| 锦鲤墨蝶呤还原酶基因的克隆、表达和定位分析 |
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| 引用本文： | 胡菊,冯彩,马晓,吴利敏,刘慧芬,宋红梅,胡隐昌,田雪,李学军.锦鲤墨蝶呤还原酶基因的克隆、表达和定位分析[J].水产学报,2020,44(4):551-561. |
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| 作者姓名： | 胡菊 冯彩 马晓 吴利敏 刘慧芬 宋红梅 胡隐昌 田雪 李学军 |
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| 作者单位： | 河南师范大学水产学院,河南省水产动物养殖工程技术研究中心,河南新乡 453007;中国水产科学研究院珠江水产研究所,农业农村部休闲渔业重点实验室,广东广州 510380 |
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| 基金项目： | 国家自然科学基金青年科学基金(31402294)；河南省重点研发与推广专项(182102110164，192102110192)；农业农村部休闲渔业重点实验室开放基金课题(2019N06) |
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| 摘 要： | 为探究SPR在锦鲤体色形成中的作用,实验利用RACE技术获得spr cDNA全长序列,并分析其时空表达模式,同时利用Western blot和免疫组织化学方法检测SPR蛋白在皮肤、鳍条和鳞片中的分布和表达情况。结果显示,spr cDNA全长879 bp,包含132 bp和134 bp的5′和3′非编码区,开放阅读框510 bp,编码170个氨基酸残基。氨基酸序列比对和系统进化树分析显示,锦鲤SPR具有保守的adh_short_C2结构域,与金鱼相似性高达97.7%。spr在各组织中均有表达,其中皮肤的表达量最高。spr在锦鲤个体发育的4个阶段表现为先降后升。纯红、纯白及红白3种体色锦鲤皮肤、鳞片和鳍条中spr mRNA和蛋白表达水平基本一致,在纯红锦鲤皮肤中表达量最高,红白锦鲤白色皮肤、鳞片和鳍条的表达量最低。SPR组织定位分析显示,红色锦鲤和白色锦鲤皮肤中均检测到阳性信号,其中红色皮肤阳性信号强度高于白色皮肤。研究表明,spr可能与锦鲤红/黄色素细胞的分化和形成具有一定相关性,参与了锦鲤体色的形成。
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| 关 键 词： | 锦鲤 spr 基因克隆 蝶啶代谢 体色 |
| 收稿时间： | 2019/7/7 0:00:00 |
| 修稿时间： | 2019/10/12 0:00:00 |
Molecular cloning and expression of sepiapterin reductase in Japanese ornamental carp (Cyprinus carpio var. koi) |
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| HU Ju,FENG Cai,MA Xiao,WU Limin,LIU Huifen,SONG Hongmei,HU Yinchang,TIAN Xue and LI Xuejun.Molecular cloning and expression of sepiapterin reductase in Japanese ornamental carp (Cyprinus carpio var. koi)[J].Journal of Fisheries of China,2020,44(4):551-561. |
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| Authors: | HU Ju FENG Cai MA Xiao WU Limin LIU Huifen SONG Hongmei HU Yinchang TIAN Xue and LI Xuejun |
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| Institution: | College of Fisheries, Engineering Technology Research Center of Henan Province for Aquatic Animal Cultivation, Henan Normal University, Xinxiang 453007, China,College of Fisheries, Engineering Technology Research Center of Henan Province for Aquatic Animal Cultivation, Henan Normal University, Xinxiang 453007, China,College of Fisheries, Engineering Technology Research Center of Henan Province for Aquatic Animal Cultivation, Henan Normal University, Xinxiang 453007, China,College of Fisheries, Engineering Technology Research Center of Henan Province for Aquatic Animal Cultivation, Henan Normal University, Xinxiang 453007, China,College of Fisheries, Engineering Technology Research Center of Henan Province for Aquatic Animal Cultivation, Henan Normal University, Xinxiang 453007, China,Key Laboratory of Recreational Fisheries, Ministry of Agriculture and Rural Affairs, Pearl River Fisheries Research Institute, Chinese Academy of Fishery Sciences, Guangzhou 510380, China,Key Laboratory of Recreational Fisheries, Ministry of Agriculture and Rural Affairs, Pearl River Fisheries Research Institute, Chinese Academy of Fishery Sciences, Guangzhou 510380, China,College of Fisheries, Engineering Technology Research Center of Henan Province for Aquatic Animal Cultivation, Henan Normal University, Xinxiang 453007, China and College of Fisheries, Engineering Technology Research Center of Henan Province for Aquatic Animal Cultivation, Henan Normal University, Xinxiang 453007, China |
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| Abstract: | The origin of teleost skin color is from chromatophores. Different chromatophores synthesize distinct pigments, including melanin, carotenoid, pteridine and purine. Sepiapterin is a yellow pteridines, which could be transformed into tetrahydrobiopterin (BH4) and yellow/red pteridines pigments together with sepiapterin reductase (SPR), dihydrofolate reductase (DHFR) and other enzymes. SPR is the last enzyme in the process of de novo BH4 synthesis. In order to explore the function of spr in koi carp color formation, this study amplified the whole cDNA of spr and analyzed the spatio-temporal profile. Furthermore, we also detected the expression and distribution of SPR in the skin, fins and scales of koi carp with different colors by Western blot and immunochemistry methods. The results showed that the size of spr cDNA was 879 bp, including 132 bp and 134 bp 5'' and 3'' untranslated regions, and a 510 bp open reading frame encoding 170 amino acids. Sequences alignment and phylogenetic analysis revealed the spr gene of koi carp contained a adh_short_C2 conserved domain and had 97.65% similarity with gold fish. spr was expressed in every tissue, especially highest expressed in skin. In the four ontogenetic stages, the expression level of spr firstly decreased, then rose. The expression level of spr mRNA and protein in skins, fins and scales displayed the same condition among three colors (whole red koi carp, whole white koi carp and kohaku koi carp). The highest expression level was detected in whole red koi carp and rarely in white skin, fins and scales of kohaku koi carp. The immunohistochemical positive signals were detected in both skins of whole red and whole white koi carp, and intensively exhibited in red skin compared with white skin. All the results might indicate that the spr gene has relationship with the xanthophores/erythrophores differentiation and formation, involved in koi carp color formation. |
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| Keywords: | Cyprinus carpio var koi spr cloning pteridine metabolism color formation |
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