Regulatory Role of Retinoic Acid in Male Pregnancy of the Seahorse

Summary: Seahorses epitomize the exuberance of evolution. They have the unique characteristic of male pregnancy, which includes the carrying of many embryos in a brood pouch that incubates and nourishes the embryos, similar to the mammalian placenta. However, the regulatory networks underlying brood...

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Main Authors: Chunyan Li, Yongxin Li, Geng Qin, Zelin Chen, Meng Qu, Bo Zhang, Xue Han, Xin Wang, Pei-yuan Qian, Qiang Lin
Format: Article
Language:English
Published: Elsevier 2020-11-01
Series:The Innovation
Subjects:
Online Access:http://www.sciencedirect.com/science/article/pii/S2666675820300552
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record_format Article
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language English
format Article
sources DOAJ
author Chunyan Li
Yongxin Li
Geng Qin
Zelin Chen
Meng Qu
Bo Zhang
Xue Han
Xin Wang
Pei-yuan Qian
Qiang Lin
spellingShingle Chunyan Li
Yongxin Li
Geng Qin
Zelin Chen
Meng Qu
Bo Zhang
Xue Han
Xin Wang
Pei-yuan Qian
Qiang Lin
Regulatory Role of Retinoic Acid in Male Pregnancy of the Seahorse
The Innovation
seahorse
male pregnancy
brood pouch
integrative omics
retinoic acid
antioxidant defense
author_facet Chunyan Li
Yongxin Li
Geng Qin
Zelin Chen
Meng Qu
Bo Zhang
Xue Han
Xin Wang
Pei-yuan Qian
Qiang Lin
author_sort Chunyan Li
title Regulatory Role of Retinoic Acid in Male Pregnancy of the Seahorse
title_short Regulatory Role of Retinoic Acid in Male Pregnancy of the Seahorse
title_full Regulatory Role of Retinoic Acid in Male Pregnancy of the Seahorse
title_fullStr Regulatory Role of Retinoic Acid in Male Pregnancy of the Seahorse
title_full_unstemmed Regulatory Role of Retinoic Acid in Male Pregnancy of the Seahorse
title_sort regulatory role of retinoic acid in male pregnancy of the seahorse
publisher Elsevier
series The Innovation
issn 2666-6758
publishDate 2020-11-01
description Summary: Seahorses epitomize the exuberance of evolution. They have the unique characteristic of male pregnancy, which includes the carrying of many embryos in a brood pouch that incubates and nourishes the embryos, similar to the mammalian placenta. However, the regulatory networks underlying brood pouch formation and pregnancy remain largely unknown. In this study, comparative transcriptomic and metabolomic profiling on the lined seahorse Hippocampus erectus, with unformed, newly formed, and pregnant brood pouches identified a total of 141 and 2,533 differentially expressed genes together with 73 and 121 significantly differential metabolites related to brood pouch formation and pregnancy, respectively. Specifically, integrative omics analysis revealed that retinoic acid (RA) synthesis and signaling pathway played essential roles in the formation of the brood pouch and pregnancy. RA might function upstream of testosterone and progesterone, thereby directly influencing brood pouch formation by regulating the expression of fshr and cyp7a1. Our results also revealed that RA regulates antioxidant defenses, particularly during male pregnancy. Alternatively, pregnancy caused a consistent decrease in RA, canthaxanthin, astaxanthin, and glutathione synthetase, and an increase in susceptibility to oxidative stress, which may balance brood pouch development and reproduction in seahorses and pave the way to successful gestation.
topic seahorse
male pregnancy
brood pouch
integrative omics
retinoic acid
antioxidant defense
url http://www.sciencedirect.com/science/article/pii/S2666675820300552
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AT yongxinli regulatoryroleofretinoicacidinmalepregnancyoftheseahorse
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AT zelinchen regulatoryroleofretinoicacidinmalepregnancyoftheseahorse
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spelling doaj-48d302149923432f8b2682bdac0b91582020-11-27T04:24:38ZengElsevierThe Innovation2666-67582020-11-0113100052Regulatory Role of Retinoic Acid in Male Pregnancy of the SeahorseChunyan Li0Yongxin Li1Geng Qin2Zelin Chen3Meng Qu4Bo Zhang5Xue Han6Xin Wang7Pei-yuan Qian8Qiang Lin9CAS Key Laboratory of Tropical Marine Bio-Resources and Ecology, South China Sea Institute of Oceanology, Innovation of South China Sea Ecology and Environmental Engineering, Chinese Academy of Sciences, 510301 Guangzhou, China; Southern Marine Science and Engineering Guangdong Laboratory (Guangzhou), 511458 Guangzhou, ChinaSouthern Marine Science and Engineering Guangdong Laboratory (Guangzhou), 511458 Guangzhou, China; Department of Chemistry, The University of Hong Kong, Pokfulam, Hong Kong, Hong Kong SAR, ChinaCAS Key Laboratory of Tropical Marine Bio-Resources and Ecology, South China Sea Institute of Oceanology, Innovation of South China Sea Ecology and Environmental Engineering, Chinese Academy of Sciences, 510301 Guangzhou, ChinaCAS Key Laboratory of Tropical Marine Bio-Resources and Ecology, South China Sea Institute of Oceanology, Innovation of South China Sea Ecology and Environmental Engineering, Chinese Academy of Sciences, 510301 Guangzhou, ChinaCAS Key Laboratory of Tropical Marine Bio-Resources and Ecology, South China Sea Institute of Oceanology, Innovation of South China Sea Ecology and Environmental Engineering, Chinese Academy of Sciences, 510301 Guangzhou, ChinaCAS Key Laboratory of Tropical Marine Bio-Resources and Ecology, South China Sea Institute of Oceanology, Innovation of South China Sea Ecology and Environmental Engineering, Chinese Academy of Sciences, 510301 Guangzhou, ChinaCAS Key Laboratory of Tropical Marine Bio-Resources and Ecology, South China Sea Institute of Oceanology, Innovation of South China Sea Ecology and Environmental Engineering, Chinese Academy of Sciences, 510301 Guangzhou, ChinaCAS Key Laboratory of Tropical Marine Bio-Resources and Ecology, South China Sea Institute of Oceanology, Innovation of South China Sea Ecology and Environmental Engineering, Chinese Academy of Sciences, 510301 Guangzhou, ChinaSouthern Marine Science and Engineering Guangdong Laboratory (Guangzhou), 511458 Guangzhou, China; Department of Ocean Science and Hong Kong Branch of Southern Marine Science and Engineering Guangdong Laboratory (Guangzhou), Hong Kong University of Science and Technology, Kowloon, Hong Kong, China; Corresponding authorCAS Key Laboratory of Tropical Marine Bio-Resources and Ecology, South China Sea Institute of Oceanology, Innovation of South China Sea Ecology and Environmental Engineering, Chinese Academy of Sciences, 510301 Guangzhou, China; Southern Marine Science and Engineering Guangdong Laboratory (Guangzhou), 511458 Guangzhou, China; Corresponding authorSummary: Seahorses epitomize the exuberance of evolution. They have the unique characteristic of male pregnancy, which includes the carrying of many embryos in a brood pouch that incubates and nourishes the embryos, similar to the mammalian placenta. However, the regulatory networks underlying brood pouch formation and pregnancy remain largely unknown. In this study, comparative transcriptomic and metabolomic profiling on the lined seahorse Hippocampus erectus, with unformed, newly formed, and pregnant brood pouches identified a total of 141 and 2,533 differentially expressed genes together with 73 and 121 significantly differential metabolites related to brood pouch formation and pregnancy, respectively. Specifically, integrative omics analysis revealed that retinoic acid (RA) synthesis and signaling pathway played essential roles in the formation of the brood pouch and pregnancy. RA might function upstream of testosterone and progesterone, thereby directly influencing brood pouch formation by regulating the expression of fshr and cyp7a1. Our results also revealed that RA regulates antioxidant defenses, particularly during male pregnancy. Alternatively, pregnancy caused a consistent decrease in RA, canthaxanthin, astaxanthin, and glutathione synthetase, and an increase in susceptibility to oxidative stress, which may balance brood pouch development and reproduction in seahorses and pave the way to successful gestation.http://www.sciencedirect.com/science/article/pii/S2666675820300552seahorsemale pregnancybrood pouchintegrative omicsretinoic acidantioxidant defense