首页> 美国卫生研究院文献>Nucleic Acids Research >5 proximal sequences of a soybean ribulose-15-bisphosphate carboxylase small subunit gene direct light and phytochrome controlled transcription.
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5 proximal sequences of a soybean ribulose-15-bisphosphate carboxylase small subunit gene direct light and phytochrome controlled transcription.

机译:大豆核糖-15-二磷酸羧化酶小亚基基因的5近端序列指导光和植物色素控制的转录。

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摘要

Two closely related ribulose-1,5-bisphosphate carboxylase small subunit (SSU) genes, SRS1 and SRS4, are transcribed at high levels in soybean plants in response to light. Transgenic petunia plants containing 5' sequences from SRS1 or SRS4 fused to the polypeptide encoding region of a neomycin phosphotransferase (NPTII) gene exhibit selectable kanamycin resistance. Deletion of three ATG codons from the region preceding the normal NPTII translation start site has little effect on the levels of kanamycin resistance in transformed plants. Run-on transcription assays in isolated nuclei demonstrate that transcription of the SRS1/NPTII chimera and the native petunia SSU11A gene subfamily is light regulated and under phytochrome control in leaves of transgenic plants. In young expanding leaves of fully light grown plants, transcription of these genes is markedly reduced within minutes of far-red treatment, while ribosomal DNA and actin gene transcription remains unchanged. This is analogous to the transcriptional response we observed for SRS1 and SRS4 in soybean seedlings. These data suggest (1) that transcription of SSU genes in both soybean and petunia require the continued presence or synthesis of phytochrome in the Pfr form and (2) that 5' sequences are sufficient to direct the phytochrome controlled transcriptional response of the SRS1 gene. In fully expanded mature leaves we found the transcription rates of the native SSU11A gene subfamily, the chimeric SRS1/NPTII gene, the rDNA genes, and several other control genes to be reduced markedly after far-red treatment or after extended periods of darkness. The contrast between results in young and mature leaves is discussed.
机译:大豆中的两个紧密相关的核糖-1,5-二磷酸羧化酶小亚基(SSU)基因SRS1和SRS4在高光下转录。含有融合到新霉素磷酸转移酶(NPTII)基因的多肽编码区的SRS1或SRS4的5'序列的转基因矮牵牛植物表现出选择性的卡那霉素抗性。从正常NPTII翻译起始位点之前的区域删除三个ATG密码子对转化植物中卡那霉素抗性的水平影响很小。在分离的核中进行连续转录测定表明,SRS1 / NPTII嵌合体和天然矮牵牛SSU11A基因亚科的转录是光调节的,并且在转基因植物叶片中处于植物色素的控制之下。在完全光照生长的植物的年轻膨胀叶片中,这些基因的转录在远红外线处理后的数分钟内明显减少,而核糖体DNA和肌动蛋白基因的转录保持不变。这类似于我们在大豆幼苗中观察到的针对SRS1和SRS4的转录反应。这些数据表明(1)大豆和矮牵牛中SSU基因的转录需要Pfr形式的植物色素的持续存在或合成,以及(2)5'序列足以指导SRS1基因的植物色素控制的转录反应。在完全扩展的成熟叶片中,我们发现天然SSU11A基因亚家族,嵌合SRS1 / NPTII基因,rDNA基因和其他几个控制基因的转录速率在远红处理或长时间黑暗后均显着降低。讨论了幼叶和成熟叶片结果之间的对比。

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