Evidence map›Paper›PMID 11029047›Full record

ArticleMolecular biology of the cell2000

Expression of multiple UNC-13 proteins in the Caenorhabditis elegans nervous system.

R E Kohn, J S Duerr, J R McManus, A Duke, T L Rakow, H Maruyama, G Moulder, I N Maruyama, R J Barstead, J B Rand

Abstract read
In one paragraph

Article in Molecular biology of the cell, 2000. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 51 papers.

0numbers the graph read from it
0cells of the map it votes in
51citing papers in PubMed
1.1field-weighted citation impact, top 25% of its field
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

51 citing papers in PubMed, 86 citations in OpenAlex.

  1. Article
  2. ImmatureProceedings of the National Academy of Sciences of the United States of America · 2026
    Article
  3. ImmaturebioRxiv : the preprint server for biology · 2025
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  9. Proceedings of the National Academy of Sciences of the United States of America · 2023
    Article
  10. Article
  11. Review
  12. Article
  13. Article
  14. A unique C2 domain at the C terminus of Munc13 promotes synaptic vesicle priming.Proceedings of the National Academy of Sciences of the United States of America · 2021
    Article
  15. Article
  16. Disentangling the Roles of RIM and Munc13 in Synaptic Vesicle Localization and Neurotransmission.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2020
    Article
  17. AlternativeFrontiers in immunology · 2020
    Article
  18. Article
  19. Review
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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 at 2 institutions in 1 country.

R E KohnProgram in Molecular and Cell Biology, Oklahoma Medical Research Foundation, Oklahoma City, Oklahoma 73104, USA.
J S Duerr
J R McManus
A Duke
T L Rakow
H Maruyama
G Moulder
I N Maruyama
R J Barstead
J B Rand
Oklahoma Medical Research Foundation · USScripps Research Institute · US

Funding

MOLECULAR AND GENETIC ANALYSIS OF PRESYNAPTIC PROTEINSR01GM059642 · NIGMS · OKLAHOMA MEDICAL RESEARCH FOUNDATION · PI RAND, JAMES B. · 1999 to 2006
$2.3M
NOVEL SIGNAL TRANSDUCTION PATHWAY IN THE NERVOUS SYSTEMR29NS031439 · NINDS · SCRIPPS RESEARCH INSTITUTE · PI MARUYAMA, ICHIRO · 1996 to 2000
$125k
MOLELULAR AND GENETIC ANALYSIS OF PRESYNAPTIC PROTEINSR01NS033187 · NINDS · OKLAHOMA MEDICAL RESEARCH FOUNDATION · PI RAND, JAMES B. · 1994 to 1997
–
NIGMS NIH HHS R01 GM059642NINDS NIH HHS NS31439NINDS NIH HHS NS33187
6 · The paper itself

Abstract

The Caenorhabditis elegans UNC-13 protein and its mammalian homologues are important for normal neurotransmitter release. We have identified a set of transcripts from the unc-13 locus in C. elegans resulting from alternative splicing and apparent alternative promoters. These transcripts encode proteins that are identical in their C-terminal regions but that vary in their N-terminal regions. The most abundant protein form is localized to most or all synapses. We have analyzed the sequence alterations, immunostaining patterns, and behavioral phenotypes of 31 independent unc-13 alleles. Many of these mutations are transcript-specific; their phenotypes suggest that the different UNC-13 forms have different cellular functions. We have also isolated a deletion allele that is predicted to disrupt all UNC-13 protein products; animals homozygous for this null allele are able to complete embryogenesis and hatch, but they die as paralyzed first-stage larvae. Transgenic expression of the entire gene rescues the behavior of mutants fully; transgenic overexpression of one of the transcripts can partially compensate for the genetic loss of another. This finding suggests some degree of functional overlap of the different protein products.

Indexed as

Caenorhabditis elegans ProteinsMutationTranscription, GeneticAnimalsAnimals, Genetically ModifiedCaenorhabditis elegansCarrier ProteinsExonsFemaleFertilityHelminth ProteinsNervous SystemPolymerase Chain ReactionProtein IsoformsRecombinant ProteinsRestriction MappingCaenorhabditis elegans ProteinsCarrier ProteinsHelminth Proteinsphorbol ester binding proteinProtein IsoformsRecombinant Proteins

Identifiers

PMID11029047
PMCPMC15005
OpenAlexW2116928584

What OpenQuestion holds

Textmetadata
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.