Evidence map›Paper›PMID 39187487›Full record

ArticleNature communications2024

Calibrated ribosome profiling assesses the dynamics of ribosomal flux on transcripts.

Kotaro Tomuro, Mari Mito, Hirotaka Toh, Naohiro Kawamoto, Takahito Miyake, Siu Yu A Chow, Masao Doi, Yoshiho Ikeuchi, Yuichi Shichino, Shintaro Iwasaki

Abstract read
In one paragraph

Article in Nature communications, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

19 citing papers in PubMed.

  1. Review
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  10. Article
  11. Article
  12. Detection and Characterization of the Eukaryotic Vacant Ribosome.International journal of molecular sciences · 2025
    Review
  13. Article
  14. Advances in ribosome profiling technologies.Biochemical Society transactions · 2025
    Review
  15. Review
  16. Article
  17. Review
  18. Article
  19. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors.

Kotaro Tomuro *RNA Systems Biochemistry Laboratory, RIKEN Cluster for Pioneering Research, Wako, Saitama, 351-0198, Japan.ORCID 0009-0008-3513-4507
Mari Mito *RNA Systems Biochemistry Laboratory, RIKEN Cluster for Pioneering Research, Wako, Saitama, 351-0198, Japan.
Hirotaka TohRNA Systems Biochemistry Laboratory, RIKEN Cluster for Pioneering Research, Wako, Saitama, 351-0198, Japan.ORCID 0000-0003-0753-0787
Naohiro KawamotoRNA Systems Biochemistry Laboratory, RIKEN Cluster for Pioneering Research, Wako, Saitama, 351-0198, Japan.ORCID 0000-0003-4252-0963
Takahito MiyakeDepartment of Systems Biology, Graduate School of Pharmaceutical Sciences, Kyoto University, Sakyō-ku, Kyoto, 606-8501, Japan.ORCID 0000-0002-4356-5883
Siu Yu A ChowInstitute of Industrial Science, The University of Tokyo, Meguro-ku, Tokyo, 153-8505, Japan.
Masao DoiDepartment of Systems Biology, Graduate School of Pharmaceutical Sciences, Kyoto University, Sakyō-ku, Kyoto, 606-8501, Japan.ORCID 0000-0001-6264-9217
Yoshiho IkeuchiInstitute of Industrial Science, The University of Tokyo, Meguro-ku, Tokyo, 153-8505, Japan.ORCID 0000-0002-2829-3840
Yuichi ShichinoRNA Systems Biochemistry Laboratory, RIKEN Cluster for Pioneering Research, Wako, Saitama, 351-0198, Japan. yuichi.shichino@riken.jp.ORCID 0000-0002-0093-1185
Shintaro IwasakiRNA Systems Biochemistry Laboratory, RIKEN Cluster for Pioneering Research, Wako, Saitama, 351-0198, Japan. shintaro.iwasaki@riken.jp.ORCID 0000-0001-7724-3754

Funding

Pacific Biosciences PacBio RS Single Molecule Real Time SequencerS10OD018174 · OD · UNIVERSITY OF CALIFORNIA BERKELEY · PI ROKHSAR, DANIEL SOLEYMAN · 2014 to 2014
$600k
Japan Agency for Medical Research and Development (AMED) JP20gm1410001Japan Agency for Medical Research and Development (AMED) JP22fk0108570Japan Agency for Medical Research and Development (AMED) JP23gm6910005MEXT | Japan Science and Technology Agency (JST) JPMJBS2418MEXT | Japan Science and Technology Agency (JST) JPMJFR226FMEXT | Japan Society for the Promotion of Science (JSPS) JP21K15023MEXT | Japan Society for the Promotion of Science (JSPS) JP22K20765MEXT | Japan Society for the Promotion of Science (JSPS) JP23H00095MEXT | Japan Society for the Promotion of Science (JSPS) JP23H02415MEXT | Japan Society for the Promotion of Science (JSPS) JP23K05648MEXT | Japan Society for the Promotion of Science (JSPS) JP23K14173MEXT | Japan Society for the Promotion of Science (JSPS) JP23KJ2175MEXT | Japan Society for the Promotion of Science (JSPS) JP23KJ2178MEXT | RIKEN Pioneering ProjectMEXT | RIKEN RIKEN TRIP initiative "TRIP-AGIS"Ministry of Education, Culture, Sports, Science and Technology (MEXT) JP20H05782Ministry of Education, Culture, Sports, Science and Technology (MEXT) JP20H05784Ministry of Education, Culture, Sports, Science and Technology (MEXT) JP20H05786Ministry of Education, Culture, Sports, Science and Technology (MEXT) JP21H05734Ministry of Education, Culture, Sports, Science and Technology (MEXT) JP23H04268Ministry of Education, Culture, Sports, Science and Technology (MEXT) JP24H02306Ministry of Education, Culture, Sports, Science and Technology (MEXT) JP24H02307NIH HHS S10 OD018174
6 · The paper itself

Abstract

Ribosome profiling, which is based on deep sequencing of ribosome footprints, has served as a powerful tool for elucidating the regulatory mechanism of protein synthesis. However, the current method has substantial issues: contamination by rRNAs and the lack of appropriate methods to measure ribosome numbers in transcripts. Here, we overcome these hurdles through the development of "Ribo-FilterOut", which is based on the separation of footprints from ribosome subunits by ultrafiltration, and "Ribo-Calibration", which relies on external spike-ins of stoichiometrically defined mRNA-ribosome complexes. A combination of these approaches estimates the number of ribosomes on a transcript, the translation initiation rate, and the overall number of translation events before its decay, all in a genome-wide manner. Moreover, our method reveals the allocation of ribosomes under heat shock stress, during aging, and across cell types. Our strategy of modified ribosome profiling measures kinetic and stoichiometric parameters of cellular translation across the transcriptome.

Indexed as

Protein BiosynthesisRibosomesRNA, MessengerCalibrationHeat-Shock ResponseHigh-Throughput Nucleotide SequencingHumansRibosome ProfilingRNA, RibosomalTranscriptomeRNA, MessengerRNA, Ribosomal

Identifiers

PMID39187487
PMCPMC11347596

What OpenQuestion holds

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LicenceCC BY-NC-ND
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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.