{"title":"微阵列识别拟南芥中可能参与向地性信号转导的转录因子","authors":"C. Cook, Avery E. Tucker, K. Shen, S. Wyatt","doi":"10.2478/gsr-2015-0008","DOIUrl":null,"url":null,"abstract":"ABSTRACT Gravity is a fundamental stimulus that affects plant growth and development. The gravity persistent signal (GPS) treatment uses a cold treatment to isolate the events of signal transduction. Plants are reoriented horizontally in the dark at 4°C for 1 hour and then returned to vertical at room temperature. A gene expression microarray was designed to identify genes that are regulated during the GPS treatment. Arabidopsis thaliana var. Columbia was grown to maturity with inflorescence stems of 8-10 cm. Total mRNA was collected from inflorescence stems at 2, 4, 10, and 30 min after reorientation in the cold. cDNA was synthesized from the mRNA and then probed against an Arabidopsis gene expression array with 4 replicates per time point. Analyses presented here focus on transcription factors because of their regulatory functions in response pathways. Five transcription factors (AtAIB, WRKY18, WRKY26, WRKY33, and BT2) were selected for further study based on their expression at 4 min. Quantitative real-time polymerase chain reaction ((PCR) RT-qPCR) was performed to confirm expression seen in the microarray data. Seeds of Arabidopsis lines containing T-DNA insertions in the genes were obtained, plants bred to homozygosity, and the mutants analyzed for GPS phenotype. Mutant analysis shows significant differences in curvature of inflorescence stems between mutants and wild type.","PeriodicalId":90510,"journal":{"name":"Gravitational and space research : publication of the American Society for Gravitational and Space Research","volume":"33 1","pages":"20 - 29"},"PeriodicalIF":0.0000,"publicationDate":"2015-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Microarray Identifies Transcription Factors Potentially Involved in Gravitropic Signal Transduction in Arabidopsis\",\"authors\":\"C. Cook, Avery E. Tucker, K. Shen, S. Wyatt\",\"doi\":\"10.2478/gsr-2015-0008\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"ABSTRACT Gravity is a fundamental stimulus that affects plant growth and development. The gravity persistent signal (GPS) treatment uses a cold treatment to isolate the events of signal transduction. Plants are reoriented horizontally in the dark at 4°C for 1 hour and then returned to vertical at room temperature. A gene expression microarray was designed to identify genes that are regulated during the GPS treatment. Arabidopsis thaliana var. Columbia was grown to maturity with inflorescence stems of 8-10 cm. Total mRNA was collected from inflorescence stems at 2, 4, 10, and 30 min after reorientation in the cold. cDNA was synthesized from the mRNA and then probed against an Arabidopsis gene expression array with 4 replicates per time point. Analyses presented here focus on transcription factors because of their regulatory functions in response pathways. Five transcription factors (AtAIB, WRKY18, WRKY26, WRKY33, and BT2) were selected for further study based on their expression at 4 min. Quantitative real-time polymerase chain reaction ((PCR) RT-qPCR) was performed to confirm expression seen in the microarray data. Seeds of Arabidopsis lines containing T-DNA insertions in the genes were obtained, plants bred to homozygosity, and the mutants analyzed for GPS phenotype. Mutant analysis shows significant differences in curvature of inflorescence stems between mutants and wild type.\",\"PeriodicalId\":90510,\"journal\":{\"name\":\"Gravitational and space research : publication of the American Society for Gravitational and Space Research\",\"volume\":\"33 1\",\"pages\":\"20 - 29\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2015-12-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Gravitational and space research : publication of the American Society for Gravitational and Space Research\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.2478/gsr-2015-0008\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Gravitational and space research : publication of the American Society for Gravitational and Space Research","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.2478/gsr-2015-0008","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
摘要
重力是影响植物生长发育的基本刺激。重力持续信号(GPS)处理采用冷处理来隔离信号转导事件。在4°C的黑暗中,植物重新水平定向1小时,然后在室温下恢复垂直。设计了基因表达微阵列来鉴定在GPS治疗期间受调节的基因。拟南芥(Arabidopsis thaliana var. Columbia)生长至成熟,花序茎长8- 10cm。在低温下重新定向后的2、4、10和30分钟,从花序茎中收集总mRNA。从mRNA合成cDNA,然后在拟南芥基因表达阵列上进行探针,每个时间点4个重复。本文主要分析转录因子,因为它们在反应通路中的调节功能。选择5个转录因子(AtAIB、WRKY18、WRKY26、WRKY33和BT2),根据其在4 min的表达情况进行进一步研究。采用实时定量聚合酶链反应(PCR) RT-qPCR验证芯片数据中的表达。获得含有T-DNA插入基因的拟南芥株系种子,进行纯合育种,并对突变体进行GPS表型分析。突变体分析表明,突变体与野生型在花序茎的弯曲度上存在显著差异。
Microarray Identifies Transcription Factors Potentially Involved in Gravitropic Signal Transduction in Arabidopsis
ABSTRACT Gravity is a fundamental stimulus that affects plant growth and development. The gravity persistent signal (GPS) treatment uses a cold treatment to isolate the events of signal transduction. Plants are reoriented horizontally in the dark at 4°C for 1 hour and then returned to vertical at room temperature. A gene expression microarray was designed to identify genes that are regulated during the GPS treatment. Arabidopsis thaliana var. Columbia was grown to maturity with inflorescence stems of 8-10 cm. Total mRNA was collected from inflorescence stems at 2, 4, 10, and 30 min after reorientation in the cold. cDNA was synthesized from the mRNA and then probed against an Arabidopsis gene expression array with 4 replicates per time point. Analyses presented here focus on transcription factors because of their regulatory functions in response pathways. Five transcription factors (AtAIB, WRKY18, WRKY26, WRKY33, and BT2) were selected for further study based on their expression at 4 min. Quantitative real-time polymerase chain reaction ((PCR) RT-qPCR) was performed to confirm expression seen in the microarray data. Seeds of Arabidopsis lines containing T-DNA insertions in the genes were obtained, plants bred to homozygosity, and the mutants analyzed for GPS phenotype. Mutant analysis shows significant differences in curvature of inflorescence stems between mutants and wild type.