小麦谷氨酰胺合成酶前体Ⅱ基因的克隆与分析  被引量:4

Cloning and Analysis of Glutamine SynthaseⅡ Precursor in Triticum aestivum L.

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作  者:韩娜 葛荣朝[1] 赵宝存[1] 沈银柱[1] 黄占景[1] 

机构地区:[1]河北师范大学生命科学学院,河北石家庄050016

出  处:《作物学报》2006年第11期1756-1758,共3页Acta Agronomica Sinica

基  金:国家自然科学基金项目(30070471);河北省自然科学基金项目(C2005000164)

摘  要:采用RACE方法,从小麦耐盐突变体RH8706-49的转录产物中获得谷氨酰胺合成酶Ⅱ(GS2)前体基因的全长cDNA序列,共包含1 690 bp,其中ORF区1 284 bp,编码427氨基酸。该基因已提交GenBank(登录号:DQ103756)。经Blast比对,该基因与大麦、水稻、玉米GS2的同源性分别达94.6%、87.0%和90.4%。经Northern blotting分析,发现GS2基因在小麦耐盐突变体RH8706-49和其同属”一粒传”后代的敏盐突变体H8706-34中盐胁迫前后均有表达,但前者高于后者。盐胁迫后二者的表达量均有所下降,不过在敏盐突变体中下降的更为明显,说明GS2基因是盐抑制基因,属于转录水平上的调控,且与小麦耐盐性密切相关。In this study, we were cloned the sequence of glutamine synthoze 2 ( GS2 ) in the wheat salt-resistant mutant RH8706-49. It contains 1 690 bp and the coding sequence has 1 284 bp which can code 427 amino acid. We have submitted this gene to GenBank (Accession No. : QD103756). The coding area of GS2 in wheat showed 94.6%, 87.0% and 90.4% similarities with barley, rice and maize, respectively. The result of Northern blotting showed that GS2 expressed both in salt-resistant wheat RH8706-49 and salt-sensitive wheat H8706-34 which were the offsprings propagated by “One Seed” mutant. The expression of GS2 in RH8706-49 was obviously higher than that in H8706-34. The expression of GS2 was reduced by salt-stress, and the amount of GS2 reduced more in H8706-34. It is demonstrated that GS2 is a kind of salt-inhibitory gene and may be regulated at the transcription level.

关 键 词:耐盐 小麦 谷氨酰胺合成酶 RACE 基因克隆 

分 类 号:S512.1[农业科学—作物学]

 

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