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The wright stuff: reimagining path analysis reveals novel components of the sex determination hierarchy in drosophila melanogaster

机译:赖特的东西:重新想象路径分析揭示了果蝇中性别决定层次的新组成部分

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Background The Drosophila sex determination hierarchy is a classic example of a transcriptional regulatory hierarchy, with sex-specific isoforms regulating morphology and behavior. We use a structural equation modeling approach, leveraging natural genetic variation from two studies on Drosophila female head tissues – DSPR collection (596?F1-hybrids from crosses between DSPR sub-populations) and CEGS population (75?F1-hybrids from crosses between DGRP/Winters lines to a reference strain w1118) – to expand understanding of the sex hierarchy gene regulatory network (GRN). This approach is completely generalizable to any natural population, including humans. Results We expanded the sex hierarchy GRN adding novel links among genes, including a link from fruitless (fru) to Sex-lethal (Sxl) identified in both populations. This link is further supported by the presence of fru binding sites in the Sxl locus. 754 candidate genes were added to the pathway, including the splicing factors male-specific lethal 2 and Rm62 as downstream targets of Sxl which are well-supported links in males. Independent studies of doublesex and transformer mutants support many additions, including evidence for a link between the sex hierarchy and metabolism, via Insulin-like receptor. Conclusions The genes added in the CEGS population were enriched for genes with sex-biased splicing and components of the spliceosome. A common goal of molecular biologists is to expand understanding about regulatory interactions among genes. Using natural alleles we can not only identify novel relationships, but using supervised approaches can order genes into a regulatory hierarchy. Combining these results with independent large effect mutation studies, allows clear candidates for detailed molecular follow-up to emerge.
机译:背景技术果蝇性别决定体系是转录调控体系的经典例子,其性别特异性同工型可调控形态和行为。我们使用结构方程模型化方法,利用果蝇雌性头部组织的两项研究的自然遗传变异– DSPR集合(来自DSPR亚群的杂交的596?F1杂种)和CEGS群体(来自DGRP之间的杂交的75?F1杂种) / Winters将品系转到参考菌株w1118),以加深对性别等级基因调控网络(GRN)的了解。这种方法可以完全推广到包括人类在内的任何自然人口。结果我们扩展了性别等级GRN,在基因之间添加了新颖的联系,包括从两个种群中鉴定出的无结果(fru)到性致命(Sxl)的联系。 Sx1基因座中fru结合位点的存在进一步支持了该链接。将754个候选基因添加到该途径中,包括剪接因子雄性特异性致死因子2和Rm62作为Sxl的下游靶标,而Sxl是雄性中得到良好支持的链接。对双性恋和变形突变体的独立研究支持许多补充研究,包括通过胰岛素样受体证明性别等级与新陈代谢之间存在联系的证据。结论CEGS群体中添加的基因富含具有性别偏向剪接和剪接体成分的基因。分子生物学家的共同目标是扩大对基因之间调控相互作用的了解。使用自然等位基因,我们不仅可以识别新的关系,而且可以使用监督的方法将基因排序到调节层次中。将这些结果与独立的大效应突变研究相结合,可以为详细的分子随访提供明确的候选对象。

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