转录组和代谢组分析揭示了 Pinctada fucata martensii 性腺中与性别有关的差异。

IF 2.2 2区 生物学 Q4 BIOCHEMISTRY & MOLECULAR BIOLOGY
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引用次数: 0

摘要

Pinctada fucata martensii 是一种具有重要经济价值的双壳软体动物,因为该物种对海水珍珠生产做出了重大贡献。P. f. martensii的珍珠生产效率因性别而异,但P. f. martensii性别决定和性别分化的分子机制的许多方面仍不清楚。在此,我们进行了转录组学和代谢组学分析,以确定与性别决定和配子发生相关的主要基因和代谢变化。我们共发现了 3426 个雌性和雄性之间的差异表达基因(DEGs)。其中包括参与性别决定和性别分化的Fem-1c和Foxl2,以及参与配子发生的SOHLH2、Nanos1和TSSK4。我们还发现了 5231 个雌性和雄性之间的显著差异代谢物(SDMs)。这些DEGs富集在47个代谢途径中,包括 "ABC转运体"、"嘌呤代谢 "和 "甘油磷脂代谢"。我们的研究结果为性别决定、性别分化和配子发生的分子机制提供了新的见解,并将有助于今后对貂蝉的研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Transcriptomic and metabolomic analyses reveal sex-related differences in the gonads of Pinctada fucata martensii

Transcriptomic and metabolomic analyses reveal sex-related differences in the gonads of Pinctada fucata martensii

Pinctada fucata martensii is an economically important bivalve mollusk, as this species makes a major contribution to seawater pearl production. Pearl production efficiency varies between the sexes of P. f. martensii, but many aspects of the molecular mechanisms underlying sex determination and sex differentiation in P. f. martensii remain unclear. Here, transcriptomic and metabonomic analyses were conducted to identify the major genes and metabolic changes associated with sex determination and gametogenesis. We identified a total of 3426 differentially expressed genes (DEGs) between females and males. These included Fem-1c and Foxl2, which are involved in sex determination and sex differentiation, and SOHLH2, Nanos1 and TSSK4, which are involved in gametogenesis. We also identified a total of 5231 significant differential metabolites (SDMs) between females and males. These DEGs were enriched in 47 metabolic pathways, including “ABC transporters,” “purine metabolism,” and “glycerophospholipid metabolism.” Our findings provide new insights into the molecular mechanisms underlying sex determination, sex differentiation, and gametogenesis and will aid future studies of P. f. martensii.

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来源期刊
CiteScore
5.10
自引率
3.30%
发文量
69
审稿时长
33 days
期刊介绍: Comparative Biochemistry & Physiology (CBP) publishes papers in comparative, environmental and evolutionary physiology. Part D: Genomics and Proteomics (CBPD), focuses on “omics” approaches to physiology, including comparative and functional genomics, metagenomics, transcriptomics, proteomics, metabolomics, and lipidomics. Most studies employ “omics” and/or system biology to test specific hypotheses about molecular and biochemical mechanisms underlying physiological responses to the environment. We encourage papers that address fundamental questions in comparative physiology and biochemistry rather than studies with a focus that is purely technical, methodological or descriptive in nature.
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