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Changes in Accumulation and Synthesis of Transcripts Encoding Phycobilisome Components during Acclimation of Fremyella diplosiphon to Different Light Qualities

机译:复盖弗氏菌适应不同光质期间编码藻胆体成分的转录本积累和合成的变化

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摘要

We have used gene-specific DNA fragments as hybridization probes to quantitate the levels of transcripts encoding several phycobilisome polypeptides in the cyanobacterium Fremyella diplosiphon in response to changes in the light environment. While the levels of transcripts encoding allophycocyanin, the core linker polypeptide, and the constitutive phycocyanin subunits are similar in F. diplosiphon grown either in red or green light, the levels of other transcripts change dramatically. Transcripts encoding the inducible phycocyanin subunits are barely detected in green light-grown cells and very abundant in red light-grown cells, while the level of phycoerythrin mRNA is approximately 10-fold more in green than red light-grown cells. Quantitation of the phycoerythrin and inducible phycocyanin transcripts after transfer of cultures from green to red light and red to green light demonstrate that both increase rapidly upon exposure of cells to inductive illumination. The decrease in the phycoerythrin mRNA level in red light is much slower than the decline in the levels of the inducible phycocyanin transcripts in green light. Since the half-lives of the inducible phycocyanin and phycoerythrin transcripts do not change when F. diplosiphon is exposed to red or green illumination, the steady state levels of these mRNAs are primarily controlled by the rate of transcription. Therefore, the high level of phycoerythrin mRNA maintained for several hours after cultures are transferred from green to red illumination must result from continued transcription of the phycoerythrin gene set. Differences in expression from the phycoerythrin and inducible phycocyanin gene sets in response to light quality are discussed in terms of possible mechanisms involved in their regulation.
机译:我们已经使用了基因特异性的DNA片段作为杂交探针来定量编码蓝细菌弗雷米氏菌双歧双歧杆菌中几种藻胆体多肽的转录本水平,以响应光照环境的变化。尽管在红色或绿色光下生长的二倍体拟南芥中编码别藻蓝蛋白,核心接头多肽和组成型藻蓝蛋白亚基的转录本水平相似,但其他转录本的水平却发生了巨大变化。在绿光生长的细胞中几乎未检测到编码诱导型藻蓝蛋白亚基的转录物,在红光生长的细胞中含量非常丰富,而绿藻中的藻红蛋白mRNA的水平大约是红光生长细胞的十倍。在将培养物从绿光转移到红光以及从红光转移到绿光后,对藻红蛋白和可诱导性藻蓝蛋白转录本的定量表明,当细胞暴露于感应照明时,两者都会迅速增加。红光中藻红蛋白mRNA水平的下降比绿光中可诱导的藻蓝蛋白转录本水平的下降慢得多。由于当二倍抗镰刀菌暴露于红色或绿色光照下时,可诱导的藻蓝蛋白和藻红蛋白转录本的半衰期不会改变,因此这些mRNA的稳态水平主要受转录速率控制。因此,培养物从绿色向红色照明转移后,维持数小时的高水平藻红蛋白mRNA必须归因于藻红蛋白基因集的持续转录。根据它们调控的可能机制,讨论了藻红蛋白和诱导型藻蓝蛋白基因组在响应光质量方面的表达差异。

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