VLDB 2026 Research / reviewers in the wild / expert
Jonathan S. Weissman
dblp:130/7302
· DBLP profile ↗
1ranked-venue papers
0as first author
0since 2021 · last 2013
0000-0003-2445-670XORCID · verified
Domains — the database's venue-derived domains; a paper can count in several
Applied, interdisciplinary, general and emerging computing · 1
Expertise — from the expertise taxonomy: the topics of the expert's papers under the CCF categories. A weight counts papers with recency: 1 for a paper about the topic, 0.3 when the topic is its context, halved every five years.
| Interdisciplinary, comprehensive, and emerging computing
1 paper |
Bioinformatics and computational biology · 100% |
Topics — the 2 heaviest of 2, each with the papers that count most for it
| Topic | Weight | Papers | Last | Evidence papers |
|---|---|---|---|---|
Bioinformatics and computational biology › transcriptomics
ribosome profiling |
0.2 | 1 | 2013 | rRNA: mRNA pairing alters the length and the symmetry of mRNA-protected fragments in ribosome profiling experiments · Bioinform. 2013 |
Bioinformatics and computational biology › RNA biology
translation |
0.2 | 1 | 2013 | rRNA: mRNA pairing alters the length and the symmetry of mRNA-protected fragments in ribosome profiling experiments · Bioinform. 2013 |
Methods — techniques the papers use, named apart from their topics
statistical modeling · 0.2
| Year | Publication | Venue | Position |
|---|---|---|---|
| 2013 | rRNA: mRNA pairing alters the length and the symmetry of mRNA-protected fragments in ribosome profiling experimentsabstractMOTIVATION: Ribosome profiling is a new technique that allows monitoring locations of translating ribosomes on mRNA at a whole transcriptome level. A recent ribosome profiling study demonstrated that internal Shine-Dalgarno (SD) sequences have a major global effect on translation rates in bacteria: ribosomes pause at SD sites in mRNA. Therefore, it is important to understand how SD sites effect mRNA movement through the ribosome and generation of ribosome footprints. RESULTS: Here, we provide evidence that in addition to pausing effect, internal SD sequences induce a caterpillar-like movement of mRNA through the ribosome cavity. Once an SD site binds to the ribosome, it remains attached to it while the ribosome decodes a few subsequent codons. This leads to asymmetric progressive elongation of ribosome footprints at the 3'-end. It is likely that internal SD sequences induce a pause not on a single, but on several adjacent codons. This finding is important for our understanding of mRNA movement through the ribosome and also should facilitate interpretation of ribosome profiling data. Patrick B. F. O'Connor, Gene-Wei Li, Jonathan S. Weissman, John F. Atkins, Pavel V. Baranov |
Bioinform. | 3 |