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首页> 外文期刊>Plant Science: An International Journal of Experimental Plant Biology >A Japanese plum alpha-L-arabinofuranosidase/beta-D-xylosidase gene is developmentally regulated by alternative splicing
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A Japanese plum alpha-L-arabinofuranosidase/beta-D-xylosidase gene is developmentally regulated by alternative splicing

机译:日本李子α-L-阿拉伯呋喃糖苷酶/β-D-木糖苷酶基因通过选择性剪接受到发育调控。

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A full-length cDNA clone named PsARF/XYL was obtained from Prunus salicina Lindl., and determined to encode a putative alpha-L-arabinofuranosidase/beta-D-xylosidase belonging to glycoside hydrolase (GH, EC 3.2.1.-) family 3. Two related PsARF/XYL cDNAs were amplified, one from a fully-spliced transcript (PsARF/XYLa) and another one from an intron-retained transcript (PsARF/XYLb). The protein deduced from PsARF/XYLb is a truncated peptide at C-terminus that conserves the active-site amino acid sequence. High levels of PsARF/XYLa and PsARF/XYLb transcripts are detectable in several plant tissues. PsARF/XYLb transcripts accumulate progressively during the phase of exponential fruit growth but they become barely noticeable during on-tree ripening, or after a 6-h exposure of preclimacteric full-size plums to ethylene. In contrast, PsARF/XYLa is expressed throughout fruit development, and transcript accumulation parallels the climacteric rise in ethylene production during ripening. PsARF/XYLa expression is strongly induced in preclimacteric full-size plums after a 6-h treatment with physiologically active concentrations of ethylene. These findings suggest that PsARF/XYL gene is post-transcriptionally regulated by alternative splicing during development and that ethylene may be involved in this regulation. The isolation of a partial cDNA clone, PsARF1, is also reported. It encodes a putative cell-wall alpha-L-arabinofuranosidase, and its transcription is rapidly inhibited by ethylene in mature green plums. (C) 2014 Elsevier Ireland Ltd. All rights reserved.
机译:从Prunus salicina Lindl。获得全长cDNA克隆,命名为PsARF / XYL,并确定其编码属于糖苷水解酶(GH,EC 3.2.1-)家族的推定的α-L-阿拉伯呋喃糖苷酶/β-D-木糖苷酶。 3.扩增了两个相关的PsARF / XYL cDNA,一个来自完全剪接的转录本(PsARF / XYLa),另一个来自内含子保留的转录本(PsARF / XYLb)。从PsARF / XYLb推导的蛋白质是C端的截短肽,保留了活性位点氨基酸序列。在几种植物组织中可检测到高水平的PsARF / XYLa和PsARF / XYLb转录物。 PsARF / XYLb转录本在指数果实生长阶段逐渐积累,但在树上成熟期间或将更年期前的全尺寸李子暴露于乙烯6小时后,它们几乎不显着。相反,PsARF / XYLa在整个果实发育过程中表达,并且转录产物的积累与成熟期间乙烯产量的更年期上升平行。在生理活性浓度的乙烯处理6小时后,在更年期前的全尺寸李子中强烈诱导PsARF / XYLa表达。这些发现表明,PsARF / XYL基因在发育过程中受到选择性剪接的转录后调控,乙烯可能参与了这种调控。还报道了部分cDNA克隆PsARF1的分离。它编码一种假定的细胞壁α-L-阿拉伯呋喃糖苷酶,其转录在成熟的青李中被乙烯迅速抑制。 (C)2014 Elsevier Ireland Ltd.保留所有权利。

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