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太平洋白虾中阴离子交换蛋白3的分子鉴定:组织、个体发育、蜕皮和卵巢发育的mRNA表达谱及其在应激诱导鳃损伤中的潜在作用

Molecular Identification of Anion Exchange Protein 3 in Pacific White Shrimp (): mRNA Profiles for Tissues, Ontogeny, Molting, and Ovarian Development and Its Potential Role in Stress-Induced Gill Damage.

作者信息

Zhang Xin, Yang Hao, Li Hongmei, Chen Ting, Ruan Yao, Ren Chunhua, Luo Peng, Wang Yanhong, Liu Bing, Li Huo, Zhong Ping, Zhang Jiquan, Jiang Xiao, Hu Chaoqun

机构信息

CAS Key Laboratory of Tropical Marine Bio-resources and Ecology (LMB), Guangdong Provincial Key Laboratory of Applied Marine Biology (LAMB), South China Sea Institute of Oceanology, Chinese Academy of Sciences, Guangzhou, China.

College of Earth and Planetary Sciences, University of Chinese Academy of Sciences, Beijing, China.

出版信息

Front Physiol. 2021 Sep 30;12:726600. doi: 10.3389/fphys.2021.726600. eCollection 2021.

DOI:10.3389/fphys.2021.726600
PMID:34658912
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8514663/
Abstract

Bicarbonate (HCO ) transport mechanisms play an essential role in the acid-base homeostasis of aquatic animals, and anion exchange protein 3 (AE3) is a membrane transport protein that exchanges Cl/HCO across the cell membrane to regulate the intracellular pH. In this study, the full-length cDNA of () was obtained from the Pacific white shrimp (). The cDNA is 4,943 bp in length, contains an open reading frame of 2,850 bp, coding for a protein of 949 amino acids with 12 transmembrane domains. -AE3 shows high sequence homology with other AE3 at the protein level. mRNA was ubiquitously detected in all tissues selected, with the highest expression level in the gill, followed by the ovary, eyestalk and brain. By hybridization, positive cells were shown predominant localization in the secondary gill filaments. The expression levels of were further investigated during the essential life processes of shrimp, including ontogeny, molting, and ovarian development. In this case, the spatiotemporal expression profiles of in were highly correlated with the activities of water and ion absorption; for example, increased mRNA levels were present after hatching, during embryonic development, after ecdysis during the molt cycle, and in the stage IV ovary during gonadal development. After low/high pH and low/high salinity challenges, the transcript levels of were reduced in the gill, while the cell apoptosis rate increased. In addition, knockdown of mRNA expression induced cell apoptosis in the gill, indicating a potential link between -AE3 and gill damage. Altogether, this study thoroughly investigated the relationship between the mRNA expression profiles of and multiple developmental and physiological processes in , and it may benefit the protection of crustaceans from fluctuated aquatic environments.

摘要

碳酸氢根(HCO₃⁻)转运机制在水生动物的酸碱平衡中起着至关重要的作用,阴离子交换蛋白3(AE3)是一种膜转运蛋白,可跨细胞膜交换Cl⁻/HCO₃⁻以调节细胞内pH值。在本研究中,从太平洋白虾(Litopenaeus vannamei)中获得了(LvAE3)的全长cDNA。该cDNA长度为4943 bp,包含一个2850 bp的开放阅读框,编码一个含有12个跨膜结构域的949个氨基酸的蛋白质。Lv -AE3在蛋白质水平上与其他AE3具有高度的序列同源性。在所选的所有组织中均普遍检测到LvAE3 mRNA,在鳃中的表达水平最高,其次是卵巢、眼柄和脑。通过原位杂交,阳性细胞主要定位于次级鳃丝。在虾的重要生命过程中,包括个体发育、蜕皮和卵巢发育,进一步研究了LvAE3的表达水平。在这种情况下,LvAE3在凡纳滨对虾中的时空表达谱与水和离子吸收活动高度相关;例如,在孵化后、胚胎发育期间、蜕皮周期中的蜕皮后以及性腺发育期间的IV期卵巢中,mRNA水平升高。在低/高pH和低/高盐度挑战后,鳃中LvAE3的转录水平降低,而细胞凋亡率增加。此外,敲低LvAE3 mRNA表达会诱导鳃细胞凋亡,表明Lv -AE3与鳃损伤之间存在潜在联系。总之,本研究全面调查了凡纳滨对虾中LvAE3 mRNA表达谱与多个发育和生理过程之间的关系,这可能有助于保护甲壳类动物免受波动的水生环境的影响。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8225/8514663/02fdacf1d77b/fphys-12-726600-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8225/8514663/16b7121812cc/fphys-12-726600-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8225/8514663/afc84117b888/fphys-12-726600-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8225/8514663/26b1277e342a/fphys-12-726600-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8225/8514663/947659f18226/fphys-12-726600-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8225/8514663/65373dd48b7b/fphys-12-726600-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8225/8514663/8a7c2264a251/fphys-12-726600-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8225/8514663/02fdacf1d77b/fphys-12-726600-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8225/8514663/16b7121812cc/fphys-12-726600-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8225/8514663/afc84117b888/fphys-12-726600-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8225/8514663/26b1277e342a/fphys-12-726600-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8225/8514663/947659f18226/fphys-12-726600-g004.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8225/8514663/8a7c2264a251/fphys-12-726600-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8225/8514663/02fdacf1d77b/fphys-12-726600-g007.jpg

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