农业科学与技术(英文版)
農業科學與技術(英文版)
농업과학여기술(영문판)
Agricultural Science & Technology
2015年
10期
2197-2201,2237
,共6页
于二汝%李小冬%舒健虹%吴佳海%王小利
于二汝%李小鼕%舒健虹%吳佳海%王小利
우이여%리소동%서건홍%오가해%왕소리
高羊茅%SRP基因%克隆%表达分析
高羊茅%SRP基因%剋隆%錶達分析
고양모%SRP기인%극륭%표체분석
Festuca arundinacea%SRP gene%Cloning%Expression analysis
[目的]了解高羊茅 SRP基因结构与功能以及在多种逆境胁迫下的表达变化。[方法]以高羊茅转录组学测序获得的 SRP序列为基础,从高羊茅叶片 cDNA中应用3’ RACE和5’RACE方法扩增出 SRP基因全长 cDNA序列。[结果] SRP基因 cDNA全长为1165 bp,具有一个完整的长度为855 bp的开放阅读框,编码蛋白为284个氨基酸,包含一个REF结构域。通过生物信息学的方法预测SRP基因的结构及功能发现, FaSRP与单子叶植物 SRP蛋白具有相对较高的序列同源性。应用荧光定量 PCR技术分析了 SRP基因在低氮、干旱、高热以及高盐逆境胁迫下的表达变化发现 SRP基因能够应答低氮、干旱、高温等胁迫,但应答机制不一样,可能是通过不同途径调节植物抗逆性,FaSRP对高盐胁迫不敏感。[结论]该研究为培育抗旱、耐热、营养高效的高羊茅品种提供候选基因与技术储备。
[目的]瞭解高羊茅 SRP基因結構與功能以及在多種逆境脅迫下的錶達變化。[方法]以高羊茅轉錄組學測序穫得的 SRP序列為基礎,從高羊茅葉片 cDNA中應用3’ RACE和5’RACE方法擴增齣 SRP基因全長 cDNA序列。[結果] SRP基因 cDNA全長為1165 bp,具有一箇完整的長度為855 bp的開放閱讀框,編碼蛋白為284箇氨基痠,包含一箇REF結構域。通過生物信息學的方法預測SRP基因的結構及功能髮現, FaSRP與單子葉植物 SRP蛋白具有相對較高的序列同源性。應用熒光定量 PCR技術分析瞭 SRP基因在低氮、榦旱、高熱以及高鹽逆境脅迫下的錶達變化髮現 SRP基因能夠應答低氮、榦旱、高溫等脅迫,但應答機製不一樣,可能是通過不同途徑調節植物抗逆性,FaSRP對高鹽脅迫不敏感。[結論]該研究為培育抗旱、耐熱、營養高效的高羊茅品種提供候選基因與技術儲備。
[목적]료해고양모 SRP기인결구여공능이급재다충역경협박하적표체변화。[방법]이고양모전록조학측서획득적 SRP서렬위기출,종고양모협편 cDNA중응용3’ RACE화5’RACE방법확증출 SRP기인전장 cDNA서렬。[결과] SRP기인 cDNA전장위1165 bp,구유일개완정적장도위855 bp적개방열독광,편마단백위284개안기산,포함일개REF결구역。통과생물신식학적방법예측SRP기인적결구급공능발현, FaSRP여단자협식물 SRP단백구유상대교고적서렬동원성。응용형광정량 PCR기술분석료 SRP기인재저담、간한、고열이급고염역경협박하적표체변화발현 SRP기인능구응답저담、간한、고온등협박,단응답궤제불일양,가능시통과불동도경조절식물항역성,FaSRP대고염협박불민감。[결론]해연구위배육항한、내열、영양고효적고양모품충제공후선기인여기술저비。
Objective] This study aimed to study the structure and functions of SRP gene and variation in its expression under abiotic stresses. [Method] Using the SRP sequence obtained from transcriptome sequencing as the template, the ful-length cDNA sequence of SRP gene in Festuca arundinacea was amplified using the 3’RACE and 5’RACE methods. [Result] The cDNA sequence of SRP gene has a ful length of 1 165 bp, and it contains an open reading frame in ful length of 855 bp. The encoded protein by SRP gene is composed of 284 amino acids, and contains a REF domain. The bioinformatic researches on structures and functions of SRPs show that the SRP gene in Festuca arundinacea (FaSRP) has relatively high ho-mologies with SRP s in monocots. Under low nitrogen, drought, high temperature and high salt stresses, the variations in expression of FaSRP gene were studied using fluorescence quantitative PCR. The results showed that FaSRP gene makes responses to low nitrogen, drought and high temperature stresses, but the relevant response mechanisms are not the same, indicating different pathways regulating re-sistance of plants. The expression of FaSRP gene is insensitive to high salt stress. [Conclusion] This study wil provide certain candidate gene and technical reserve for breeding of drought- and high temperature-tolerant, nutritious and highly efficient Festuca arundinacea cultivars.