多组织代谢组学分析揭示了与扇贝生长相关的关键代谢物和途径。

IF 3.5 2区 生物学 Q2 BIOTECHNOLOGY & APPLIED MICROBIOLOGY
Yihan Zhang, Huizhen Wang, Shiqi Liu, Xiangfu Kong, Lirong Chang, Liang Zhao, Zhenmin Bao, Xiaoli Hu
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引用次数: 0

摘要

背景:双壳贝类因其高产和广泛的市场需求而成为水产养殖业的重要经济资源。生长是双壳贝类最重要和最理想的水产养殖性状之一,受多个层面的调节,尤其是复杂的代谢过程。然而,人们对影响双壳类动物生长的代谢特征的了解还很有限,尤其是从多组织的角度来看:本研究采用超高效液相色谱-四极杆飞行时间质谱(UPLC-Q-TOF-MS)系统地研究了具有不同生长性能的 Chlamys farreri 的多个组织的代谢概况。通过比较快速生长(FG)扇贝和慢速生长(SG)扇贝之间的代谢变化,在扇贝的套膜、鳃、内收肌和消化腺中分别鉴定出了613、509、105和192种显著不同的代谢物(SDMs)。在所有四种组织中都发现了与生长相关的代谢途径,包括鞘脂代谢、脂肪酸生物合成和ABC转运途径,以及与生长性状相关的11种SDMs,这意味着它们参与了扇贝多种组织的生长。组织特异性代谢分析表明,贝壳中的含硫氨基酸代谢可能有助于贝壳的生长,而鳃通过各种代谢过程协同参与贝壳的生长,如酪氨酸代谢、甘氨酸、丝氨酸和苏氨酸代谢以及黑色素生成;能量代谢对内收肌的生长至关重要;消化腺中的营养物质消化和吸收与扇贝的生长有关:我们的研究结果首次全面分析了与扇贝生长相关的关键途径和代谢物,为未来双壳贝类水产养殖生产提供了宝贵的见解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Multi-tissue metabolomic profiling reveals the crucial metabolites and pathways associated with scallop growth.

Background: Bivalves represent a vital economic resource in aquaculture for their high productivity and extensive market demand. Growth is one of the most important and desired aquaculture traits for bivalves, regulated by multiple levels, notably intricate metabolic processes. However, the understanding of the metabolic profiles that influence bivalve growth is limited, particularly from a multi-tissue perspective.

Results: In this study, metabolic profiles of multiple tissues of Chlamys farreri with different growth performance were systematically investigated by ultraperformance liquid chromatography quadrupole time-of-flight mass spectrometry (UPLC-Q-TOF-MS). Through comparing the metabolic variation between fast-growing (FG) scallops and slow-growing (SG) scallops, 613, 509, 105, and 192 significantly different metabolites (SDMs) were identified in the mantle, gill, adductor muscle, and digestive gland, respectively. Growth-related metabolic pathways including sphingolipid metabolism, fatty acid biosynthesis, and ABC transporter pathway, along with 11 SDMs associated with growth traits were identified in all four tissues, implying they were involved in the growth of multiple tissues in scallops. Tissue-specific metabolic profiling indicated that sulfur-containing amino acid metabolism in the mantle potentially contributed to shell growth, while the gill synergistically participated with the mantle through various metabolic processes, such as tyrosine metabolism, glycine, serine, and threonine metabolism and melanogenesis; energy metabolism was crucial for adductor muscle growth; and nutrients digestion and absorption in the digestive gland were linked to scallop growth.

Conclusions: Our results represent the first comprehensive analysis of the crucial pathways and metabolites associated with the growth of C. farreri, offering valuable insights for future bivalve aquaculture production.

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来源期刊
BMC Genomics
BMC Genomics 生物-生物工程与应用微生物
CiteScore
7.40
自引率
4.50%
发文量
769
审稿时长
6.4 months
期刊介绍: BMC Genomics is an open access, peer-reviewed journal that considers articles on all aspects of genome-scale analysis, functional genomics, and proteomics. BMC Genomics is part of the BMC series which publishes subject-specific journals focused on the needs of individual research communities across all areas of biology and medicine. We offer an efficient, fair and friendly peer review service, and are committed to publishing all sound science, provided that there is some advance in knowledge presented by the work.
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