Escola de Artes, Ciências e Humanidades da Universidade de São Paulo, São Paulo, Brazil.
Departamento de Radiologia e Oncologia, Instituto do Câncer do Estado de São Paulo, Hospital das Clínicas, Faculdade de Medicina, Universidade de São Paulo, São Paulo, Brazil.
Dev Biol. 2024 Jan;505:11-23. doi: 10.1016/j.ydbio.2023.09.014. Epub 2023 Oct 24.
The orphan nuclear receptor Tailless (Tll) exhibits conserved roles in brain formation and maintenance that are shared, for example, with vertebrate orthologous forms (Tlx). However, the early expression of tll in two gap domains in the segmentation cascade of Drosophila is unusual even for most other insects. Here we investigate tll regulation on pair-rule stripes. With ectopic misexpression of tll we detected unexpected repression of almost all pair-rule stripes of hairy (h), even-skipped (eve), runt (run), and fushi-tarazu (ftz). Examining Tll embryonic ChIP-chip data with regions mapped as Cis-Regulatory Modules (CRMs) of pair-rule stripes we verified Tll interactions to these regions. With the ChIP-chip data we also verified Tll interactions to the CRMs of gap domains and in the misexpression assay, Tll-mediated repression on Kruppel (Kr), kni (kni) and giant (gt) according to their differential sensitivity to Tll. These results with gap genes confirmed previous data from the literature and argue against indirect repression roles of Tll in the striped pattern. Moreover, the prediction of Tll binding sites in the CRMs of eve stripes and the mathematical modeling of their removal using an experimentally validated theoretical framework shows effects on eve stripes compatible with the absence of a repressor binding to the CRMs. In addition, modeling increased tll levels in the embryo results in the differential repression of eve stripes, agreeing well with the results of the misexpression assay. In genetic assays we investigated eve 5, that is strongly repressed by the ectopic domain and representative of more central stripes not previously implied to be under direct regulation of tll. While this stripe is little affected in tll-, its posterior border is expanded in gt- but detected with even greater expansion in gt-;tll-. We end up by discussing tll with key roles in combinatorial repression mechanisms to contain the expression of medial patterns of the segmentation cascade in the extremities of the embryo.
孤儿核受体 Tailless(Tll)在脑形成和维持中表现出保守作用,例如与脊椎动物同源形式(Tlx)共享。然而,tll 在果蝇分节级联的两个缺口域中的早期表达甚至对大多数其他昆虫来说也是不寻常的。在这里,我们研究了 tll 对配对规则条纹的调节。通过异位过表达 tll,我们检测到几乎所有 hairy(h)、even-skipped(eve)、 runt(run)和 fushi-tarazu(ftz)的配对规则条纹都受到意外抑制。在用区域映射为配对规则条纹的顺式调控模块(CRM)的 Tll 胚胎 ChIP-chip 数据进行检查时,我们验证了 Tll 与这些区域的相互作用。使用 ChIP-chip 数据,我们还验证了 Tll 与缺口基因 CRM 的相互作用,并且在过表达实验中,Tll 对 Kruppel(Kr)、kni(kni)和 giant(gt)的抑制作用与其对 Tll 的不同敏感性相对应。这些与缺口基因的结果证实了文献中的先前数据,并排除了 Tll 在条纹图案中间接抑制作用的可能性。此外,对 eve 条纹 CRM 中的 Tll 结合位点的预测以及使用经过实验验证的理论框架去除它们的数学建模表明,与 CRM 中不存在抑制因子结合的情况一致,对 eve 条纹具有影响。此外,对胚胎中 tll 水平的建模增加导致 eve 条纹的差异抑制,与过表达实验的结果非常吻合。在遗传实验中,我们研究了 eve 5,它被异位域强烈抑制,是以前没有被认为受 tll 直接调控的更中央条纹的代表。虽然这个条纹在 tll-中几乎没有受到影响,但它的后边界在 gt-中扩展,但在 gt-;tll-中检测到更大的扩展。最后,我们讨论了 tll 在组合抑制机制中的关键作用,以在胚胎的末端限制分节级联中中间图案的表达。