泥蟹甜菜碱同型半胱氨酸s -甲基转移酶基因1 (BHMT1)的表征及调控分析:一个对盐度和摄食行为敏感的基因

IF 1 Q4 GENETICS & HEREDITY Gene Reports Pub Date : 2024-11-28 DOI:10.1016/j.genrep.2024.102102
Jinju Yin , Zhiqiang Liu , Xin Jin , Wei Wang , Lingbo Ma , Ming Zhao
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引用次数: 0

摘要

甜菜碱同型半胱氨酸s -甲基转移酶基因1 (BHMT1)编码甜菜碱同型半胱氨酸s -甲基转移酶(BHMT),以甜菜碱为甲基供体催化同型半胱氨酸-蛋氨酸反应。此前,我们发现BHMT在节肢动物昆虫支系的基因组中缺失,但在泥蟹Scylla paramosain (Sp)的下颌器官(MO)中高表达。为了进一步探讨其意义,我们对泥蟹的BHMT进行了初步的调控分析。Sp-BHMT1的开放阅读框长度为1203 bp,编码400个氨基酸。序列比对表明,BHMT1在不同动物中具有高度保守性,在亲缘关系较近的物种中具有较高的同源性。Sp-BHMT1在两性MO中的表达量最高,其在雄性MO中的表达量是雌性MO的1.6倍;在脑神经节、肝胰腺和胸神经节组织中也发现了类似的结果。在幼虫发育过程中,Sp-BHMT1在大部分时间表达较弱,但在Z2和Z3期的第一天表达显著升高。Sp-BHMT1在盐度为10‰时表达量最高,在盐度为30‰时表达量最低。随着盐度的降低,Sp-BHMT1的表达在6 h时显著升高,8 h时恢复到基线水平。饥饿处理后,Sp-BHMT1的表达在所有检测时间点均较饲料组显著上调,饥饿组在第3天18:00达到表达高峰。法诺酸甲酯(methyl farnesoate, MF)信号基因kr ppel同源基因1 (Kr-h1)在低盐度和饥饿条件下可增加Sp-BHMT1的表达,提示蟹体内可能存在“盐度/饥饿→BHMT1→MF生物合成”调控轴。本研究为Sp-BHMT1的功能研究和MF生物合成调控提供了有价值的见解。
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Characterization and regulatory analysis of betaine homocysteine S-methyltransferase gene 1 (BHMT1) in mud crab: A gene responsive to salinity and feeding behavior
Betaine homocysteine S-methyltransferase gene 1 (BHMT1) encoded betaine homocysteine S-methyltransferase (BHMT) catalyzes the homocysteine-to-methionine reaction using betaine as a methyl donor. Previously, we found that BHMT was lost in the genome of the insect clade of arthropods, but was highly expressed in the mandibular organ (MO) of the mud crab Scylla paramamosain (Sp). To further explore its significance, we performed a primary regulatory analysis of BHMT in mud crabs. The open reading frame (ORF) length of Sp-BHMT1 was 1203 bp, encoding 400 amino acids. Sequence alignment revealed that BHMT1 was highly conserved in different animals, and its identity was higher in more closely related species. Sp-BHMT1 had the highest expression in the MO of both sexes, while its expression in the MO was 1.6-fold higher in males than in females; similar results were also found in the cerebral ganglion, hepatopancreas, and thoracic ganglia tissues. During larval development, Sp-BHMT1 was weakly expressed on most days but was significantly elevated on the first day of the Zoea 2nd (Z2) and Z3 stages. Sp-BHMT1 exhibited the highest expression at a salinity of 10 ‰ and the lowest at a salinity of 30 ‰. With decreasing salinity, the expression of Sp-BHMT1 increased significantly at 6 h and then returned to baseline at 8 h. After starvation treatment, the expression of Sp-BHMT1 was significantly upregulated compared to that in the feed group at all examined time points, with a peak expression at 18:00 on the third day in the starvation group. Krüppel homolog 1 (Kr-h1), a methyl farnesoate (MF) signal gene, could increase Sp-BHMT1 expression under low salinity and starvation, suggesting that a “salinity/starvation→BHMT1 → MF biosynthesis” regulatory axis might exist in crabs. This study provides valuable insights into the functional study of Sp-BHMT1 and MF biosynthetic regulation.
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来源期刊
Gene Reports
Gene Reports Biochemistry, Genetics and Molecular Biology-Genetics
CiteScore
3.30
自引率
7.70%
发文量
246
审稿时长
49 days
期刊介绍: Gene Reports publishes papers that focus on the regulation, expression, function and evolution of genes in all biological contexts, including all prokaryotic and eukaryotic organisms, as well as viruses. Gene Reports strives to be a very diverse journal and topics in all fields will be considered for publication. Although not limited to the following, some general topics include: DNA Organization, Replication & Evolution -Focus on genomic DNA (chromosomal organization, comparative genomics, DNA replication, DNA repair, mobile DNA, mitochondrial DNA, chloroplast DNA). Expression & Function - Focus on functional RNAs (microRNAs, tRNAs, rRNAs, mRNA splicing, alternative polyadenylation) Regulation - Focus on processes that mediate gene-read out (epigenetics, chromatin, histone code, transcription, translation, protein degradation). Cell Signaling - Focus on mechanisms that control information flow into the nucleus to control gene expression (kinase and phosphatase pathways controlled by extra-cellular ligands, Wnt, Notch, TGFbeta/BMPs, FGFs, IGFs etc.) Profiling of gene expression and genetic variation - Focus on high throughput approaches (e.g., DeepSeq, ChIP-Seq, Affymetrix microarrays, proteomics) that define gene regulatory circuitry, molecular pathways and protein/protein networks. Genetics - Focus on development in model organisms (e.g., mouse, frog, fruit fly, worm), human genetic variation, population genetics, as well as agricultural and veterinary genetics. Molecular Pathology & Regenerative Medicine - Focus on the deregulation of molecular processes in human diseases and mechanisms supporting regeneration of tissues through pluripotent or multipotent stem cells.
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