首页> 外文学位 >Regulation of the cyanobacterialpsbA genes in response to light intensity: cis-regulatory elements and their interactions withtrans-acting factor(s).
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Regulation of the cyanobacterialpsbA genes in response to light intensity: cis-regulatory elements and their interactions withtrans-acting factor(s).

机译:蓝细菌对光强度的响应:顺式调控元件及其与反式作用因子的相互作用。

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摘要

Three psbA genes encoding the D1 protein of the photosystem II reaction center are differentially expressed under different light intensities in the cyanobacterium Synechococcus sp. strain PCC 7942. When light intensity is increased from 125 ;Soluble proteins from Synechococcus enriched for DNA-binding activity was demonstrated to specifically bind to the psbAII enhancer and high-light-responsive DNA sequences downstream of the transcription start site. In vivo, protein binding to the upstream region of psbAII was observed only in high-light exposed cell samples but not in those maintained at low light. When 12 bp from the psbAII protein binding sites were deleted, protein binding was impaired and high-light induction of both transcriptional and translational lacZ reporters was significantly reduced, indicating that the protein binding to this region is required for high-light-induced psbAII gene expression. The mutant element also showed impaired enhancer activity when combined with the heterologous E. coli conII promoter.
机译:编码光系统II反应中心D1蛋白的三个psbA基因在蓝藻Synechococcus sp。中以不同的光强度差异表达。菌株PCC7942。当光强度从125增加时,来自Synechococcus的富含DNA结合活性的可溶性蛋白被证明与psbAII增强子和转录起始位点下游的高光响应性DNA序列特异性结合。在体内,仅在暴露于高光的细胞样品中观察到了蛋白质与psbAII上游区域的结合,而在维持低光照的细胞样品中则未观察到。当从psbAII蛋白结合位点删除12 bp时,蛋白结合受到损害,转录和翻译lacZ报告基因的高光诱导均显着降低,这表明高光诱导的psbAII基因需要与该区域结合的蛋白表达。当与异源大肠杆菌conII启动子结合时,突变元件还显示出增强子活性受损。

著录项

  • 作者

    Li, Rixin.;

  • 作者单位

    Texas A&M University.;

  • 授予单位 Texas A&M University.;
  • 学科 Biology Molecular.;Biology Genetics.;Biology Microbiology.
  • 学位 Ph.D.
  • 年度 1994
  • 页码 102 p.
  • 总页数 102
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

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