草鱼foxo4的基因克隆及其对饲料蛋白质营养调控的响应OA北大核心CSTPCD
Molecular cloning and dietary protein regulation of foxo4 in grass carp(Ctenopharyngodon idella)
为探讨草鱼(Ctenopharyngodon idella)foxo4的分子特征及其对饲料蛋白营养调控响应的关系,通过同源克隆获得草鱼foxo4基因序列,其开放阅读框为1875 bp,编码624个氨基酸;系统进化树分析表明草鱼foxo4基因与黑头呆鱼(Pimephales promelas)亲缘关系最近.对foxo4进行组织表达分析,发现foxo4基因mRNA在草鱼肌肉中表达水平最高(P<0.05),其次是心脏和肝,最后是肠、脑、脾和肾.此外,昼夜节律分析显示,foxo4在18:00表达量最高,而在24:00表达量最低.本研究进一步探究了菜粕、鱼粉和豆粕作为饲料蛋白对foxo4表达的调控,实验结果表明,在养殖14d、21d和35 d后,草鱼肠道中foxo4基因在菜粕组和鱼粉组相对于豆粕组均出现显著的上调(P<0.05),这表明草鱼foxo4基因的表达与饲料中蛋白源种类密切相关.不同比例L-丙氨酰-L-谷氨酰胺二肽(丙谷二肽)养殖实验结果显示,在0.5%~2%添加量范围内,随着饲料中丙谷二肽添加比例的增加,草鱼肠道中foxo4基因的表达呈逐渐下降趋势,其中在对照组表达量最高,在1.5%丙谷二肽添加组表达量最低.综上所述,草鱼foxo4基因表达具有组织特异性,且受到饲料蛋白源和二肽水平的调控影响.本研究为揭示foxo4基因在鱼类中的分子特征及其对蛋白质营养调控的响应提供了基础数据.
The Forkhead box(Fox)protein family is a family of transcription factors with wing-like helical structured DNA-binding region and is widely distributed in biological groups ranging from yeast to mammals.The Fox protein family is divided into 19 subfamilies,A to S,among which the forkhead box O(FoxO)subfamily is the most intensively studied.Forkhead box O4(FoxO4)is a member of the FoxO subfamily,which includes FoxO1,FoxO3,and FoxO6 in mammals.These members share structural and functional similarities as well as regulations.In certain fish species,seven highly homologous members of the FoxO subfamily exist:FoxO1a,FoxO1b,FoxO3a,FoxO3b,FoxO4,FoxO6a,and Fox06b.The involvement of FoxO in the regulation of various physiological functions,including the cell cycle,apoptosis,DNA damage repair,oxidative stress,cell differentiation,and glucose metabolism,has been demonstrated in multiple studies.Furthermore,its activity is modulated through diverse mechanisms such as phosphorylation,acetylation,and ubiquitination.To explore the molecular characteristics offoxo4 in grass carp(Ctenopharyngodon idella)and its relationship with the nutritional regulation of dietary proteins,we obtained the grass carp foxo4 sequence through homologous cloning.Its open reading frame is 1875 bp,encoding 624 amino acids,and it consists of three functional domains:FH,Pfam(FOXO_KIX_bdg),and Pfam(FOXO_TAD).Amino acid sequence alignment analysis showed that the foxo4 gene in C.idella is highly homologous to that in Danio rerio,Homo sapiens,Mus musculus,and Electrophorus electricus.Analysis of codon usage bias revealed that foxo4 exhibited a strong preference for CUG and AGC codons across all examined species,whereas C.idella and Pimephales promelas shared certain similarities in their codon preferences,suggesting a close evolutionary relationship between them.Phylogenetic tree analysis showed that the foxo4 gene of grass carp has the highest homology to that of Pimephales promelas.Tissue expression analysis of foxo4 revealed that the mRNA expression level of foxo4 was most significant in grass carp muscle(P<0.05),followed by the heart,liver,intestine,brain,spleen,and kidney.In addition,circadian rhythm analysis showed that the expression offoxo4 was the highest at 18:00 and lowest at 24:00.This study also explored the effects of dietary protein on the expression of foxo4.The results of different protein source experiments showed that after 14,21,and 35 days of the feeding trial,the expression of the foxo4 gene in the intestinal tissue of grass carp was significantly upregulated in both the rapeseed meal and fish meal groups compared with that in the soybean meal group(P<0.05).These findings suggest a close association between the expression offoxo4 gene in grass carp and dietary protein sources.A feeding trial with different levels of 1-alanyl-l-glutamine dipeptide(Ala-Gln)showed a gradual decrease in the expression of foxo4 in the intestines of grass carp as the ratio of Ala-Gln in the feed increased.The control group showed the highest expression level,whereas the 1.5%addition group displayed the lowest expression level.In summary,the expression of foxo4 in grass carp exhibits tissue specificity and is regulated by dietary protein sources and dipeptide levels.This study establishes a foundation for revealing the molecular characteristics of foxo4 in fish and its protein nutritional response and provides basic data for subsequent studies on the molecular mechanism of foxo4 gene regulation in fish protein metabolism in teleosts.
徐哲华;刘臻;曹申平;易成琳;莫郁坚;杨立权;左安丽;杨瑞瑶;张鸣宇;瞿符发;唐建洲
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||湖南师范大学生命科学学院,淡水鱼类发育生物学国家重点实验室,湖南长沙 410081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
水产学
草鱼foxo4基因克隆组织分布蛋白源丙谷二肽
Ctenopharyngodon idellafoxo4gene cloningtissue distributionprotein sourceAla-Gln
《中国水产科学》 2024 (001)
FoxOs-CDX2信号通路调控草鱼肠道PepT1转运小肽的分子机制研究
14-28 / 15
国家自然科学基金项目(32102813);湖南省自然科学基金项目(2021JJ40627);淡水生态与生物技术国家重点实验室开放课题项目(2022FB08).
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