西北植物学报
西北植物學報
서북식물학보
ACTA BOTANICA BOREALI-OCCIDENTALIA SINICA
2012年
7期
1295-1303
,共9页
水稻%Na+/H+逆向转运蛋白%启动子%C末端%非生物胁迫
水稻%Na+/H+逆嚮轉運蛋白%啟動子%C末耑%非生物脅迫
수도%Na+/H+역향전운단백%계동자%C말단%비생물협박
rice(Orvza sativa)%Na+/H+ antiporter%promoter%C-terminal%abiotic stress
为了解水稻Na+/H+逆向转运蛋白(OsNHX1)在植物应答非生物胁迫中的分子调控机制,采用RT-PCR方法克隆OsNHX1基因上游2000 bp的启动子序列,并通过基因枪轰击瞬时转化洋葱表皮细胞,检测不同非生物胁迫下启动子的活性和表达模式;同时,分别克隆全长和C末端缺失的OsNHX1基因,通过花序浸染法转化拟南芥,研究OsNHX1基因及其C末端的功能.结果显示:OsNHX1启动子受逆境胁迫诱导,在盐、干旱、脱落酸胁迫处理下GUS表达活性明显升高;过表达OsNHX1的转基因拟南芥中,种子萌发率、根长、丙二醛含量和相对含水量的测定结果均显示其胁迫耐受性得到改善,但过表达OsNHX1 C末端缺失基因对转基因植株的胁迫耐受性无明显影响.研究表明,Na+/H+逆向转运蛋白有助于提高植物耐盐性,且其C末端区域对该转运蛋白活性的发挥具有关键作用.
為瞭解水稻Na+/H+逆嚮轉運蛋白(OsNHX1)在植物應答非生物脅迫中的分子調控機製,採用RT-PCR方法剋隆OsNHX1基因上遊2000 bp的啟動子序列,併通過基因鎗轟擊瞬時轉化洋蔥錶皮細胞,檢測不同非生物脅迫下啟動子的活性和錶達模式;同時,分彆剋隆全長和C末耑缺失的OsNHX1基因,通過花序浸染法轉化擬南芥,研究OsNHX1基因及其C末耑的功能.結果顯示:OsNHX1啟動子受逆境脅迫誘導,在鹽、榦旱、脫落痠脅迫處理下GUS錶達活性明顯升高;過錶達OsNHX1的轉基因擬南芥中,種子萌髮率、根長、丙二醛含量和相對含水量的測定結果均顯示其脅迫耐受性得到改善,但過錶達OsNHX1 C末耑缺失基因對轉基因植株的脅迫耐受性無明顯影響.研究錶明,Na+/H+逆嚮轉運蛋白有助于提高植物耐鹽性,且其C末耑區域對該轉運蛋白活性的髮揮具有關鍵作用.
위료해수도Na+/H+역향전운단백(OsNHX1)재식물응답비생물협박중적분자조공궤제,채용RT-PCR방법극륭OsNHX1기인상유2000 bp적계동자서렬,병통과기인창굉격순시전화양총표피세포,검측불동비생물협박하계동자적활성화표체모식;동시,분별극륭전장화C말단결실적OsNHX1기인,통과화서침염법전화의남개,연구OsNHX1기인급기C말단적공능.결과현시:OsNHX1계동자수역경협박유도,재염、간한、탈락산협박처리하GUS표체활성명현승고;과표체OsNHX1적전기인의남개중,충자맹발솔、근장、병이철함량화상대함수량적측정결과균현시기협박내수성득도개선,단과표체OsNHX1 C말단결실기인대전기인식주적협박내수성무명현영향.연구표명,Na+/H+역향전운단백유조우제고식물내염성,차기C말단구역대해전운단백활성적발휘구유관건작용.
In order to understand the molecular regulative mechanism of rice (Oryza sativa ) Na+/H+ antiporter(OsNHX1) in plantresponse to abiotic stresses,a 2 000 bp upstream region of OsNHX1 gene was cloned and transformed into onion epidermal cells by particle bombardment to detect the promoter's activity and expression pattern under various abiotic stresses. Full length OsNHX1 and C-terminal truncated OsNHX1 (OsNHX1dC) gene were also cloned and transformed into Arabidopsis thaliana separately by floral dipping method to investigate the function of OsNHX1 C-terminal. The results showed that the OsNHX1 promoter was induced by abiotic stresses and the GUS activity
was enhanced significantly under salt, drought and ABA treatments. The assays of germination rate, root length, MDA and relative water content (RWC) exhibited that over-expression of OsNHX1 improved the salt and drought tolerance of transgenic plants,whereas no distinguishing difference was found between the OsNHX1dC transgenic and wild-type plants, suggesting that OsNHX1 contributed to an improved tolerance to salt stress in plants and the C-terminal tail was critical for the activity of Na+/H+ antiporter.