Evidence map›Paper›PMID 25078267›Full record

ArticlePLoS genetics2014

The coding and noncoding architecture of the Caulobacter crescentus genome.

Jared M Schrader, Bo Zhou, Gene-Wei Li, Keren Lasker, W Seth Childers, Brandon Williams, Tao Long, Sean Crosson, Harley H McAdams, Jonathan S Weissman and 1 more

Abstract read
In one paragraph

Article in PLoS genetics, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 95 papers.

0numbers the graph read from it
0cells of the map it votes in
95citing 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

95 citing papers in PubMed.

  1. Article
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  8. Molecular biology of the cell · 2024
    Article
  9. Article
  10. bioRxiv : the preprint server for biology · 2023
    Article
  11. Article
  12. Article
  13. Article
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  15. Article
  16. Article
  17. Review
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  19. Review
  20. Article

35 more citing papers are in PubMed but not listed here.

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

11 authors.

Jared M SchraderDepartment of Developmental Biology, Stanford University, Stanford, California, United States of America.
Bo ZhouDepartment of Developmental Biology, Stanford University, Stanford, California, United States of America.
Gene-Wei LiDepartment of Cellular and Molecular Pharmacology, California Institute of Quantitative Biology, Center for RNA Systems Biology, Howard Hughes Medical Institute, University of California, San Francisco, San Francisco, California, United States of America.
Keren LaskerDepartment of Developmental Biology, Stanford University, Stanford, California, United States of America.
W Seth ChildersDepartment of Developmental Biology, Stanford University, Stanford, California, United States of America.
Brandon WilliamsDepartment of Developmental Biology, Stanford University, Stanford, California, United States of America.
Tao LongDepartment of Developmental Biology, Stanford University, Stanford, California, United States of America.
Sean CrossonDepartment of Biochemistry and Molecular Biology, University of Chicago, Chicago, Illinois, United States of America.
Harley H McAdamsDepartment of Developmental Biology, Stanford University, Stanford, California, United States of America.
Jonathan S WeissmanDepartment of Cellular and Molecular Pharmacology, California Institute of Quantitative Biology, Center for RNA Systems Biology, Howard Hughes Medical Institute, University of California, San Francisco, San Francisco, California, United States of America.
Lucy ShapiroDepartment of Developmental Biology, Stanford University, Stanford, California, United States of America.

Funding

INSTITUTIONAL TRAINING GRANT IN GENOME SCIENCET32HG000044 · NHGRI · STANFORD UNIVERSITY · PI MICHAEL P. SNYDER · 1995 to 2026
$32.2M
Re-Engineering Translational Research at the University of ChicagoUL1TR000430 · NCATS · UNIVERSITY OF CHICAGO · PI SOLWAY, JULIAN · 2012 to 2016
$20.2M
GENETICS TRAINING PROGRAM FOR PHD CANDIDATEST32GM007790 · NIGMS · STANFORD UNIVERSITY · PI BRUNET, ANNE, KINGSLEY, DAVID M · 1985 to 2020
$12.8M
REGULATION OF DIFFERENTIATION IN CAULOBACTERR01GM032506 · NIGMS · YESHIVA UNIVERSITY · PI SHAPIRO, LUCILLE · 1985 to 2014
$7.1M
DEVELOPMENT CONTROL OF DNA REPLICATION IN CAULOBACTERR01GM051426 · NIGMS · STANFORD UNIVERSITY · PI SHAPIRO, LUCILLE · 1994 to 2013
$3.8M
Probing the function of translational pausing in bacterial protein synthesisR00GM105913 · NIGMS · MASSACHUSETTS INSTITUTE OF TECHNOLOGY · PI LI, GENE-WEI · 2015 to 2017
$747k
Probing the function of translational pausing in bacterial protein synthesisK99GM105913 · NIGMS · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI LI, GENE-WEI · 2013 to 2014
$180k
A systems approach to understand translation and sRNA-mediated gene regulation inF32GM100732 · NIGMS · STANFORD UNIVERSITY · PI SCHRADER, JARED MICHAEL · 2012 to 2014
$150k
NCATS NIH HHS UL1 TR000430NHGRI NIH HHS T32 HG000044NIGMS NIH HHS 32 GM100732NIGMS NIH HHS F32 GM100732NIGMS NIH HHS F R01 GM32506NIGMS NIH HHS GM07790NIGMS NIH HHS GM105913NIGMS NIH HHS K99 GM105913NIGMS NIH HHS R00 GM105913NIGMS NIH HHS R01 GM032506NIGMS NIH HHS R01 GM051426NIGMS NIH HHS R01 GM51426NIGMS NIH HHS T32 GM007790
6 · The paper itself

Abstract

Caulobacter crescentus undergoes an asymmetric cell division controlled by a genetic circuit that cycles in space and time. We provide a universal strategy for defining the coding potential of bacterial genomes by applying ribosome profiling, RNA-seq, global 5'-RACE, and liquid chromatography coupled with tandem mass spectrometry (LC-MS) data to the 4-megabase C. crescentus genome. We mapped transcript units at single base-pair resolution using RNA-seq together with global 5'-RACE. Additionally, using ribosome profiling and LC-MS, we mapped translation start sites and coding regions with near complete coverage. We found most start codons lacked corresponding Shine-Dalgarno sites although ribosomes were observed to pause at internal Shine-Dalgarno sites within the coding DNA sequence (CDS). These data suggest a more prevalent use of the Shine-Dalgarno sequence for ribosome pausing rather than translation initiation in C. crescentus. Overall 19% of the transcribed and translated genomic elements were newly identified or significantly improved by this approach, providing a valuable genomic resource to elucidate the complete C. crescentus genetic circuitry that controls asymmetric cell division.

Indexed as

GenomeHigh-Throughput Nucleotide SequencingMolecular Sequence AnnotationCaulobacter crescentusCell DivisionOpen Reading FramesProtein BiosynthesisRibosomes

Identifiers

PMID25078267
PMCPMC4117421

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.