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首页> 外文期刊>Plant Science: An International Journal of Experimental Plant Biology >A new cDNA encoding a xyloglucan endo-transglycosylase-related polypeptide (AtXTR8) preferentially expressed in seedling, root and stem of Arabidopsis thaliana.
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A new cDNA encoding a xyloglucan endo-transglycosylase-related polypeptide (AtXTR8) preferentially expressed in seedling, root and stem of Arabidopsis thaliana.

机译:编码木葡聚糖内转糖基化酶相关多肽(AtXTR8)的新cDNA优先在拟南芥的幼苗,根和茎中表达。

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摘要

A new cDNA clone (AtXTR8) encoding a xyloglucan endo-transglycosylase (XET)-related protein was isolated from an Arabidopsis thaliana germinating seed cDNA library using a differential screen. The predicted amino acid sequence displays only 38 to 42% amino acid identity with other members of the Arabidopsis XTR (XET-related) protein family, but shows 64% identity to a xyloglucan endo-transglycosylase enzyme (TmNXG1) expressed in nasturtium (Tropaeolum majus) germinating seeds. The AtXTR8 transciptsare expressed in germinating seeds as early as 24 h after imbibition, with the highest level of accumulation being reached at about 72 h. In adult plants, transcripts are mainly detected in roots and to a lower extent in inflorescence stems. During imbibition of the severely gibberellin-deficient ga1-3 mutant seeds, transcripts are detected only if exogenous gibberellins are supplied in the medium, suggesting that gibberellins are directly or indirectly required for AtXTR8 gene expression. Unlike otherXET genes such as TCH4, EXT and XTR3, which are rapidly activated by auxins in wild type Arabidopsis, the steady state level of AtXTR8 transcripts is not markedly increased by auxin treatment of 6-day-old seedlings. Phylogenetic analysis confirms that the XET and XTR protein sequences so far identified in various plant species can be divided into three groups; the Arabidopsis AtXTR8 protein, whose enzymatic activity has not yet been assessed, belongs to the least related group III.
机译:使用差异筛选从拟南芥发芽种子cDNA文库中分离出编码木糖葡聚糖内转糖基化酶(XET)相关蛋白的新cDNA克隆(AtXTR8)。预测的氨基酸序列与拟南芥XTR(XET相关)蛋白家族的其他成员仅显示38%至42%的氨基酸同一性,但与在金莲花(Tropaeolum majus)中表达的木葡聚糖内转糖苷酶(TmNXG1)显示64%的同一性)发芽种子。吸水后24 h内,AtXTR8转录表达的种子开始发芽,在约72 h达到最高积累水平。在成年植物中,转录本主要在根中检出,而在花序茎中检出率较低。在吸收严重赤霉素缺乏的ga1-3突变体种子期间,仅当在培养基中提供外源赤霉素时才检测到转录本,这表明赤霉素是AtXTR8基因表达直接或间接需要的。与其他XET基因(例如TCH4,EXT和XTR3)在野生型拟南芥中被生长素迅速激活的基因不同,通过生长素处理6天龄幼苗,AtXTR8转录本的稳态水平并未显着提高。系统发育分析证实,到目前为止,在各种植物中鉴定出的XET和XTR蛋白序列可分为三类。尚未评估其酶活性的拟南芥AtXTR8蛋白属于最不相关的III类。

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