首页    期刊浏览 2025年02月17日 星期一
登录注册

文章基本信息

  • 标题:Author Correction: Loss of mRNA surveillance pathways results in widespread protein aggregation
  • 本地全文:下载
  • 作者:Nur Hidayah Jamar ; Paraskevi Kritsiligkou ; Chris M. Grant
  • 期刊名称:Scientific Reports
  • 电子版ISSN:2045-2322
  • 出版年度:2021
  • 卷号:11
  • DOI:10.1038/s41598-021-95596-1
  • 语种:English
  • 出版社:Springer Nature
  • 摘要:Correction to: Scientific Reports 10.1038/s41598-018-22183-2 published online 01 March 2018 The original version of this Article contained errors. Panels upf1 and dom34 in Figure  1 looked to have originated from the same sample. The Authors now reviewed the original data and for clarity all representative images in Figure  1 have been replaced. Additionally, the Authors recalculated the results shown in Figure  1B using the original data and the graph has also been updated. The original Figure  1 is shown below, for reference: Figure 1 Strains lacking components of mRNA surveillance pathways have higher levels of protein aggregation. ( A) Hsp104-RFP was visualized in wild-type and mutant strains disrupted for NGD ( dom34, hbs1), NMD ( upf1, upf2), NSD ( ski7) and the Ski complex ( ski8). Examples of cells containing visible puncta are shown. ( B) The percentage of cells containing visible Hsp104-RFP puncta is quantified for each strain. Data shown are the means of three independent biological repeat experiments ± SD. Significance is shown compared with the wild-type strain; *** p  < 0.001. ( C) Western blot analysis of Hsp104 protein levels. Blots were probed with a Pgk1 antibody as a loading control. The full blots are shown in Supplementary Fig. 1. The original version of the Article has been corrected.
国家哲学社会科学文献中心版权所有