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非质体SAC结构域蛋白突变导致拟南芥叶绿体ATP合酶的缓慢暗失活。

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

作者信息

Gong Ping, Wu Guosheng, Ort Donald R

机构信息

Department of Plant Biology, University of Illinois, 190 ERML, Urbana, IL 61801, USA.

出版信息

Photosynth Res. 2006 May;88(2):133-42. doi: 10.1007/s11120-006-9041-4. Epub 2006 Feb 2.

Abstract

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.

摘要

偶联因子缓慢恢复(cfs)是拟南芥的一个隐性突变体,具有异常的ATP合酶激活/失活特性以及独特的生长表型。该突变体最显著的特征是,相对于野生型,ATP合酶在暗适应下的失活非常缓慢,这表明其对ATP合酶调节存在干扰。通过物理定位,该突变被限定在一对细菌人工染色体克隆的一个区域内。对位于该区域的所有34个推定基因的T-DNA插入系进行检测,鉴定出同一基因At3g59770的两个纯合T-DNA插入系,其表型与cfs突变体无法区分。At3g59770此前被鉴定为肌动蛋白9(SAC9)的抑制因子,SAC9是一种具有SAC结构域的蛋白质,该结构域是一种蛋白质-蛋白质相互作用模块,包含两个保守的色氨酸,即WW结构域,以及一个ATP/GTP结合位点基序A。对cfs的序列分析显示,一个从G到A的点突变导致氨基酸从色氨酸替换为终止密码子,从而编码一种截短的蛋白质。对基因特异性片段进行实时PCR扩增表明,T-DNA突变体没有全长转录本,而cfs突变体转录出全长的突变转录本。通过RT-PCR对野生型植物不同组织中SAC9 RNA表达水平进行进一步研究,结果显示在叶片中表达最高。SAC9功能障碍可能通过改变磷酸肌醇信号传导诱导应激模拟反应来干扰ATP合酶的失活。

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