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首页> 外文期刊>Plant Molecular Biology >A phosphate-starvation inducible beta-glucosidase gene (psr3.2) isolated from Arabidopsis thaliana is a member of a distinct subfamily of the BGA family.
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A phosphate-starvation inducible beta-glucosidase gene (psr3.2) isolated from Arabidopsis thaliana is a member of a distinct subfamily of the BGA family.

机译:从拟南芥中分离的磷酸饥饿诱导β-葡萄糖苷酶基因(psr3.2)是BGA家族一个独特的亚家族的成员。

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摘要

A phosphate starvation-response (psr) cDNA clone, psr3.1, which encodes a beta-glucosidase has been previously isolated from Brassica nigra. Southern blots of Arabidopsis thaliana genomic DNA probed with the psr3.1 cDNA indicated that this gene exists as a single locus. A genomic library of A. thaliana was screened at high stringency to isolate the corresponding genomic clone. The resultant clone was designated psr3.2 because of its sequence divergence from isolated psr3.1 cDNA clones. Northern blotting with probes derived from the coding region of the genomic clone showed that this gene is expressed at high levels in Pi-starved roots and the enhancement occurred within two days of growth in medium lacking Pi. The expression of this gene is repressed by heat shock and anaerobic conditions, and it is not significantly induced by high salinity, or by nitrogen or sulfur deprivation. Sequence analysis of the genomic clone revealed the existence of 13 exons interrupted by 12 AT-rich introns and it possessed a high homology with the B. nigra psr3.1 as well as various other beta-glucosidase genes from other species. Sequence similarity and divergence percentages between the deduced amino acid sequences of the psr3 clones and other beta-glycosidases suggests that they should be included along with two other Brassicaceae genes in a distinct subfamily of the BGA glycosidase gene family. The presence of an endoplasmic reticulum retention signal at the carboxy terminus indicates the likely cellular location of PSR3.2. The possible metabolic and regulatory roles of this enzyme during the Pi-starvation response are discussed.
机译:先前已从黑芸苔中分离出编码β-葡糖苷酶的磷酸饥饿响应(psr)cDNA克隆psr3.1。用psr3.1 cDNA探测的拟南芥基因组DNA的Southern印迹表明该基因以单个位点存在。高严格度筛选拟南芥的基因组文库以分离相应的基因组克隆。由于所得克隆与分离的psr3.1 cDNA克隆序列不同,因此命名为psr3.2。用来自基因组克隆的编码区的探针进行的RNA印迹显示,该基因在缺乏Pi的根中高水平表达,并且增强在缺乏Pi的培养基中生长两天内发生。该基因的表达受热休克和厌氧条件的抑制,并且没有被高盐度或氮或硫的剥夺显着诱导。基因组克隆的序列分析显示存在被12个富含AT的内含子打断的13个外显子,它与黑芽孢杆菌psr3.1以及其他物种的其他各种β-葡萄糖苷酶基因具有高度同源性。 psr3克隆的推导氨基酸序列与其他β-糖苷酶之间的序列相似性和差异百分比表明,它们应与BGA糖苷酶基因家族的一个不同亚家族中的其他两个十字花科基因一起包括在内。羧基末端存在内质网保留信号表明PSR3.2可能位于细胞内。讨论了该酶在Pi饥饿反应中可能的代谢和调节作用。

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