...
首页> 外文期刊>Photosynthesis Research >Slow dark deactivation of Arabidopsis chloroplast ATP synthase caused by a mutation in a nonplastidic SAC domain protein
【24h】

Slow dark deactivation of Arabidopsis chloroplast ATP synthase caused by a mutation in a nonplastidic SAC domain protein

机译:非塑性SAC域蛋白突变引起的拟南芥叶绿体ATP合酶的缓慢暗灭活

获取原文
获取原文并翻译 | 示例
           

摘要

Coupling factor slow recovery (cfs) is a recessive mutant of Arabidopsis with anomalous ATP synthase activation/deactivation characteristics as well as a distinct growth phenotype. The most significant feature of this mutant is that the dark-adapted deactivation of ATP synthase is a very slow relative to the wild type, indicating interference with ATP synthase regulation. Physical mapping of the mutation delimited it to a region in a pair of bacterial artificial chromosome clones. Examination of T-DNA insertion lines of all 34 putative genes located in this region identified two homozygous T-DNA insertion lines of the same gene, At3g59770, possessing phenotypes indistinguishable from the cfs mutant. At3g59770 had been previously identified as suppressor of actin 9 (SAC9), a protein with a SAC domain, a protein–protein interaction module containing two conserved tryptophans known as a WW domain, and an ATP/GTP-binding site motif A. Sequence analysis of cfs revealed a point mutation of G to A resulting in an amino acid substitution from tryptophan to STOP, thereby coding a truncated protein. Real-time-PCR amplification of the gene specific fragments showed that the T-DNA mutants did not have full-length transcripts whereas the cfs mutant transcribed a full-length mutated transcript. Further investigation of SAC9 RNA expression levels in different tissues of wild-type plants by RT-PCR revealed the highest expression in leaves. SAC 9 dysfunction interferes with ATP synthase deactivation, possibly by an alteration in phosphoinositide signaling inducing a stress mimicry response.
机译:耦合因子缓慢恢复(cfs)是拟南芥的隐性突变体,具有异常的ATP合酶激活/失活特征以及独特的生长表型。该突变体最显着的特征是,暗适应性的ATP合酶失活相对于野生型而言非常缓慢,表明干扰了ATP合酶的调控。突变的物理作图将其限定在一对细菌人工染色体克隆中的一个区域。对位于该区域的所有34个推定基因的T-DNA插入线进行检查,鉴定出同一基因At3g59770的两条纯合T-DNA插入线,它们的表型与cfs突变体没有区别。 At3g59770先前已被鉴定为肌动蛋白9(SAC9)的抑制剂,它是具有SAC结构域的蛋白质,包含两个保守色氨酸的蛋白-蛋白质相互作用模块(称为WW域)和ATP / GTP结合位点基序A。序列分析cfs的图谱显示G点突变为A点,导致氨基酸从色氨酸取代为STOP,从而编码截短的蛋白质。基因特异性片段的实时PCR扩增表明,T-DNA突变体没有全长转录本,而cfs突变体转录了全长突变转录本。通过RT-PCR进一步研究野生型植物不同组织中SAC9 RNA的表达水平,发现其在叶片中的表达最高。 SAC 9功能障碍可能通过磷酸肌醇信号转导诱导应激模拟反应而干扰ATP合酶失活。

著录项

  • 来源
    《Photosynthesis Research》 |2006年第2期|133-142|共10页
  • 作者单位

    Department of Plant Biology University of Illinois;

    Department of Plant Biology University of Illinois;

    Department of Plant Biology University of IllinoisDepartment of Crop Science University of IllinoisInstitute for Genomic Biology University of IllinoisPhotosynthesis Research Unit United States Department of Agriculture Agricultural Research Service;

  • 收录信息
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

    ATP synthase; SAC;

    机译:ATP合酶;SAC;

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号