草鱼cdk2的分子特征、表达调控及其蛋白与CDX2的相互作用
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1.长沙学院生物与化学工程学院, 水生动物营养与品质调控湖南省重点实验室, 湖南 长沙 410022 ;2.湖南师范大学生命科学学院, 动物肠道功能调控湖南省重点实验室, 湖南 长沙 410081

作者简介:

何志敏,副教授,研究方向为水生动物分子营养.E-mail:z20180831@ccsu.edu.cn

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S917

基金项目:

国家自然科学基金项目(U21A2026731902345); 湖南省自然科学基金面上项目(2023JJ30075); 湖南省教育厅重点项目(22A0597); 湖南省领军人才计划项目(2023RC1072); 湖南省现代农业产业技术体系项目(HARS-07).


Molecular characteristics, expression regulation and its coding protein’s interaction with CDX2 of cdk2 in Ctenopharyngodon idella
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1.Hunan Provincial Key Laboratory of Nutrition and Quality Control of Aquatic Animals, Department of Biological andChemical Engineering, Changsha University, Changsha 410022 , China ;2.Hunan Provincial Key Laboratory of Animal Intestinal Function Regulation, College of Life Sciences, Hunan NormalUniversity, Changsha 410081 , China

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    摘要:

    为探究草鱼(Ctenopharyngodon idella) cdk2 的分子特征、CDK2 蛋白与 CDX2 的相互作用及其表达营养调控, 本研究通过克隆获得草鱼 cdk2 基因序列, 其开放阅读框 897 bp, 编码 298 个氨基酸, 与其他物种 CDK2 氨基酸序列同源性达到 80%以上, 且具有保守 S_TKc 功能域; 基于 cdk2的密码子偏好性及聚类分析均表明, 草鱼与斑马鱼 (Danio rerio)的亲缘关系最近; 相对基于 cdk2 RSCU 的聚类分析, 基于 CDK2 氨基酸序列的系统进化树分析更符合传统物种的分类; 组织表达分析结果表明, 草鱼 cdk2 mRNA 在血液组织表达水平最高(P<0.05), 肝脏和脾脏次之。 通过分子对接和酵母双杂交分析了草鱼 CDK2 与其下游磷酸化底物蛋白 CDX2 的相互作用, 结果表明草鱼 CDK2 与 CDX2 具有相互作用。本研究进一步通过养殖实验探究了饲料中添加不同水平的游离氨基酸 CAA (游离 lys 和 glu)、二肽 KE (lys-glu, KE), 三肽 GHK (gly-his-lys, GHK)对 cdk2 的表达调控, 结果表明, 相比对照组, 0.5% GHK 对草鱼 cdk2 mRNA 的表达促进作用最大, 氨基酸 CAA 相比具有同样氨基酸组成的 KE 二肽, 更能促进 cdk2 的表达。综上认为, 草鱼 cdk2 基因表达具有组织特异性, CDK2 与 CDX2 相互作用, cdk2 表达水平受到饲料中氨基酸和小肽水平的影响。本研究可为研究其他硬骨鱼类 cdk2 分子特征,肠道功能基因的调控机制提供新的线索, 并为后续开展 cdk2 基因调控氨基酸及小肽的转运吸收分子机制研究提供理论基础。

    Abstract:

    To investigate the molecular characteristics, interaction, and nutritional regulation of CDK2 in grass carp (Ctenopharyngodon idella), we obtained the grass carp cdk2 sequence by cloning; its open reading frame is 897 bp, encoding 298 amino acids. It exhibited a high degree of sequence and structure conservation in the analyzed species. The results of codon bias and cluster analyses based on CDK2 suggested that the grass carp has the closest relationship with zebrafish. Compared with clustering based on cdk2 RSCU, a phylogenetic tree analysis based on CDK2 sequence was more consistent with the conventional species classification. Tissue expression analysis showed the highest cdk2 mRNA levels in blood (P<0.05), liver, and spleen; molecular docking and yeast two-hybrid assays were employed to analyze the interaction between grass carp CDK2 and its downstream phosphorylated substrate protein CDX2. The results showed that grass carp CDK2 interacted with CDK2. Furthermore, the regulation of different inclusion levels of free amino acid CAA (free amino acids: lys and glu), dipeptide KE (lys-glu, KE), tripeptide GHK (gly-his-glu, GHK) on cdk2 expression were examined, and the results revealed that compared with the control and other treatment groups, cdk2 expression showed the highest expression in the 0.5% GHK group; cdk2 expression of the CAA groups was higher than those of the KE dipeptide group which showed similar amino acids as the CAA group. In summary, cdk2 expression in grass carp exhibits tissue specificity; CDK2 interacted with CDX2; and its expression was regulated by the inclusion level of amino acids and oligopeptides. This study provides new clues for studying the molecular characteristics of grass carp cdk2 exploring the regulatory mechanism of intestinal function in other teleost fish, and provides a theoretical basis for further study on the molecular regulating mechanism of cdk2 on transporting and absorption of amino acids and oligopeptides.

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何志敏,罗君涵,王辰浩洋,唐翔,蒋然,王麒翔,刘晶,李艳芳,高星,曾鹏,卿艳玲,罗雅楠,刘臻.草鱼cdk2的分子特征、表达调控及其蛋白与CDX2的相互作用[J].中国水产科学,2025,32(5):581-594
HE Zhimin, LUO Junhan, WANG Chenhaoyang, TANG Xiang, JIANG Ran, WANG Qixiang, LIU Jing, LI Yanfang, GAO Xing, ZENG Peng, QING Yanling, LUO Yanan, LIU Zhen. Molecular characteristics, expression regulation and its coding protein’s interaction with CDX2 of cdk2 in Ctenopharyngodon idella[J]. Journal of Fishery Sciences of China,2025,32(5):581-594

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  • 收稿日期:2025-02-08
  • 最后修改日期:2025-03-23
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  • 在线发布日期: 2025-08-04
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