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Differential light regulated expression of nuclear genes encoding chloroplast and cytosolic glyceraldehyde-3-phosphate dehydrogenase in Nicotiana tabacum

机译:烟草中编码叶绿体和胞质甘油醛-3-磷酸脱氢酶的核基因的差异调光表达

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摘要

When tobacco (Nicotiana tabacum) plants were transferred from the dark to continuous white light, the steady-state mRNA levels transcribed from the nuclear genes encoding chloroplast (GapA and GapB) glyceraldehyde-3-phosphate dehydrogenase increased at least 30- to 50-fold, while the mRNA level for the cytosolic enzyme (GapC) increased only 10-fold. Kinetic analyses show that the rates of mRNA accumulation for GapA and GapB are identical reaching steady-state levels after 24-48 h in light. In contrast, mRNA accumulation for the GapC gene shows a completely different kinetic pattern, accumulating much faster than that of GapA and GapB. These results suggest that expression of GapC and GapA/B genes are controlled by different light regulated mechanisms and nuclear run-on analyses suggest that these effects are primarily due to increased transcription.
机译:当烟草(Nicotiana tabacum)植物从黑暗转移到连续白光时,从编码叶绿体(GapA和GapB)甘油醛-3-磷酸脱氢酶的核基因转录的稳态mRNA水平增加了至少30到50倍。 ,而胞质酶(GapC)的mRNA水平仅增加10倍。动力学分析表明,GapA和GapB的mRNA积累速率在光照24-48小时后达到稳态水平是相同的。相反,GapC基因的mRNA积累显示出完全不同的动力学模式,其积累速度远快于GapA和GapB。这些结果表明,GapC和GapA / B基因的表达受不同的光调节机制控制,核运行分析表明,这些作用主要是由于转录增加所致。

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