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首页> 外文期刊>Science China Life Sciences >TinII intron, an enhancer to affect the function of the cytoplasmic male sterility related gene T in Brassica juncea
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TinII intron, an enhancer to affect the function of the cytoplasmic male sterility related gene T in Brassica juncea

机译:TinII内含子,影响芥菜胞质雄性不育相关基因T功能的增强子

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The T gene, which was cloned from the mitochondria of tumorous stem mustard (Brassica juncea var. tumida), is a cytoplasmic male sterility (CMS)-related gene that can produce two transcripts, T1170 and T1243. The latter is transcribed with the uncleaved intron TinII. In our previous study, transgenic Arabidopsis thaliana plants over-expressing the T1243 transcript (OE-T1243) showed a severe male-sterile phenotype, whereas OE-T1170 plants did not. However, the functional mechanism of the T gene in B. Juncea remained unknown. In this study, microscopic analyses of paraffin sections of anthers confirmed that OE-T1243 plants did not produce normal pollen, whereas OE-T1170 plants did. We analyzed the transcription of 15 anther development-related genes and found that transcript levels of nozzle/sporocyteless and barely any meristem 1 and 2 were markedly lower in OE-T1243 plants than those in wild type, while the transcript levels of these genes in OE-T1170 plants were unchanged. To investigate the potential roles of TinII, we inserted the TinII sequence upstream of a minimal region (?60) of the cauliflower mosaic virus 35S promoter fused to the 5′ end of the β-glucuronidase (GUS) reporter gene. Analysis of the transgenic plants suggested that TinII acted as an enhancer to significantly increase GUS expression. The potential action mechanism is that the TinII intron acts as an enhancer to affect the function of the CMS-related gene T.
机译:从肿瘤茎芥菜(Brassica juncea var。tumida)的线粒体克隆的T基因是细胞质雄性不育(CMS)相关基因,可产生两个转录本,T1170和T1243。后者与未切割的内含子TinII转录。在我们先前的研究中,过表达T1243转录本(OE-T1243)的转基因拟南芥植物显示出严重的雄性不育表型,而OE-T1170植物没有。然而,在芥菜中T基因的功能机制仍然未知。在这项研究中,对花药石蜡切片的显微分析证实,OE-T1243植物不产生正常的花粉,而OE-T1170植物却产生。我们分析了15个与花药发育相关的基因的转录,发现OE-T1243植物中的无喷嘴/无孢子的和几乎没有分生组织1和2的转录水平显着低于野生型,而这些基因的转录水平在OE-T1243中-T1170植物没有变化。为了研究TinII的潜在作用,我们将TinII序列插入到与β-葡糖醛酸糖苷酶(GUS)报告基因5'末端融合的花椰菜花叶病毒35S启动子的最小区域(?60)的上游。对转基因植物的分析表明,TinII充当了显着增加GUS表达的增强子。潜在的作用机制是TinII内含子充当增强子,影响CMS相关基因T的功能。

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