神经肽 HGAP 调节太平洋鲍鱼的生长、繁殖、变态、组织损伤修复以及对饥饿的反应。

IF 3.2 2区 医学 Q2 ENDOCRINOLOGY & METABOLISM
Neuroendocrinology Pub Date : 2024-01-01 Epub Date: 2023-12-23 DOI:10.1159/000535945
Md Abu Hanif, Shaharior Hossen, Doo Hyun Cho, Kang Hee Kho
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引用次数: 0

摘要

引言神经肽调节多细胞生物的重要生理过程,包括生长、繁殖、变态和摄食。最近的转录组分析揭示了在脊椎动物和无脊椎动物生长和繁殖过程中可能发挥作用的神经肽基因。在这些基因中,卤代生长相关肽(HGAP)被确定为鲍鱼中的一个新基因:本研究的重点是太平洋鲍鱼(Haliotis discus hannai)中的 HGAP,已鉴定并描述了名为 Hdh-HGAP 的完整 cDNA 序列。研究人员收集了鲍鱼变态、幼鲍生长、性腺发育阶段、肌肉重塑和饥饿等不同实验的样本进行 mRNA 表达分析:结果:Hdh-HRNA序列长达552 bp,编码96个氨基酸,分子量为10.96 kDa。表达分析表明,Hdh-HGAP在肌肉组织中含量较高。值得注意的是,在变态过程中,Hdh-HGAP 在蝌蚪期、绒毛期和幼体期的表达量高于细胞分裂期。在生长模式方面,Hdh-HGAP在快速生长期的表达量高于生长迟缓期、极小生长期和正常生长期。在性腺发育过程中,Hdh-HGAP mRNA在成熟期达到最高表达水平,表明其在性腺细胞增殖和成熟过程中可能发挥作用。体内 GnRH 对性腺发育的影响以及 Hdh-HGAP 神经肽的表达表明,它参与了太平洋鲍的繁殖调节。虽然组织重塑主要由免疫基因控制,但在肌肉组织重塑过程中,Hdh-HGAP 也被上调。相反,在长期饥饿过程中,Hdh-HGAP 会下调:本研究首次全面探讨了太平洋鲍鱼的 Hdh-HGAP 神经肽基因,揭示了该基因参与生长、繁殖、变态、组织重塑和对饥饿的反应,但其调控机制大多尚不清楚。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The Neuropeptide HGAP Regulates Growth, Reproduction, Metamorphosis, Tissue Damage Repair, and Response against Starvation in Pacific Abalone.

Introduction: Neuropeptides regulate vital physiological processes in multicellular organisms, including growth, reproduction, metamorphosis, and feeding. Recent transcriptome analyses have revealed neuropeptide genes with potential roles in vertebrate and invertebrate growth and reproduction. Among these genes, haliotid growth-associated peptide (HGAP) was identified as a novel gene in abalone.

Methods: This study focused on HGAP in Pacific abalone (Haliotis discus hannai), where the complete cDNA sequence named Hdh-HGAP was identified and characterized. Samples from different experiments, such as metamorphosis, juvenile abalone growth, gonad development stages, muscle remodeling, and starvation, were collected for mRNA expression analysis.

Results: The sequence spans 552 bp, encoding 96 amino acids with a molecular weight of 10.96 kDa. Expression analysis revealed that Hdh-HGAP exhibited higher levels in muscle tissue. Notably, during metamorphosis, Hdh-HGAP exhibited greater expression in the trochophore, veliger, and juvenile stages than in the cell division stages. Regarding growth patterns, Hdh-HGAP was highly expressed during rapid growth compared to stunted, minimal, and normal growth. In gonadal development, Hdh-HGAP mRNA reached its highest expression level during the ripening stage, indicating a potential role in gonadal cell proliferation and maturation. The in vivo effects of GnRH on gonad development and the expression of the Hdh-HGAP neuropeptide indicate its involvement in regulating reproduction in Pacific abalone. While tissue remodeling is primarily governed by immune genes, Hdh-HGAP was also upregulated during muscle tissue remodeling. Conversely, Hdh-HGAP was downregulated during prolonged starvation.

Conclusion: This study marks the first comprehensive exploration of the Hdh-HGAP neuropeptide gene in Pacific abalone, shedding light on its involvement in growth, reproduction, metamorphosis, tissue remodeling, and response to starvation, although regulatory mechanisms are mostly unknown.

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来源期刊
Neuroendocrinology
Neuroendocrinology 医学-内分泌学与代谢
CiteScore
8.30
自引率
2.40%
发文量
50
审稿时长
6-12 weeks
期刊介绍: ''Neuroendocrinology'' publishes papers reporting original research in basic and clinical neuroendocrinology. The journal explores the complex interactions between neuronal networks and endocrine glands (in some instances also immunecells) in both central and peripheral nervous systems. Original contributions cover all aspects of the field, from molecular and cellular neuroendocrinology, physiology, pharmacology, and the neuroanatomy of neuroendocrine systems to neuroendocrine correlates of behaviour, clinical neuroendocrinology and neuroendocrine cancers. Readers also benefit from reviews by noted experts, which highlight especially active areas of current research, and special focus editions of topical interest.
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