|本期目录/Table of Contents|

[1]陶思怡,林颖辉,许凯,等.NhDGK-1调控坛紫菜丝状体成熟的分子机制[J].集美大学学报(自然科学版),2025,(5):409-419.
 TAO Siyi,LIN Yinghui,XU Kai,et al.Molecular Mechanism of NhDGK1 Regulating the Maturation of Conchocelis in Neoporphyra haitanensis[J].Journal of Jimei University,2025,(5):409-419.
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《集美大学学报(自然科学版)》[ISSN:1007-7405/CN:35-1186/N]

卷:
期数:
2025年第5期
页码:
409-419
栏目:
水产、食品与生物技术
出版日期:
2025-09-28

文章信息/Info

Title:
Molecular Mechanism of NhDGK1 Regulating the Maturation of Conchocelis in Neoporphyra haitanensis
作者:
陶思怡林颖辉许凯徐燕纪德华王文磊谢潮添
(集美大学水产学院,福建 厦门 361021)
Author(s):
TAO SiyiLIN YinghuiXU KaiXU YanJI DehuaWANG WenleiXIE Chaotian
(Fisheries College,Jimei University,Xiamen 361021,China)
关键词:
坛紫菜孢子囊枝二酰甘油激酶互作因子酵母双杂交
Keywords:
Neoporphyra haitanensissporangial branchletsdiacylglycerol kinaseinteraction factorsyeast two-hybrid
分类号:
-
DOI:
-
文献标志码:
A
摘要:
坛紫菜新品种在推广的过程中均会遇到“良种难育”的瓶颈,即自由丝状体不容易成熟,难以集中获得大量壳孢子,严重制约了坛紫菜良种的推广。由于二酰甘油激酶(DGK)基因在坛紫菜丝状体成熟过程中发挥着重要作用,因此本研究通过抑制二酰甘油激酶的活性,发现坛紫菜孢子囊枝形成率明显降低。之后,利用酵母双杂交技术鉴定到了7个与NhDGK1互作的蛋白质,即电压依赖性阴离子通道蛋白VDAC、葡萄糖-6磷酸-1-差向异构酶G6P1E、伴侣蛋白DnaJ、细胞质蛋白复合物外被体蛋白亚基COP1、肌环己六氢醇脱氢酶Idh、磷酸吡哆醛合成酶PDX1-1和3-酮脂酰-ACP还原酶FabG。这些互作蛋白广泛参与多种物质的合成与代谢、囊泡运输、光合作用和转录调控等生命过程,当NhDGK1活性被抑制后,这些互作蛋白编码基因的表达量同样受到抑制。其中,G6P1E与NhDGK1互作提高了孢子囊枝形成过程中的糖代谢水平,促进了藻体中碳水化合物的积累;FabG与NhDGK1互作可以促进脂肪酸的合成,提高丝状体的耐受性并促进孢子囊枝的形成;COP1介导的囊泡运输可能也调控了坛紫菜中PLC/DGK途径产生磷脂酸(phosphatidic acid,PA)的过程。
Abstract:
During the promotion of new varieties of Neoporphyra haitanensis,there exists a “difficult breeding” bottleneck,that is,the free-living filaments are not easily matured,making it challenging to obtain a large amount of sporangial branchlets,which seriously restaicts the propagation of high-quality N.haitanensis strains.Previous studies found that the diacylglycerol kinase gene(DGK) plays an important role in the maturation process of free-living filaments in N.haitanensis.This study found that the formation rate of sporangial branches in N.haitanensis was significantly reduced by inhibiting the activity of diacylglycerol kinase.Then,seven proteins interacting with NhDGK1 were identified by yeast two-hybrid technology,namely voltage-dependent anion channel protein(VDAC),glucose-6-phosphate-1-epimerase (G6P1E),chaperone protein (DnaJ),coatomer delta1subunit (COP1),myo-inositol 2-dehydrogenase (Idh),pyridoxal 5-phosphate synthase subunit (PDX1-1),and 3oxoacylacylcarrierprotein reductase (FabG).These interacting proteins are widely involved in various life processes such as the synthesis and metabolism of multiple substances,vesicle transport,photosynthesis,and transcriptional regulation.When the activity of NhDGK1 was inhibited,the expression levels of the genes encoding these interacting proteins were also suppressed.Among them,the interaction between G6P1E and NhDGK1 increases the level of sugar metabolism during the formation of sporangial branch and promotes the accumulation of carbohydrates in the algal;the interaction between FabG and NhDGK1 can promote the synthesis of fatty acids,enhance the tolerance of filamentpis bodies,and promote the formation of sporangial branches;COP1-mediated vesicle transport may also regulate the process of phosphatidic acid (PA) production through the PLC/DGK pathway in N.haitanensis.

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备注/Memo

备注/Memo:
更新日期/Last Update: 2025-11-02