Sex-specific plasticity and the nutritional geometry of insulin-signaling gene expression in Drosophila melanogaster.

IF 4.1 2区 生物学 Q1 DEVELOPMENTAL BIOLOGY Evodevo Pub Date : 2021-05-14 DOI:10.1186/s13227-021-00175-0
Jeanne M C McDonald, Pegah Nabili, Lily Thorsen, Sohee Jeon, Alexander W Shingleton
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Abstract

Background: Sexual-size dimorphism (SSD) is replete among animals, but while the selective pressures that drive the evolution of SSD have been well studied, the developmental mechanisms upon which these pressures act are poorly understood. Ours and others' research has shown that SSD in D. melanogaster reflects elevated levels of nutritional plasticity in females versus males, such that SSD increases with dietary intake and body size, a phenomenon called sex-specific plasticity (SSP). Additional data indicate that while body size in both sexes responds to variation in protein level, only female body size is sensitive to variation in carbohydrate level. Here, we explore whether these difference in sensitivity at the morphological level are reflected by differences in how the insulin/IGF-signaling (IIS) and TOR-signaling pathways respond to changes in carbohydrates and proteins in females versus males, using a nutritional geometry approach.

Results: The IIS-regulated transcripts of 4E-BP and InR most strongly correlated with body size in females and males, respectively, but neither responded to carbohydrate level and so could not explain the sex-specific response to body size to dietary carbohydrate. Transcripts regulated by TOR-signaling did, however, respond to dietary carbohydrate in a sex-specific manner. In females, expression of dILP5 positively correlated with body size, while expression of dILP2,3 and 8, was elevated on diets with a low concentration of both carbohydrate and protein. In contrast, we detected lower levels of dILP2 and 5 protein in the brains of females fed on low concentration diets. We could not detect any effect of diet on dILP expression in males.

Conclusion: Although females and males show sex-specific transcriptional responses to changes in protein and carbohydrate, the patterns of expression do not support a simple model of the regulation of body-size SSP by either insulin- or TOR-signaling. The data also indicate a complex relationship between carbohydrate and protein level, dILP expression and dILP peptide levels in the brain. In general, diet quality and sex both affect the transcriptional response to changes in diet quantity, and so should be considered in future studies that explore the effect of nutrition on body size.

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黑腹果蝇胰岛素信号基因表达的性别特异性可塑性和营养几何学
背景:动物中普遍存在性大小二形性(SSD),但尽管对驱动SSD进化的选择性压力进行了深入研究,但对这些压力作用的发育机制却知之甚少。我们和其他人的研究表明,黑腹蝇中的SSD反映了雌性相对于雄性的营养可塑性水平的提高,例如SSD会随着饮食摄入量和体型的增加而增加,这种现象被称为性别特异性可塑性(SSP)。其他数据表明,虽然雌雄体型都会对蛋白质水平的变化做出反应,但只有雌性体型对碳水化合物水平的变化敏感。在此,我们采用营养几何学方法,探讨雌性与雄性的胰岛素/IGF信号(IIS)和TOR信号通路对碳水化合物和蛋白质变化的反应是否反映了形态水平上的敏感性差异:结果:IIS调控的转录本4E-BP和InR分别与雌性和雄性的体型相关性最强,但两者都不对碳水化合物水平做出反应,因此不能解释体型对饮食碳水化合物的性别特异性反应。然而,受 TOR 信号调控的转录本确实以性别特异性的方式对饮食碳水化合物做出了反应。在雌性动物中,dILP5的表达与体型呈正相关,而在碳水化合物和蛋白质浓度都较低的膳食中,dILP2、3和8的表达都有所升高。相反,我们在低浓度日粮喂养的雌性动物大脑中检测到的 dILP2 和 5 蛋白水平较低。我们无法检测到饮食对雄性 dILP 表达的任何影响:结论:尽管雌性和雄性对蛋白质和碳水化合物的变化表现出性别特异性转录反应,但其表达模式并不支持由胰岛素或 TOR 信号调节体型 SSP 的简单模型。数据还表明,大脑中的碳水化合物和蛋白质水平、dILP 表达和 dILP 肽水平之间存在复杂的关系。总的来说,饮食质量和性别都会影响饮食数量变化的转录反应,因此在今后探讨营养对体型影响的研究中应加以考虑。
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来源期刊
Evodevo
Evodevo EVOLUTIONARY BIOLOGY-DEVELOPMENTAL BIOLOGY
CiteScore
7.50
自引率
0.00%
发文量
18
审稿时长
>12 weeks
期刊介绍: EvoDevo publishes articles on a broad range of topics associated with the translation of genotype to phenotype in a phylogenetic context. Understanding the history of life, the evolution of novelty and the generation of form, whether through embryogenesis, budding, or regeneration are amongst the greatest challenges in biology. We support the understanding of these processes through the many complementary approaches that characterize the field of evo-devo. The focus of the journal is on research that promotes understanding of the pattern and process of morphological evolution. All articles that fulfill this aim will be welcome, in particular: evolution of pattern; formation comparative gene function/expression; life history evolution; homology and character evolution; comparative genomics; phylogenetics and palaeontology
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