to be involved in tissue-specific Sgs3 expression. Experiments employing a set of oligonucleotide competitors revealed that Fork head binding was prevented by the same single base substitutions that were previously shown to interfere with the TGTTTGC element function in vivo. Furthermore, the anti-Fork head antibody bound to >60 sites of polytene chromosomes, including the puffs of all Sgs genes and Fork head protein was detected in the nuclei of salivary glands of larvae of all examined stages. These data provide experimental evidence for the hypothesis that the protein encoded by the fork head gene is required initially for salivary gland formation and is utilized subsequently in the control of larval genes specifically expressed in this organ.
机译:果蝇叉头蛋白参与唾液腺的形成,因为叉头胚胎中缺少唾液腺。在这里,我们显示叉头编码的蛋白结合到幼虫唾液腺胶蛋白基因Sgs3的上游调控区域。在存在抗-Fork头抗体的情况下进行的迁移率变动分析表明,Fork头因子与TGTTTGC盒相互作用,该TGTTTGC盒显示与组织特异性Sgs3表达有关。使用一组寡核苷酸竞争者的实验表明,相同的单碱基取代阻止了叉头的结合,先前已证明在体内干扰TGTTTGC元件的功能。此外,在所有受检阶段的幼虫唾液腺细胞核中都检测到与> 60个多态染色体染色体结合的抗Fork头抗体,包括所有Sgs基因的粉扑和Fork头蛋白。这些数据为以下假设提供了实验证据:由叉头基因编码的蛋白质最初是唾液腺形成所必需的,随后被用于控制在该器官中特异性表达的幼虫基因。

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