نتایج جستجو برای: ribosome rescue

تعداد نتایج: 45218  

Journal: :Philosophical transactions of the Royal Society of London. Series B, Biological sciences 2017
Allen R Buskirk Rachel Green

Ribosomes translate genetic information into polypeptides in several basic steps: initiation, elongation, termination and recycling. When ribosomes are arrested during elongation or termination, the cell's capacity for protein synthesis is reduced. There are numerous quality control systems in place to distinguish between paused ribosomes that need some extra input to proceed and terminally sta...

2014
Hiroyuki Kogure Yoshihiro Handa Masahiro Nagata Naoto Kanai Peter Güntert Kenji Kubota Nobukazu Nameki

The YaeJ protein is a codon-independent release factor with peptidyl-tRNA hydrolysis (PTH) activity, and functions as a stalled-ribosome rescue factor in Escherichia coli. To identify residues required for YaeJ function, we performed mutational analysis for in vitro PTH activity towards rescue of ribosomes stalled on a non-stop mRNA, and for ribosome-binding efficiency. We focused on residues c...

Journal: :Journal of molecular biology 2012
Serafín Vivanco-Domínguez José Bueno-Martínez Gloria León-Avila Nobuhiro Iwakura Akira Kaji Hideko Kaji Gabriel Guarneros

During translation, ribosomes stall on mRNA when the aminoacyl-tRNA to be read is not readily available. The stalled ribosomes are deleterious to the cell and should be rescued to maintain its viability. To investigate the contribution of some of the cellular translation factors on ribosome rescuing, we provoked stalling at AGA codons in mutants that affected the factors and then analyzed the a...

Journal: :Mechanisms of Development 2009
Valeria Pappas Stephen M. Miller

The Zuotin-family J protein chaperone GlsA is essential for the asymmetric divisions that establish germ and somatic cell initials during embryogenesis in the green alga Volvox carteri, but it is not known on what cellular process GlsA acts to carry out this function. Most GlsA protein is nuclear, and GlsA possesses two SANT domains, suggesting that GlsA may function as a transcriptional regula...

2014
Zofia Maria Chrzanowska-Lightowlers Robert Neil Lightowlers Nils-Göran Larsson

Release factors (RFs) govern the termination phase of protein synthesis. Human mitochondria harbor four different members of the class 1 RF family: RF1Lmt/mtRF1a, RF1mt, C12orf65 and ICT1. The homolog of the essential ICT1 factor is widely distributed in bacteria and organelles and has the peculiar feature in human mitochondria to be part of the ribosome as a ribosomal protein of the large subu...

Journal: :Genes & genetic systems 2011
Yuhei Chadani Emi Matsumoto Hiroaki Aso Takeo Wada Kazuhiro Kutsukake Shizuyo Sutou Tatsuhiko Abo

Ribosomes translating mRNA without an in-frame stop codon (non-stop mRNA) stall at its 3' end. In eubacteria, such ribosomes are rescued by SsrA-mediated trans-translation. Recently, we have shown that Escherichia coli ArfA (formerly YhdL) also rescues stalled ribosomes by a mechanism distinct from that of trans-translation. Synthetic lethality phenotype of ssrA arfA double mutants suggests tha...

2017
Nicholas R Guydosh Philipp Kimmig Peter Walter Rachel Green

The unfolded protein response (UPR) monitors and adjusts the protein folding capacity of the endoplasmic reticulum (ER). In S. pombe, the ER membrane-resident kinase/endoribonuclease Ire1 utilizes a mechanism of selective degradation of ER-bound mRNAs (RIDD) to maintain homeostasis. We used a genetic screen to identify factors critical to the Ire1-mediated UPR and found several proteins, Dom34,...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 2012
Georgina Cox Gary S Thompson Huw T Jenkins Frank Peske Andreas Savelsbergh Marina V Rodnina Wolfgang Wintermeyer Steve W Homans Thomas A Edwards Alexander J O'Neill

Resistance to the antibiotic fusidic acid (FA) in the human pathogen Staphylococcus aureus usually results from expression of FusB-type proteins (FusB or FusC). These proteins bind to elongation factor G (EF-G), the target of FA, and rescue translation from FA-mediated inhibition by an unknown mechanism. Here we show that the FusB family are two-domain metalloproteins, the C-terminal domain of ...

نمودار تعداد نتایج جستجو در هر سال

با کلیک روی نمودار نتایج را به سال انتشار فیلتر کنید