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Posttranscriptional gene silencing of gn1 in tobacco triggers accumulation of truncated gn1-derived RNA species.

机译:烟草中gn1的转录后基因沉默触发了gn1截短的RNA物种的积累。

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摘要

Posttranscriptional silencing of basic beta-1,3-glucanase genes in the tobacco line T17 is manifested by reduced transcript levels of the gn1 transgene and homologous, endogenous basic beta-1,3-glucanase genes. An RNA ligation-mediated rapid amplification of cDNA ends (RLM-RACE) technique was used to compare the 3' termini of gn1 RNAs present in expressing (hemizygous and young homozygous) and silenced (mature homozygous) T17 plants. Full-length, polyadenylated gn1 transcripts primarily accumulated in expressing plants, whereas in silenced T17 plants, mainly 3'-truncated, nonpolyadenylated gn1 RNAs were detected. The relative abundance of these 3'-truncated gn1 RNA species gradually increased during the establishment of silencing in homozygous T17 plants. Similar 3'-truncated, nonpolyadenylated gn1 RNA products were observed in an independent case of beta-1,3-glucanase posttranscriptional gene silencing. This suggests that these 3'-truncated gn1 RNAs are a general feature of tobacco plants showing posttranscriptional silencing of the gn1 transgene.
机译:烟草品系T17中基本β-1,3-葡聚糖酶基因的转录后沉默表现为gn1转基因和同源内源性基本β-1,3-葡聚糖酶基因的转录水平降低。 RNA连接介导的cDNA末端快速扩增(RLM-RACE)技术用于比较gn1 RNA的3'末端存在于表达(杂合和年轻纯合)和沉默(成熟纯合)的T17植物中。全长聚腺苷酸gn1转录物主要在表达植物中积累,而在沉默的T17植物中,主要检测到3'截短的非聚腺苷酸gn1 RNA。这些3'截断的gn1 RNA种类的相对丰度在纯合T17植物中建立沉默期间逐渐增加。在独立的β-1,3-葡聚糖酶转录后基因沉默案例中,观察到了类似的3'截短的,非聚腺苷酸的gn1 RNA产物。这表明这些3'截短的gn1 RNA是烟草植物的一般特征,显示gn1转基因的转录后沉默。

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