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Identification of the autophagy pathway in a mollusk bivalve Crassostrea gigas

机译:在MOLLUSK双级克萨斯特拉省Gigas鉴定自噬途径

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摘要

The Pacific oyster, Crassostrea gigas, is a mollusk bivalve commercially important as a food source. Pacific oysters are subjected to stress and diseases during culture. The autophagy pathway is involved in numerous cellular processes, including responses to starvation, cell death, and microorganism elimination. Autophagy also exists in C. gigas, and plays a role in the immune response against infections. Although this process is well-documented and conserved in most animals, it is still poorly understood in mollusks. To date, no study has provided a complete overview of the molecular mechanism of autophagy in mollusk bivalves. In this study, human and yeast ATG protein sequences and public databases (Uniprot and NCBI) were used to identify protein members of the C. gigas autophagy pathway. A total of 35 autophagy related proteins were found in the Pacific oyster. RACE-PCR was performed on several genes. Using molecular (real-time PCR) and protein-based (western blot and immunohistochemistry) approaches, the expression and localization of ATG12, ATG9, BECN1, MAP1LC3, MTOR, and SQSTM1, was investigated in different tissues of the Pacific oyster. Comparison with human and yeast counterparts demonstrated a high homology with the human autophagy pathway. The results also demonstrated that the key autophagy genes and their protein products were expressed in all the analyzed tissues of C. gigas. This study allows the characterization of the complete C. gigas autophagy pathway for the first time.
机译:太平洋牡蛎,克萨斯特拉·吉斯,是一种商业化重要的家伙作为食物来源。太平洋牡蛎在文化期间受到压力和疾病。自噬途径涉及许多细胞过程,包括对饥饿,细胞死亡和微生物消除的反应。 C. gigas中还存在自噬,并在免疫反应中起作用。虽然这种过程在大多数动物中被良好撰写和保守,但在软体动物中仍然明白。迄今为止,尚无研究概述了软体动物双抗体中自噬的分子机制概述。在该研究中,使用人和酵母ATG蛋白质序列和公共数据库(UNIPROT和NCBI)来鉴定C.Gigas自噬途径的蛋白质成员。在太平洋牡蛎中发现了总共35个自噬相关蛋白质。种族PCR在几种基因上进行。使用分子(实时PCR)和基于蛋白质(Western印迹和免疫组织化学)的方法,在太平洋牡蛎的不同组织中研究了ATG12,ATG9,BECN1,MAP1LC3,MTOR和SQSTM1的表达和定位。与人和酵母对应物的比较展示了人类自噬途径的高同源性。结果还证明了关键的自噬基因及其蛋白质产物在C.Gigas的所有分析组织中表达。该研究首次允许完成完整的C. Gigas自噬途径的表征。

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