Histone deacetylases regulate organ-specific growth in a horned beetle

IF 4.1 2区 生物学 Q1 DEVELOPMENTAL BIOLOGY Evodevo Pub Date : 2024-04-05 DOI:10.1186/s13227-024-00223-5
Yonggang Hu, Jordan R. Crabtree, Anna L. M. Macagno, Armin P. Moczek
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Abstract

Nutrient availability is among the most widespread means by which environmental variability affects developmental outcomes. Because almost all cells within an individual organism share the same genome, structure-specific growth responses must result from changes in gene regulation. Earlier work suggested that histone deacetylases (HDACs) may serve as epigenetic regulators linking nutritional conditions to trait-specific development. Here we expand on this work by assessing the function of diverse HDACs in the structure-specific growth of both sex-shared and sex-specific traits including evolutionarily novel structures in the horned dung beetle Onthophagus taurus. We identified five HDAC members whose downregulation yielded highly variable mortality depending on which HDAC member was targeted. We then show that HDAC1, 3, and 4 operate in both a gene- and trait-specific manner in the regulation of nutrition-responsiveness of appendage size and shape. Specifically, HDAC 1, 3, or 4 knockdown diminished wing size similarly while leg development was differentially affected by RNAi targeting HDAC3 and HDAC4. In addition, depletion of HDAC3 transcript resulted in a more rounded shape of genitalia at the pupal stage and decreased the length of adult aedeagus across all body sizes. Most importantly, we find that HDAC3 and HDAC4 pattern the morphology and regulate the scaling of evolutionarily novel head and thoracic horns as a function of nutritional variation. Collectively, our results suggest that both functional overlap and division of labor among HDAC members contribute to morphological diversification of both conventional and recently evolved appendages. More generally, our work raises the possibility that HDAC-mediated scaling relationships and their evolution may underpin morphological diversification within and across insect species broadly.
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组蛋白去乙酰化酶调控角甲虫器官特异性生长
营养供应是环境变异影响发育结果的最普遍手段之一。由于生物个体内的几乎所有细胞都具有相同的基因组,因此结构特异性生长反应必须是基因调控变化的结果。早先的研究表明,组蛋白去乙酰化酶(HDACs)可能是连接营养条件和特异性发育的表观遗传调控因子。在此基础上,我们评估了不同的 HDAC 在角蜣螂(Onthophagus taurus)性别共享和性别特异性(包括进化中的新结构)结构特异性生长中的功能。我们发现了五种 HDAC 成员,根据所针对的 HDAC 成员的不同,其下调所产生的死亡率也大不相同。然后,我们发现 HDAC1、3 和 4 以基因和性状特异的方式调节附肢大小和形状的营养反应性。具体来说,敲除 HDAC 1、3 或 4 会同样减小翅膀的大小,而针对 HDAC3 和 HDAC4 的 RNAi 则会不同程度地影响腿的发育。此外,HDAC3转录本的耗竭导致蛹期生殖器的形状更加圆润,并降低了所有体型的成虫雌蕊的长度。最重要的是,我们发现HDAC3和HDAC4能改变进化过程中新颖的头角和胸角的形态并调节其缩放,这与营养变异有关。总之,我们的研究结果表明,HDAC成员之间的功能重叠和分工有助于传统附肢和新近进化附肢的形态多样化。更广泛地说,我们的研究提出了一种可能性,即HDAC介导的缩放关系及其进化可能是昆虫物种内部和物种之间形态多样化的基础。
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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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