کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
2035142 1072142 2015 12 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Ribosome Excursions during mRNA Translocation Mediate Broad Branching of Frameshift Pathways
موضوعات مرتبط
علوم زیستی و بیوفناوری بیوشیمی، ژنتیک و زیست شناسی مولکولی بیوشیمی، ژنتیک و زیست شناسی مولکولی (عمومی)
پیش نمایش صفحه اول مقاله
Ribosome Excursions during mRNA Translocation Mediate Broad Branching of Frameshift Pathways
چکیده انگلیسی


• Ribosome translocation excursions occur before adopting a frame to resume translation
• Ribosomes achieve −1, −4, and +2 nt slips to enter the −1 frame on the mRNA
• Ribosomes frameshift not from one specific codon but from a range of codon positions
• The presence of incomplete translation products underscores fidelity maintenance

SummaryProgrammed ribosomal frameshifting produces alternative proteins from a single transcript. −1 frameshifting occurs on Escherichia coli’s dnaX mRNA containing a slippery sequence AAAAAAG and peripheral mRNA structural barriers. Here, we reveal hidden aspects of the frameshifting process, including its exact location on the mRNA and its timing within the translation cycle. Mass spectrometry of translated products shows that ribosomes enter the −1 frame from not one specific codon but various codons along the slippery sequence and slip by not just −1 but also −4 or +2 nucleotides. Single-ribosome translation trajectories detect distinctive codon-scale fluctuations in ribosome-mRNA displacement across the slippery sequence, representing multiple ribosomal translocation attempts during frameshifting. Flanking mRNA structural barriers mechanically stimulate the ribosome to undergo back-and-forth translocation excursions, broadly exploring reading frames. Both experiments reveal aborted translation around mutant slippery sequences, indicating that subsequent fidelity checks on newly adopted codon position base pairings lead to either resumed translation or early termination.

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ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: - Volume 160, Issue 5, 26 February 2015, Pages 870–881
نویسندگان
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