跳轉至內容
Merck
  • Xrn1p acts at multiple steps in the budding-yeast RNAi pathway to enhance the efficiency of silencing.

Xrn1p acts at multiple steps in the budding-yeast RNAi pathway to enhance the efficiency of silencing.

Nucleic acids research (2020-06-06)
Matthew A Getz, David E Weinberg, Ines A Drinnenberg, Gerald R Fink, David P Bartel
摘要

RNA interference (RNAi) is a gene-silencing pathway that can play roles in viral defense, transposon silencing, heterochromatin formation and post-transcriptional gene silencing. Although absent from Saccharomyces cerevisiae, RNAi is present in other budding-yeast species, including Naumovozyma castellii, which have an unusual Dicer and a conventional Argonaute that are both required for gene silencing. To identify other factors that act in the budding-yeast pathway, we performed an unbiased genetic selection. This selection identified Xrn1p, the cytoplasmic 5'-to-3' exoribonuclease, as a cofactor of RNAi in budding yeast. Deletion of XRN1 impaired gene silencing in N. castellii, and this impaired silencing was attributable to multiple functions of Xrn1p, including affecting the composition of siRNA species in the cell, influencing the efficiency of siRNA loading into Argonaute, degradation of cleaved passenger strand and degradation of sliced target RNA.

材料
產品編號
品牌
產品描述

Sigma-Aldrich
抗HA抗体,小鼠单克隆抗体 小鼠抗, clone HA-7, purified from hybridoma cell culture
Millipore
EZview Red 抗-FLAG® M2 亲和凝胶, clone M2
Sigma-Aldrich
核糖核酸,转移 来源于面包酵母(酿酒酵母), buffered aqueous solution
Sigma-Aldrich
抗FLAG® BioM2单克隆抗体 小鼠抗, clone M2, purified immunoglobulin, buffered aqueous glycerol solution
Millipore
EZview Red 抗-HA 亲和凝胶