文石欠饱和多重驱动下东部牡蛎幼虫转录组对表型组的响应

IF 2.3 2区 生物学 Q2 ECOLOGY
Samuel J. Gurr, Shannon L. Meseck, Genevieve Bernatchez, Dylan Redman, Mark S. Dixon, Lisa Guy, Aaron MacDonald, Sheila Stiles, Katherine McFarland
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引用次数: 0

摘要

了解相互作用的环境挑战如何影响海洋物种对全球变化下的长期生态和经济稳定至关重要。海洋钙化剂被认为容易受到海洋酸化的影响(OA;二氧化碳分压升高);文石的活性溶解(Ωar)与双壳类幼虫的发育、存活和基因表达中断有关,导致早期生命阶段的瓶颈。沿海系统中的动态碳酸盐化学强调了多种压力源的重要性,例如,相对于OA,变暖和低盐度事件可能改变生物体的反应。本研究采用全因子实验设计,在温度(23°C和27°C)、盐度(17和27)和pCO2浓度(~700 μatm和1850 μatm pCO2)两种条件下,将东部牡蛎幼虫(Crassostrea virginica)置于Ωar条件0.3-1.7中。Ωar由于低盐度、二氧化碳分压升高和低温而减少,每一种都减缓了早期发育并降低了存活率。低盐度×升高的pCO2与严重的Ωar欠饱和(< 0.5)有关,这抑制了碳酸氢盐运输、生物矿化的表达,并增加了纤毛运动、蛋白质停滞和组蛋白修饰因子的表达。在隔离和中等Ωar强度(0.5 <; Ωar < 1)下,幼虫在低盐度条件下增加渗透调节活性和内吞作用的转录,在pCO2升高条件下抑制铁代谢的转录。虽然Ωar欠饱和会影响牡蛎壳的生长和存活,但d期牡蛎幼虫和幼牡蛎的基因表达模式表明它们对动态河口环境具有耐受性。赋予蜕变后牡蛎生存的基因和表达模式可以提高我们对环境-生物体相互作用的理解,并改善育种计划,使其能够实现可持续生产。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Transcriptome-To-Phenome Response of Larval Eastern Oysters Under Multiple Drivers of Aragonite Undersaturation

Transcriptome-To-Phenome Response of Larval Eastern Oysters Under Multiple Drivers of Aragonite Undersaturation

Understanding how interactive environmental challenges affect marine species is critical to long-term ecological and economic stability under global change. Marine calcifiers are thought to be vulnerable to ocean acidification (OA; elevated pCO2); active dissolution of aragonite (Ωar) is associated with disrupted development, survivorship, and gene expression in bivalve larvae, resulting in an early life-stage bottleneck. Dynamic carbonate chemistry in coastal systems emphasizes the importance of multiple stressors, e.g., warming and low salinity events may change organismal responses relative to OA alone. We exposed Eastern oyster larvae (Crassostrea virginica) to a full-factorial experimental design using two temperatures (23°C and 27°C), salinities (17 and 27), and pCO2 levels (~700 μatm and 1850 μatm pCO2), resulting in Ωar conditions 0.3–1.7. Ωar reduced by low salinity, elevated pCO2, and low temperature, each slowed early development and reduced survival. Low salinity × elevated pCO2 was linked to severe Ωar undersaturation (< 0.5) that suppressed expression of bicarbonate transport, biomineralization and augmented expression for ciliary locomotion, proteostasis, and histone modifiers. In isolation and under moderate Ωar intensity (0.5 < Ωar < 1), larvae increased transcription for osmoregulatory activity and endocytosis under low salinity, and suppressed transcription for iron metabolism under elevated pCO2. Although shell growth and survival were affected by Ωar undersaturation, gene expression patterns of D-stage oyster larvae and oyster juveniles suggests tolerance to dynamic estuarine environments. Genes and expression patterns that confer survival of postmetamorphosed oysters can improve our understanding of environmental-organismal interactions and improve breeding programs enabling sustainable production.

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来源期刊
CiteScore
4.40
自引率
3.80%
发文量
1027
审稿时长
3-6 weeks
期刊介绍: Ecology and Evolution is the peer reviewed journal for rapid dissemination of research in all areas of ecology, evolution and conservation science. The journal gives priority to quality research reports, theoretical or empirical, that develop our understanding of organisms and their diversity, interactions between them, and the natural environment. Ecology and Evolution gives prompt and equal consideration to papers reporting theoretical, experimental, applied and descriptive work in terrestrial and aquatic environments. The journal will consider submissions across taxa in areas including but not limited to micro and macro ecological and evolutionary processes, characteristics of and interactions between individuals, populations, communities and the environment, physiological responses to environmental change, population genetics and phylogenetics, relatedness and kin selection, life histories, systematics and taxonomy, conservation genetics, extinction, speciation, adaption, behaviour, biodiversity, species abundance, macroecology, population and ecosystem dynamics, and conservation policy.
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