不同藜麦品种甜菜碱醛脱氢酶(BADH)基因的硅晶分析

IF 3.9 4区 生物学 Q1 GENETICS & HEREDITY
Ali Reza Mirzaei, Bahman Fazeli-Nasab, Mehrnaz Hatami, Ali Salehi Sardoei, Mansour Ghorbanpour
{"title":"不同藜麦品种甜菜碱醛脱氢酶(BADH)基因的硅晶分析","authors":"Ali Reza Mirzaei,&nbsp;Bahman Fazeli-Nasab,&nbsp;Mehrnaz Hatami,&nbsp;Ali Salehi Sardoei,&nbsp;Mansour Ghorbanpour","doi":"10.1007/s10142-025-01577-2","DOIUrl":null,"url":null,"abstract":"<div><p><i>Chenopodium quinoa</i> is an emerging halophyte plant that has gained significant attention from researchers in recent years due to its high nutritional value and resilience to environmental stress. This plant serves as an excellent substitute for rice and wheat. However, there has been limited research on it, leaving many of its genes still unidentified. The objective of this research was to identify gene patterns and conduct a bioinformatics analysis across various fields. The expression sequence of the <i>betaine aldehyde dehydrogenase</i> (<i>BADH</i>) gene was predicted using bioinformatics software such as PlantCARE and PlantPan. The findings indicated that different cultivars provide valuable information regarding resistance to the binding sites of MYB transcription factors, hormone response regions, and both promoter and enhancer regions, which contain 32 <i>cis</i>-regulatory elements. This emphasized the role of the <i>BADH</i> gene in responding to abiotic stress. Additionally, the research revealed that the <i>BADH</i> gene activates oxidoreductase activity across different cultivars, influencing NAD or NADP receptors that contribute to stress resistance. The protein lengths identified were 454 and 500 amino acids, respectively. Chloroplast analysis revealed that the GC content for the <i>BADH</i> gene was 37%. From this analysis, it was determined that out of 128 distinct functional genes in the genome, approximately 84 are protein-coding genes. An examination of the domains and motifs in the target genes showed that they contain two conserved sequences: Aldedh and DUF1487. Furthermore, miRNA analysis and promoter investigations indicated that the <i>BADH</i> gene plays a vital role in activating processes related to arginase, protein kinases, superoxide dismutase, tubulins, and membrane proteins. The gene is also crucial for activating nuclear transcription factors through receptor activation. In conclusion, the results suggest that <i>BADH</i> genes contribute to the plant's resistance to salt stress through various mechanisms. Stress acts as a trigger for the activation of this gene, effectively safeguarding the plant against the detrimental effects of environmental stresses.</p></div>","PeriodicalId":574,"journal":{"name":"Functional & Integrative Genomics","volume":"25 1","pages":""},"PeriodicalIF":3.9000,"publicationDate":"2025-04-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"In silico analysis of betaine aldehyde dehydrogenase (BADH) gene in different cultivars of Chenopodium quinoa\",\"authors\":\"Ali Reza Mirzaei,&nbsp;Bahman Fazeli-Nasab,&nbsp;Mehrnaz Hatami,&nbsp;Ali Salehi Sardoei,&nbsp;Mansour Ghorbanpour\",\"doi\":\"10.1007/s10142-025-01577-2\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p><i>Chenopodium quinoa</i> is an emerging halophyte plant that has gained significant attention from researchers in recent years due to its high nutritional value and resilience to environmental stress. This plant serves as an excellent substitute for rice and wheat. However, there has been limited research on it, leaving many of its genes still unidentified. The objective of this research was to identify gene patterns and conduct a bioinformatics analysis across various fields. The expression sequence of the <i>betaine aldehyde dehydrogenase</i> (<i>BADH</i>) gene was predicted using bioinformatics software such as PlantCARE and PlantPan. The findings indicated that different cultivars provide valuable information regarding resistance to the binding sites of MYB transcription factors, hormone response regions, and both promoter and enhancer regions, which contain 32 <i>cis</i>-regulatory elements. This emphasized the role of the <i>BADH</i> gene in responding to abiotic stress. Additionally, the research revealed that the <i>BADH</i> gene activates oxidoreductase activity across different cultivars, influencing NAD or NADP receptors that contribute to stress resistance. The protein lengths identified were 454 and 500 amino acids, respectively. Chloroplast analysis revealed that the GC content for the <i>BADH</i> gene was 37%. From this analysis, it was determined that out of 128 distinct functional genes in the genome, approximately 84 are protein-coding genes. An examination of the domains and motifs in the target genes showed that they contain two conserved sequences: Aldedh and DUF1487. Furthermore, miRNA analysis and promoter investigations indicated that the <i>BADH</i> gene plays a vital role in activating processes related to arginase, protein kinases, superoxide dismutase, tubulins, and membrane proteins. The gene is also crucial for activating nuclear transcription factors through receptor activation. In conclusion, the results suggest that <i>BADH</i> genes contribute to the plant's resistance to salt stress through various mechanisms. Stress acts as a trigger for the activation of this gene, effectively safeguarding the plant against the detrimental effects of environmental stresses.</p></div>\",\"PeriodicalId\":574,\"journal\":{\"name\":\"Functional & Integrative Genomics\",\"volume\":\"25 1\",\"pages\":\"\"},\"PeriodicalIF\":3.9000,\"publicationDate\":\"2025-04-02\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Functional & Integrative Genomics\",\"FirstCategoryId\":\"99\",\"ListUrlMain\":\"https://link.springer.com/article/10.1007/s10142-025-01577-2\",\"RegionNum\":4,\"RegionCategory\":\"生物学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"GENETICS & HEREDITY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Functional & Integrative Genomics","FirstCategoryId":"99","ListUrlMain":"https://link.springer.com/article/10.1007/s10142-025-01577-2","RegionNum":4,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"GENETICS & HEREDITY","Score":null,"Total":0}
引用次数: 0

摘要

藜麦(Chenopodium quinoa)是一种新兴的盐生植物,因其具有较高的营养价值和抗环境胁迫能力,近年来受到了研究人员的广泛关注。这种植物是水稻和小麦的极好的替代品。然而,对它的研究有限,它的许多基因仍未被识别。本研究的目的是识别基因模式,并在各个领域进行生物信息学分析。利用PlantCARE、PlantPan等生物信息学软件预测甜菜碱醛脱氢酶(BADH)基因的表达序列。结果表明,不同品种对MYB转录因子结合位点、激素反应区以及包含32个顺式调控元件的启动子和增强子区域的抗性提供了有价值的信息。这强调了BADH基因在应对非生物胁迫中的作用。此外,研究表明,BADH基因激活不同品种的氧化还原酶活性,影响NAD或NADP受体,这些受体有助于抗逆性。鉴定出的蛋白质长度分别为454和500个氨基酸。叶绿体分析表明,BADH基因GC含量为37%。从这一分析中,确定了在基因组中128个不同的功能基因中,大约84个是蛋白质编码基因。对靶基因结构域和基序的分析表明,它们包含两个保守序列:Aldedh和DUF1487。此外,miRNA分析和启动子研究表明,BADH基因在激活精氨酸酶、蛋白激酶、超氧化物歧化酶、小管蛋白和膜蛋白等相关过程中起着至关重要的作用。该基因也是通过受体激活激活核转录因子的关键基因。综上所述,BADH基因通过多种机制参与了植物对盐胁迫的抗性。压力作为激活该基因的触发器,有效地保护植物免受环境压力的有害影响。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
In silico analysis of betaine aldehyde dehydrogenase (BADH) gene in different cultivars of Chenopodium quinoa

Chenopodium quinoa is an emerging halophyte plant that has gained significant attention from researchers in recent years due to its high nutritional value and resilience to environmental stress. This plant serves as an excellent substitute for rice and wheat. However, there has been limited research on it, leaving many of its genes still unidentified. The objective of this research was to identify gene patterns and conduct a bioinformatics analysis across various fields. The expression sequence of the betaine aldehyde dehydrogenase (BADH) gene was predicted using bioinformatics software such as PlantCARE and PlantPan. The findings indicated that different cultivars provide valuable information regarding resistance to the binding sites of MYB transcription factors, hormone response regions, and both promoter and enhancer regions, which contain 32 cis-regulatory elements. This emphasized the role of the BADH gene in responding to abiotic stress. Additionally, the research revealed that the BADH gene activates oxidoreductase activity across different cultivars, influencing NAD or NADP receptors that contribute to stress resistance. The protein lengths identified were 454 and 500 amino acids, respectively. Chloroplast analysis revealed that the GC content for the BADH gene was 37%. From this analysis, it was determined that out of 128 distinct functional genes in the genome, approximately 84 are protein-coding genes. An examination of the domains and motifs in the target genes showed that they contain two conserved sequences: Aldedh and DUF1487. Furthermore, miRNA analysis and promoter investigations indicated that the BADH gene plays a vital role in activating processes related to arginase, protein kinases, superoxide dismutase, tubulins, and membrane proteins. The gene is also crucial for activating nuclear transcription factors through receptor activation. In conclusion, the results suggest that BADH genes contribute to the plant's resistance to salt stress through various mechanisms. Stress acts as a trigger for the activation of this gene, effectively safeguarding the plant against the detrimental effects of environmental stresses.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
CiteScore
3.50
自引率
3.40%
发文量
92
审稿时长
2 months
期刊介绍: Functional & Integrative Genomics is devoted to large-scale studies of genomes and their functions, including systems analyses of biological processes. The journal will provide the research community an integrated platform where researchers can share, review and discuss their findings on important biological questions that will ultimately enable us to answer the fundamental question: How do genomes work?
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信